Viruses Flashcards

Alex Lecture 2 (24 cards)

1
Q

how are viruses imaged?

A

using electron microscopy.
electron beams to look at structures

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2
Q

what are polymorphic viruses?

A

viruses with no defined shape

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3
Q

what is a bacteriophage?

A

a virus that infects and replicates within bacteria

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4
Q

why are all viruses described as “obligate” intracellular parasites?

A

obligate = cannot REPRODUCE outside of host cell

vs facultative intracellular parasites can live / reproduce either inside or outside of cells

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5
Q

key features of viruses

A
  1. evolve rapidly, highly error prone
  2. hijack the host’s synthetic/energy/transport systems

also: diversity of morphology (shape)

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6
Q

what is the Baltimore Classification of viruses based on? explain the classes.

A

how viruses produce mRNA (necessary to hijack host’s translation machinery to produce viral proteins).

type: DNA or RNA
strand: Single or Double
Polarity: + or - for ssRNA
replication strategy

–> 7 classes

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7
Q

what is the difference between positive and negative sense RNA viruses?

A

+ve sense: orientation is same sense as mRNA, can be directly translated.

-ve sense: complementary to mRNA, must first be TRANSCRIBED to +RNA using RNA dependent RNA polymerase before translation

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8
Q

approximately spherical viruses are described as what shape?

A

icosahedral (20 faces)

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9
Q

what does a pleomorphic mean? (shape)

A

pleomorphic = varying morphology, varied shapes and sizes due to lipid envelope

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10
Q

define subunit (of a virus)

A

single folded polypeptide chains (ie protein molecule) making up part of the viral capsid

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11
Q

define structural unit (virus)

A

protomer = repeating assembly of subunits, forming the basic building block of the capsid

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12
Q

define capsid

A

the protein shell that encloses the viral genome, made up by assembling protomers (which are made up of subunits) into capsomers

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13
Q

define nucleocapsid

A

the viral genome + the capsid

can be the whole virion for non-enveloped viruses.

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14
Q
A
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15
Q

what does the concept of “Genetic economy” refer to in general?

A

viruses, due to limited genomic space, adopt a design that minimises the number of protein subunits needed

ie. max efficiency in protein product/structure

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16
Q

what does the Caspar-Klug theory refer to?

A

a construction theory, building on the idea of genetic economy.

allows for the construction of large, complex capsids from a small number of protein subunits, using triangulation numbers to describe the organisation of subunits on the capsid surface

17
Q

name the give key stages of the virus replication cycle (ie. how viruses interact with cells)

A
  1. Absorption / Attachment
  2. Penetration (endocytosis), viral DNA enters host cell
  3. Eclipse phase (biosynthesis of viral proteins)
  4. Assembly / maturation
  5. Virion release / exocytosis

DRAW DIAGRAM

18
Q

why is understanding the virus replication cycle important for biotech?

A

the replication offers lots of opportunity to develop antiviral strategies (literally possible to inhibit at every step)

19
Q

how do viruses attach themselves to host cells?

A

interactions between viral proteins on the envelope/capsid and receptors on the host cell membrane (eg. GPCRs)

HIGHLY SPECIFIC binding – viruses can only infect cells with the appropriate receptor

20
Q

two methods of virion release (final stage of replication cycle)

A

lytic or non-lytic (virion particles can be exocytosed)

21
Q

what are prodrugs?

A

a compound with little/no pharmacological activity, until metabolised in the body it converts to the active drug

eg. being converted to a triphosphate by some enzyme –> active form

22
Q

how can antiviral drugs use virus specific kinases?

A

use these kinases to selectively activate only in infected cells

ie. prodrug activated by virus specific kinase by phosphorylation

23
Q

why are a cocktail of drugs often used to treat viral infections?

A
  • viruses mutate rapidly, would evolve resistance to one type of drug quickly
  • complete viral suppression - different drugs block multiple steps

eg. HAART, to treat HIV

24
Q

what technology derived from viruses may be a viable antibody alternative?

A

phage therapy