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module 7
Infectious diseasestudent notes
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Module 7: Infectious Disease
Content Focus
This module examines the treatment, prevention and control of infectious disease both locally and globally. It includes study of the human immune system and its response to an infectious disease.
The value of studying infectious disease and its causes and effects is highlighted by the cost to humans in terms of losses in productivity and production and the impact on overall health. The module also considers medical and agricultural applications that draw on the work of a variety of scientists.
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Causes of Infectious DiseaseInquiry question: How are diseases transmitted?
Students:● describe a variety of infectious diseases caused by pathogens, including microorganisms,
macroorganisms and non-cellular pathogens, and collect primary and secondary-sourced
data and information relating to disease transmission, including:
– classifying different pathogens that cause disease in plants and animals
Disease can be defined as “any condition that disturbs the normal functioning of the
body”.
A pathogen or infectious agent is a biological agent that causes disease or illness to
its host.
Pathogen Characteristics Example3
Prion Defective proteins: proteinaceous infectious particle
Minuscule Not cellular No nucleic acids Causes degeneration of brain
tissue Diseases can be both hereditary and infectious
Fatal Familial Insomnia
Virus Tiny: 30 to 300 nm Not cellular Can only reproduce using
host cells Can be crystallised
Influenza
Bacteria Small: 0.5 to 5 µm Cellular Prokaryotic: no membrane
bound organelles Single strand of DNA Reproduce by binary fission
quickly inside a host Waste products (toxins) often
harm host Classified by shape
Tuberculosis
Protozoa
Small: 2 to 1000 µm Eukaryotic: membrane-bound
nucleus No cell wall Many are free-living Classified by the way they
move
Amoebic dysentery
Fungi
Range in size, unicellular to multicellular
Eukaryotic: membrane-bound nucleus
Cell wall No chloroplasts Saprophytic (living on dead
matter) or parasitic
Thrush
Macro-parasites
Visible by the naked eye Endoparasites or exoparasites Endoparasites usually have
long association with host Ectoparasites usually have
brief association with host
Tapeworm, lice
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Prion
Virus
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Bacteria
Protozoa
Investigation 10.1
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– investigating the transmission of a disease during an epidemic– investigate modes of transmission of infectious diseases, including direct contact,
indirect contact and vector transmission
Epidemic
An epidemic is a widespread occurrence of an infectious disease in a community at
a particular time.
Pandemic
A pandemic is when the disease is prevalent over a whole country or the world.
Modes of transmission of infectious disease.
Transmission of infectious diseases involves the carrying or transfer of a pathogen
from an infected host to a non-infected organism.
For a disease to spread between organisms, a “chain of infection” must be present.
This chain has three elements:
1. A host that is susceptible to the disease2. A pathogen that is capable of causing the disease3. A mode of transmission: a way for the pathogen to get from host to host
There are three models of transmission, or ways that a pathogen can get from host to
host:
1. Direct contact: transfer of the pathogens via exposure to infected skin or body
secretions
2. Indirect contact: transfer of the pathogen to a new host via a non-living host
3. Vector transmission: transfer of the pathogen via another organism such as an
arthropod
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Direct ContactTransmission by direct contact occurs when there is physical contact between the
host and a non-infected organism.
Contact between organisms of the same generation, or between organisms that are
non-parent and child, is known as horizontal transmission.
Contact between offspring a parent is known as vertical transmission.
Physical contact includes:
Touching
Sexual contact
Kissing
Contact with the nasal or oral secretions
Biting
Direct contact with any blood or other body fluids
Direct contact with wounds
Prenatal all perinatal transmission
STI’s
Indirect Contact
Transmission by indirect contact occurs when the host organisms have no direct
contact with each other.
Infection occurs from a reservoir created by the host outside itself, such as
contaminated materials, surfaces or objects.
A fomite is in the object or substance that carries infection.
Some indirect means of transmission include:
Airborne transmission, e.g. Coughing or sneezing
Touching an infected surface
Contaminated food or water
Infected surgical instruments
Vectors transmissions through arthropods such as mosquitoes, ticks and fleas
Measles virus from infected droplets such as from body fluids
Gastroenteritis, for example, caused by the bacterium E. coli
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Diseases spread by vector transmission include:
Chagas disease – also termed American trypanosomiasis is an infection caused by
a protozoan parasite, (Trypansoma cruzi) that can result in acute inflammatory skin
changes (chagomas) and eventually cause infection and inflammation of many
other body tissues, especially those of the heart and intestinal tract.
Malaria
Dengue fever
Canine and feline heart worm
Hendra and Nipah viruses
Students read and summarise case study: equine influenza virus, page 334 of the textbook
Investigation 10.2
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– design and conduct a practical investigation relating to the microbial testing of water or food samples
Detection of microbes in food and water is not possible with the naked eye.
However, when microbes such as bacteria and fungi reproduce, they form clusters
which are visible to the naked eye. These clusters are called colonies.
Bacterial colonies can be smooth, glossy and coloured.
Whereas, fungal colonies are furry and large.
Bacterial colonies can be identified according to their:
Colour
Margin
Form (basic shape)
Elevation (shape of the cross-section)
Surface features (smooth, dull and wrinkled)
Investigation 10.3 page 338Check Your Understanding 10.1a p331 and 10.1b p339
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● investigate the work of Robert Koch and Louis Pasteur, to explain the causes and transmission of infectious diseases, including:– Koch’s postulates– Pasteur’s experiments on microbial contamination
During the second half of the nineteenth century, the work of Pasteur and Koch and other scientists stimulated the search for microbes as causes of disease
Pasteur’s FlasksPasteur’s early research suggested the existence of spores. He hypothesised that
these spores were carried in air, where they were inactive. They developed into
active microorganisms when nutrients became available.
Pasteur designed the experiment as shown below. The flasks with the S shaped
neck allowed air to enter but dust and spores were trapped in the neck and could
not reach the broth. The other flask was directly open to the air.
Pasteur boiled the broth and subjected the glassware to steam to kill any microbes
present.
As Pasteur predicted the glassware with the S bend did not become contaminated
proving that the organisms that contaminated the broth must be carried in the air.
Pasteur’s flasks are still on display in the Pasteur Institute in Paris and after 150
years they are still not contaminated.
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Investigation 10.4 page 343
Koch’s PostulatesKoch developed a set of procedures to follow, which will definitely and scientifically identify the pathogen. These procedures are known as “Koch’s Postulates” and are still used today when previously unknown infectious diseases are discovered.Koch was the first person to develop a set of rules (postulates) which linked a particular organism with a particular disease.
He was the first to develop a way of growing pure cultures of bacteria on agar in a Petri dish.He stained, described and identified many bacteria including TB, cholera and anthrax.
Koch’s Postulates
The organism believed to be the cause of the disease must always be present
when the disease occurs.
The organism must be isolated from the host and grown in pure culture.
Organisms from the pure culture, when inoculated into healthy, suitable,
susceptible hosts must produce the disease.
The organism must be re-isolated, grown in pure culture and compared to the
organism first injected.
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Summary of Pasteur’s and Koch’s work
Louis Pasteur (1822-1895) Robert Koch (1843-1910)Created the science of microbiology Developed many bacteriological techniquesDemonstrated that microbes caused the souring of wine and beer (lactobacilli)
Developed the agar plate technique for growing microorganisms
Development of the process of pasteurisation to kill bacteria
Identified the bacterium Bacillus anthracis responsible for anthrax disease.
Conducted the swan-necked flask experiment to disprove spontaneous generation
Demonstrated that specific microbes are responsible for causing specific diseases
Established the germ theory of disease, that microbes caused disease Developed Koch’s postulates
Developed a vaccine for chicken cholera Identified the bacterium responsible for tuberculosis and cholera
Used Koch’s work on anthrax to develop a vaccine for anthraxDeveloped a vaccine against rabies and used it on humans for the first timeEstablished the principle of immunity and developed an effective way to prevent infectious disease
Check Your Understanding 10.2 page 344
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● assess the causes and effects of diseases on agricultural production, including but not limited to:
– plant diseases– animal diseases
Causes and effects of disease in agricultural production.
Culture involves cultivation of crops and pastures and the rearing of animals.
Infectious diseases in Australian agriculture
Two types of plant and animal diseases are of concern in agriculture in Australia:
1. Endemic diseases: these are diseases consistently present in a country or
region, such as bovine Johne’s disease in sheep and cattle and footrot in sheep.
2. Exotic (introduced) diseases: such foot and mouth disease, avian influenza and
bovine tuberculosis as examples.
The complex interplay of three factors may contribute to the development of
infectious disease in organisms of agricultural imports.
Host factors - susceptibility to disease, access to pathogens, concurrent disease
or poor nutrition leading to weakened immune response, drought and heatwave
stress on the host.
Pathogen factors – the pathogens availability, its ability to transfer between
hosts, as well as virulence factors including adhesion and invasion of host
tissues, and successful establishment inside host tissues.
Environmental Factors – overcrowding and lack of hygiene and to a build-up of
wastes, which provide a suitable environment for pathogen reservoirs
The favourable environment within the host for pathogens to establish and cause
disease.
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Students summarise case study: Footrot in sheep page 345
Factors contributing to the risk of infectious disease
Increased mobility of human populations
Rise of intensive and industrial types of agriculture.
Changing patterns of land use
Climate change
Antimicrobial resistance (e.g. Resistance to antibiotics)
Pesticide resistance
Loss of genetic diversity
Increasing the number of hobby farmers – if farmers with little experience in animal
husbandry or crop production
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Plant diseases of agricultural significance
Commercially grown plants in Australia include:
Grains
Fruits and vegetables
Fodder
Fibre
Horticultural plants
Forestry planets
The main causes of infectious diseases in plants include:
Fungi – are by far the most common cause of plant disease.
Terms such as rust, blight, smut and mildew are all fungal diseases in plants.
Reservoirs of fungal spores exist in contaminated seeds, farm machinery, and
soil and nearby weeds.
These pathogens can be transmitted by wind, water and direct contact with the
reservoirs.
Fungi move into plants through their stomata or other openings in the plant.
They damage the plant by destroying conducting tissues and absorbing nutrients
from the plants.
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Insects and mitesInsects and mites cause direct damage to plant tissue but can also act as vectors for
other pathogens.
Examples include aphids, fruit fly, citrus leaf miner and mealy bugs.
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Bacteria
Reservoirs of pathogenic bacteria may occur in soil, weeds, seeds and humans.
Bacteria need certain conditions to be to multiply and spread. These may include
humid and warm conditions.
An example is bacterial canker of tomatoes.
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Nematodes (Microscopic Worms)
Thousands of these live in the soil but only a few act as plant pathogens.
The nematodes attacks plant roots, creating galls and lumps.
The plants subsequently wilt, turn yellow and die.
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Viruses
Plant viruses are obligate (by necessity) intracellular parasites.
For example the tomato mosaic virus.
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The students summarise the case study: Panama disease of bananas page 349
Investigation 10.5
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● compare the adaptations of different pathogens that facilitate their entry into and transmission between hosts
Adaptations of pathogens to facilitate their transfer.
For a pathogen to successfully establish an infection, it must find a way to adhere
to the hosts cells, colonise the host tissues, and persist in the host long enough to
reproduce.
For an organism to cause disease it must:
1. Enter the host
2. Multiply within the host tissues
3. Resist or not stimulate host defence mechanisms
4. Damage the host
The following table summarises some of the strategies that the various cellular and
non-cellular pathogens use to gain access and colonise host tissues.
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Responses to Pathogens
Inquiry question: How does a plant or animal respond to infection?
Students:● investigate the response of a named Australian plant to a named pathogen through
practical and/or secondary-sourced investigation, for example:– fungal pathogens– viral pathogens
Students to complete Investigation 11.1
Immunity
Inquiry question: How does the human immune system respond to exposure to a pathogen?
Students:● analyse responses to the presence of pathogens by assessing the physical and chemical
changes that occur in the host animals cells and tissues
● investigate and model the innate and adaptive immune systems in the human body
● explain how the immune system responds after primary exposure to a pathogen, including innate and acquired immunity
Pathogens: a bacterium, virus, or other microorganism that can cause disease.
Antigens: are molecules which trigger an immune response e.g. bacteria, viruses
and a foreign marker on cell membrane.
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Lines of DefenceInnate Immunity
Innate immunity is present at birth and is genetically determined.
Its response to pathogens are non-specific, and include both physical and
chemical (first line of defence) as well as cellular responses (second line of
defence).https://www.youtube.com/watch?v=GIJK3dwCWCw
Adaptive Immunity
Adaptive immunity is the third line of defence.
This is a specific defence mechanism consisting of specialised cells that act if the
pathogen persists in its invasion.
https://www.youtube.com/watch?v=2DFN4IBZ3rI
First Line Defence mechanisms30
Barrier Method of defence
Skin
Tough physical barrier
Dry, outer layer of cells inhibits bacterial growth.
Oil and sweat glands produce antibacterial and antifungal substances.
Beneficial bacteria live off the oil secreted by sebaceous (oil) glands and produce acids that prevent pathogen growth.
Mucus membranes
Pathogens get caught in mucus which is coughed up or swallowed.
Contains antibody to prevent pathogens attaching.
Harmless microbes produce substances that inhibit growth and entry of pathogens.
Cilia Move mucus containing pathogens out of
the lungs
Chemical barriers – urinary and vaginal tracts
Acidic conditions inhibit growth and entry of pathogens.
Chemical barriers – alimentary canal
Acid of the stomach is intolerable for many pathogens.
Other pathogens cannot tolerate the basicity of the intestines.
Other body secretions – Saliva
Washes bacteria from between teeth
Contains chemicals to destroy microbes
Other body secretions – tears
Contains enzyme lysozyme that destroys some bacterial cell walls
Wash pathogens are away from eyes
Other body secretions – urine
Acidity prevents growth of pathogens
Flushes and cleans urinary system
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Second Line of DefenceAdaptation Method of defence
Inflammation response
Tissue around the wound becomes hot to inhibit activity of pathogens by denaturing the enzymes of the pathogen. Chemicals such as histamine are released, causing the tissue becomes swollen as capillaries swell to increase blood circulation to the area, allowing more white blood cells to be released to attack pathogens.
Phagocytosis
A phagocyte is a cell that can flow about another cell and engulf it. Neutrophils, manufactured in the bone marrow and found in blood-lymph and body tissues, ingest bacteria and the enzymes break down the bacterium. Macrophages engulf foreign particles and poisons, common in the liver and lymph glands, and are more commonly involved in fighting off long infections.
Lymph system
Lymph nodes filter the lymph fluid and remove pathogens, dead cells and other debris. Lymph nodes contain phagocytes to destroy any foreign material.
Cell death
If other responses cannot control the pathogen, a layer of dead cells (granuloma) is formed around infection site, followed by a layer of macrophages. Pathogens eventually die and are consumed by macrophages.
Third Line of Defence - Acquired Immunity32
MacFarlane Burnet’s work in the middle of the twentieth century contributed to a better understanding of the immune response and the effectiveness of immunisation programs.
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Description Role
Antibodies
Proteins that the body produces when it detects specific antigens
Different antigens stimulate the production of different corresponding antibodies
Join with antigens, causing them to clump together to form an antibody-antigen complex
Antigen-antibody complex is more easily recognised and destroyed by macrophages than antigens alone
B cell
Special kind of lymphocyte
Produced in bone marrow
Control antibody-mediated immunity
When a B cell recognises an antigen, it is cloned to produce a mass of identical cells.
The B cells work as antibody producers (plasma cells) or memory B cells which provide long-term immunity.
T cell
Special kind of lymphocyte
Produced in bone marrow
Mature in thymus gland
Control cell-mediated immunity
Cytotoxic T cells produce toxic substances that destroy cells that have been invaded by a pathogen. They defend the body cancer cells and transplanted tissue.
Helper T cells help B cells divide rapidly.
Suppressor T cells turn off the immune response and suppress the production of antibodies when they are not needed.
Memory T cells recognise the antigen if it is re-introduced, providing long-term immunity.
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Both B and T lymphocytes attack the same antigen and must interact.
Antigen presenting B cells are inspected by helper T cells.
Helper T cells stimulate B cells and T cells to clone.
Helper T cells stimulate the production of antibodies by plasma cells.
Suppressor T cells stop the production of B cells and T cells when the antigen is
destroyed.
Your body can produce the most effective weapons against the invaders, which
may be bacteria, viruses or parasites. Other types of T-cells recognise and kill
virus-infected cells directly. Some help B-cells to make antibodies, which
circulate and bind to antigens.
With the help of T-cells, B-cells make special Y-shaped proteins called
antibodies. Antibodies stick to antigens on the surface of germs, stopping them
in their tracks, creating clumps that alert your body to the presence of intruders.
Your body then starts to make toxic substances to fight them. Patrolling
defender cells called phagocytes engulf and destroy antibody-covered intruders
Mechanisms that allow interaction between B and T lymphocytes
Interaction occurs through cell contact or the production of chemicals by the T cells e.g. interleukins which cause B cells to divide.Helper T cells (T4 cells) are able to recognise “self” molecules that mark the surfaces of B cells, preventing T cells from attacking the person’s own B cells if the B cell has an antigen on its surface.
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Range of T lymphocyte types and the difference in their roles
Type of T lymphocyte Role
Killer (cytotoxic) T cells (Tc cells)
Attack and destroy body cells that have been infected by an antigen by producing toxic chemicals (perforins) which cause the cell membrane to rupture and the cell lyses
Helper T cells (T4 cells)
Secrete chemicals such as lymphokines and interleukins that stimulate cloning in B and T cells and stimulate macrophages for phagocytosis
Memory T cellsRemain in the body and reactivate quickly with subsequent infections by the same antigen
Suppressor T cells (T8 cells)Stop the production of B and T cells and suppress antibody production when the antigen is destroyed
Prevention, Treatment and Control
Inquiry question: How can the spread of infectious diseases be controlled?
Students:● investigate and analyse the wide range of interrelated factors involved in limiting local,
regional and global spread of a named infectious disease
Factors involved in monitoring and control.
The three main factors to consider in monitoring and control:
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Local factors
Local factors include neighbourhoods, towns, cities etc.
Regional factors
The United Nations divides the world into five regions: Africa, the Americas, Asia,
Europe and Oceania.
Global factors
The global factors encompasses the whole world. Increasing the amount of people
around the globe has increased the difficulty in limiting the spread of infectious
disease.
Factors involved in disease transmission.
The causes of the spread of disease can be multi-factorial involving local, regional
and global factors.
Pathogen factors
Some pathogens are virulent (and can cause disease in small numbers. (A virulent
disease is dangerous and spreads or affects people very quickly)
Other pathogens need to be present in large numbers to cause of these rates.
Some pathogens form reserves in food, water or the environment.
Others must be a transferred directly from host to host.
Host factors
The fact that the host is invaded by a pathogen does not mean that the host will get
the disease.
The immune system of the host may prevent the disease from developing.
The health of the host also plays a role in the development of the disease.
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The environmental and geological factors
Certain environments may predispose the spread of infectious diseases.
Pathogens may build-up a large reservoir in certain environments which produces a
greater risk of outbreaks. For example, in areas of natural disasters such as
earthquakes and floods.
Societal factorsSocietal factors may further enhance the spread of disease.For example diseases such as chickenpox and measles can return in society due to anti-vaccination campaigns.
Case Study P451Students read and summarise Pages 451 to 453 in context of the syllabus dot point.
● investigate procedures that can be employed to prevent the spread of disease, including but not limited to:
- hygiene practices- quarantine- vaccination, including passive and active immunity - public health campaigns- use of pesticides- genetic engineering
HygieneHygiene can be divided into two types: personal and community hygiene.
Personal hygiene involves keeping the body and any openings on it clean.
This reduces the risk of pathogens and entering the body or the transmission of
pathogens to others.
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Community hygiene
Community hygiene helps prevent the build-up of pathogenic organisms in a
community.
Community hygiene includes the following measures:
Sewage and garbage disposal
Sterilization and disinfection of equipment in medical practices.
City planning
Clean food and water prevents the transfer all pathogens
QuarantineDue to Australia’s geographical isolation it remains one of the world’s countries
least affected by serious diseases and pests.
The Department of Agriculture and Water Resources (DWAR) is responsible for
Australia’s biosecurity.
The role of quarantine is to minimize the risk of exotic pests and diseases entering
Australia, in order to protect our native flora and fauna, our agricultural industries
and our health.
Plants and animals that are placed into quarantine when entering Australia. Sick
passengers are also quarantined when entering Australia. The Australian
Quarantine and Inspection Services (AQIS) is responsible for this.
VaccinationVaccination involves the introduction of a vaccine (A vaccine is a biological
preparation that provides active acquired immunity to a particular disease.)
Immunization is the process in which the body reacts to a vaccine by going through
the immune response.
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Active acquired immunity
Active acquired immunity is when the immune response occurs and memory cells are
produced.
It can be naturally induced or be artificially induced (through vaccination).
Vaccines contain cultures of micro-organisms, which may be either:
1. Living but attenuated (weakened) and therefore harmless, e.g rabies and
measles
2. Dead, e.g typhoid and whooping cough
Passive acquired immunityPassive acquired immunity involves the introduction of the antibodies (the
immunoglobulins) into the body to prevent a disease from developing.
The antibodies have been produced by another organism that has had the disease.
For example, if you have been exposed to hepatitis A, you may be given injections
of the antibodies to prevent you from catching the disease. This is the only a short
term immunity.
Public health campaignsThe approach to controlling infectious diseases can be that and down into four
categories, known as RICE.
Resolution of governments and health organizations to find solutions to
infectious diseases.
Information in the form of epidemiological studies and scientific studies of
the pathogen and it’s mode of transmission so that the solution it is based on
accurate data.
Coordination of efforts on a local, regional and global scale so that resources
are used efficiently.
Education of human populations on a local, regional and global scale
regarding factors affecting infectious disease transmission.
Notifiable diseases include measles, botulism, cholera, meningococcal
infection, pertussis (whooping cough) and malaria.
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Use of pesticides
Pesticides are chemicals used to kill the pests of plants and animals, including
the vectors that transmit them.
Pesticides can be classified into three groups:
1. Insecticides – kill insects e.g. DDT
2. Fungicides – kill fungal pathogens
3. Herbicides – kill weeds and sometimes or plants
Genetic engineering
Genetic engineering involves altering the genetic composition of an organism.
This can give the organism resistance to disease or other designed characteristics.
Procedures used include gene cloning, forming transgenic species and genetic
engineering to give disease resistance, (for example BT cotton).
Check your understanding 13.2 b 1, 2, 3, 5, 6 & 7
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● investigate and assess the effectiveness of pharmaceuticals as treatment strategies for the control of infectious disease, for example: – antivirals– antibiotics
Pharmaceuticals for controlling infectious diseaseChemotherapy is a general term that means the use of any drug to treat any disease,
(it does not just mean the treatment of cancer).
Antimicrobial agents are designed to control infectious diseases caused by microbes.
The main classes of antimicrobials are:
Antiviral medicationsViruses enter as cells which then reproduce the virus.
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The genetics of viruses vary in the following ways:
They may contain DNA or RNA
The antiviral medications are used to control viral infections.
They do not kill viruses, but inhibit their development inside affected cells.
They do not do cure the disease but simply slow down its progress, allowing the
body’s natural defences to take over.
They stop the spread of viral diseases, and therefore, are a useful addition to the
control of the epidemics and pandemics.
The viruses most commonly targeted by antiviral drugs include:
HIV
Seasonal influenza A
Herpes
Hepatitis B and C
Three antiviral medicines to treat influenza and registered for use in Australia:
Oseltamivir (Tamiflu ®)
Zanamivir (Relenza ®)
Amantadine (Symmetrel ®)
These compounds are effective against seasonal influenza A strains.
Efficacy is important, (efficacy of a medication is its ability to produce the desired
outcome.), as nations stockpile the medications in case of a pandemic.
These drugs have greater efficacy when taken early in the course of the illness.
Antibiotics
Antibiotics are used to control bacterial infections.
They work by either killing or slowing down the growth of bacteria.
Antibiotics are not effective against viruses.
Antibiotics are most effective when:
They are used solely for the treatment of bacterial infections.
Bacterial antibiotics are used to kill rather than inhibit growth of the bacteria,
(penicillins and cephalosporins).
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Narrow spectrum antibiotics are chosen that target the specific pathogen.
They are able to get to the site of the infection and kill the bacteria.
The whole course is taken to reduce the risk of bacterial resistance.
A Gram stain and culture and sensitivity tests are done to ensure that the
appropriate antibiotic has been chosen.
(Gram staining is a common technique used to differentiate two large groups
of bacteria based on their cell wall constituents.
Check Your Understanding 13.3 p451 1, 2, 4, 5
● investigate and evaluate environmental management and quarantine methods used to control an epidemic or pandemic
Environmental management and quarantine methods.Case study: Ebola virus disease 2014 – 2016Students read and summarise pages 451 to 453
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● interpret data relating to the incidence and prevalence of infectious disease in populations, for example:– mobility of individuals and the portion that are immune or immunised – Malaria or Dengue Fever in South East Asia
The accumulation of real-time data on infectious diseases is currently managed in
Australia by both Federal and State/Territory governments.
The constant threat of new and emerging diseases as well as the re-emergence of
old diseases (e.g. tuberculosis and measles) requires a robust system of data
gathering and analysis.
The type of data that must be collected includes:
Incidence and prevalence of the disease – determines what pathogens are
present in a population.
Mobility of the population
Percentage of the population that is immunised against an infectious disease.
Incidence
The incidence of an infectious disease is the number of new cases occurring
during a specified time.
To calculate the incidence of a disease as a percentage, the following formula can
be used:
For example, a survey was conducted in a school with 1000 students. Over the winter period 150 students contracted influenza. The prevalence is:
Prevalence = 150 x 100 = 15%1000
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Mobility
The mobility of a population determines the rate at which a disease will spread.
The rate of immunisation of a population is a key factor in analysing data relating
to infectious disease.
When a significant proportion of the population have been immunised, this
creates herd immunity.
Herd immunity relies on high numbers of individuals being vaccinated, to reduce
the chances of unvaccinated individuals coming into contact with the disease-
causing microbe.
When the population has herd immunity, everyone in that population, including
unvaccinated individuals, are protected against epidemics.
- Malaria or Dengue Fever in South East Asia
Investigation 13.5aCheck Your Understanding 13.5 p457 1, 3, 5
● evaluate historical, culturally diverse and current strategies to predict and control the spread of disease
Historical Control of a Disease Outbreak
Investigation 13.6
Cultural Control of the Spread of Disease.
Culture refers to the integrated patterns of human behaviour, including the
language, thoughts, communications, actions, customs, beliefs, values and
institutions of racial, ethnic, religious or social groups.
In 2014 control of the Ebola outbreak in South Africa was made it difficult
through local culture. The traditional ritual of paying respects to the deceased
through close contact with the corpse promoted the spread of the disease.
Control measures needed to include educating the public to abandon these
traditional cultural belief systems.
Check Your Understanding 13.6
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● investigate the contemporary application of Aboriginal protocols in the development of particular medicines and biological materials in Australia and how recognition and protection of Indigenous cultural and intellectual property is important, for example:
– bush medicine– smoke bush in Western Australia
Students Read and Summarise p 459 to 460“Aboriginal protocols in the development of medicines.”
Investigation 13.7 Students produce the table in the method.
For example, The Emu bushhttp://anpsa.org.au/APOL22/jun01-2.html
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