pathogenesis chapter32 prepared by : riham alakhras

69
Pathogenesi s CHapter32 Prepared by : Riham Alakhras

Post on 21-Dec-2015

215 views

Category:

Documents


1 download

TRANSCRIPT

Page 1: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Pathogenesis

CHapter32

Prepared by : Riham Alakhras

Page 2: Pathogenesis CHapter32 Prepared by : Riham Alakhras

•Introduction• The ability of viruses to cause

disease can be viewed on two distinct levels: (1) the changes that occur within individual cells and (2) the process that takes place in the infected patient.

Page 3: Pathogenesis CHapter32 Prepared by : Riham Alakhras

•The Infected Cell• There are four main effects of virus infection

on the cell:

• (1) death,

• (2) fusion of cells to form multinucleated cells,

• (3) malignant transformation, and

• (4) no apparent morphologic or functional

change.

Page 4: Pathogenesis CHapter32 Prepared by : Riham Alakhras

•Death of the cell is probably due to inhibition of macromolecular synthesis. Inhibition of host cell protein synthesis frequently occurs first and is probably the most important effect.

Page 5: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• Inhibition of DNA and RNA synthesis may be a secondary effect. It is important to note that synthesis of cellular proteins is inhibited but viral protein synthesis still occurs.

Page 6: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• For example, poliovirus inactivates an initiation factor (IF) required for cellular mRNA to be translated into cellular proteins, but poliovirus mRNA has a special ribosome-initiating site that allows it to bypass the IF so that viral proteins can be synthesized.

Page 7: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• Infected cells frequently contain inclusion bodies, which are discrete areas containing viral proteins or viral particles. They have a characteristic intranuclear or intracytoplasmic location and appearance depending on the virus.

Page 8: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• One of the best examples of inclusion bodies that can assist in clinical diagnosis is that of Negri bodies, which are eosinophilic cytoplasmic inclusions found in rabies virus–infected brain neurons.

Page 9: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• Another important example is the owl's eye inclusion seen in the nucleus of cytomegalovirus-infected cells. Electron micrographs of inclusion bodies can also aid in the diagnosis when virus particles of typical morphology are visualized.

Page 10: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• Fusion of virus-infected cells produces multinucleated giant cells, which characteristically form after infection with herpesviruses and paramyxoviruses. Fusion occurs as a result of cell membrane changes, which are probably caused by the insertion of viral proteins into the membrane.

Page 11: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• The clinical diagnosis of herpesvirus skin infections is aided by the finding of

• 1-multinucleated giant cells

• 2-eosinophilic intranuclear inclusions in skin scrapings.

Page 12: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• A hallmark of viral infection of the cell is the cytopathic effect (CPE). This change in the appearance of the infected cell usually begins with a rounding and darkening of the cell and culminates in either lysis (disintegration) or giant cell formation.

• is an important method for quantifying the amount of virus in a sample.

Page 13: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• Infection with certain viruses causes malignant transformation, which is characterized by unrestrained growth, prolonged survival, and morphologic changes such as focal areas of rounded, piled-up cells

Page 14: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• Infection of the cell accompanied by virus production can occur

without morphologic or gross functional changes.

Page 15: Pathogenesis CHapter32 Prepared by : Riham Alakhras

•The Infected Patient• Pathogenesis in the infected patient

involves

• (1) transmission of the virus and its entry into the host;

• (2) replication of the virus and damage to cells;

• (3) spread of the virus to other cells and organs;

Page 16: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• (4) the immune response, both as a host defense and as a contributing cause of certain diseases; and

• (5) persistence of the virus in some instances.

Page 17: Pathogenesis CHapter32 Prepared by : Riham Alakhras

•The stages of a typical viral infection are the same as those described for a bacterial infection

•These stages are•?????

Page 18: Pathogenesis CHapter32 Prepared by : Riham Alakhras

•incubation period•prodromal period •specific-illness period •recovery period

Page 19: Pathogenesis CHapter32 Prepared by : Riham Alakhras

•Transmission & Portal of Entry

• Viruses are transmitted to the individual by many different routes, and their portals of entry are varied

Page 20: Pathogenesis CHapter32 Prepared by : Riham Alakhras

•Main Portal of Entry of Important Viral Pathogens.

Page 21: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Portal of Entry

VirusDisease

Respiratory tract1Influenza virusInfluenza

RhinovirusCommon cold

Respiratory syncytial virus

Bronchiolitis

Epstein-Barr virusInfectious mononucleosis

Varicella-zoster virusChickenpox

Herpes simplex virus type 1

Herpes labialis

CytomegalovirusMononucleosis syndrome

Measles virusMeasles

Mumps virusMumps

Rubella virusRubella

HantavirusPneumonia

AdenovirusPneumonia

Page 22: Pathogenesis CHapter32 Prepared by : Riham Alakhras

influenza virus

Page 23: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Rhinovirus

Page 24: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Respiratory Syncytial Virus.

Page 25: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Epstein-Barr virus 

Page 26: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Varicella zoster virus

Page 27: Pathogenesis CHapter32 Prepared by : Riham Alakhras
Page 28: Pathogenesis CHapter32 Prepared by : Riham Alakhras

herpes simplex virus 1

Page 29: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Cytomegalovirus

Page 30: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Measles

Page 31: Pathogenesis CHapter32 Prepared by : Riham Alakhras

mumps virus

Page 32: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Rubella virus

Page 33: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Hantavirus

Page 34: Pathogenesis CHapter32 Prepared by : Riham Alakhras

adenovirus

Page 35: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Gastrointestinal tract

Hepatitis A virus

Hepatitis A

PoliovirusPoliomyelitis

RotavirusDiarrhea

SkinRabies virus Rabies

Yellow fever virus

Yellow fever

Dengue virus Dengue

Human papillomavirus

Papillomas (warts)

Page 36: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Hepatitis A virus

Page 37: Pathogenesis CHapter32 Prepared by : Riham Alakhras

poliovirus

Page 38: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Rotavirus

Page 39: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Rabies virus

Page 40: Pathogenesis CHapter32 Prepared by : Riham Alakhras

yellow fever virus 

Page 41: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Dengue virus

Page 42: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Human papillomavirus

Page 43: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Genital tractHuman papillomavirus

Papillomas (warts)

Hepatitis B virus

Hepatitis B

Human immunodeficiency virus

AIDS

Herpes simplex virus type 2

Herpes genitalis and neonatal herpes

Page 44: Pathogenesis CHapter32 Prepared by : Riham Alakhras

hepatitis B

Page 45: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Human Immunodeficiency Virus

Page 46: Pathogenesis CHapter32 Prepared by : Riham Alakhras

herpes simplex virus type 2

Page 47: Pathogenesis CHapter32 Prepared by : Riham Alakhras

BloodHepatitis B virusHepatitis B

Hepatitis C virusHepatitis C

Hepatitis D virusHepatitis D

Human T-cell lymphotropic virus

Leukemia

Human immunodeficiency virus

AIDS

CytomegalovirusMononucleosis syndrome or pneumonia

TransplacentalCytomegalovirusCongenital abnormalities

RubellaCongenital abnormalities

Page 48: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Hepatitis C

Page 49: Pathogenesis CHapter32 Prepared by : Riham Alakhras

HEPATITIS D

Page 50: Pathogenesis CHapter32 Prepared by : Riham Alakhras

associated cutaneous

lymphoma

Human T-cell lymphotropic virus

Page 51: Pathogenesis CHapter32 Prepared by : Riham Alakhras

•Viruses that Commonly Cause Perinatal Infections

Page 52: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Type of Transmission

Virus

Transplacental Cytomegalovirus 

Parvovirus B19

Rubella virus

Page 53: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Parvovirus B19 virus

Page 54: Pathogenesis CHapter32 Prepared by : Riham Alakhras

At time of birthHepatitis B virus

Hepatitis C virus

Herpes simplex virus type-2

Human immunodeficiency virus

Human papillomavirus

Breast feedingCytomegalovirus

Human T-cell lymphotropic virus

Page 55: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• Animal-to-human transmission can take place either directly from the bite of a reservoir host as in rabies or indirectly through the bite of an insect vector, such as a mosquito, which transfers the virus from an animal reservoir to the person.

Page 56: Pathogenesis CHapter32 Prepared by : Riham Alakhras

•Medically Important Viruses that Have an Animal Reservoir.

Page 57: Pathogenesis CHapter32 Prepared by : Riham Alakhras
Page 58: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• Localized or Disseminated Infections

• Viral infections are either localized to the portal of entry or spread systemically through the body. The best example of the localized infection is the common cold, which involves only the upper respiratory tract

Page 59: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• Influenza is localized primarily to the upper and lower respiratory tracts.

• One of the best-understood systemic viral infections is paralytic poliomyelitis

Page 60: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• After poliovirus is ingested, it infects and multiplies within the cells of the small intestine and then spreads to the mesenteric lymph nodes, where it multiplies again. It then enters the bloodstream and is transmitted to certain internal organs, where it multiplies again.

Page 61: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• The virus reenters the bloodstream and is transmitted to the central nervous system, where damage to the anterior horn cells occurs, resulting in the characteristic muscle paralysis.

Page 62: Pathogenesis CHapter32 Prepared by : Riham Alakhras
Page 63: Pathogenesis CHapter32 Prepared by : Riham Alakhras

Primary viremia refers to the initial spread of virus in the blood from the first site of infection.

Secondary viremia occurs when primary viremia has resulted in infection of additional tissues via bloodstream, in which the virus has replicated and once more entered the circulation.

Page 64: Pathogenesis CHapter32 Prepared by : Riham Alakhras

poliomyelitis

Page 65: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• Viral replication in the gastrointestinal tract results in the presence of poliovirus in the feces, thus perpetuating its transmission to others.

Page 66: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• Some of the molecular determinants of pathogenesis have been determined by using reovirus infection in mice as a model system. This virus has three different outer capsid proteins, each of which has a distinct function in determining the course of the infection.

Page 67: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• One of the proteins binds to specific receptors on the cell surface and thereby determines tissue tropism. A second protein conveys resistance to proteolytic enzymes in the gastrointestinal tract and acts as the antigen that stimulates the cellular immune response.

Page 68: Pathogenesis CHapter32 Prepared by : Riham Alakhras

• The third protein inhibits cellular RNA and protein synthesis, leading to death of the cell. Alternatively, this third protein can play a role in the initiation of persistent viral infection.

Page 69: Pathogenesis CHapter32 Prepared by : Riham Alakhras

•MAY ALLAH LEAD

YOU ALL TO

SUCCESS !!!