Intro to Virology Flashcards

1
Q

Compare the attachment sites of enveloped vs. non-enveloped viruses.

A

Attachment sites in non-enveloped viruses have a 3D structure; while glycoprotein spikes in enveloped viruses serve that purpose.

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2
Q

Describe the significance of the negative (-) ss RNA strands and how they differ from the (+).

A

(-) ss RNA strands must be TRANSCRIBED first into message before being translated.

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3
Q

Define tissue tropism in regards to viral entry.

A

Tissue tropism refers to a specific cell that a virus will attach to due to its receptor.

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4
Q

Compare/contrast the mode of entry between enveloped and non-enveloped viruses into host tissues.

A

Non-enveloped viruses use 3D proteins to enable their endocytosis into the host cell. Enveloped viruses (2 mechs) can fuse with host membrane via glycoprotein-receptor interaction (uncoated).

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5
Q

Distinguish the way in which RNA and DNA viruses replicate in the host cell. What are the exceptions of each.

A

RNA viruses replicate in the cytoplasm (exc. influenza). DNA viruses replicate in the nucleus (exc. POX virus).

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6
Q

Briefly describe viral replication in 6 steps.

A
  1. enters via receptors
  2. Makes enzymes
  3. makes more genome
  4. makes structural proteins
  5. packages new viral particles; assembly
  6. envelope buds out of host cell for release
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7
Q

Describe the 2 ways in which new viral progeny can be released from host cell.

A
  1. ) Lysis

2. ) Budding off - where virus acquires glycoproteins and envelope on the way out

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8
Q

Briefly describe the 4 effects that viruses have on host cells.

A
  1. No apparent effect
  2. Kill host cells (LYSIS)
  3. Fuse infected cells (multi-nucleated GIANT cells)
  4. Transform cells (MALIGNANT)
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9
Q

Describe what enables the fusion of virally-infected cells.

A

Glycoprotein spikes that were activated by the viral progeny facilitates fusion of infected cells.

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10
Q

Briefly describe the protocol for viral plaque assay in 3 steps.

A
  1. Dilute a viral stock
  2. infect a monolayer of cells
  3. Each area of clearing represents a functional, LIVE PARTICLE
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11
Q

Define Hem-agglutination and how it can be used to detect a virus.

A

the ability to agglutinate RBCs (i.e. measles or influenza) will be shown as a pale sheen of RBCs in test tubes; negative result will show as a pellet at the bottom.

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12
Q

Define hemagglutination inhibition and the significance of a (+) result.

A

If the patient has antibodies against the virus, they will be neutralized and no hemagglutination will result. This is shown as a red pellet at the bottom of the tube.

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13
Q

Distinguish a virion from a virus.

A

A virion is a viral particle; whereas each virus has a specific morphology to its virion. For example, the polio virus has an “icosahedral virion”

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14
Q

What viral component do neutralizing antibodies bind to in the case of Polio virus?

A

Nucleocapsid protein

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15
Q

Define the limitation of serologic diagnosis of viral infections.

A

Presence of antibody in a single sample may not be sufficient for a diagnosis of current infection.

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16
Q

Which of the following assays will detect only infectious virions: ELISA, PCR, Hemagglutination, Plaque assay, Western Blot? Define it.

A

Plaque assay - a method to count the number of LIVE VIRAL particles that may be infectious

17
Q

What is the function of nucleocapsid in all viruses?

A

Protect the genome from nuc leases

18
Q

Where does the variation which creates multiple serotypes occur in viruses?

A

Structural variation of proteins at the virus surface

19
Q

Differentiate the early phase from the late phase of the viral replication cycle.

A

Early phase = production of viral enzymes;

Late phase = production of structural proteins and assembly of new virions

20
Q

What mode of immune defense does a virus escape by spreading from one cell to another by induction of uninfected cells with infected cells?

A

Neutralization of virions by antibody. This is possible since the virus doesn’t need to go into circulation to spread from one cell to the next.