03/09f Diagnostic Virology Flashcards

1
Q

Is there such thing as a ‘broad-spectrum’ antiviral?

A

NO - antivirals are specific to certain viruses

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2
Q

Why do we need specific diagnoses for viruses?

A

To treat infections with specific antiviral chemotherapy
To institute appropriate control measures
To decrease inappropriate therapy and unnecessary hospitalization
For education and awareness of viral disease

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3
Q

What are the strategies to diagnose viral infections in the lab? Name four

A

1) Viral isolation in cell culture systems
2) Antigen detection of proteins unique to specific viruses
3) Nucleic acid detection through PCR
4) Detection of immune response in the host

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4
Q

Why is viral isolation a nonspecific means of detecting virus?

A

ANY virus might result from culture isolation, including one that was not in your differential

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5
Q

What information must be used in conjunction with viral cell culture in order to make a preliminary diagnosis?

A

Clinical history
Source of specimen
Timing and characteristics of cytopathic effects
Host range of virus in vitro

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6
Q

What is a shell vial?

A

A vial that contains an enhanced environment to encourage fast virus growth

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7
Q

What are the advantages of viral isolation? List three

A

1) Gold standard of diagnosis for viruses that will growth in cell culture
2) Permits detection of unexpected viruses
3) Permits the performance of additional assays such as identification and speciation, antiviral susceptibility, and PCR/sequencing

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8
Q

What are the disadvantages of viral isolation? List four

A

1) Maintenance of cell culture is expensive, labor-intensive, and slow
2) Not available in all labs
3) Some viruses only grow in certain cell culture systems
4) Some viruses won’t grow in culture at all

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9
Q

What is viral antigen detection?

A

Method that uses tagged monoclonal antibodies to identify specific viral epitopes
Must have an idea of what virus it might be

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10
Q

What are the advantages of antigen detection?

A

1) Rapid (1-2 hours)
2) Does not require the presence of infectious or viable virus
3) Does not require cold-chain specimen transport
4) Amenable to batch testing
5) Able to assess specimen quality

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11
Q

What are the disadvantages of antigen detection?

A

1) Less sensitive than other methods because there is no amplification of the sample
2) Requires specific reagents, some of which can be carcinogenic
3) Some specimens are not suitable for antigen detection (result in nonspecific reactions)
4) Not applicable to all viruses

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12
Q

What is fluorescent antibody staining?

A

Method that uses a monoclonal antibody specific to a viral epitope, and a fluorescent marker
Widely used for viral antigen detection

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13
Q

What are the two procedures possible for fluorescent antibody staining?

A

Direct - antiviral antibody is conjugated with a fluorescent marker
Indirect - uses fluorescently-tagged secondary antibody

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14
Q

What are the advantages of fluorescent antibody techniques?

A

Direct - simple, fast

Indirect - more sensitive

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15
Q

What are the disadvantages of fluorescent antibody techniques?

A

Direct - requires fluorescent conjugation to each antiviral antibody, which is expensive
Indirect - more time-consuming
Both are subjective and complex tests

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16
Q

What is an enzyme immunoassay?

A

Method that uses a ‘capture’ antibody that is fixed to a solid surface and binds the antigen of interest
Antigen is directly or indirectly detected with a secondary antibody
Substrate produces a quantifiable color change (read with a spectrophotometer)

17
Q

What are the advantages to EIAs?

A

1) Rapid
2) Can be batched and automated for large volumes of specimens
3) Can also be performed individually on a STAT basis
4) Can be applied to diverse type of specimens
5) Does not require intact live virus

18
Q

What are the disadvantages of EIAs?

A

1) Less sensitive than culture
2) Most monoclonal antibody has low affinity - can be washed away
3) Requires very specific reagents
4) Not applicable to all viruses

19
Q

What are three methods of nucleic acid detection of viruses?

A

1) Direct hybridization
2) Target (template) amplification - PCR, used most often
3) Signal amplification

20
Q

What is direct hybridization? What specific assays rely on this technique?

A

Direct detection of viral nucleic acid without amplification, using a nucleic acid probe
Assays include dot blot, liquid hybridization, and Southern blot
Lack sensitivity - best for specimens with a high titer of target protein (like Hepatitis B)

21
Q

What is target amplification?

A

PCR

22
Q

What are the advantages of PCR?

A

Highly sensitive

Rapid

23
Q

What are the disadvantages of PCR?

A

Too sensitive for some applications (latent viruses)
Expensive
Reaction can be inhibited by a variety of substances

24
Q

What is signal amplification?

A

Method in which nucleic acid is hybridized to a probe (nucleic acid is NOT amplified)
Signal is amplified by binding many detector molecules to each target-probe hybrid
Example - hybrid capture assay

25
Q

What are the advantages of signal amplification?

A

Simpler than target amplification

Not susceptible to carryover contamination (unlike PCR)

26
Q

What are the disadvantages of signal amplification?

A

Not as sensitive as PCR

27
Q

How do you obtain serologic evidence of an acute infection?

A

Look for seroconversion in serial specimens - rising or falling titer of virus-specific antibodies from acute to convalescent phase
Presence of virus-specific IgM in an acute phase specimen can indicate infection

28
Q

In what types of viral infections do you want to test CSF in addition to serum?

A

Rabies - virus-specific antibody in CSF is diagnostic

Encephalitis viruses - virus-specific IgM is diagnostic

29
Q

What are the advantages of serological tests?

A

Useful for viruses that can’t be cultured
For certain viruses (that usually cause chronic infection), the presence of antibodies is diagnostic
Determines patient’s immune status to specific viruses

30
Q

What are the disadvantages of serological tests?

A

May take a long time (need both acute and convalescent samples)
May not be accurate for patients who have received a number of blood transfusions
Some viral infections may react non-specifically (false positive)