viral zoonoses (rabies and vhfs)- 2013 (fn) [compatibility mode].pdf
TRANSCRIPT
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Viral ZoonosesViral Zoonoses -- Rabies andRabies andViral haemorrhagic feversViral haemorrhagic fevers
Dr F Noordeen
Department of Microbiology
Faculty of Medicine
University of Peradeniya
May 2013
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Modes of transmission and the pathogenesis of viral
zoonoses including rabies in humans
Clinical features of viral zoonoses including rabies
Principles of diagnosis, management and prevention
viral zoonoses including rabies in Sri Lanka
Learning outcomes
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Aim:
Make students aware pathogenesis &ake students aware pathogenesis &clinical significance of rabies virusclinical significance of rabies virus
Objectives:
1. to diagnose a clinical presentation of
rabies (History + Symptoms + Lab)
2. to prevent disease progression after anexposure (post exposure immunization)
3. to prevent/control rabies in Sri Lanka
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Rabies and rabies virus Rabies - Acute viral infection resulting
in encephalomyelitis
Family - RHABDOviridae - (Bullet shaped)
Genus - LYSSAvirus - (Madness)
Genome - ssRNA
Envelope - Lipoprotein envelope Hosts - All warm blooded animals + man
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EM appearanceEM appearance Rabies virusRabies virus
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PathogenesisPathogenesis
Animal biteAnimal bite C N SC N S
Salivary glands +
hair bearing tissues
Sensory nerves
Centripetal spread
Neuronal axons
Centrifugal
spreadAerosol
Conjunctiv
al/
olfactory nerve
1. Virusacquisition
2. Virus acquisition
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ClinicoClinico--pathological aspectspathological aspects
Incubation periodIncubation period -- 10 days to year or >
1. Quantity of virus deposited
2. Distance of bite site from head
OnsetOnset -- Insidious with 1-10 days of prodrome
malaise, fever, headache, psychological
disturbances, pain and tingling
around the bite - neurological phase
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Clinical presentationClinical presentation
Furious rabies
80% patients Hyperactive to
various stimuli
Dumb rabies
20% patients Hyperactivity
is absent
Paralysis
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Furious form of rabies
1. After 3/4 days
symptoms
become worse
2. Restless and
hypersensitive
to stimuli
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3. Hydrophobia
4. On attempting/site of
water produces violentspasms in respiratory& swallowing actions
5. Respiratory & cardiacarrest Death
Furious form of rabies cont...
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Dumb rabiesDumb rabies1. 20% patients may
present with this form
2. Hyperactivity is absent
3. Expressionless
4. Paralysis and death
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Infection of brain - coma and death
Antibody response is apparent only in latterstage of the disease when virus has entered
the CNS and other tissues
Rx with antibodies X progression to C N S
Rabies is fatal unless the vaccine is given
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DiagnosisDiagnosis
Clinical - History of animal bite and
neurological signs
Lab tests - to confirm diagnosis
Viral antigen in skin by FAT (AM)
Viral specific inclusion bodies (70-90%)
hippocampus of brain (PM)(Sellers stain or Mann stain)
Antibodies in serum + CSF in terminal
disease
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Negri bodies in the brain section
Rabies virus antigen -IFA
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Epidemiology
Spread - Zoonosis
Urban rabies - Unvaccinated dogs & catsWild rabies - Wild animals
Transmission - Animal bite or aerosols
Risk group - Veterinarians, veterinarystudents, animal handlers, wild lifeofficers, students/scientists involve inecological/zoological camping
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Occurrence - Worldwide, common in Sri
Lanka, India and Latin AmericaFree in Australia and some islands
Prevention1. Vaccination of reservoirs
(pet dogs/cats)
2. Vaccination of high risk personals3. Stray dog elimination
4. Proper post exposure immunization
5. Public education programs on rabies
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TreatmentTreatment
Human vaccine - human diploid cellculture vaccine - HDCV (killed by
formaldehyde or propiolactone) Post exposure treatment - prevent
disease
Immediate cleaning of wound
Vaccination with killed vaccine
Administration of human rabies Igs (ARS)
Symptoms - Death is inevitable
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Rabies immunisation (HDVC)
Pre-exposure Rx
3 dose regime
Day 0, 7, 21 or 28
Route - deep
subcutaneous/IM
Post-exposure Rx
5 dose regime
Day 0, 3, 7, 14, 28
Route - deepsubcutaneous/IM
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Human rabies
a. May be transmitted by the bite of cats
b. May be prevented by adequate immunization and
control of dogs
c. The best available vaccine is the human diploidcell culture vaccine
d. Specific immunoglobulin should be injected
around the bite wound as soon as possible after
the bitee. The development of hypersensitivity reactions are
major complication of the human diploid cell
culture vaccine
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RNA viruses includeRNA viruses include
a. Chicken pox virus
b. Rabies virus
c. Hepatitis A virus
d. Hepatitis C virus
e. Hepatitis B virus
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Viral haemorrhagic fevers (VHFs)Viral haemorrhagic fevers (VHFs)
Aetiology:A number of arboviruses (Toga
and Bunyaviruses) and some similar viruses
(Arena and Filoviruses)
Disease: Similar to the rather non-specific
flu-like illness but which rapidly progresses to
a severe disseminated illness with a markedbleeding tendency and multi-organ failure
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There is usually a considerable mortality
in VHFs
The following may produce a similar
clinical picture & requires to be excluded
Meningococcal disease
Rickettsial disease
Leptospirosis
Hepatitis
Malaria
Snake bites
Tryponosomiasis
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Crimean Congo Haemorrhagic Fever (CCHF)
Eastern Europe, Central and Southern Africa
Yellow fever Could be urban
Lassa fever West Africa
Ebola Africa
Marburg Central Africa
Hanta Africa and Asia
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FAMILY Bunyaviridae
GENUS Hantavirus
More than 30 different hantavirus
species have been found (20 of whichare known to be pathogenic to humans)
Hantavirus infection/disease
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Hantavirus diseaseHantavirus disease
1. Hemorrhagic fever with renal syndrome (HFRS)
2. Hantavirus pulmonary disease (HPS)
Deer mouse Cotton rat
Rice rat White footed mouse
Hantavirus
vectors
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PreventionPrevention
Avoid contact with rodents and their habitats
Do not keep rodents as pets
Keep all food in sealed containers
Virions may be stable for 2 days on a dry surface sodisinfect areas contaminated by rodents
Disinfect using a 10% solution of household bleach
Eradication unlikely due to the large percentage ofrodents which carry these viruses
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Three young men presented to Pollunnaruwa hospital with a 2 day
history of high fever with chills, intense myalgia and deteoriating
renal function. Two required ventilation due to respiratorycomplications. They all gave a history of exposure to rats during
different activities they perform in the paddy stores and
warehouses they work.
1. What 2 infective diseases may produce these clinicalfeatures and what is the route of transmission in each of the
diseases? (30 Marks)
2.How can you make an aetiological diagnosis of ONE
disease that you have identified in 2.2. (50 Marks)
3.How can you advise those who work in similar settings to
prevent exposure to infective agent responsible for the above
clinical scenario. (20 marks)