LG 6.8 - Medical Virology Flashcards

1
Q
Pandemic
Epidemic
Outbreak
Endemic
Seasonal
Sporadic
Eliminated
Eradicated
A
  • Present in a widespread region, possibly worldwide
  • Present at a higher level than usually found in a community or population
  • Suddenly present in a distinct population
  • Present at a fairly constant level
  • Incidence peaks during a specific time of year
  • Random, not associated with an outbreak
  • No longer circulating in a given geographic region, control measures still necessary
  • Permanently eliminated from circulation worldwide, controls measures no longer necessary
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2
Q

(1) Emerging infectious diseases?
Re-emerging infectious diseases?
Deliberating emerging infectious diseases?

A
  • Previously unknown or undetected infectious agents
  • Known pathogens who incidence had decreased in the past but has reappeared
  • Agents with potential to be used for bioterrism
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3
Q

(1) Activities that increase exposure to infectious agents?

A
  • Population movements
  • Urbanization (old tires - mosquitos)
  • Long-distance travel
  • Natural disaster
  • Global climate change
  • Technologies (blod transfusions)
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4
Q

(1) Activities that increase susceptibility to infectious agents?

A
  • Microbial adaptation
  • Poverty and social inequality
  • War and famine
  • Lack of public will
  • Immunosuppresion
  • opting out of vaccine.
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5
Q

(6) What type of viruses replicate in the cytoplasm which in the nucleus?

A
  • RNA is cytoplasm for the most part.

- DNA is nucleus for the most part.

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6
Q

(6) For translation, what is the name of the site for the start of translation and what is the name of the end site on the DNA?

A
  • Start = promotor region.

- End = polyadenylation site.

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7
Q

(6) What do (-) sense RNA viruses have to bring with them, why?

A
  • Bring their own RNA transcriptase.

- In order to replicate their (-) RNA into (+) RNA to be translated.

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8
Q

(6) How do retroviruses translate their RNA?

A
  • Reverse transcriptase into DNA back into RNA then translate.
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9
Q

(7) How are mutations in viruses beneficial but also harmful for humans?

A
  • Beneficial: can use these mutations to make viruses that are non-virulent in vaccines that will stimulate immune system but trigger no immune response. DI.
  • Harmful: can use these mutations to evade our immune system (influenza). Phenotype mixing.
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10
Q

(7) What is the difference between antigenic drift and shift?

A
  • Antigenic drift: random mutations and virus genotypes drift from the origin.
  • Antigenic shift: genetic shuffling between viruses to create new genotypes.
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11
Q

How do naked (capsid-only) viruses enter host cell?

A

endocytosis (viroplexis)

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12
Q

How do enveloped viruses enter the host cell?

A

endocytosis (virplexis) and direct fusion (only enveloped viruses can do this)

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13
Q

how do enveloped viruses exit the host cell?

A

budding

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14
Q

how do naked viruses leave the host cell?

A

lysis

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15
Q

What are some characteristics of viral translation?

A

The most always follow rules of eukaryotic translation: 1. Contain a 5’ cap & 3’ poly(A) tail

  1. Splicing in the nucleus, then exported
  2. Be monocistronic (one mRNA = one protein) with initiation at first AUG
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