Bornaviridae, Astroviridae & Prions Flashcards

1
Q
Borna disease virus is mostly detected in? 
USA
Iceland
Africa
Central Europe
A

Central Europe

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2
Q
The fatal form of Borna disease is:
the neurological disease 
      the gastrointestinal disease
the reproductive tract disease
the mucosal disease
A

the neurological disease

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3
Q

“Dribbling and champing of jaws” is a clinical sign of Borna disease.
True
False

A

True

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4
Q

Eosinophilic intranuclear inclusion bodies in neurons called “Joest-Degen” bodies are pathognomonic for Borna disease Virus infection.
True
False

A

True

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5
Q
Ante-mortem diagnosis is of Borna disease is difficult mainly because of similarities in neurological manifestation. Which is of following diseasescan be considered as differentials?

EHV-1 infection
rabies
West Nile
       All above options are valid
A

All above options are valid

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6
Q
What disease does the avian bornavirus cause?
rhinotracheitis
osteopetrosis
“Big leg” syndrome
Proventricular dilatation disease
A

Proventricular dilatation disease

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7
Q

During infection with the avian bornavirus, proventricular dilatation is a direct result of:
progressive indigestion
progressive neurological dysfunction
diarrhoea
inappetence

A

progressive neurological dysfunction

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8
Q
Although Astroviruses are known to cause diarrhoea in many animal species, however, a fatal diarrheic disease can be observed only in:
birds
humans
pigs
cattle
A

birds

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9
Q
Astroviruses have a linear, positive sense, single-stranded RNA and the RNA is:
semi-infectious
quiescent
non-infectious
infectious
A

infectious

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10
Q
The term prion means:
primitive form of virus
infectious protein or rogue protein
non-infectious protein
precarious protein
A

infectious protein or rogue protein

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11
Q

What classification system is used for prions?
microorganism classification system
Bergey’s manual of systematic bacteriology
There is no classification system for prions yet
International committee on taxonomy of viruses

A

There is no classification system for prions yet

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12
Q
What is the abnormal form of the prion protein?
PrPsc
PrPc
PrP
PrPs
A

PrPsc

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13
Q
Prion proteins are mostly expressed in:
muscle cells
enterocytes
neurons and lymphoreticular cells
skull osteocytes
A

neurons and lymphoreticular cells

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14
Q

Why are prions difficult to eliminate?
there envelope coat is resistant to proteases
they are resistant to chemical and physical conditions
they are made of RNA that is resistant to ultraviolet light
they are invisible

A

they are resistant to chemical and physical conditions

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15
Q

How do prions replicate?
they use reverse transcriptase to transcribe their genetic material
they are amplified by Taq polymerase
by transduction
the PrPsc catalyses the conversion of PrPc into PrPsc

A

the PrPsc catalyses the conversion of PrPc into PrPs

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16
Q
Scrapie is a prion disease mainly found in:
pigs
sheep
camels
cattle
A

sheep

17
Q

In animals infected with the scrapie prion, histopathological lesions are characterized by wide spread inflammatory reaction in the brain.
True
False

A

False

18
Q

Why has prion infection in cattle been termed “mad cow disease”?
constant mooing of the affected animal
aimless wondering of the affected animal
Abnormal posture and progressive apprehensive behaviour of the affected animal
weight loss of the affected animal

A

Abnormal posture and progressive apprehensive behaviour of the affected animal

19
Q
Although the transmission of prions is not fully known, what is the accepted mode of transmission currently?
oral route
ticks
mosquitoes
thrips
A

oral route

20
Q

Histopathological examination of a brain from a cow suspected to have died from Bovine spongiform encephalopathy would show:
Astrocytic hypoplasia
Neuronal vacuolation and degeneration
lymphocytes infiltration around neurons
vestibular neuronitis

A

Neuronal vacuolation and degeneration