MM0 Flashcards

(32 cards)

1
Q

Viruses were first described as?

A

Filterable agents

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2
Q

Mimivirus genome is how large?

A

1.2 million base pairs

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3
Q

What virus suggested that viruses may represent the fourth domain of life?

A

Mimivirus

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4
Q

Why did mimivirus suggest viruses may represent the fourth domain of life?

A
  • Genome larger than some bacteria
  • Larger than Rickettsia bacterial species
  • Contained genes associated with translation
  • Genes encoding proteins for amino/nucleotide synthesis, does not rely on the host for these pathways
  • Can be infected by virophages including Sputnik
  • Although, does not encode a ribosome
  • Also undergoes assembly of progeny instead of division
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5
Q

What is pathogenesis?

A

Pathogenesis is a qualitative description of disease

It includes the biological mechanisms a pathogen uses to cause disease and the ability of a pathogen to cause disease

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6
Q

What is virulence?

A

It is quantitative and relative (non-scalar)

It is the extent of disease caused

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7
Q

How can virulence be measured?

A

Morbidity
Mortality
Temperature during fever etc…

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8
Q

Before the advent of tissue culture how were viruses studied?

A

In vivo passage

In ovo passage

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9
Q

How can the number of infectious particles present be measured?

A

Plaque assays

End point assays

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10
Q

Which assay was used first?

A

End-point essay

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11
Q

What is the end point?

A

The dilution at which 50% of cells/animals are infected

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12
Q

Why are end-point assays still used today?

A

For viruses that do not produce plaques

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13
Q

Describe how a plaque assay works?

A

10 fold dilutions
Inoculate a tissue monolayer with aliquots
Allow time for the viruses to attach
Place agar layer on top to restrict infection of viruses to neighbouring cells only
Use a dye to colour the cells, areas of cell death are represented by a colourless plaque

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14
Q

What is the pfu?

A

Plaque forming unit

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15
Q

How can the titre of the original virus stock be calculated?

A

Using the number of plaque forming units obtained

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16
Q

What is the particle/pfu ratio?

A

When using an electron microscope particles of viruses can be identified. If this is higher than the pfu it means that many of the virus particles assembled were non-infectious e.g. did not contain viral genome/ functioning viral genome

17
Q

What does MOI stand for?

A

Multiplicity of infection

18
Q

What is moi?

A

The number of viral particles to cells present

19
Q

MOI of 1?

A

There is one viral particle per cell present

20
Q

What is virulence?

A

Virulence is non-scalar (relative). It is a quantitative measure of the extent of disease.

21
Q

How can virulence be measured?

A

Virulence can be measured by:

  • Mortality
  • Morbidity
  • Temperature change (fever)
  • Weightloss
22
Q

What is pathogenicity?

A

Pathogenicity is a qualitative description of the ability of a pathogen to cause disease. Includes the biological mechanisms by which the pathogen causes disease

23
Q

What were the two strains of smallpox?

A

Variola major and variola minor

24
Q

Which strain of smallpox was more virulent?

A

Variola major was more virulent as it had a fatality rate of 20%, variola minor only had a fatality rate of around 1-2%

25
Describe viruses which result in acute infection?
Influenza Ebola Smallpox
26
Describe viruses which have a latent lifestyle?
Herpes virus
27
Describe viruses which have a chronic lifestyle:
HBV HCV HIV
28
Example of a localised infection caused by a virus?
HPV infection is restricted to the genitals
29
Example of a virus capable of systemic infection and their route of spread?
Rabies spreads via the nerves HSV can spread via the nerves Polio can spread via the blood HIV can spread via the blood
30
What can determine the tropism of a virus?
Viral tropism can be determined by the cell receptors- the receptors by which it gains cell entry
31
What determines the tropism of HIV?
The presence of the chemokine receptors | Only present on white blood cells which is why it infects these
32
What determines the tropism of HCV?
A micro RNA miRNA-122 This is produced in abundance in hepatocytes It binds upstream of the IRES in the 5' UTR and stabilises the genome allowing translation to begin