13 - Viral interactions Flashcards

Viral interactions (recombination, complementation, phenotype mixing, interference, virus exaltation).

1
Q

What is defined as viral environment?

A
  • Another virus
  • Host cell
  • Host organism
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2
Q

When does viral interaction occur?

A
  • Only during multiplication (vegetative virus)
  • Simultaneous infection of the same cell
  • Only between certain viruses (usually related viruses, but not always)
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3
Q

Types of viral interactions

A
  • Advantagous
    • On nucleic acid level (recombination)
    • On protein level (complementation, phenotype mixing)
  • Disadvantageous (interference)
  • Neutral (virusexaltation)
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4
Q

Advantagous interaction

Recombination

A
  • On nucleic acid level
  • Excange of genetic information → new virus generation - inherited new properties
  • At least 20-40 nucleotide homology between the viruses is needed
  • Intramolecular recombination:
    • Derailing of the polymerase during replication
    • Aujeszky’s disease virus: even 70% transfer
    • Sometimes between non-related viruses (Polyomavirus ⟷ adenovirus)
    • Also with RNA virus (i.e. FMDV)
  • Genetic reassortment:
    • Viruses with segmented genome (ie. orthomyxoviridae)
    • Excange of segments during viral assembly
    • Sudden, major antigenic cahnges → antigenic shift
  • Reactivation;
    • Cross-reactivation:
      • Attenuated vaccine strain + related virus
      • Repair of the defected virulence-genes
      • i.e herpesviruses
    • Multiple reactivation:
      • Between two attenuated virus-strains
      • Different defected genome regions
      • Mutual completion

→ Do not use different live vaccines within a short time interval!

Figure: intramolecular recombination

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5
Q

Advantagous interaction

Complementation

A
  • On protein level
  • Between defective and cometent (helper) viruses
  • Exchange of enzymes (mainly polymerase) → multiplication of the defected virus
    • Heat sensitive mutant + wild type virus
    • Avirulent virus + inactivated virulent virus (pox)
    • Dependovirus + adenovirus
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6
Q

Advantagous interaction

Phenotype mixing

A
  • On protein level
  • Exchange of structural proteins
  • Leukosis virus + sarcoma virus: acquiring envelope proteins
  • Transcapsidation if a similar capsid (poliovirus + coxsackievirus)
  • Non-heritable!
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7
Q

Disadvantageous interaction

Interference

A
  • One virus inhibits the multiplication of the other
  • Adsorption interference:
    • Competition for the same cell-surface receptor, either:
      • Related viruses
      • After phenotype mixing
      • Different viruses, but the same receptor (ie. CAR)
  • Autointerference:
    • _​_Complete and incomplete forms of the same virus
    • Also at adsorption
    • Incomplete virion: shorter nucleic acid → higher mobility, polymerase affinity
    • Competition for enzymes, ribosomes → defective interfering particles
    • Large amounts of incomplete progeny viruses → self-limiting infections (paramyxoviridae, rhabdoviridae)
  • Heterologous interference:
    • _​_Non-related viruses
    • Viral suppressor protein production
    • Ie.: herpesvirus, adenovirus, inhibits pox
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8
Q

Neutral interaction

Virusexaltation

A
  • The viruses are able to multiplicate independently
  • The simultaneous infection does not effect the multiplication

But….

  • Changes the viral influence on the host cell or organism:
    • Increased pathogenicity (Poliovirus + Coxsackievirus in monkey)
    • Cytopathic effect appears (Classical swine fever virus, BVDV + Newcastle disease virus)
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