Viruses 4 - Classification Flashcards

look at the graphs on the PowerPoint - These cards focus mainly on Avian Influenza

1
Q

What are acute self-limiting infections?
and
What are examples?

A
  • virus causes rapid, self limiting infection
  • infection cleared by the immune system, leading to recovery
  • influenza virus
  • rotavirus
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2
Q

Whare are chronic infections with a carrier?

A
  • viruses can persist fir many months in animal after symptoms have cleared such as FMDV in cattle = 24 months
  • will eventually be eliminated
  • doesn’t tend to kill the host so we have to
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3
Q

What is a latent infection?

A
  • Virus persists at very low levels
  • limited recognition by immune system of infected cells
  • no/few viral proteins expressed
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4
Q

Where do latent infections replicate?

A
  • in immune privileged sites
  • special relationship between tissue and immune system
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5
Q

Latent infections have the potential to reactivate - what does this mean and what is this usually due to?

A
  • switch from latent to productive infection
  • usually due to immunosuppression/external stimuli (sunlight/stress)
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6
Q

Name some examples of latent viruses?

A
  • IBR virus invades via nasopharynx or genital tract - proceeds to ganglionic neuron - latency
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7
Q

What is a chronic infection?

A
  • virus persists at very low levels in immune privileged sites, with slow growth
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8
Q

Name toe examples of chronic infection?

A
  • FeLV - retrovirus in oncornavirus group - causes cancer - slow, progressive disease, can persist after initial infection
  • Jaagsiekte “chase disease” = slow continuous growth
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9
Q

Classification is the same for all organisms how are they classed?

A
  • species
  • genus
  • family
  • order
  • class
  • phylum
  • kingdom
  • realm
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10
Q

What is the Baltimore system of classification based on?

A
  • based on system of messenger RNA (mRNA) synthesis
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11
Q

The Baltimore system of classification has 7 groups what are the specifications for each of these groups?

A
  • group I = double stranded DNA viruses - DsDNA
  • Group II = single stranded DNA viruses ssDNA
  • Group III = double stranded RNA viruses dsRNA
  • Group IV = positive sense single stranded RNA viruses = ssRNA (positive sense)
  • group V = negative sense single stranded RNA viruse = ssRNA (negative sense)
  • Group VI = single stransed RNA viruses with DNA intermediate in lifecycles = ssRNA (positive sense, reverse transcribing)
    Group VII = double stranded DNA viruses with an RNA intermediate in their lifecycle = dsDNA (reverse transcribing)
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12
Q

What is Avian Influenza?

A
  • 7 genera but only 1 (A) known to infect birds
  • highly contagious disease if birds - domestic and wild
  • significant economic impact
  • potential zoonosis
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13
Q

What is the mortality rate in affected flock? (AI)

A
  • up to 50% mortality
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14
Q

How is AI spread?

A
  • spread by migratory wild birds
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15
Q

What are the two forms of AI?

A
  • highly pathogenic
  • low pathogenic
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16
Q

How do you determine if AI is highly or low pathogenic?

A
  • determined by IVPI (intravenous pathogenicity index)
17
Q

How do you asses Intravenous pathogenicity index?

A
  • inoculate virus into wing vein of 10 x6 (4-8) week old chicks
  • examine every 24hrs for 10 days
  • score number if birds on symptoms = normal, sick, paralysed or dead
  • add up score after 10days = have an index
  • IVPI > 1.2 = HPAI (max 3)
  • or H5 or H7 with specified amino acid at Haemagglutinin cleavage site)
18
Q

Group VI -Group VI viruses have a positive sense, single-stranded RNA genome (so normally would replicate in cytoplasm as can be read directly into the ribosome and translation into proteins) but what do they do instead?

A
  • but replicate through a DNA intermediate.
  • The RNA is converted to DNA by reverse transcriptase
  • then the DNA is spliced into the host genome for subsequent transcription and translation using the enzyme integrase.
19
Q

Group VII - viruses have a double-stranded DNA genome, but unlike Class I viruses, how would they replicate?

A
  • they replicate via a ssRNA intermediate.
  • The dsDNA genome is gapped, and subsequently filled in to form a closed circle serving as a template for production of viral mRNA.
  • To reproduce the genome, RNA is reverse transcribed back to DNA.
20
Q

What is Haemagglutinin?

A
  • homotrimeric (3 identical polypeptide chains) glycoprotein on the surface of influenza viruses
  • amino acid sequence of the connecting peptide that cleaves H - critical factor
21
Q

What is Haemagglutinin important for?

A
  • HA important for entering cells
22
Q

What is Neuraminidase important for?

A
  • NA important for exiting cells
23
Q

How is an genome released into cytoplasm?

A
  • As pH dops , structure of HA changes, virus and ,lysosome membranes fuse and release genome into cytoplasm
24
Q

What is HA essential for? and how dies this work in AI?

A
  • binding viruses to cell surface
  • binds to sialic acid-containing receptors in target cells in respiratory tract
  • results in endocytosis - internalisation of the virus
  • creates endosome =- cell digests contents - dropping pH transformation to lysosome
25
Q

Where is the HA cleavage site?

A
  • protein cleaved unit HA1 and HA2
26
Q

What happens if there is no cleavage?

A
  • no fusion
  • no cell penetration
27
Q

What does cleavage require?

A
  • require specific enzyme
28
Q

What is LPAI HA?

A
  • Single type of amino acid = arginine at the hemagglutinin cleavage site
  • trypsin-like proteases catalyse the cleavage process
29
Q

What happens in LPAI HA acquires multiple amino acids?

A
  • open to multiple proteases (e.g., furin, PC6)
  • virus can then multiply systemically (proteases elsewhere)
  • significant increase in replication , virulence, pathogenicity
30
Q

What does virulence mean?

A
  • Virulence, a term often used interchangeably with pathogenicity, refers to the degree of pathology caused by the organism.
31
Q

What is the extent of virulence usually correlated with?

A
  • The extent of the virulence is usually correlated with the ability of the pathogen to multiply within the host and may be affected by other factors
32
Q

What is the difference between ducks and chickens AI?

A
  • Chickens – excessive, delayed cytokine response; poor cellular immune response
  • Ducks - fast, lower cytokine response; strong cellular response
33
Q

What are the general carrier of AI?

A
  • In general: waterfowl and waders – carriers – disseminate virus; get localised/widespread outbreaks in wild birds
34
Q

Where do outbreaks of AI in poultry mostly occur?

A
  • Outbreaks in poultry mostly occurred in areas where the location of farms or trade areas overlapped with habitats for wild birds
35
Q

Where do outbreaks in wild birds mainly occur?

A
  • Outbreaks in wild birds…mainly found in areas where food and shelters..” Spread to poultry via both poultry and wild birds
  • Contact with wild birds alone seems to drive the outbreaks in wild birds.