Influenza Flashcards

You may prefer our related Brainscape-certified flashcards:
1
Q

What viral family does Influenza belong to?

A

Orthomyxoviridae

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What type of genome does Influenza have?

A

segmented negative RNA genome, 8 segments

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

How are influenza isolates named?

A

Species infected; H and N type

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

H and N are… ? In relation to the influenza virus

A

the spikes on the surface of the virus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

H produces _____?

Why?

A

hemagglutinin (16 types)

Cell attachment, important for host tropism; has cleavage site that controls tissue tropism and spread, affects disease severity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

N produces _____?

Why?

A

neuramidase (9t types)

aids in release of the virus from the cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Why is a segmented genome good for a virus like influenza?

A

allows for rapid genetic evolution (mix n’ match)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Why can influenza rapidly evolve genetically?

A

segmented genome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is an antigenic change?

A

When a viral genome changes enough so as to to prevent immune protection (not quite the same virus as last time)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is antigenic drift?

why does this happen in influenza?

A

accumulation of single nucleotide changes, gradual over a long period of time

no prrofreading mechanism, mistakes are passed to progeny

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is antigenic shift?

how does this happen in relation to influenza?

A

genetic reassortment/change in combination of segments

animal infected with 2 different strains can produce new strains from genomic mix n match

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Viral replication?

A

H involved with adsorption

N involved with Release

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

It was formerly believed that pigs were the “melting pot” for new flus, however…

A

we as humans may be!

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Is an epidemic more likely to come from an antigenic drift or shift?

A

antigenic shift; antigenic drift is responsible for allowing people to be infected multiple times by the “same” virus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Anti virals were first discovered in ____ against herpesvirus by ____

A

1960s; “hit or miss”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

____ in 1980s turned attention to antivirals

A

AIDS

17
Q

Antivirals are difficult to design because _____.

Typically ____ an enzyme required for _____.

Must be take _____ or _____.

A
  • most also damage host cells
  • inactivate
  • viral replication
  • prophylactically
  • early in infection
18
Q

There are drugs that block various stages of the viral replication cycle, such as…

A
  • entry (amantadine)
  • viral component synthesis (AZT)
  • release (neuraminidase inhibitors)
19
Q

H5N1 - High Path Avian Influenza

A
  • Low pathology strain exits in US poultry and wildlife, no clinical signs in most poultry or wild birds
  • High pathology strain arose in Asia in 1996, found in Africa, Europe and Asia, has killed thousands of turkeys, chickens, and geese
  • First human case 1997, 562 human cases in 15 countries 59% fatality
20
Q

Swine Flu vs Novel H1N1

A
  • Influenza isolated from swine 1930
  • Shifted from seasonal disease to year round endemic
  • H1N1 in US swine at least 75 years; not the most predominant now and not the “novel H1N1”
  • Zoonotic disease
  • Novel H1N1 does not appear more severe for swine, may be for some subgroups of humans
21
Q

National Animal Health Laboratories Network (NAHLN) diagnostic testing in Emergency responses

A
  • Same PCR protocol for all laboratories
  • Positives confirmed by appropriate government agency, only virus isolation positive samples considered “true” positives

Avian

  • Avian flu surveillance in migratory wild birds, ended Spring 2011
  • State organizations sampling poultry

Swine (H1N1)

  • Focus on clinically ill animals and those associated with human cases
  • A basis for further study of what influenzas are circulating in swine
  • Addition of testing feral swine
22
Q

A POSITIVE result is defined as the presence of a product and is typically interpreted to indicate that the pathogen in question was present in the sample.

  • Reasons for “false positives” include: _____
  • “True positive” results can be difficult to interpret:_____
A
  • Contamination (field, lab)
  • Recent use of MLV vaccines
  • Residual nucleic acid from past infections (e.g. a latent herpesvirus infection)
  • Nonspecific amplification that produces a product of the same size, less of a problem in real-time
  • The extreme sensitivity of PCR allows detection of very small quantities of genomic material.
  • Numerous examples exist where the virus/bacteria may be present yet cause no disease (FIP/FeCV, PCV-2).
23
Q

A negative result is defined as the absence of a product.

Reasons for “false negatives” include:_____

A
  • Divergence between the sequence of the pathogen and that of the nucleotide primers
  • Presence of endogenous inhibitors in the sample
  • Fecal samples require additional steps for nucleic acid extraction
  • Hemoglobin is a known inhibitor of PCR
  • Heparin is a known inhibitor of PCR
  • Autolysis/sample degradation (probably more of a concern with RNA viruses)
  • Improper sample selection (wrong tissue, wrong time)
24
Q

Other tests:

A
  • Virus isolation-viable virus
  • Serology- rapid testing, subtype testing, confirms exposure