epidemiological and clinical investigations on bovine
TRANSCRIPT
Epidemiological and Clinical Investigations
On Bovine fasciolosis among Beef Cattle in Gezira State, Sudan
Arwa Babiker Abdalla Babiker
Bachelor of Veterinary Medicine, University of Sudan for Science
and Technology (2004)
A Thesis
Submitted to the University of Gezira in Fulfillment of the
Requirements for the Award of the Degree of Master of
Veterinary Medicine
In
Department of Medicine, Pharmacology and Toxicology
Faculty Veterinary Medicine
March, 2014
Epidemiological and Clinical Investigations
On Bovine fasciolosis among Beef Cattle in Gezira State,
Sudan(2013)
Arwa Babiker Abdalla Babiker
Supervision Committee:
Name Position Signature
Prof. Adam Dawoud Abakar Salim Main supervisor …………….
Dr. Abuagla Yousif Mohamed Adam Co. Supervisor ……………
Date : March 2014
I
Epidemiological and Epidemiological and Clinical Investigations
On Bovine fasciolosis among Beef Cattle in Gezira State,
Sudan(2013)
Arwa Babiker Abdalla Babiker
Examination Committee:
Name Position Signature
Prof. Adam Dawoud Abakar Salim Chair Person …………..
Dr . Ibrahim Elhag Elmahdi Elgizooli Internal Examiner …………..
Dr. Husna Mohammed El Bashir External Examiner …………..
Date of Examination 2/3/2014
Ii
Dedication
To
Memory of my late father,
My lovely mother,
Friendly sisters and brothers
I dedicate this work
Arwa Babekir
Iii
ACKNOWLEDGMENTS
First of all, my thanks are due to Almighty God , the Great who gave me the power and strength
to complete this work.
My gratitude and deepest thanks are extended to my supervisor Professor Adam Dawoud
Abakar, Department of Medical Parasitology, faculty of veterinary Medical Laboratory Sciences
.University of Gezira for his unfailing guidance, help and critical supervision and encouragement
throughout this work. My great thanks are due to my Co - supervisor Dr. Abu Agla Yousif
Mohammed, Department of Biochemistry, Faculty of Veterinary Medicine University of Al-
Butana. This research has been possible by a scholarship from University of Gezira; I would like
to thank the Vice-Chancellor and Dean Faculty of Veterinary Medicine. The nomination for this
scholarship came through Veterinary Medical Association of the Gezira State. My gratitude and
deepest thanks extended to Dr. Abdall Azim Tag-Alsir and Dr, Abobaker Ammar Sunni,
Veterinary Hospital, Barakat Administrative unit, for their assistance throughout this work. My
acknowledgments are extended to Director General, Ministry of Agriculture and Animal
Resources, Gezira State, and special gratitude to my colleagues at Barakat Veterinary hospital
for their support .Special thanks are due to Dr. Yasir M. Gesmaseed and Mr. Saeed M .Saeed for
their helpful assistance during this work. This work was generously typed by Ustaz Nagwa
Mohammed Osman from Faculty of Medical Laboratory Science, University of Gezira. Finally I
would to regret for those which are not mentioned here and help me in a way or another.
Iv
Epidemiological and Clinical Investigations
On Bovine fasciolosis among Beef Cattle in Gezira State,
Sudan
By
ArwaBabikerAbdallaBabiker
ABSTRACT
Fasciolagigantica is considered as one of the most important parasites affecting beef
cattle in the Gezira state. The disease is seriously affecting beef industry in the Sudan.
The disease is characterized by high morbidity rate and has an endemic course in the
Gezira State. Although several techniques were utilized, yet, the diagnosis of the
parasites is not well established.In the present study, retrospective, prospective,
knowledge attitude and practise (KAP) methods were conducted to diagnose and
determine the epidemiological picture of infection with Fasciola gigantica among beef
cattle in the Gezira State. Retrospective study was conducted on data of meat inspection
obtained from different meat inspection departments of the Gezira State, represented by
western, southern and central localities between the years 2010-2012. On average, 54819
cases were admitted annually to the abattoirs, the cases underwent routine anti mortem
and post mortem examination. Out of 164459, 12738 livers were found infected giving an
overall prevalence of infection of 7.74% .The infection rates within the examined beef
cattle were recorded to be 6.3,8.9and8.2 for the years 2010,2011and 2012, respectively .
Infections with Fasciolosis were significantly higher for beef cattle slaughtered in
abattoirs of west Gezira (10.9%). The prevalence of the parasite in south and central
Gezira State was 7.9% ,5.3% respectively. The Fasciola gigantica showed different rates
of infection with the season of the year.The highest infection rate was recorded during the
hotdry months (8.4%,8.1, 6.7%) within beef cattle in west, south and central Gezira State,
respectively. The diagnosis of infection using faecal examination revealed an infection
rate of 10.4% of the examined population. The prevalence among adult cattle was 12.9%.
Survey showed that cattle owners have a good endogenous knowledge about diagnosis
and risk factors of bovine fasciolosis. The study recommends a combination of
endogenous knowledge coupled with faecal examination and good clinical examination
for the diagnosis of bovine fasciola in the Gezira State .
v
السودان ،داء الكبد البقري وسط أبقار اللحوم بولاية الجزيرةعن وبائيه وسريريه دراسة
أروى بابكر عبد الله بابكر
ملخص الدراسة
تعد الدودة الكبدية العملاقة من أهم الطفيليات التي تصيب أبقار اللحوم بولاية الجزيرة. يعتبر المرض من
الأمراض الخطيرةالتي تصيب جميع فصائل الحيوانات المجترة ويشكل خطورة لصناعة اللحوم بالسودان.
زيرة. علي الرغم من أن هنالك يمتاز المرض بنسبه الإصابة العالية ويؤخذ المسار المتوطن في ولاية الج
تقنيات متعددة استخدمت إلا أن تشخيص الطفيل لم يؤسس له بصوره جيدة بعد. في الدراسة الحالية، تم
استخدام طرائق دراسات سابقه ، وحاليه وطرق تتعلق بالمعرفة والاتجاهات والممارسة لتشخيص وتحديد
لاقة وسط أبقار اللحوم بولاية الجزيرة. تم إجراء الدراسات الصورة الوبائية للإصابة بالدودة الكبدية العم
السابقة على البيانات الخاصة بتفتيش اللحوم التي تم الحصول عليها من أقسام تفتيش اللحوم في ولاية الجزيرة
في المتوسط تم إدخال 2012ـ 2010ممثله بمحليات غرب، جنوب ، ووسط ولاية الجزيرة بين الأعوام من
حاله سنويا للمسالخ بولاية الجزيرة. وهذه الحالات تم أجراء فحص دوري لها ما قبل وبعد الذبح 54819
، % 7.7كبدا مصابه وأعطت إصابة كليه تساوي 12738وجد أن 164459علي هذه الحالات من أصل
2012، 2010،2011، للأعوام %6.3، %8.9، %8.2سجلت نسبه الإصابة وسط أبقار اللحوم المفحوصة
أظهرت زيادة معنوية لأبقار اللحوم المذبوحة بسلخانات غرب الدوده الكبديه علي التوالي الإصابة بداء
%5.29، %7.97( سجلت بنسبه الإصابة بالطفيل في جنوب ووسط ولاية الجزيرة بـ %10.93الجزيرة )
العملاقة معدلات مختلفة خلال فصول السنة، سجلت اعلي علي التوالي أظهرت نسبه الإصابة بالدودة الكبدية
( وسط أبقار اللحوم في غرب %6.7،%8.1،%8.4نسبه إصابة في خلال فصول الفصل الجاف الحار )
وجنوب ووسط ولاية الجزيرة علي التوالي. التشخيص عن طريق فحص البراز اظهر معدل إصابة بلغ
. مسح الاستبيان اظهر %12.9الإصابة وسط الأبقار البالغة ( من القطيع المفحوص. وكانت نسبه10.4%)
أن ملاك الأبقار لهم معرفه فطريه جيده عن تشخيص وعوامل الخطر المرتبطة بمرض الدودة الكبدية البقرية
ومن اجل تشخيص طفيل الدودة الكبدية العملاقة بولاية الجزيرة أوصت الدراسة بضرورة تطبيق المزج بين
طرية مقرونة بفحص البراز والفحص السريري .المعرفة الف
vi
LIST OF CONTENTS
iii DEDICATION…………………………………………………….…
Iv ACKNOWLEDGMENTS…………….……………….……….…...
V ABSTRACT (ENGLISH)…..…………….…………………….…
Vi ABSTRACT (ARABIC)……..………………………….……...…
Vii LIST OF CONTENTS ……………………………………………...
Ix LIST OF TABLES……………………………….….……………....
Xi LIST OF MAP………………………………………………………
Xii LIST OF APPENDIX.........................................................................
CHAPTER ONE: INTRODUCTION
1 Introduction………………………………………………………….
3 Objectives of the Study ………………………………………….....
CHAPTER TWO: REVIEW OF LITERATURE
4 2.1. Morphology and classification of Fasciola gigantic………………
5 2.2. Life cycle of Fasciola species………………………………….
7 2.3. Epidemiology of bovine Fasciolosis……………………………
9 2.3.1. Prevalence and ecology of Lymnaea natalensis………………
10 2.4. Pathogensis of Fascilosis………………………………………...
10 2.4.1. Acute bovine Fasciolosis…………………………………
11 2.4.2. Sub acute bovine Fasciolosis……………………………
12 2.4.3. Chronic bovine Fasciolosis…………………………….
15 2.5. Diagnosis of bovine Fasciolosis……………………………
16 2.6. Control of bovine Fasciolosis…………………………………
17 2.6.1. Education…………………………………………………….
17 2.6.2. Control of Grazing………………………………………….
17 2.6.3. Pasture Management……………………………………….
18 2.6.4. Improved Water Supplies…………………………………
19 2.6.5. Snail Control………………………………………………... vii
20 2.6.6. Chemotherapy……………………………………………..
21 2.6.7. Environmental sanitation and manipulation……………
CHAPTER THREE: MATERIALS AND METHODS
23 3.1 study area ………………………………….
23 3.2 Animal of the study
24 3.3 Retrospective study
25 3.4 Prospective study
26 3.5 Parasitological diagnosis of Fasciola gigantic
26 3.5.1 Collection of faecal samples
26 3.5.1.1 Faecal samples examination
27 3.5.1.2 Floatation method
27 3.5.1.3 Sedimentation method
27 3.5.2 Egg identification
27 3.5.3 Total egg count
27 3.6 Liver inspection
27 3.6.1 Adult worm identification
27 3.7 Statistical analysis
CHAPTER FOUR: RESULTS
29 4.1 Retrospective study
35 4.2 Questionnaire data
41 4.3 Parasitological diagnosis of Fasciola gigantic
42 CHAPTER FIVE : DISCUSSION
CHAPTER SIX: CONCLUSION/AND RECOMMENDATIONS
45 6-1 conclusion
45 6-2 Recommendations
45 REFERENCES………………………..…………………………..
47
viii
LIST OF TABLES
Page Table.
NO
29
Prevalence of Fasciola gigantica infection among beef cattle
Slaughtered in abattoirs of Gezira state during the Period 2010 -2012.....
4.1
30
Prevalence of Fasciola gigantica infection recorded among beef cattle
slaughtered in west Gezira State abattoirs during the period 2010, 2011
and 2012...........................................................................................................
4.2
31 Prevalence of Fasciloa gigantica infection recorded among beef cattle
slaughtered in Southeren Gezira State abattoirs during the period 2010,
2011 and 2012................................................................................................
4.3
32
Prevalence of Fasciola gigantica infection among beef cattle slaughtered in
abattoirs of central Gezira state.................................................................
4.4
33
prevalence of infection with Fasciloa gigantica among beef cattle in
slaughter houses of Gezira State...................................................................
4.5
34
Prevalence of Fasciola gigantica infection among beef cattle slaughtered in
abattoirs of Gezira State according to Season during the survey period
2010, 2011 and 2012.........................................................................................
4.6
35
Frequency of herd data concerning herd men and herd structure in Gezira
State..................................................................................................................
4.7
37
Estimated prevalence of Fasciola gigantica among beef cattle by risk factor
pertains to Knowledge.........................................................................
4.8
39 Estimated prevalence of Fasciola gigantica among beef cattle by risk
factors pertain to attitude............................................................................
4.9
Ix
40
Estimated prevalence of Fasciola gigantica among beef cattle by risk
factors pertain to practice ...............................................................................
4.10
41 Prevalence of Fasciloa gigantica eggs according to animal sex...................... 4.11
41 prevalence of Fasciola. gigantica eggs according to animal breed................ 4.12
41 Prevalence of Fasciola. Gigantica eggs according to animal age...................... 4.13
x
LIST OF MAP
Map Page
Gezira State…………………………………………………………25
xi
LIST OF APPENDIX
Page Appe. No
55
Knowledge, Attitudes and Practices ( KAP) of cattle owners
towards bovine Fasciolosis in Gezira State …………………..
1
Xii
CHAPTER ONE
INTRODUCTION
Hepatic Fasciolosis is a parasitic disease that affects the bile ducts of ruminants, horses,
rabbits and other herbivores as well as-man. In addition, wild life such as rabbits, kangaroos,
elephants and deer were also affected. The adult worms are located in bile canaliculi of affected
hosts, but in other cases can be located under the skin or lung, among other locations. This
parasite “Fasciola species” is found in many places of the world, where conditions of moisture
and temperature exist for their development (Urquhart et. al., 2001). Fasciola hepatica is a
cosmopolitan in distribution. On other hand, Fasciola gigantica is common fluke of domestic
animals in Africa including Sudan (EL khawad et. al., 1978).
Infection rate of Fasciola gigantica in the Upper Nile province varied (Esia, 1966 a)
between 37-68%, in Equatoria province, 33% and in Bahar Elghazal province 56%. About 26%
of cattle livers were condemned (Esia, 1966) in meat inspection in Upper Nile province due to
Fasciolosis. Along the banks and tributaries of White Nile River Karib (1962), reported Fasciola
gigantica is enzootic along the white Nile. It was observed that the immature flukes were first
seen in cattle, in February which meant that cattle had gotten the infection in November and that
patent infection reach their peak in June and July. It was therefore, suggested that cattle must be
treated against fasciolosis between November and February with second dose in April /May
(Karib, 1962) Lymnaea snail are the intermediate host (Elkhawad et. al., 1976). The diagnosis of
fasciolosis may based on clinical signs, presence of the intermediate host, a history of grazing in
endemic areas and demonstration of typical ova in faeces using sedimentation (Marquardt and
Demaree 1986) and or floatation tests. The egg shell is yellow and the operculum is indistinct.
Also diagnosis can be aided by plasma concentration of gammaglutamy transferase which
increased with bile duct damage. At necropsy the nature of liver damage is diagnostic. Adult
flukes are readily seen in the bile duct and
immature stages, may be squeezed or teased from the cut surface. Serological tests are
used during the prepatent period and in chronic cases. (Tristram, et. al., 2006). Recently,
molecular diagnosis based on PCR techniques was also adopted (Rokni, et. al., 2010).
Fasciolosis is a disease that has been described extensively in the United States, England,
Ireland, the middle East, Afrcia and Australia. In most countries the animal’s liver parasitized by
Fasciola is condemned and unfit for human consumption. Recent appointments indicate that
fasciolosis is emerging as human parasitic disease (Hillyer et.al ;1997; Mas-Coma et . al; 2007).
The fluke has serious economic losses and impact on productive animals such as cattle, sheep,
goat and buffaloes. Bovine Fasciolosis in the Sudan is usually subacute or chronic. The acute
form being less common even in endemic areas. Sporadic cases of fasciolosis are sometimes
seen in other parts of the country following the implementation of water development schemes.
It is increasingly evident that parasitic diseases represent a major draw- back to cattle production
in the Sudan. However, proper evaluation of economic losses due to bovine fasciolosis is
lacking. The financial loss caused by the disease is commonly estimated from liver
condemnation rates alone.
Many infections are acquired in the dry season when cattle graze around infected
shrinking areas along the White Nile and drink from infected irrigation canals. The prophylaxis
or control measures of Fasciola infection ideally should involve control of intermediate host and
removal of fluke in affected animals, reduction of intermediate host snail populations and
prevention of access of live stock to infected snails. Use of Molluscacides can be effective to
reduce lymnaeid snail population. Also control of Molluscan habitat by improving drainage
fencing, drainage ditches and springs. Tremendous advances have been made in both the
efficacy and safety of drugs against adult and immature flukes. This study compared the
diagnostic efficiency of faecal examination, Knowledge, attitudes and practice (KAP), and
postmortem examination with ultimal goal to improve diagnosis of bovine fasciolosis in Gezira
state which may help to assess the economic significance of bovine fasciolosis due to liver
condemnation in the abattoir.
Objectives of the study:
To study the prevalence of bovine fasciolosis in Gezira State.
To determine the different factors that affect, the transmission of the fasciola spp.
To compare the diagnostic efficiency of KAP, faecal examination and post mortem
examination records.
CHAPTER TWO
REVIEW OF LITERATURE
2.1. Morphology and classification of Fasciola gigantica
Fasciola gigantica is a parasitic flat worm of the class Trematoda which causes tropical
fasciolosis. It is regarded as one of the most important single platy helminth infections of
ruminants in Asia and Africa. Estimates of infection rates are as high as 80-100% in some
countries. The infection is commonly called fasciolosis. The prevalence of Fasciola gigantica
often overlaps with that of Fasciola hepatica and the two species are so closely related in terms
of genetics behavior, morphological and anatomical structures.(ItagakiT et.al.2011) therefore
sophisticated molecular techniques are required to correctly identify and diagnose the infection
(Rokni et. al.,2010).
Fasciola gigantica is leaf- shaped and tapers at both ends. Adult Fasciola gigentica may
reach a size of 75 by 25 mm. it is leaf- shaped broader interiorly, with an anterior cone shaped
projection which is followed by a pair of broad shoulder. It is grayish brown in color changing
to grey when preserved. The ventral sucker is situated at the level of the shoulders and is about a
large as the oral one. The surface of Fasciola gigantica appears rough due to abundant
microscopic spines and surface folding. Spines increase in size in their middle section and are
smaller on the surface near the suckers, spikers range from 30 mm to 58 mm and have serrated
edges with any where from 16 to 20 sharp points. This species has both an oral and ventral
suckers for feeding and attaching to the inside of it is host. Fasciola gigantica has three different
types of surface papillae which are used as sensory receptors Dang Prasert, et. al.,2001, Kumar,
1998). A pharynx and a short esophagus are present and the intestinal caeca are commonly
much branched, especially laterally. The excretory bladder is also much branched. The genital
pore is medial and directed anterior to the ventral sucker. In about the second and third quarters
of the body, there is well developed cirrus and the cirrus, sac. The prostate and seminal vesicle.
The ovary is situated to the right of the middle, anterior to testes, and is branched, the vitelline
glands consist of filling the lateral fields and the ducts of follicles unite to form two transverse
ducts which pass in wards to open into a median yolk
reservoir, from which a duct passes to ootype. The uterus lies anterior to testes Testes are
tandem, or branched. The vitelleria strongly developed and filling the lateral fields and extending
medially as well The egg of Fasciola gignatica can reach sizes of 0.2 mm length (Dang prasert,
et. al.,2001 Kumar, 1998).
Also the eggs of "Fasciola species" have barrel shape, with thin shells and are
operculated. (Soulsby, 1986). Fasciola gigntica is the common liver fluke of domestic stock in
Africa, it occurs frequently in Asia the Philippines, southern USA, southern Europe, European
Russia and the Middle East. Mixed infection of Fasciola hepatica and Fasciola gignetica might
be occurring for example, in Pakistan. Kendall (1954) found mixed infection on the boundaries
of high land areas. Fasciola gigntica resembles Fasciola hepatic but is readily recognized by up
to 12mm in breadth. The anterior cone is smaller than that of Fasciola heptica, the shoulders are
not as prominent and the body is more transparent. The eggs measure 156 – 197 – 90-104 mm
(Soulsby, 1986).
The detailed classification of fasciola has been given by Yamaguti (1958) and schell (1970) as
follows:
Kingdom Animalia
Phylum Platy helminthes
Class Trematoda (Rudollph,1808)
Subclass Digenea (Van Benden, 1858)
Suborder Prosos toneatce (odhner, 1905)
Family Fasciolidae (Railier1895)
Genus Fasciola (Linnaeus, 1858)
Species Fasciola gigantica
Fasciola hepatica
2.2. Life cycle of Fasciola gigantica
Sexually mature adult reside and presumably mate in biliary ducts of their mammalian host
(Cheesbrough,2005) Fasciola gigantica reproduce sexually as adults and asexually in other
stages of it is life cycle. The flukes are in the metacercariae stage before becoming sexual adults.
After residing in their mammal host's duodenum, the metacercariae penetrate the liver and
become mature in the biliary tract. The adult flukes have both sexes organs but fertilization
between adult female and male flukes is the most
common source of sexual reproduction adult flukes produce eggs that are then passed in the
host's faeces (Cheesbrough, 2005; Read, 1973).
Non embryonic eggs are laid within the mammalian host and are passed through to the intestinal
tract where they are expelled in the faeces (Cheesbrough,2005).
Egg reach the out side by passing down the common bile duct and being voided with faeces.
They are undeveloped when passed and require a minimum of -10days to reach the mircidial
stage. The eggs are ready to hatch immediately on reaching the out side and do so mostly under
the influence of lowered osmotic pressure; the temperature at which development occurs are 10
to 26Co ; below 10Co, there is only marginal development of eggs and larval stages and no
emergence of cercariae. Hatching is controlled by a number of factors such as light, temperature
and salinity (Soulsby,1986 and Marquardt and Demaree- 1986).
The life span for each stage of Fasciola gigantica varies greatly after being ingested, it takes
3-4 months for adult flukes to become mature and begin producing eggs. Adult flukes can live
for multiple years in their definitive host, embryos of “Fasciola species” are able to persist
outside the host for several months. After produced embryos are then shed through digestive
system with its host faeces. When water and temperature condition are favorable, the embryos
develop in to ciliated larva called, Miracidium which is able to swim and it will die soon after
hatching if it doesn’t contact a secondary host. Miracidum are able to swim and locate it’s
secondary snail host with help of it’s cilia. If miracidium to come in contact with a snail it
actively penetrates it. The cilia are then shed and it is transformed into sporocyst (Read,1973), an
undifferentiated mass of cells. The penetration is associated by the boring action of the miracidia
and probably by enzymes secretions from the apical gland. within the sporocyst the germinal
cells multiply and produce daughter sporocyst or redia. The redia has an oral sucker, apharynx,
asac-like intestine, an excretory system and birth pore, through which cercariae produced inside
it escape. (Soulsby, 1986; Marquardt and Demaree, 1986).
According to (Read, 1973), the rediae move to the snail’s digestive gland known as the hepato
pancreas, over time this is where the redia will form cercariae. One sporocyst and two redial
generations give rise to gymnocephalous cercariae about 6 weeks later (Soulsby , 1986 ;
Marquardt and Demaree, 1986). The cercariae develop tails and leave
snail in search for vegetation to encyst. Once the cysts are formed become metacercariae and
these infect a mammal host if they are accidentally ingested with the vegetation (Read, 1973). If
conditions are favorable metacercariae are able to persist for up to one year (Miliotis and Bier,
2003; Read, 1973). Metacercariae which are eaten with herbage, excyst in the small intestine and
migrate through the gut wall to the abdominal cavity. They reach the liver at about day 5 and
penetrate its capsule. Juvenile flukes migrate in the liver parenchyma, reaching bile ducts and
producing eggs 8 to 12 weeks post- infection (Soulsby-1986; Marquardt and Demaree1986).
Adult fluke live longer than 10 years in sheep (Durbin, 1952), but generally less than a year in
cattle (Delcon, et. al.,1980). When the adult Fasciola are in bile ducts of a host it obtain a small
portion of it’s nutrients from active blood suckling. In day's time, a single adult fluke can take
about 0.2 ml of blood. There is evidence that adult flukes need around 100 times the amount of
glucose the Fasciola receives from active ingestion. There fore adult flukes also receive nutrients
by absorption of glucose through their tegument. The free swimming miracidia were once
thought to be a non- feeding stage, but it has been shown that they metabolize glucose when it is
present (Read, 1973). A variety of general aquatic predators are known to feed on the free-
living stages of Fasciola gignatica including the miracidia and the cercariae stages (Johnson and
the Thieltges, 2009).
. The eggs measure 130-150 by 63-90 um; and the miracidium develops only after the eggs
have been laid (Soulsby; 1986 and Marquardt and Demaree, 1986).
2.3. Epidemiology of bovine Fasciolosis
Fasciolosis due to infection by Fasciola hepatica or Fasciola gigantica is currently
believed to affect as many 17 Million people worldwide, (Hopkins,1992) with91.1million
individuals at risk for infection (KeiserJ and UtzingerJ, 2005). Fasciola gigantica infection is
more geographically constricted, occurring in the tropical regions of Africa, the Middle East, and
Asia, where infection due to either species may occur (KeiserJ and Utzinger J 2009). Contrary to
early thinking prevalence of veterinary disease is not predictive of prevalence of human disease.
(Mas-Comas et. al 2005). Prior to 1980; fasciolsis was thought to be a zoonosis of only mild,
sporadic, or local importance. In the past 20years however, more complete understanding of
disease epidemiology has emerged (Mas-Coma et, al. 1999) have proposed an epidemiologically
useful clarification, based on more recent studies, to better understand fasciolosis. Epidemic
outbreaks can be characterized as occurring in areas where fasciolosis is endemic in animals but
not humans and in areas where the disease is endemic in both animals and human.
Areas of the world with the highest prevalence of fasciolosis include the highland of Bolivia,
the Bolivian Altiphano has- the highest prevalence in the world (Mas-Coma et. al.1999).
Equador, Peru, Cuba, Portugal ,Spain, Turkey, the Nile Delta of Egypt and other countries in
Africa, the northern regions of the Islamic Republic of Iran and elsewhere in Asia; and central
Vietnam (World Health organization 2010).
Humans most often become accidental hosts of fasciola when they ingest aquatic vegetation
on which the metacercariae have encysted. Implicated plants include (most commonly)
watercress, (Tolan , 2001). water Moring glory (Pak boong), (Price TA , TuazonCU,
Siomon,1993). Other aquatic plant, salads in endemic areas such as the high land of south
America, (Marcosl, et. al. 2006) and alfalfa juice which are used as medicinal tonic in Peru .
Another source of infection is drinking water contaminated with free-living (non encysted)
metacercariae and the least common mode of transmission is the consumption of raw
undercooked liver infected with immature or adult worms.
In Sudan Fasciola gigantica is the only fluke reported as causing fasciolosis in cattle
(Karib,1962). Fascioloa gigantica was reported to present in large number and to be causing
severe liver damage in infected cattle in the Upper Nile province (Eisa, 1966 a). Karib (1962)
reported that Fasciola gigantica is enzootic along the white Nile. The area most affected is lying
between Dueim and Malakal towns and about 300 miles long. The author had toured the area
during 1956/57 examining over 600 cattle and he found 32 percent of them were infected with
Fasciloa gigantica and that 50 percent of the affected livers were totally condemned. Kraib
(1962) also studied the prevalence of Fascilosis in cattle slaughtered in the central municipal
abttoir in Omdurman City. He derived the prevalence of Fascilosis in cattle throughout the
country from the data obtained from abattoirs at provincial head quarters. These studies revealed
a high prevalence of 26 percent for cattle in the Upper Nile Region. To provide further
information on the helminthes of cattle in western regions of the Sudan, a survey carried out by
(Elkhawd,
et. al., 1978), two hundred and seventy carcasses were examined from El-Fashir and Nyala
central Abattoirs at Darfur Region. Investigations revealed 10 % were infected with Fasciola
gigantica. Magzoub and Adam (1977) transported 251 male zebu cattle, two to five years of age
to Omdurman central Abattoir in Khartoum province. These animals were reared under different
nomadic conditions and were from different parts of the country. The animals were slaughtered
and the livers were dissected for worm collection. Of these cattle 66.1 percent were infected with
Fasciola gigantica, a higher prevalence than that reported by Karib, (1962) 15 years earlier from
the prevalence rates it can be seen that bovine Fascilosis is a serious problem in cattle of white
Nile province, Equatoria and Bahr-Elghzal Regions.
2.3.1. Prevalence and ecology of Lymnaea natalensis
Lymnaea natalensis is the only snail intermediate host of Fasciola gigantica in the Sudan
(Elkhawad, et . al,1976). This snail has been found along the while and the Bule Nile and their
subsidiaries Lymnaea natalensis was found to build up in October and November in the white
Nile and the infected snails with Fascila gigantica were observed from December til April with a
peak, infection rate during February (Elazazy and Schillhorn,1983). Amin (1972) reported the
presence of the snail in the northern part of the Gezira irrigation area where considerable
breeding occurred during February –March; Elkhawad et, al. (1976) examined 22pools at water
in pastures along the banks of the white Nile at Malakal and found that six out of 22 pools of
water contained snails Lymnaea natalensis and infected snails were encountered in three out of
six infected pools of water. The intensity of water infestation with Lymnaea natalensis was 15
snails per cubic metre. Malek, (1969) looked at Gebel Aulia dam in the Sudan. The dam is
situated on the White Nile 25 miles south of Khartoum. It impounds water for about 300 miles to
the south and forms shallow flowing (reservoir) flood water in July and the reservoir is full until
March. The extent flooding the banks varies from one place to another and after the water has
reached them at the end of march several ponds in the flood plains retain water almost until the
next flooding season. The flood plain, which is shallow at the edge, is very rich in aquatic
vegetation and snail fauna. Considerable human activity takes place in the area and herds cattle
are brought to be watered (Lymnaea natalensis was identified in the flood plain.
In Sudan Abdelrazig (1983) reported that the infection rate of Lymnaea snails follow a
seasonal pattern, with a peak in summer months. Mohammed Ali (1983) showed that the
environmental condition in hot summer were suitable for higher rate of transmission of
fasciolosis in White Nile area. Recently, Atta, Elmanan, et, al. (2001) reported some aspects of
the epidemiology of fasciolosis in northern part of Gezira. Their result revealed that the average
population of Lymnaea snails was different in the four sites of the study. The number of the
snails increased during summer and rainy season and decreased during winter. The author also
reported that the snail infection rate with Fasciola gigantica varied between 17% and 29%.
2.4. Pathogensis of Fascoilosis
The development of infection in definitive host is divided into two phases; the
parenchymal (migratory) phase and the biliary phase (DubinskyA,1993). The parenchymal phase
begins when excysted juvenile flukes penetrate the intestinal wall. After the penetration of the
intestine flukes migrate within the abdominal cavity and penetrate the liver or other organs.
During the migration of flukes, tissues are mechanically destroyed and inflammation appears
around migratory tracts of flukes. The fluke principally migrate in the ventral lobe of the liver
where they produce extensive necrosis of necrotic and haemorrhages which later organize to
form post necrotic scars (Sewell, 1966; Rushton and Murray, 1977)
The second phase (the biliary phase) begins when the parasite enters the biliary duct of the
liver, in biliary duct the flukes mature feed on blood, and produce eggs. Hypertrophy of biliary
ducts associated with obstruction of the lumen occurs as a result of tissue damage. Also the
presence of the adult fluke in the main bile ducts further induces considerable hyperplasia of the
bile duct epithelium and periductal fibrosis (Dawes, 1963).
Fasciola gigantic infection of cattle showed three types of infection.
2.4.1. Acute bovine Fasciolosis
Acute fasciolosis is less common in cattle than the sub acute or chronic form of the disease
(Karib1962) and it is essentially a traumatic hepatitis caused by the simultaneous migration of
large numbers of immature flukes into the liver. The animal dies suddenly and blood stained
froth in the nostrils. Blood is also discharged through the anus as in the
case of anthrax. Acute and fatal fasciolosis is observed from time to time in young cattle
even in enzootic areas and in rare cases in adult cattle in the Sudan. However, such infections
were found when cattle being away for several months were brought to infected localities. (Karib
1962). Heavy infections were reported in the White Nile area when river grazing was used from
April to July (Eisa1966a).
The greater damage is really done from the passage of these flukes through the liver causing
haemorrhages and the affected animal usually dies suddenly from liver destruction (Soliman and
Zaki,1964). Animals may die within few days of the onset of the clinical signs and in this case
the liver is enlarged, pale and friable. It shows numerous haemorrhagic track and clots on the
surface and through out the peritoneal cavity. (Soulsby,1986,Goraish,1987)
2.4.2. Sub acute bovine Fasciolosis
The liver is covered with the flukes migratory tracks. With infiltration of leukocytes and
hepatic, fibrosis (Solusby 1986). Subacute fasciolsis may occur during a chronic form of the
disease with marked cellular response possibly indicating a form of an immune response. Acute
and subacute fasciolosis may occur in animals of all ages and states of nutrition. Death ensues
rapidly or after several days. Affected animals when observed alive are reluctant to move are
anorexic and show distended abdomen which is painful to the touch. One of the complication of
the acute and sub acute fasciolsis is "black disease" caused by the bacteria clostridumo
edamatiens. The organism is a saprophyte and the infection occurs only after liver damage. The
disease is common in Australia and vaccine is available.
Oganrinade (1983) found that infection with 5000 cysts of Fasciola gigantic took 150 days to
cause death in adult Fulani cattle in Nigeria, while Sewell (1966) indicated that even 2000.
Metacercariae of Fasciola giganatica giving rise to 7000 young flukes in the liver took 11 weeks
to cause a two – year old steer to die at sub acute fasciolosis. There was rapid loss of weight and
rapid progressive anaemia but this did not commence until eight weeks after infection. Jaundice
was very marked in the later stage and there was an increase in both the total and direct serum
bilirubin concentrations. Hammond and Sewell (1986) in their experimental infection with
Fasciola gigantica in cattle in the Kenyatsh land found that infection within the range at 500-
2000 metacercariae in young
cattle consistently resulted in retarded growth from about 10 weeks after infection but only
animals given 2000 metacercariae showed clinical signs of lost weight even during this period
from 10 weeks after infection they found that the mean pre-patent period for all the single
infections was 90±5 days with some tendency for the pre-patent period to be shorter in heavier
infections. Although it is generally believed that flukes ingest blood, recent evidence suggests
that young flukes on their way through liver parenchyma feeding mainly on hepatic cells
(Sinclair,1962. Dawes, 1963)
2.4.3. Chronic bovine Fasciolosis
It is the most common form of the disease affecting cattle and other animals including
human. The infection causes mainly hepatic fibrosis. The disease in cattle is characterized by
digestive disturbance with alternating diarrhea and constipation in the terminal stage. Emaciation
ensues rapidly and weakness soon leads to prostration, especially in calves.
Chronic fasciolosis is the type usually encountered and it is a persistent wasting disease which
can be recognized in live, dead or slaughtered animals (Soliman and Zaki,1964) . although
diagnosis of fasciolsis may be difficult in the presence of other diseases such as trypansomosis or
haemonchosis cattle owners and field veterinarians in the Sudan regard the gradual development
of oedematous swelling at the dewlap as almost a pathognomonic sign of liver fluke infection
(Karib,1962).
In chronic fasciolosis . animals become unthrifty, emaciated and weak, the mucosa becomes
pale and there is oedema particularly between the angles of the jaw and the abdomen. Animals
on a high plain of nutrition are more resistant to the disease and conversely the disease is
exacerbated by inadequate nutrition particularly during a savannah dry season (British veterinary
Association,1970).
Graber (1952) found, from his studies on the affect of young zebu cattle artificially infected
with Fasciola gigantica, that a ration based on straw complemented by cotton seed was
sufficient to maintain the host parasite balance in the case at a moderate infestation with 500
metacercariae. When the infection was only 100 -200metacercariae, he found the daily gain in
weight to be normal but a deficient ration at straw is followed either by a speedy loss of weight
or heavy morbidity when the infection is severe (1000-6000 metacercariae) .
Chronic fasciolosis a ppears to be the form of the disease which is the most economically
important. Subclinical infections are not readily recognized by cattle owners and may greatly
reduce the productivity at adult cattle and retard normal growth in young animals. The lesions of
chronic fasciolosis are mostly confined to the liver in severe cases, the substances of the liver is
more or less completely replaced by fibrous tissue, such livers, are totally condemned as the
extensive fibrosis associated with the lesions reduces their value and for aesthetic reasons. There
is no pubic health risk involved (Sewell 1976).
Haruon and Hussein (1975) investigated the pathological aspects of naturally occurring
bovine fasciolosis in the Sudan. They found that car cases of the infected cattle were generally
emaciated an showing subcutaneous oedema. In most cases specific lesions were confined to the
liver although occasionally other organ such as the lung and pancreas were affected. In the liver
from 7 -745 flukes with an average of 100 flukes were found but there was no correlation
between the worm burden and the severity of the hepatic tensions. This confirmed observations
by Coyle (1958) in Uganda and it is difficult to escape the conclusion that many flukes die in the
liver naturally or partly as a result at becoming locked in heavily calcified ducts. The livers were
enlarged and fibrosed and had a leathery consistency. Sometimes there were adhesions with the
neighboring organs. Areas of degeneration, hemorrhages and telengiactsis were found. The bile
ducts were thickened, fibrozed and calcified of even ossified and their Lumina were distended
with exudates containing flukes or remnants of flukes and occasionally biliary calculi Umo and
IKewe (1978) investigated the hepatic changes in natural Fasciola gigantica infestation in Fulani
zebu cattle. The gross lesions which they described are similar to those of Haroun and Hussein
(1975). They included a hard liver structures with thickened prominent bile ducts, some at which
on incision contained varying number of adult Fasciola gigantica. Of the livers they examined
22 percent and 87 percent were respectively totally or partially condemned. Laboratory
investigation on naturally infected zebu cattle with Fasciola gigantica in the Sudan was carried
out by Magzoub and Adam (1977). Nomadic male cattle were slaughtered and then investigated
post mortem. The hepatic damage caused by Fasciola gigantica in moderate cases showed
thickening of the liver capsule and grayish, white tracts in the liver substance.
Microscopically, there was thickening of the walls of the bile ducts which contained flukes,
infiltration by eosinophils and lymphatic cells and proliferation at the bile ducts with foci or
superficial necrosis. In severe cases the surface of the liver was distorted, irregular and fibrotic.
In large animals including cattle anaemia and hypoalbuminaemia are being the most common
and glaring manifestations, constant of fasciolosis (Kumar et al.1982; Ganga et, al. 2007; Edith
et, al.2010b). The developing Fasciola gigantica juveniles and the adults have considered non-
haematophagous and tissue feeding parasites yet cause severe anaemia in the host suffering from
acute and/or chronic disease (Ganga et al .2004b). Thus, pathogenesis of anaemia in Fasciolsis
has therefore been debatable. Various factors, such as haematophagic, haemorrhages during
migratory phase and injurious nature of the fluke. Metabolites discharged into the host
circulation significantly contribute to the development of anaemia (Ganga et al.2004). With
mean fluke load of 300 and above had a significant fall in erythrocytic anaemia (Yadav et al.
1999; Ganga et al 2007). Where as in the chronic phase, hypoalbuminaemia is more marked
than anaemia and an immune carrier host on partial recovery from the acute course of disease
(Edith et al.2010b) continues to suffer from normocytic hypochromic anaemia (Edith,et.al
2010b). It was strongly speculated that the fluke metabolites discharged into the circulation
coupled with generalized oxygen starvation at tissue level, incidental to the severe and prolonged
anaemia could influence normal functioning of the hypothalamus. Pituitary axis and
consequently, the altered physiological plasma levels of the tropic hormones leading to
dysfunction of the target endocrine glands, especially thyroid and adrenal glands that influence
and shift the entire metabolism in the host (Ganga et. al 2007; Edith et. al 2010a). The
histopathological evidence of hypothyroidism in the diseased host were, the appearance of
peripheral vacuoles and atrophy of the thyroid follicles and lymphocytic thyroiditis with diffuse
mononuclear cell infiltration in inter and intra cellular spaces, causing progressive destruction of
thyroid hormones secretary cells and follicles. (Ganga et.al.,2007). Altered serum enzyme levels
and the elevated serum enzyme concentration in fasciolsis were exploited for early and semi
quantitative diagnosis of the disease before the animal is coproscopically positive for the fluke
eggs (Kumar et al.1982; Swarup and Pachauri 1987; Edith et al .2010a).
The recent experimental finding on the liver specific enzyme concentrations periodically
refluxed by the damaged hepatic tissues in the circulation of Fasciola gigantica infected animals
during the course of the disease revealed that the elevated levels of serum Aspartate
transaminase (AST) and Alanine transaminase (ALT) were suggestive of the hepatic tissue
injury, where as the elevated level of alkaline phosphatas (AP) indicated establishment of adult
flukes in the bile ducts (Edith et, al. 2010b). The increasing patterns of the serum enzyme
concentration revealed two clearly demarcated stages. The first stage of massive invasion and
traumatic hepatitis caused by the fluke juveniles during prepatency was coinciding with the onset
and significant increase in the AST and ALT in the host circulation. The second phase (Patency)
in the infected animals increase of the serum AP concentration. In contrast to AST and ALT, the
elevated levels of AP are scribed to decrease biliary excretion of the enzyme or obstruction of
bile flow stimulate denovosynthesis of the hepatic AP and synthesized enzyme is refluxed into
the host circulation. Over 28% increase in AP concentration indicates obstructive hepato-bitiary
lesions and less than 8% increased AP concentration was suggestive of chronic form of the
disease or post –patency immune carrier status of the host (Edith et, al. 2010b). Histologically,
there were fibrosis and proliferation. Bile ducts and old fluke tracks were in many places luded
by connective tissue infiltrated with eosinophils and fibroblast.
2.5. Diagnosis of bovine Fasciolosis
Diagnosis of Fasciolosis may consist of tentative and confirmatory procedures. Atentative
diagnosis of fascilosis may be established based on prior knowledge of the epidemiology of
clinical signs, information of grazing history and seasonal occurrence. Confirmatory diagnosis
however , is based on demonstration of fasciloa eggs. Through standard examination of feaces in
the laboratory, postmortem examination of infected animals and demonstration of immature and
mature of flukes in the liver. The latter is helpful in deciding the intensity of infection. The
diagnosis of fasciolosis is of prime important for planning treatment and the eradication program
from the endemic area. Faecal examination is of little consequence in the host suffering from the
acute course of the disease because the onset of adverse effects appear much before appearing of
fluke eggs in faeces (Gupta and Yadav 1994; Dixit et, al.2008). Quantitative examination of
faeces and assessing hepatic fluke load at necropsy are also not sensitive enough to precisely
predict severity of the disease (Garg et. al. 2009). However it is possible to predict and suspect
fasciolosis during early pre-patency (Day 40 post infection ) by periodical monitoring the
elevated levels of marker enzymes (AST and ALT) in the host circulation (Edith et,al.2010 b).
Serological demonstration of anti Fasciola specific antibody, Fasciola gigantica antigens and
immune complexes in host circulation during prepotency appears to be useful alternate option to
coproscopic detection of fluke eggs (Yadav et, al.1999; Dixit et. al 2008). Amongst various
immune diagnostic techniques used , ELISA is the most sensitive and acceptable technique but at
time suffers from false positive reporting cross reactivity with other in situmetazoan infection
and that is a major limitation and it prompted a search for specific immune- dominant moieties in
complex somatic and excretory antigens. The role of metabolites released during the
development of olds cercariae in conferring acquired immunity in the host, immune evasion
and diagnosis of the disease was thoroughly investigated (Dixit et,al.2008). Ultimately,
Glutathionestranferase (GST) and Cathepsin Lcysteine proteinase (CS) molecules were
identified as specific for the purpose. Cathepsin Lcysteins proteinase was further purified,
characterized and designated as Fgcl-3 antigens .
The Fgcl-3 ELISA showed 100% and 97% sensitivity under experimental and field situations,
respectively in the diagnosis of the disease. The infection could be detected as early as two wpi
(Dixit et. al. 2004; Raina et. al.2006). The Fgcl-3 was also evaluated for its potential in the
detection of early prepatent infection in experimentally infected bovine calves infected with
Fasciola gigantica as early as 4thwpi, while using sensitive antibody detection assays with 100%
sensitivity (Sriveny et. al.2006).
2.6. Control of bovine Fasciolosis
Several control methods against ruminant fasciolosis are available and either be used
independently and as combination of two or more of them. These methods involve thefollowing
:-
2.6.1. Education
Behavioural changes have the potential to be the most effective and cost efficient
approaches to disease control and thus, education is an essential aspect of any public health
effort. The primary message of Fasciola gigantica campaigns is to keep domestic animal herds
separate from the growing sites of aquatic. This limits the risk of contaminating the vegetation
and thus decrease the transmission for both human and animal infection.
2.6.5. Control of Grazing
Before a rational grazing control scheme can be instituted it is first necessary to carefully
identify and survey all suitable habitats for the snail intermediate host, Lymnea natalensis. This
is best done in the dry season and control measures may then be directed towards preventing
access of cattle to the habitats where metacarcariae have been found. However, excluding cattle
from infested areas cannot be relied upon to eliminate the infection because wild species act as
reservoirs of infection (Hammond and Sewell, 1986).
Nevertheless, where animals have to graze infected areas due to the lack of grazing in dry
areas, this should be delayed for as long as possible until the pastures are well dried out and so
became relatively safe for grazing stock, through the destruction of any metacarcariae by
desiccation Hammand and Sewell,1986). This will be effective, but will involve loss of pasture
and the lack of alternative grazing during the recurring drought makes this approach rather
impractical. The most effective procedure for controlling the disease is zero- grazing where
animals are closely penned, while their food is produced else where and brought to them. If this
is not possible for economic and logistic reasons with all the cattle a more restricted system
could be practiced. For example, zero- grazing may be utilized only with young animals or in the
period of the seasonal prevalence of the parasites, when the grazed pasture is heavily
contaminated (Sewell, 1976).
2.6.6. Pasture Management
The possibility of this form of control is limited under the communed grazing systems
which prevail in almost all parts of the Sudan. After the harvest in the irrigated areas, the
population of cattle including nomadic herds from long distances away becomes great, attracted
by grazing on the stubble fields (Khuele, 1983). The use of
irrigation for growing cattle feed, e.g. alfalfa, were the crop is grown and then allowed to
dry for some weeks and it is used as standing hay is relatively safe (Sewell,1976). No
satisfactory grazing control strategies have evolved within traditional systems. Some isolate
enclosures have been established and could provide useful dry season grazing but there was no
incentive to develop this further since they were frequently trespassed upon and benefits accrued
mainly to other users of the communal resources.
2.6.7. Improved Water Supplies
The sue of water troughs sited on the dry ground filled with water form wells is the
traditional among some pastoral tribes. So far, no deliberate attempts to control the snail
intermediate host have been made in connection with animal Fasciolosis, but certain steps have
been taken to prevent the infestation of newly dug water reservoirs (haffirs) for watering animals
and or people. This is achieved by adopting a design where by the reservoir has perpendicular
edges and square corners so that the formation at shallow edges is avoided and the infestation of
snails made impossible (Karib, 1962). The water supply for cattle from these reservoirs should
be fed into deep troughs, with the outlet pipe fitted with affine screen to prevent infected snails
form passing through. In any case, the land immediately around the reservoir should, if possible,
be enclosed with a stock proof fence. A study at control measures applied in Tanzania is given
by Hammond (1965). In Uganda, Coyle (1958) described boreholes as the completes answer to
the liver fluke problem provided that all the natural watering places which harbour snails are
fenced off. In the Sudan and elsewhere, in dry pastoral areas, the use of bore holes with
hydraulic rams to pump the water to a high level from where it can be fed to water troughs sited
on dry ground, is relatively safe.
In the dry season the River Nile and its associated water courses, the irrigation canals
associated with crop production schemes and pools found in the flood plains after the water has
recede, are the main sources of water for livestock in the eastern, central and southern parts of
the Sudan. At present the only thing that might be done is to try to persuade livestock owners to
water their animals only at selected areas which are naturally unsuitable as hip tats for the snail
intermediate host. In this respect it might be helpful if livestock owners were taught to recognize
the various snail infested areas particularly near villages and know infected areas were clearly
sign posted.
2.6.5. Snail Control
Control of parasitic diseases is crucial to improve the productivity of the animals. In most
fasciolosis endemic areas, the control of the intermediate snail host population offers a good
opportunity for the reduction of transmission and is generally effective when combined with one
environmental sanitation.
Although eradication of the snail host is the most effective method of total fluke controls this,
however is often very difficult in low wet areas with a mild climate. Snails multiply extremely
rapidly and hence eradication is almost impossible in irrigation areas There are different types of
snail poison available that are safe for stock but need care and precision in their application.
Other useful methods of fluke control include biological control of intermediate host based on
the introduction of natural enemies i.e. predator, competitors or parasites. Predators are active
organisms which seek their food and consume a number of preys during their life time. Predators
of fresh water snails include species of virtually every major group of the animal kingdom i.e.
Mammalian to planarian (Madsen, 1992). Protoptreus annectans has controlling effects on snail
population (Daffalla et. al., 1985). The use of Molluscicides for control of snail intermediate
host, is a potential tool for the control of the infections. Before considering chemical control of
snails, it should be noted that many habitats are topographically unsuitable for the use of
molluscides and it is often very difficult to apply them effectively. They are toxic to the
environment, cooperation between neighboring properties is required for effective cover and
regular (at least yearly) application is required because rapid repopulation of snail may occur.
Where as, they are not species- specific, may destroy edible snails highly, valued as food in some
communities, and expensive (Hansen and Perry,1994). A great number of chemicals have been
used as molluscicides in the past, but at present Niclosamide (Baylascide or Mollotor) and
copper sulphate are used in different parts of African countries (Brown, 1980).
Brown (1980) indicated that molluscicidal properties have been demonstrated in extracts from
a variety of plants. Asubstance ' Endod' or Lemma toxins derived from the fruits of shrubs
phytolacca dodecandra Substance such as 'Endod' might provide means of snail control less
costly to developing countries than synthesized molluscides but the production of natural
molluscides on a commercial scale has yet to a achieved. Tadesse
and Getachew, (2002) from their finding they also indicated that 'Endod' was used for the
control of Fasciola transmitting snails particularly lymnaea natalensis and lymnaea truncatula .
2.6.6. Chemotherapy
Effective control of most trematode infections is based on strategically applied
chemotherapy (Hansen and Perry, 1994). Combination of chemotherapy, intermediate host
control, sanitation and environmental manipulation are believed to be more efficient but very
expensive. Aflukicidal drug of choice must full. fill the following:
It must act against both immature and mature flukes
It must not be toxic to the recipient animal
It must be cheap and available
Chemotherapy with drugs remains the most effective way of treating parasitic diseases, and is
usually at the heart of any major control campaign. Compared to, drug treatment is very cheap
(Gaasenbeek, et. al., 2001). The drugs used against flukes should ideally destroy the migrating
immature flukes as well as adults in the bile duct. Chemotherapy has been used for years in
animal populations to decrease the animal reservoir and reduce agricultural losses. Until
recently, however, bithionol was the only treatment available for Fascioliasis and its cost, high
doses, and the extended length of treatment effectively prohibited its use for large-scale
campaigns. The antihelmintic triclabendazole is not yet approved in most countries, but shows
great promise for its utility single - dose chemotherapy efforts to control morbidity and
transmission in endemic areas. A number of drugs have been used to control fasciolosis in
animals. Drugs differ in their efficacy, mode of action price and viability. Fasciolicides (drug
against fasciola SPP), fall into five main chemical groups ;(Fair weather, Boray JC September
1999).
Halogenated phenols: bithionol (Bitin), hexachlorophene (Bilevon): nitroxynil (Trodax)
Salicylanilides : closantel (flukiver supaverm), rafoxanide (Flukanide, Ranizole)
Benzimidazoles: Triclabendazole (Fasinex), albendazole (vermitan, valbazen) , mebendazole
(Telmin), Luxabendazole (Fluxacut) Phenoxyalkanes diamphenetide (coriban) Triclabendazole
(fasinex) is considered as the most common drug due to its high efficacy against adult in control
of fasciolosis of live stock in many countries. Nevertheless, long- term veterinary use of
triclabendezole has caused appearance of resistance in Fasciloa hepatica. In animals,
triclabendazole resistance was first described in Australia (Overend DJ, Bowen FL,1995).
Scientists have started to work on the development of new drug. Recently, anew Fasciolicide
was successfully tested in naturally and experimentally infected cattle in Mexico. This new drug
is called compound Alpha and is chemically very similar to triclabendazole (IbarraF, VeraY,
QuirozH, et. al., (2004). Chemotherapy normally reduces the prevalence and intensity of
infection as measured by faecal egg counts (Hansen, et. al., 1999). Other drugs salicylanilides ,
closantel, oxyclozanide, and substituted phenol (nitroxynil) are the drugs of choice in use against
Fasciola gigantica, with an efficacy ranging from 20 to 100% depending upon the drug, dosage
and administration modalities used (Gupta et. al., 1989; Sanyal and Gupta 1996; Pal et. al,
2003). Use of Triclabendazole incorporated feed pellets and strategic application of the
antihelemintic delivery device have also been claimed to reduce flukes burden (Sanyal, 1998). In
the endemic areas, epizootiology based specific therapeutic management of the disease in mild
summer (May- June) in autumn (October), and in late winter (January), when animals are
confined to indoor housing and are stall fed, have been advised and practiced. In the endemic
areas, metrological forecasting facilitates early warning of disease occurrence, so that control
measures, are timely applied, prior to shelling of cercariae by the infected snails and intake of
metacariae by the host.
2.6.7. Environmental sanitation and manipulation
Draining swamps, building sewage system and providing clean water
supplies are used to control water – borne diseases including snail borne/ helminthes but is very
expensive compare to chemotherapy, (Hansen and Perry,1994; Gaasen Beek, et. al., 2001).
Strategies for the treatment and prophylaxis of infections with Fasciloa are developed based on
epidemiological data. Effective treatment during the prepatent period
for an extended duration could eliminate Fasciola infection or reduce contamination of pasture
to a very low level, requiring less frequent treatment for a considerable time (Hansen and Perry
1994; Yilma and Malone, 1998). Retardation of immature flukes, which survive treatment,
appears to be applicable to all antihelmintics and the degree of retardation depend on the efficacy
of the drugs against the immature stages. This phenomenon has a great advantage in strategic
control by reducing early posture contamination with eggs. Less frequent strategic treatments
with a possible yearly rotation of antihelmintic combinations that are effective against both
immature and adult flukes has been reported to provide the best method of success full control of
fasciolosis (Parr and Gray 2000). Other control methods include rotational grazing (i.e-grazing
animals in divided paddocks; grazing equines, then sheep etc and avoiding mixture grazing of
animals of different age groups (NB: Young animals are generally susceptible to helminthes
infections).
CHAPTER THREE
MATERIALS AND METHODS
3.1. Study area
Gezira state is located between latitudes (13- 32 ْ S- 15-30 ْ W) and longitudes (22-32 ْ W-
20-42 ْ S). Bordered from North by Khartoum state from south Sennar state, west. Algedaref
state and east White Nile state. The whole area is about 23373) kilometers square, that is to say
about 2.5 %of the total area fo the country. The state consist of seven localities. Medani is the
capital of Gezira state According to the latest cencus (2006) the total number of population is
about (2.796.330) who belong to different tribes; 19.1% of the population lives in the country
side while the rest 80.4% lives in urban areas. There are many agricultural Projects is the state.
These include, Alrahad project which lies North east Umalgora locality, Sundus and Guneid
sugar projects. The State located within the belt of the dry climate and uniforms, characterized
by seasonal rains which fall during summer dry months (July and September). Annual total rain
fall was 272.1 ml peaked in August and declined to zero in winter seasons. Humidity range
between 70 – 180 and drought it fall between 18 – 32% in dry season. Most the surface of the
state is flat plains and there are no heights just some of the hills in the eastern southern parts and
sliding surface is generally in the direction of rivers and streams. The most important rivers are
the Blue Nile River and Alrhad River. The state attracts people from other parts of the country
due to its location and presence of agricultural projects .
Economic potential of the state is based on agricultural and live stock which considered of the
best local and cross breeds . Animal health services and preventive medicine measure are taken
care by veterinary authorities . The state contains agricultural projects , besides natural pasture
that could help improved the marketing of livestock. This could help the economy of Sudan .
3.2. Animal of the study
The animals under study include beef cattle of different breeds, age and sex. The best local
breeds ( Kenana and Butana) are found in the state besides foreign breeds. Many types of
farming system are found in the state include sedentary, semi sedentary,
mixed (livestock – crop), semi nomadic and nomadic system. Cattle under study were
categorized into calves (less than 12 months old) wearers (1-2 years old) and adult over 2 years
old.
3.3. Retrospective study
The data of retrospective study were collected from records and sheets of Animals
Resources Directorate, Ministry of Agriculture and Animal Resources- Gezira state. These
animals were diagnosed as infected with Fasciloa gigantica during meat inspection. The study
period covered the years, 2010, 2011 and 2012. All cases were recorded in form of tables
clarifying upper and lower cases for different infection circumstances.
Map.1. Gezira State indicating from where samples were collected
Source: (Anon, 2006)
13 N
15 N
43 E 32 E
3.4. Prospective study( Preparation of the questionnaire )
The questionnaire used in this study had been designed to be suitable as a rapid means of
identifying Fasciola-infected beef cattle in Gezira State. The questionnaire was designed and sent
to five randomly selected Veterinarians in the study area (Managil, Medani, Kamleen, Barakat
and Hassahesa) and had been a administered by them to cattle owners and beef enterprises
personnel in seven localities of the State. The questionnaire was prepared to identify the area for
study. (Annex No.1), it was been pretested and modified as necessary before admission. Before
the questionnaire survey was conducted, the relevant regional and district Veterinary and Animal
health authorities in Gezira were
contacted and were briefed with the purpose and methodology of the survey. The individuals
who were responsible for coordinating survey activities in the area were consulted and
information on the number of cattle owners and beef enterprises personnel in Gezira State and
the methods of distribution and collection of questionnaire were discussed. A sufficient copy of
the questionnaire was produced. Questionnaires were then distributed to Veterinary officers
Managil, Madani, Hassahesa, Kamleen, Southern Gezira, Eastern Gezira and Ummelgora
localities. The responsible persons in these localities were regularly contacted during the survey
period. Completed questionnaires (120) from selected localities were collected. Data obtain were
then analyzed and tabulated.
3.5. Parasitological diagnosis of fasciola gigantic
3.5.1. Collection of faecal samples
Faecal sample were collected during the period 2010- 2012, samples were collected from
cattle and calves of local and cross breed. A total of 201 faecal samples were rectally collected
from Southern and Madani alkobra localities these animals, each sample was then labeled , the
sex of animal and age were also recorded. The faecal samples were preserved in 10% formal
saline for microscopic examination
3.5.1.1. Faecal sample Examination
Direct smear: to determine egg of “Fasciola species”, a small amount of faeces was placed
on amicroscope slide and water was added and was mixed thoroughly using an applicator stick
cover –slip was applied with forceps or finger then the sample was examined microscopically at
low and at high power magnification.
3.5.1.2. Floatation Method
Two gram of faeces were taken in beaker with sufficient water to make a fluid mixture. The
faeces thoroughly dissociated so that the egg were freed from faeces , the suspension was
poured into a test tube and more Mg sulphate was added to fill the tube to the top. A cover slip
was then placed on the surface of the liquid and left standing for
10 -50 minutes. The cover slip was then removed vertically and placed on a slide and
examined microscopically under low and high power magnification.
3.5.1.3. Sedimentation Method
Three gram of faeces homogenized with water and the suspension was passed through coarse
mesh sieve (250nm), transferred the filtrate into a conical flask made that the faeces were
dissociated. Poured the mixture into centrifuge tube and spined at a moderate. Speed for 5
minutes poured off the supernatant fluid, a small quantities of sediment were collected with a
pipette then put on glass microscope slide, cover slip were applied and examined for detection of
the trematode eggs.
3.5.2. Egg identification
The characters of Fasciola gigantica and Fasciola hepatica eggs were used for
identification of the parasite. These characters included egg shell (yellow, the operculum is
(indistinct) and embryonic cells are also (indistinct) whenseen under the microscope.
3.5.3. Total egg Count
Egg counts were made using the modified McMaster method (Anon 1977). Three gram
of faeces were mixed with 42 ml of tap water and faecal suspension was then passed through 80
um/square inch sieve to remove debris. The filtrate was collected in a clean dry bowl 15 ml of
this filtrate were taken into a centrifuge tube, centrifuged (baird and tat lock ltd, England) for 3
minutes at 3000 rpm and the supernatant was then discarded. The sediment was emulsified by
gentle agitation and saturated zinc sulphate was added until the volume became equal to the
initial aliquot of the filtrate. The centrifuge tube was inverted several times to obtain an even
suspension of the contents and the two chambers of the McMaster slide were filled using a clean
Pasteur pipette. The average number of egg present in these chambers was multiplied by 100 to
obtain the number of egg per gram of faeces.
3.6. Liver inspection
The liver was examined for the detection of any abnormal conditions whether localized,
superficially or deeply in the organ. The liver was then placed on its parietal surface where 2
incision were made one is diagonal and directly behind the caudal lobe extending to portal
fissure, while the other is perpendicular to middle plane of the
visceral surface of the liver about 10 -15 cm left of the portal fissure where the large bile
ducts were then exposed and examined for flukes.
3.6.1.Adult worm identification
Fluke recovery was performed by the method described by Rapic, et.al (1984). The infected
liver were immediately removed at postmortem labeled and placed in individual polyethylene,
they were then transported to the laboratory where they were placed in plastic dishes containing
warm normal saline. The adult flukes were first removed by slicing the main bile ducts and gall
bladder. The livers were then cut into slices approximately 1cm thick and placed in dishes
containing warm saline and soaked for 30 minutes. While in the liquid, the slices were squeezed
and macerated. The liver tissue was removed and liberated flukes were collected. The flukes
were washed and counted individually as identified by presence of the oral suckers.
3.7.Statistical analysis
The obtained data were subjected to statistical analysis using a computerized programme (Basic
stat). Chi-square test was performed to determine the significant differences in infection rates at
0.05 level.
CHAPTER FOUR
RESULTS
4.1. Retrospective study
Table (4.1) indicates that during 2010 – 2011 -2012, The slaughter houses in Gezira state
handled 164459 cases of cattle for meat inspection with annual average of 54819. The largest
number of cases presented to slaughter houses was in the year 2012 followed by the year 2010 and
lastly 2011.About12738 out of these cases were positive giving an over all prevalence 7.74 infection
for Fasciola gigantica a among beef cattle in Gezira state. The prevalence rate of infection was
significantly higher in the year 2011 (8.87%) followed by the year2010 (8.15%). The least infection
rate with the parasite was recorded during the year 2012 (6.29%)
Table 4.1. Prevalence of Fasciola gigantica infection among beef cattle
slaughtered in abattoirs of Gezira state during the Period 2010 -2012
Prevalence% NO. infected No. Examined Year
8.15 4385 53774 2010
8.87 4760 53604 2011
6.29 3593 57081 2012
7.74 12738 164459 Over all
Table (4.2) gives the prevalence of infection with Fasciloa gigantica in west Gezira state. The
overall prevalence rate was 10.93%. the highest rate of infection was recorded in year,
2010(12.38%) followed by the year 2011 (10.58%) The least infection rate was showa in the year
2012(9.66%).
Table 4.2. Prevalence of Fasciola gigantica infection recorded among Beef Cattle slaughtered
in west Gezira State abattoirs during the period 2010, 2011 and 2012
Prevalence% NO. infected No. Examined Year
12.38 2027 16365 2010
10.58 1551 14654 2011
9.66 1418 14672 2012
10.93± 4996 45691 Over all
Chi2 – test P:0.823 Not significant
Infection recorded among beef cattle slaughtered in south Gezira state abattoirs during the
period 2010 – 2011- and 2012 is depicted in table (4.3). Out of 54218 animals examined 4322 livers
were found infected giving an overall prevalence of 7.97%. The highest rate of infection was
recorded in the year 2011 (9.66%) followed by year 2010(8.40%). The least infection rate with the
parasite was reported in the year 2012 (6.26%). This infection rate was significantly lower when
compared to that recorded among cattle of west Gezira state.
Table 4.3. Prevalence of Fasciloa gigantica infection recorded among beef Cattle slaughtered
in Southeren Gezira State abattoirs during the period 2010, 2011 and 2012
Prevalence% No. infected No. Examined Year
8.40 1240 14756 2010
9.66 1734 17948 2011
6.26 1348 21514 2012
7.97± 4322 54218 Over all
Chi2 – P:0.683>0.05 Not significant
The infection of beef cattle in central Gezira state is shown in table (4.4). Out of 64550 animal
slaughtered at central Wad Medani slaughter house, 3420 were found infected with Fasciola
gigantica giving an over all prevalence of 5.29% which is lower significant (P>0.05) when
compared to either of that recorded for cattle of south or west Gezira state. The highest infection rate
was recorded in the year 2011(6.32%) while the least infection rate was recorded in the year2012
(4.66%).
Table 4.4. Prevalence of Fasciola gigantica among beef cattle in slaughtered abattoirs of
central Gezira state.
Prevalence% NO. infected No. Examined Year
4.78 1154 24102 2010
6.32 1439 22735 2011
4.66 827 17713 2012
5.29 3420 64550 Over all
Chi2 – P>0.05 Not significant
As shown in Table (4.5). through out the survey period out of 164459 cattle examined 12738
were found infected with Fasciloa gigantica giving over all prevalence rate 7.74%. The prevalence
rate of infection with the parasite in west, south and central 10.93, 7.97 and 5.29% respectively.
Higher infection rate (10.93%) was recoreded in 2010 and the least Fasciloa gigantica prevalence
was recoreded in 2012 (5.29%).
Table 4.5. prevalence of infection with Fasciloa gigantica among beef cattle in slaughter houses
of Gezira State.
Year Prevalence %
`2010 12.38 8.40 4.78
2011 10.58 9.66 6.32
2012 9.66 6.26 4.66
Overall 10.93 7.97 5.29
ANOVA-test: high significant differences between the overall infection effect of season of the
prevalence of the parasite is shown in Table (4-6): Dry hot= (March – June), Hot wet =(July –
October), dry cold = (November – February). The prevalence rate with Fasciloa gigantica showed
different rates of infections with the season of the year. The highest infection rate was recorded
during dry hot months (8.36%). followed by dry cold (8.014%) and Hot wet (6.73%). No significant
difference was recorded between different season of the year (P>0.05).
Table 4.6. Prevalence of Fasciola gigantica among beef Cattle slaughtered in abattoirs of
Gezira State according to Season during the survey period 2010 , 2011 and 2012
Prevalence% No. infected No. Examined Season
8.36 4526 54081 Dry hot
6.73 3704 54090 Hot wet
8.14 4509 55388 Dry cold
7.74 12738 164459 Over all
Chi2 – P>0.05 Not significant
4.2. Questionnaire Data
The questionnaire survey assigned for endogenous knowledge of herd men about diagnosis and
risk factors of bovine fasciolosis was conducted in seven localities in Gezira state namely Managil,
Great Mendani Southern Gezira ,Eastern Gezira, Alhassehsia, Alkamlin, and Umalogra Locality.
Menagil locality was selected to represent beef cattle located at the western part of Gezira state,
where animal are in contacts with water. The other localities were pointed out to represent cattle in
the central part of Gezira state as represented by Madani Elkobra ,south locality represented south
part of Gezira state, Alhassehisa and Alkamlain represent northern part of Gezira state while
Umalogra and Eastern Gezira represent eastern part of Gezira state. The same opportunities for
water animal contacts are also available there. The surveyed populations include 120 herd men of
which 23 were surveyed in Managil, 16 in Madani Elkobra, 16 in south Gezira, 19 in Eastern
Gezira,15 in Umalogra, 14 in Alkamlin, 17 in Alhassihessia locality.
Data analysis concerning herd men and herd structure is shown in Table (4-7) Most of herd
men(73%) are in educated levels and have an excellent level of experience. Only 27% were illiterate
and have very limited experience about cattle breeding. Half of the herd structure in Gezira state is
represented by cross breed. About 31% of cattle were Butana breed and 19% were of kenana type.
Regarding gender, females are represented by 70% of the whole herd while male percentage is only
4.2. The rest (24.2) is a combination of both sexes. Most of these animals are brought from endemic
areas(65.8%)
Table 4.7. Frequency of herd data concerning herd men and herd structure in Gezira State as
represented by 120 questionnaire
NO Parameter Respondent Percent
1 Educational level
Illiterate
Educated
Graduated
33
53
34
27.5
44.2
28.3
2 Experience
Poor
Fiar
Expert
04
13
103
3.3
10.8
85.8
3 Breed
Butana
Kenana
38
23 31.7
Crossed 59 19.2
49.2
4 Sex
Male
Female
Both equally
7
84
29
4.2
70
24.2
5 Animal source
Endemic
Non endemic
79
41 65.8
34.1
Result of endogenous knowledge of herd men about the disease and risk factors associated with
its transmission is depicted in Table (4-8) About 70% of respondent did not know the causative
agent of bovine fasciolosis and 46% did not know the season when the disease is prevailing
.Moreover, most of them (61%) are acquainted with the mode of transmission. The clinical
symptoms which characterized the disease are very well known by 60% of tested population but
only 29% of them confirmed that jaundice and sunken eyes are the cardinal signs for the disease.
The discovery of sick animals is very easy as 85% of herd men practiced this job. Knowledge about
factors which improve the diagnosis of fasciolosis are very well understood by herd men and they
are represented by mixed of other herds (63%), veterinary services provided by 98% of herd men
where as identification of current diseases is highly practiced by 80% of them. About 60.8% of the
respondents believed on the effect of fasciolosis on their animal production.
Table 4.8. Estimated prevalence of Fasciola gigantica rate among beef Cattle by risk factor
pertains to Knowledge as represented by 120 questionnaire
NO Parameter Respondent Percent
1 Mix with other herd
Exposed
Non exposed
76
41
63.3
36.7
2 Veterinary service
Applied
Not applied
118
2
98.3
1.7
3 Current disease
Identified
Not identified
97
23
80.8
19.2
4 Importance of disease
Important
Not important
62
58
51.7
48.3
5 Clinical symptoms
Known
Not known
73
47
60.8
39.2
6 Jaundice and sunken eyes
known
not known
35
85
29.2
70.8
7 Effect on production
Recorded
Not recorded
73
47
60.8
39.1
8 Causative agent
Known
Not known
34
86
28.3
71.7
9 Transmission
Known
Not known
74
46
61.7
38.3
10 Discover sick animal
Practiced
Highly practiced
102
18
85
15
11 Season
Known
Not known
56
64
46.7
53.3
12 Frequency
Known
Not known
39
81
32.5
67.5
13 Previous experience
Known
Not known
5
115
4.1
95.8
Table (4-9) reflects attitudes of herd towards the disease and risk factors associated with its
transmission. Results showed that most herd men are responded well to detect the source of outbreak
when the disease occurs (65%). Moreover, practices which increase improve diagnosis of bovine
fasciolosis like detection of signs (51%), cardinal signs (62%) and effect of treatment (73%) are well
known by tested population. Risk factor which gives indications for the disease occurrence like
(morbidity rate is practiced by 31% of the respondents where as mortality rate represented by only
15% and age category (35%)) is not well comprehended by respondents.
Table 4.9. Estimated prevalence of Fasciola gigantica rate among beef Cattle by risk factors
pertain to attitude as represented by 120 questionnaire
NO Parameter Respondent Percent
1 Source of outbreak
Practiced
Highly practiced
78
42
65
35
2 Detection of sign
Detected
Not detected
62
58
51.7
48.3
3 Effect of treatment
Applied
Highly applied
32
88
26.7
73.3
4 Cardinal sign
known
Not known
75
45
62.5
37.5
5 Age category
Known
Not known
43
77
35.8
64.2
6 Morbidity
Known
Not known
38
82
31.7
68.3
7 Mortality
Known
Not known
19
101
15.8
84.1
As shown in Table (4-10) herd men practices differ towards bovine fasciolosis diagnosis or detection. 70%
of respondents did not used Identification as improvement criterion for the disease diagnosis and 55% of
then did not practice screening prior to purchasing their herd or when they move from endemic to other
areas. Vaccination as a protective measure for contagious diseases, which facilitates the differential
diagnosis of bovine fasciolosis is extensively practiced by herd men (70%).On other hand, quarantine as
protective measure is not applied by most of tested population (58%). The type of management practiced
by (68%) herd men in the study area highly exposed their animals to infection. Furthermore, the type of
production practiced by (69%) of respondents facilitates the detection and diagnosis of the disease.
Table 4.10. Estimated prevalence of Fasciola gigantica rate among beef Cattle by risk factor
pertain to practice as represented by 120 questionnaire
NO Parameter Respondent Percent
1 Identification
Identified
Non identified
35
85
28.3
70.8
2 Screening
Screened
Not screened
54
66
45
55
3 Vaccinations
Vaccinated
Non vaccinated
84
36
70
30
4 Quarantine
Applied
Non applied
50
70
41.7
58.3
5 Type of production
Major
Minor
83
37
69.2
30.8
6 Management
Exposed
Non exposed
82
38
68.3
31.7
4.3. Parasitological diagnosis of fasciola gigantica
As shown in Tables (4-11, 4-12 and 4-13), Out of 201 faecal samples examined from cattle in
Gezira state, 21animals were found infected with Fasciola gigantica eggs giving a prevalence rate
of 10.4% the infection rate among adults was 12.9% all calves were found free from infection.
Table 4.11 Prevalence of Fasciloa gigantica eggs according to animal Sex
Sex No. Examined No. infected Prevalence
Male 80 14 17.5
Female 121 7 5.7
Total 201 21 10.4
Table 4.12 prevalence of Fasciola. Gigantica eggs according to animal Breed
Breed No. Examined No. infected Prevalence
Local 84 7 8.3
Cross 127 14 11.02
Total 201 21 10.4
Table 4.13 Prevalence of Fasciola. Gigantica eggs according to animal Age
Age No. Examined No. infected Prevalence
Calves 39 - -
Adult 162 21 12.9
Total 201 21 10.4
CHAPTER FIVE
DISCUSSION
Bovine Fasciolosis is one of the major parasitic diseases of economic and social importance,
in the tropical and subtropical countries. Fasciolosis has been a major economic threat to
development of ruminants. Despite control efforts in a number of countries, still a large number
of ruminants are infected. In Gezira state there is a high percentage of Fasciolosis where water
development project are found which are linked with the increase in Fasciolosis transmission .
Epidemiological studies of Fasciolosis in the Gezira state would enrich the data base for
Fasciolosis research in the Gezira state and Sudan at large. The objectives of the present study
were directed to wards finding the prevalence of infection with Fasciola gigantica among beef
cattle in Gezira state based on KAP, faecal examination and post-mortem examination and to
state the geographical distribution of the parasite within the state and to study it seasonal
dynamics. The first part of the study concerned with investigation of Fasciola gigantica
affecting be cattle from abattoirs records in Gezira state in the years 2010 - 2012. The overall
prevalence of infection with the parasite was 7.74%, the result was almost the same when
compared with similar studies conducted elsewhere in the Sudan (Karib, 1962; Eisa,1966,
Serrag,2004). The study showed that 2011 gave the highest prevalence rate for the parasite was
in year 2011. Results concerning infection of beef cattle in west and south Gezira state (10.93)%,
(7.97) were in agreement with reported findings in other parts of the country. Karib, (1962)
derived the prevalence of Fasciolosis was 26% for cattle in Upper Nile state Eisa and Dalil,
(1963) found that up to 19% of examined cattle in the Upper Nile state were infected with
Fasciola gigantica. Likewise, Abakar et.al (2005) reported the similar results in Darfur region.
The diagnosis of Bovine Fasciolosis recorded here, depend entirely on post-mortem examination
and in some instance on the clinical picture during the ant- mortem examination. The diagnosis
was rarely confirmed by laboratory diagnosis. For suitable and useful recording system in
slaughter houses a tentative diagnosis adopted during ant-mortem examination has to be
recorded and considered rather than leaving the cases as miscellaneous hepatic infections. After
this initial tentative record, and when cases with similar clinical manifestations and with similar
epidemiological picture are frequently admitted to slaughter houses, this will provide an interest
for reliable diagnosis to be made during post-mortem examination, which would ultimately
improve the recording system for Fasciolosis. In the present study, the prevalence of Fasciola
gigantica from abattoirs records from Gezira state showed that the highest prevalence rate of
infection with Fasciola gigantica was recorded from western part and then followed by south
Gezira and finally central Gezira state. This was solely linked with the abundance of water pools
in addition to the some suitable water bodies for reproduction of the intermediate host; the
migration of cattle to White Nile in western part of Gezira especially during the dry season might
also justify this difference. It is clear that the infection pattern with Fasciola gigantica among
beef cattle in the study area was affected by season of the year, as the infection reached its peak
on the hot dry months. The hot wet months of the year have the least infection rate. These
findings were strongly supported by many authors (Amin, 1972;Abd lrazig,1983 et. al.,2001;
Abo-Elgasimm,2003). During the hot dry months, movement of animals to graze around
infected shrinking areas where get contacted with infected intermediate host. Amin (1972)
reported that during summer (march-June) the water temperature ranges between 24-36 Co . The
drying out of irrigation canals and water bodies towards June and the turbidity and flood (
August –October) represent limiting factors for snail multiplication (Abo-Elgasim, 2003).
Abdelrazig (1984) revealed that infection of Lymnaea snails fallow seasonal pattern, with a peak
in summer months. Later, Mohammed, (1983) and Atta-Elmannan, (2001) showed that the
environmental conditions of the hot summer were suitable for high rate of transmission of
fasciolosis in White Nile and Gezira areas. In the second part of the study the result of faecal
samples surveyed indicated that 21 out of 201 faecal specimens examined at Gezira state giving
an overall prevalence of 10.4%, the infection rate with adult cattle was 12.9% .None of the
examined calves were found to be infected with the parasite. This finding similar to prevalence
rate for Fasciola gigantica reported by other workers (Abakar et. al, 2005) . Regarding gender,
male cattle were prone to infection more than females, this may be due to the fact that males are
the major source for meat production, so for finishing, males have to be moved away from water
pools where contact with causative agent is available.
The third part of the study concerned with endogenous knowledge of herd men about bovine
fasciolosis diagnosis and estimation of risk factors associated with practice and attitude. The
study showed that most of herd men are educated and got an excellent experience on beef
production. Their herd structure composed mainly of local breed and mostly obtained from
endemic areas of fasciolosis. The endogenous knowledge of cattle breeder about the causative
agent of bovine fasciolosis in the study area is very poor. Likewise, seasonal occurrence of the
disease is not well understood, this may reflect the higher prevalence of the disease when
compared to other part of the country. The clinical symptoms which characteriz hepatic
fasciolosis are very well known by almost all herd men. In addition, the cardinal signs and mode
of transmission of Fasciola infection are known as well. These findings strength and ease the
discovery of sick animals by herd men in the study area. The current study indicated that
Practices which either improve the diagnosis or control of bovine fasciolosis among beef cattle
in the study area is well comprehended by cattle owners. Most of tested subjects responded well
to source of outbreak when occur. Vaccination and good husbandry practice are extensively used
which may justify the low rate of infection with the parasite in the study area. On the other hand,
animal Identification and quarantine, to be used as diagnostic indicators for improve diagnosis
and control of bovine fasciolosis, were not practiced well by cattle owners, This may explains
the higher prevalence of the disease when compared with other similar studies.
CHAPTER SIX
CONCLUSION AND RECOMMENDATION
6.1. Conclusion
The over whelming infection with F. gigantica in Gezira state recorded in beef cattle. Such
infections resulted in serious economic losses due to reduced productivity, cattle death and
condemnations of large numbers of infected livers. In this work, retrospective study was
conducted among beef cattle slaughtered for local consumption in the abattoirs of Gezira state.
The study was planned to determine the prevalence of F. gigantica and to assess the related risk
factors to cattle raised in this state. The study concluded that:
1. The prevalence of infection recorded from slaughter house was found to be 7.74%.
2. The parasitological survey undertaken on faecal examination to assess the parasite
infection rate in cattle showed that 12.9 % of the cattle were infected.
3. The highest infection rate was reported among cattle raised in west Gezira state followed
by south Gezira state.
4. Beef cattle in central Gezira state gave the least prevalence.
5. On seasonal basis, the infection rate was significantly higher during hot dry months of the
year.
6. Questionnaire survey showed that cattle owners have good endogenous knowledge about
diagnosis and risk factors of bovine fasciolosis.
6.2 Recommendations
For further investigation and on the light of these results, good diagnosis and control of
bovine Fasciolosis might be under control through.
1. Education veterinary extension as a mean of disease control.
2. Control of animal movement can be applied and should be studied epidemiologically carefully
not to affect animal movement from their natural ecosystem to new ecosystem, so that the
productivity and health will be affected.
3. Biological control is intended to control the most effective part in the cycle of infection (Lymnea
snails by the help of the natural enemy)
4. Training of abattoirs workers for proper recording and analysis of Fasciolosis in slaughter houses
.
5. Records from animal farms and markets that can help detailed information a bout Fasciolosis
affected by species , animal type , age , breed , location and season.
REFERENCES
Abakar, A. D., Bashar, A. E., Mohammed, A., A., Serrag. A. M and Abo elgasim, A. A
(2005).: Bovinee FasciolosisI: Prevalence of Fasciola gigantica infection among beef
cattle in Darfur States based on retrospective survey: Egyptian Veterinary Medical
Society of Parasitology Journal, (11/2) 366 – 372.
Abdel Razig, Y, (1983). Epidemiological studies on bovine Fasciolosis in Darfur province,
M.V.Sc. Thesis, University of Khartoum .
Amin M.A. (1972). Large scale assessment of Moulluscicides copper sulphate and N-
Tritylmorphline (Frescon) in the north group of the Gezira irrigated Area of the Sudan.
Journal of Tropical Medicine and Hygiene, (75): 169-179.
Anon (1977). Manual of Veterinary Parasitological laboratory techniques, Ministry of
Agriculture, fisheries and food Agricultural Development Advising Services, Technical
Bulletin No.18 2nd edition .
Atta El Manan, AM;sman O.M; Bushara, H.O and Majid, A.M.(2001) some aspects of the
epidemiology of Bovine fasciolosis in North Gezira and Khartoum state. The Sudan
Journal of veterinary Research (17). 35 – 40 .
Boray, Jc; (1969) "Experimental Fascioliasis in Australia" Advances in parasitology 7: 95 ậ€
"210.
British, Veterinary Association (1970). Hand book of animal Diseases in the tropics. British
veterinary Association, London.
Brown, D. S. (1980). Fresh water snails of Africa and their medical importance. Taylor and
Francis Ltd., London, PP. 487.
Centers for Control of DiseasesControl and Prevention Laboratory Identification and
Prevention of Parasites of Public Health Concern. Available at: www.dpd. cdc. gor/dlx/
HTML ImgeLibrary/Fascioliasis-il htm Accessed July 23,2010
Cheesbrough, M. (2005). "District laboratory practice in tropical countries,volume1. Cambridge
England: Cambridge University. Parasite and Health. Accessed. January a, 2013a htt:
//www. Dpd.cdc.gov/dpdx/html/Fas.cioliasis. htm.
Coyle, T. J. (1958). Experiments in the diagnosis and treatment of fascioliasis in Uganda-
Bulletin of Epizootic Diseases of Arica,6:255 – 273)
Daffalla, A. A.; Elias, E. E., and Amin, M. A. (1985). The lung fish protopterus annectans
(owen) as bio-control agent against shistosome vector snails the Journal of Tropical
Medicine and Hygiene. (66). 131-134
Dang Prasert, T; Khawsuk W, Meepool,A C. Wanichanon. V-Viyanat,
E.Upatham,s.wongrtanacheevin,PSobhon. (2001). Fasciola gigantica : surface
topography of the adult tegument. Journal of helminthology 75: 43 - 50
Dawes, B. (1963). The migration of Juvenile forms of F.hepatica through the intestine in the
mouse, with some observations on food and feeding Parasitology (53): 109 – 120.
Delcon, D., Queens, R;and Hillyer, G. V. (1980). The present and patent period of Fasciola
Hepatica in cattle in Puerto Rico Journal of parasitology (67). 734.
Dixit Ak, Yadavsc,and Sharma Rl. (2004). Kinetics of antibody response using 28KDa
Fasciola gigantica cysteine proteinase As antigen. Trop Animal Health Prod,
2004;36: 49 – 54
Dixit D,and Sharma, Rl.(2008). Immunodiagnostic Protective role of Cathepsin L cysteine
Protein as secreted by fasciols spp a
review vet parasitol-2008;154: 177-184 .
Dubinsky A1/2/2,p.,(1993).Tremat ْ A3dyatrematodAzy.In:Jur ْ Ai ْ Aiek,V.,Dubinsk
A1/2,p ْ akoletAv, Veterin ْ Ajrna ParazitolA3gia.PrArodaa.s.,Bratslava158ậ
€’’187.(inslovakian)
Durbin, C.G (1952). longevity of the liver fluke, fasciola spp, in sheep proceedings of
Helminthological society. Washington (19):120,
Edith R; Thilagar MB; Godara R,and Sharma RL. (2010a).. Tropical liver fluke induced
stress in the experimentally infected and immunized buffaloes. Vet Rec. 2010;167:571–
575.
Edith R; Godara, R Sharma RL,and Thilagar, M.B. (2010b). Serum enzyme and
hematological profile of F.gigantica immunized and experimentally infected riverince
buffaloes. Parasitol Res.2010:106 – 947-956
Eisa , AM . and Dalil , E . A . ( 1963 ) . Incidence of parasites in bovine livers sudan Journal of
Veterinary Science and Animal Husbandary , ( 4 ) : 71 – 76
Eisa, A.M (1966a). Normal worm burden in upper Nile province. Sudan journal of Veterinary
Science and Animal Husbandry, (4): 63-71 .
Eisa A,M.(1966b). Parasitism challenge to animal wealth in the Sudan, Sudan Journal of
challenge Veterinary Science and Animal Husbandry, (7):85-94
EL khawad, SB; Eisa, AM, Ibrahim, A.M. Slepnov, IV.K and Gezuli, A. Y (1978). Incidence
of helminth Parasities of cattle, sheep and goat in southern region of the Sudan. Sudan
Journal of veterinary science and Animal Husbandary (17) 86 – 90
EL khawad, SB; Eisa, AM, Ibrahim, A.M. Slepnov, IV.K and Gezuli, A. Y (1976) . Asurvey
of helminth paraside of cattle , sheep and goats in southern region of the sudan . Sudan
Journal of Veterinary Science and Animal Husbandary (7) : 86 – 90
Fairweather,1and Boray,J.C.(1999).Fasciolicides efficacy, actions,Resistance and its
mangment "the Veterinary Journal 158(2):81-112
GaasenBeek ; C.P.H, Moll,L., Cornelissen,J.B.W. Vellema, P and Borgsteede,
F.H.M.(2001) A experimental study on triclabendazole resistance of faciola hepatica
in sheep Veterinary Parasitology 95 (1):37-45
Gang G, Varshney JP, and Sharma R. L., Varshney V, P. (2007). Kalicharan effect of F.
gigantica infection on adrenal and thyroid glands of buffaloes. Res Vet Sci. 2007; 82:
61-67.
Ganga G, Varshney JP, Sharma RL. (2004). Oxidative stress in F. gigantica infected
buffaloes. J. Vet Parasitol, 2004;18:71–71.
Garg R,Yadav Cl,Kumar RR,Banerjee Ps,Vatsyas, and Godara R. (2009) The epidemiology
of Fasciolosis on ruminants in different geo-climatic regions of north India. Trop Anim
Health Production 2009;41:1695 – 1700
Goraish. I.A. (1987). Studies on the susceptibility - to Fasciola gigantica infection in goats with
special reference to levamisole treatment M.V.Sc. thesis University of Khartoum
Graber, M.( 1952) Role of Diet in bovine and ovine fasciolosis caused by fasciola giantica.
Bulletin of Epizootic Diseases of Africa.(19).60
Gupta, Sc, and Yadavsc(1994). Emergence of Fasciola gigantica cercariae from naturally
infected L.aurcularia Indian J Parasitol 1994;18:53-56
Gupta Sc, Chandra R., and Yadav S. C. (1989). Efficacy of triclabendazole against
experimental fasciola gigantica infection in sheep, goats buffaloes and rabbit. Indian
vet J. 1989; 66: 680-682.
Hammond, J.A. ( 1965 ) . Observations on fascioliasis in Tanganyika Bulletin of Epizootic
Diseases of Africa , (13) : 55 - 65
Hammond, J.A. and sewell, MM.H(1986) Helmintholgy Notes,MSc./ Diploma in Tropical
Animal Production and Health. CTVM, University of Edinburgh
Hansen, J. and Perry, B.(1994). The Epidemiology, Diagnosis and control of Helminth parasite
of Ruminants = A Handbook. Animal production and health division, FAO, Rome.
Italy. pp.171
Hansen, D . S . , Clery , D . G . , Estuningsih , S . E ., Widjajanti , S., Partoutomo , S. and
Spithill , T. W . ( 1999 ) . Immune responses in Indonesian thin tail and Merino Sheep
during aprimary in fection with Fasciola gigantica lack of aspecific Ig G2 antibody
response is associated with increased resistance to infection in Indonesian Sheep .
International Journal for Parasitology 29 (7) : 1027 – 1035
Haroun, E. M and Hussein, M. F., (1975). Clinic opathological studies on naturally occurring
bovine fascioliasis in the Sudan. Journal of Helminthology, (49): 143-152
Hillyer, G. (1997). Food-borne Trematode infections in the Americas. Parasitol Today, Apt W,
1387-88.
Hopkins , D.R. (1992). Homing in on helminths. Am J Trop Med Hyg.;46:626-634
Ibarra F,VeraY, Quiroz H, et al February (2004) Determination of the effective dose of an
experimental Fasciolicide in naturally and experimentally infected cattle " Vet-
parasitol, 120(1ą € 2") 65ậ €74
Itagaki T, Ichinomiya M, Fuk, Fusyuku S, Carmona (2011). ''Hybridization experiments
indicate incomplete reproductive isolating mechanism between Fasciola hepatica and
Fasciola gigantica '' Parasitology 138 (10) : 1278 - ậ € '' 1284
Johnson P.,D. Thieltges 2009 Diversity decoys and the dilution effect How ecological
communities affect disease risk. Journal of Experimental Biology 213: 961 – 970
Karib, E.A.(1962). Fascioliasis in cattle & sheep in Sudan. Bulletin de L,office international
desEpizooties, (58) : 337-346
Kiser J, Utzinger J(2009). Food borne trematodiases. Clin Microbiol Rev.;22:466-483
Keiser J. and Utzinger J.(2005) Emerging food borne trematodiasis Emerg Infect Dis.;
11:1507-1514
Kendall, S.B.(1954) Fasciolasis in Pakistan Ann trop. Med. Parasite, (48) .307 – 313
Khuele, M. E. (1983). The integration of live stock into irrigated agriculture system in semi-arid
tropics with particular reference to Gezira. M. Sc. Thesis CTVM university of
Edinburgh.
Kumar M , Pathak KML , Pachaurisp (1982). Clinico – Pathological Studies on naturally
occurring bovine fasciolosis in India . Br Vet J ; 138 : 241 – 246
Kumar, V.(1998). Trematode infections and Diseases of Man and Animals AA Dordrech +, The
Nether lands: Kluwer Acaclmic Publishers.
Madsen, H. (1992). Inter-specific competition between Helisoma duryi (Wetherby, 1979) and
intermediate hosts of Schistosomes, Gasropoda-Planorbidae. An evaluation of
biological control of Schistosome intermediate host by competition snails. Ph.D.
Thesis. Danish Bilharziasis laboratory, Charlothenlum. D. Denmark.
Magzoub, M. and Adam E.I(1977). Laboratory investigation on natural infection in zebu cattle
with fasciola gigantica and S.boivs zeniraibatl for vertinarmedizin B(24): 53-62.
Malek, E. A (1969).Studies on bovine shistosomiasis in the Sudan . Annals of Tropical
Medicine and Parasitology, (63) :501-513
Marcos L Terashima A, and Gotuzzo E. :(2005) Update on hepatobiliary flukes: Fascioliasis,
opisthorchiasis and clonorchiasis. Curopin Infect Dis ;21:523-530
Marcos L, and Maco V .(2006). Risk factors for Fasciola hepatica infection in children: Acase-
control study. T trans . R.Soc Trop Med Hyg ;100: 158 -166
Marquardt , W.C., and Demaree, JR.(1986). Mechanism between Fasciola hepatica and
Fasciola gigantica. Parasitology 138: 1278-1284.
Miliotis, M., and BierJ (2003). International Hand book of food borne pathogens Imprint, New
York : Marcel Dekker Inc.
Mas-Coma, S., Angle, R., Eseban, J. G., Bargues, M. D., Buchon, P., Franken, M., and
Strauss, W. (2007). The Northern Bolivian Altiplano: A region highly endemic for
human Fascioliasis. Trop. Med and Health, 4, 454-467.
http://dx.dio.org/10.1046/j.1365-3156.1999.00418.x
Mas-Coma, S., Bargues M. D., Valero M. A (2005). Fasciolasis and other plant – borne
trematode zoonoses. In J. Parasitol. 35(11-12): 1255-78
Mas-Coma, S., Bargues M. D., and Esteban J. G (1999). Human fasciolosis. In: Fasciolosis
(Dalton J. P. ed.) CABI publishing walling ford, PP. 411 – 434.
Mohammed ,M.A (1983). – M . V. Sc . Thesis . Unuversity of Khartoum
Ogunrinade, A.F. (1983). Bovine fascioliasis in Nigeria. V. The pathologenicity of the
experimental infections in white Fulani cattle. Revued, J, Elevageetde Medicine
veterinaire des days tropicaux, 36(2); 141-149
Overend DJ and Bowen, FL(1995 )Resistance of Fasciola hepatica to triclabendazole Aust.
Vet.J.72 (7): 275
Pal, D. Kumar V., Yadav C.L, Banerjee P S (2003). Efficacy of certain drugs against naturally
acquired bubaline fasciolosis and amphistomosis, Indian vet J. 2003; 80: 3-5
Parr, S. L and Gray, J. S. (2002). A strategic dosing scheme for the control fasciolosis in cattle
and sheep in Ireland Veterinary parasitology 88(3-4): 187-197.
Price TA,; Tuazon Cu, Simon GL(1993). Fascioliasis: Case reports and review. Clin infect
Dis.1993; 17;426-430
Rainaok, Yadavsc, sriveny D, Gupta Sc (2006) Immunodiagnosis of bovine Fascilosis with
fascoila gigantica Cathepsin Land recombinant Cathepsin L1- Dproteases Actatrop.
2006; 98:145-151
Rapic, D., Dzakula, N., cankovic, and stojecevec, D. (1984). Efficacy of Triclabenzole against
Fasciola hepatic a in naturally infected sheep Veterinary (54).13-18)
Read,C.1973. Animal Parasitism. Englewood Cliffs, New Jersey: Prentice – Hall-Inc
Rokni MB; Mirhendi H. MizaniA, Mohebali M ,Sharbatkhori M, KiaEB, Abdoli H, Izadi
S(2010) "Identification and differentiation of fasciola hepatica and fasciola gigantica
using a simple PCR-restriction enzymethoid" Experimental parasitology 124(2): 209 -
213.
Rushton, B., Murry, M. (1977). Hepatic pathology of a primary experimental infection of
Fasciola hepatica in sheep. Journal of comparative pathology . (87). 459-470.
Sanyal P. K. (1998). Pharamcokinetics and efficacy of triclabendazole in corporate urea
molasses block against experimental immature fasciologsis in bovine J . Vet parasitol;
12: 25-29.
Sanyal P. K.and Gupta S.C (1996). Efficacy and pharmacokinetics of trictabendazole in
buffalo with induced fasciologsis vert parasitol ; 63 : 75-82.
Serrag, A. M (2004). Studies on bovine fascilogosis in Darfur States M.Sc. thesis, El Fashir
University.
Sewell, M.M.H.(1966). The pathogenesis of fasciolasis Veterinary Record,(78) : 98-105
Sewell, M.M.H.(1976). The role of management in the control of helminthes diseases in: Beef
cattle production in developing countries (Ed. A. J. Smith), pp 130- 149. CTVM,
University of Edinburgh.
Sinclair, K.B.(1962) observations on the clinical pathology of ovine fasciolosis `British
Veterinary Journal, (118).37.
Soliman, K. N. and Zaki, H.(1964). The present situation concerning liver fluke disease in
Egypt . Bulletin of Epizootic Diseascs of African, (12): 455- 460
Soulsaby. E. S. L. (1986). Helminths, Arthropodes and protozoa of Domesticated Animals, 7th
ed. Bailliere Tindall, London.
Sriveny. D; Raina O.k; Yadavsc. Chandra D Jayaraw AK,singhm, velusamy R,singh BP (
2006) . Cathepsin Lcysteine proteinase in diagnosis of bovine F.gigantica infection
Veterinary Parasitology ;135:25-31
Swarup. D; Pachauri SP (1987)Pathophy siology of Fasciolosis in buffaloes : some
biochemical indices . Indian J Animsci , 57:1083-1085
Tadesse Eguale and Getachew Tilahune (2002) Mollucicidal effects of Endod (phytalacca
dodecndra) on fasciola transmiting snails SINET : Ethiopia journal of science 25 (2)
:275-284
Tolan R,W, Dr.2001. Fasciolaiasis. e - Medicine from WebMD. Updated. June
15,2010.Available at: emedicine. Meds cape .Com/arricle/997890-overview. Accessed
July 6,2010
Tristam, G.P., Daniel, B.S., Abba, (2006). Report of the WHO Informal Meeting on use of
Triclabendazole in Fasciloiasis Control. WHO Headquarters. Geneva. Switzerland:
October 17-8, 2006. Available at:www.who.int/neglected-diseases/preventive-
chemotherapy/ WHO-CDS-NTD-PCT -2007.l.pdf Accessed July 6,2010
Umo and Ikewe, M. M. (1978). Hepatic change in natural fasciola gigantica infection of the
Fulani zebu cattle. Bulletin of animal heath and production in Africa 26(2): 162-167.
Urquhart ,G.M.,Armour,J.,Duncan,A.M.,and Jennings, F.W (2001). Parasitologia
Veterinaria (2ned).Acribia S.A.Zaragoza.Espana,pp117-127
World Health organization (2010). Report of the WHO informal meeting on use of
triclabendazole in fasciolaiasis control . WHO head quarters , Geneva Switzerland :
October 17-18 2006 available at www.WHO.int /neglected diseases / preventive
chemotherapy WHO-CDS –NTD-PCT 2007.I.pdf essed july2010
Yadav Sc, Mandals, sharma RL(1999).A comparative evaluation of F. gigantica antigens in
immunodiagnosis of bubaline Fasciolosis Rivista Diparassitol: 1999;16=73-81.
Yagamuti. S (1958). System aHelminthum VOI . I.the Digentic Trematodes of vertebrates ,
parts 1 and 2 new york : interscience publishers .
Yilma J; Malone, J. B. (1998). A geographical information system forecast model for strategic
control of fasciolosis in Ethiopia. Veterinary Parasitology 78(2): 103-127.
Appendex1
Knowledge, Attitudes and Practices (KAP) of cattle owners towards bovine
Fasciolosis in Gezira State.
Bovine fasciolosis Questionnaire Format for Animal owners
The purpose of this form is to assess the knowledge, attitudes and practices of cattle owners to
wards bovine fasciolosis in their herds. The forms also aimed to determine conditions present on
the farm that may increase the risk of introducing or spreading disease.
DATA COLLECTION FORMAT
No. Date: / /
State: ………………………………………….
Locality/site:………………………………….
1. General information
(a) Name:
(b) Address:
(c) Gender:
(d) Age:
(e) Educational level:
- Uneducated
- Primary School
- High School
- Secondary School
- Graduate
- Professional training
(f) Number of years of experience in animal business
………………………………………………………………………………
2. Management of herds and herd characteristics
(a) Where is the herd kept?
………………………………………………………………………………
(b) How many animals are there?
(c) Breed:
Butana
- Kenana
- Crossed
- Pure line
- Sex: All male All female Mix
(e) Which sex is the most affected?
- Males
- Females
- Both equally
- Do not know
(g) What is the source of the animals when buying?
………………………………………………………………………………
(h) Characteristics upon when the animals are bought
………………………………………………………………………………………………………
………………………………………………………………………………………………………
……………………………………………………………………..
(i) Do animals in the herd have identification numbers? Yes No
(j) What do you do when introducing new animals into the herd?
………………………………………………………………………………………………………
………………………………………………………………………………………………………
……………………………………………………………………..
iii- Vaccination and prevention programmes
(a) Do you vaccinate against the following?
(i) R pest Yes No
(ii) Bq Yes No
(iii) Anthrax Yes No
(iv) HS Yes No
(v) Lumpy skin disease Yes No
(b) When was the last time you vaccinated your animals ?
……………………………………………………………………………… (c) How many
animals were vaccinated?
………………………………………………………………………………
(d) When animals purchased from outside where do they come from most probably?
………………………………………………………………………………
(e) Do you keep the new animals in quarantine before mixing them with the old ones?
Yes No
For how long?
If clinical signs observed what is the action?
………………………………………………………………………………………………………
………………………………………………………………………………………………………
………………………………………………………………………
iv- Type of production system and changing of the herd
(a) Source of income
- Only livestock
- Mainly livestock, minor crop
- Mainly crop, minor livestock
- Livestock and crop equally important
(b) Management of the herd and farming system
- Sedentary
- Semi-sedentary
- Mixed (crop/livestock)
- Semi-nomadic
- Nomadic (Free range or grazing)
If nomadic please indicate the migratory route?
………………………………………………………………………………………………………
……………………………………………………………………………….
(c) Has the herd mixed with other herds?
………………………………………………………………………………………………………
…………………………………………………………………………………
(c) How do you breed your animals?
- Natural
- AI programme
(e) Inventory change of the herd during the year is mainly due to
- Market off take
- Non-market off ``take (home consumption, gift out, lost/stolen)
- Mortality
vi- Health problem
(a) What kind of veterinary services do you receive?
- Governmental
- Private
- Community Animal Health Workers
- Traditional medicine
- Using own prescription
(b) What are the current disease problems in the herd?
- Respiratory
- Gastro-intestinal
- Reproductive
- Skin
- External parasites
- Others
………………………………………………………….
………………………………………………………….
………………………………………………………….
………………………………………………………….
(c) Please rank the most important diseases in your area?
1- ……………………………………………………….
2- ……………………………………………………….
3- ……………………………………………………….
4- ……………………………………………………….
5- ………………………………………………………..
6- ………………………………………………………..
7- ………………………………………………………..
8- ………………………………………………………..
9- ………………………………………………………..
10- ………………………………………………………..
(d) Do you know the clinical symptoms of the bovine Fasciolosis? Yes
No
(e) Have you ever seen its signs within your herd? Yes No
(f) Can you mention these signs?
1- …………………………………………………………
2- …………………………………………………………
3- …………………………………………………………
4- …………………………………………………………
5- …………………………………………………………
(g) Which age category is the most affected?
- Less than one year
- One to two years
- Two to four years
- More than four years
- No difference between age groups
Morbidity %
(h) Mortality rate %
(i) Jaundice and sunken eyes rate within affected animals %
(j) The effect of the disease on the production
1- …………………………………………………………………….
2- …………………………………………………………………….
3- …………………………………………………………………….
4- …………………………………………………………………….
5- …………………………………………………………………….
(I) Do you know the causative agent of bovine Fasciolosis
1 . Yes
2. No
(II) Do you know how bovine Fasciolosis is transmitted
1- Yes
2- No
(k) When you discover a sick animal what do you do?
- Isolation
- Reporting to veterinary authorities
- Handling the case without reporting
(l) When an outbreak of Fasciolosis occurs in your herd, the likely source is
- Introduction of new animal(s)
- Contact with water
- Contact with wild animals
- Movement of animal(s)
- Other(indicate)…………………………………………………………
………………………………………………………………………………………………………
…………………………………………………………………………………
(m) Season of occurrence
- Dry season
- Rainy season
- Cold season
- Hot season
- Not specifically associated with season
(n) How many times have you had the disease?
- Only once
- Twice
- Three times
- Commonly occurs
(o) When was the last outbreak of Fasciolosis in your herd?
- Before 1935
- 1950 - 1975
- 19 80- 1989
- 1995-
- Had never occurred
(p) When an outbreak of Fasciolosis or any other disease occurs in the next herd, how do you
protect your animals?
- Stop movement
- Prevent contact with water
- Treat affected animals
- Report to the authorities
- Other measure
(q) What was the importance of the following clinical symptoms?
- Weight loss
- Sunken eyes
- Jaundice
- Diarrhoea and Pneumonia
- others
Relative
Importance
Weight loss Sunken Eyes Jaundice Diarrhea and
peumonia
Others
Very
important
Important
Less
important
Negligible
(r) When was the last time these clinical symptoms occurred?
- …………………………………………………………………..
(s) Have you had personal experience with this disease?
Yes No
If yes,
When…………………………………………………………………………
Where………………………………………………………………………
vii- Recording system
Do you keep such type of record files with you?
(a) Animal record files Yes No
(b) Herd production files Yes No
(c) Herd disease files Yes No
(d) Herd environment or management files Yes No
viii. Other comments
………………………………………………………………………………………………………
…………………………………………………………………………………………………….