4.7 Article

Evolution of an Eurasian Avian-like Influenza Virus in Naive and Vaccinated Pigs

Journal

PLOS PATHOGENS
Volume 8, Issue 5, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.ppat.1002730

Keywords

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Funding

  1. Wellcome Trust
  2. Veterinary Training and Research Initiative
  3. Defra [VT0105]
  4. Alborada Trust
  5. RAPIDD of the Science & Technology Directorate, Department of Homeland Security
  6. National Institutes of Health [R01 GM080533-05]
  7. Fogarty International Center, National Institutes of Health
  8. BBSRC [BBS/E/T/000PR6193] Funding Source: UKRI
  9. MRC [G0801822] Funding Source: UKRI
  10. Biotechnology and Biological Sciences Research Council [BBS/E/T/000PR6193] Funding Source: researchfish
  11. Medical Research Council [G0801822] Funding Source: researchfish

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Influenza viruses are characterized by an ability to cross species boundaries and evade host immunity, sometimes with devastating consequences. The 2009 pandemic of H1N1 influenza A virus highlights the importance of pigs in influenza emergence, particularly as intermediate hosts by which avian viruses adapt to mammals before emerging in humans. Although segment reassortment has commonly been associated with influenza emergence, an expanded host-range is also likely to be associated with the accumulation of specific beneficial point mutations. To better understand the mechanisms that shape the genetic diversity of avian-like viruses in pigs, we studied the evolutionary dynamics of an Eurasian Avian-like swine influenza virus (EA-SIV) in naive and vaccinated pigs linked by natural transmission. We analyzed multiple clones of the hemagglutinin 1 (HA1) gene derived from consecutive daily viral populations. Strikingly, we observed both transient and fixed changes in the consensus sequence along the transmission chain. Hence, the mutational spectrum of intra-host EA-SIV populations is highly dynamic and allele fixation can occur with extreme rapidity. In addition, mutations that could potentially alter host-range and antigenicity were transmitted between animals and mixed infections were commonplace, even in vaccinated pigs. Finally, we repeatedly detected distinct stop codons in virus samples from co-housed pigs, suggesting that they persisted within hosts and were transmitted among them. This implies that mutations that reduce viral fitness in one host, but which could lead to fitness benefits in a novel host, can circulate at low frequencies.

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