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Viral Evolution

Viral genomes can evolve very rapidly for a number of different reasons:

  • High rates of mutation – RNA and ss-DNA are less stable and viruses lack proofreading enzymes

  • Short generation times – Evolution occurs across successive generations and viruses have a typical infectious cycle of ~8–72 hours

  • Large population sizes – Each infectious cycle can produce large quantities of new virions (>100)

Examples of viruses that undergo rapid evolution are influenza viruses and human immunodeficiency virus (HIV)

  • Influenza viruses have an infectious cycle of 6 – 12 hours and may produce populations of up to 10,000 virions

  • HIV has one of the highest mutation rates of any virus (~0.34 mutations per replication cycle)

Mechanisms of Viral Evolution

There are two different mechanisms by which viruses may evolve to avoid immune detection and destruction

  • Viral evolution can occur progressively via antigenic drift or spontaneously via antigenic shift

Antigenic Drift:

  • Antigenic drift occurs when the accumulation of point mutations lead to a gradual change in the surface proteins of the virus

  • Consequently, antibodies produced against the original virus may no longer be able to recognise the new viral strain

  • Antigenic drift can lead to seasonal reoccurrences of a virus and require new vaccinations (booster shots) to confer protection

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Antigenic Shift:

  • Antigenic shift occurs when cells get infected with multiple viral strains and the gene segments from the two strains get reassorted

  • This results in a sudden dramatic change in antigenicity and a new viral sub-type is formed to which an entire population is susceptible

  • Antigenic shift can result in new viral sub-types that may cross species barriers and lead to massive outbreaks (i.e. pandemics)

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Treatment of Viral Diseases

Rapidly evolving viruses are able to evade detection by an organism’s immune system and consequently cause disease

  • Vaccines need to be constantly changed and updated to remain effective against different viral strains

  • Infectious individuals may need to be isolated (quarantined) to limit the spread of viral infection

  • Contact tracing and health related databases may be used for monitoring and predicting disease spread

  • Viral propagation may be reduced by targeting vectors of viral delivery (e.g. via water chlorination, fumigation)

  • Disease-resistant vectors may be introduced via genetic engineering (e.g. sterile mosquitoes)

  • Social strategies may commonly involve government legislations designed to support scientific interventions

    • Education programmes may be used to inform the public of associated risks (to help minimise exposure)

    • Laws may be passed to ensure public compliance (e.g. customs protocols or vaccination mandates)