1 Virus Classification, Structure, Replication Flashcards

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1
Q

How is a virus different from a bacterium? From a toxin

A

A virus can’t replicate on it’s own, but it can replicate (unlike toxins)

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2
Q

Theories of Virus Origin:

A

Cellular Origin- evolved from cells

Autopoietic Origin- once autopoietic, became dependent on cells for replication

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3
Q

RNA/DNA in a core that is protected by a protein coat. (Virus particle structure)

A

Nucleocapsid

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4
Q

A nucleocapsid is comprised of repeating subunits called _____

A

Capsomeres

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5
Q

Virus-modified cellular membranes acquired upon exit from host.

A

Envelopes

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6
Q

Exposure to lipid solvents in the lab (alcohol, ether, acetone, Freon) render _____ viruses noninfectious

A

Enveloped

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7
Q

Pros/Cons to large virus genome?

A

Pros- More effective genes/tools

Cons- High chance of error, detection

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8
Q

What do most DNA viruses need that RNA viruses do not?

What do RNA viruses need that DNA viruses do not?

A

DNA polymerase, Nucleus access

Need an RNA dependent RNA polymerase

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9
Q

____ is a major factor in virus eradication

A

Host range

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10
Q

_____ is a major determinant of virus tropism (host range)

A

Attachment

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11
Q

Binding of a virus receptor to a cellular receptor.

A

Attachment

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12
Q

Virus entry pathways:

A

Receptor mediated endocytosis

Direct penetration of plasma membrane

Non-enveloped viruses not well understood (pores, membrane disruption)

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13
Q

Influenza entry happens by:

A

HA protein- attachment and membrane fusion

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14
Q

Production of mRNA (messenger RNA) templates for protein synthesis. DNA viruses usually rely on cellular RNA polymerase. The genome of (+)ssRNA viruses can serve as mRNA.

A

Transcription

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15
Q

Production of proteins

A

Translation

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16
Q

Viral protein production can be regulated at the ____ level or the ____ level

A

Transcript (mRNA)

Translation

17
Q

Genome Replication:

  1. Define (+)ssRNA
  2. Define (-)ssRNA
A
  1. This genome serves as template for translation; polymerase makes (-)ssRNA copy as template for new genomes
  2. Virus practical must include viral polymerase which makes mRNA for translation; this genome replaces through (+)ssRNA intermediate
18
Q

Packaging of new genomes into functional particles.

A

Assembly

19
Q

Types of Virus Release:

A
  1. Lysis- best known for bacteriophage; viral molecules rupture cellular membrane
  2. Weak Lysis- depends on membrane breakdown after cell death
  3. Budding (enveloped only)- enveloped viruses use cell membrane as outer coat of virus particle
20
Q

Pros/Cons of Lytic vs Non-lytic infections

A

Lytic- Dump contents out of cell, has chance to infect other cells before immune system can respond

Non-Lytic- can stay undetected longer

21
Q

How does understanding a virus replication process help to design antivirals?

A

Find things unique to virus that target it without causing illness to host

22
Q

List the Virus Replication Kinetics curve phases (useful to asses mutations, cell entry, process design):

A
  1. Eclipse- attachment and uptake
  2. Exponential growth- replication/assembly
  3. Plateau- cell death
23
Q

Cell rounding, syncytia formation, and inclusion bodies would be observations of this infection assay:

A

Cytopathic Effect (CPE)

24
Q

Infect cells, expose virus antigen, stain with labeled antibody, count areas that flouresce would be observations of this infection assay:

A

Flourescent Focus Assay

25
Q

Cell monolayer, inoculate with dilute virus, infected cells die leaving a clear area would be observations of this infection assay:

A

Plaque Assay

26
Q

ID50, IU 50, TCID 50; Systems: tissue culture, eggs, animals; inoculate with different dilutions of virus; calculate concentration based on number infected– these would be observations of this infection assay:

A

Infectious Dose

27
Q

Direct image of virus particles, calibrate with latex bead standard would be observations of this particle assay:

A

Electron Microscopy

28
Q

Viruses that bind RBCs, mix constant number of RBCs with various virus dilutions, if virus concentration is sufficient then a matrix of RBCs and virus is formed, matrix does not allow RBCs to pellet–would be observations of this particle assay:

A

Hemagglutinin Assay

29
Q

DNA primer specific to virus, amplify the gene, very sensitive– would be observations of this genome assay:

A

Polymerase Chain Reaction

30
Q

Isolate DNA/RNA, separate by electrophoresis, use labeled DNA probe to detect–would be observations of this genome assay:

A

Southern (DNA) and Northern (RNA) Blots

31
Q

Antibody binding to virus can block infection, virus concentration determined by amount of antibody needed–would be observations of this serological assay:

A

Virus Neutralization

32
Q

Antibody recognition of virus, amplification by enzyme linked to antibody–would be observations of this serological assay:

A

ELISA (Enzyme Link Immunosorbant Assay)

33
Q

Separate proteins by electrophroresis, probe proteins using an antibody–would be observations of this serological assay:

A

Western (Protein) Blot

34
Q

Human viruses have diameters of ____

A

30-300 nm

35
Q

Viruses are classified by:

A
  1. Genome
  2. Virus particle
  3. Structure
  4. Replication Strategy