Genetic stability of foot-and-mouth disease virus during long-term infections in natural hosts

PLoS One. 2018 Feb 1;13(2):e0190977. doi: 10.1371/journal.pone.0190977. eCollection 2018.

Abstract

Foot-and-mouth disease (FMD) is a severe infection caused by a picornavirus that affects livestock and wildlife. Persistence in ruminants is a well-documented feature of Foot-and-mouth disease virus (FMDV) pathogenesis and a major concern for disease control. Persistently infected animals harbor virus for extended periods, providing a unique opportunity to study within-host virus evolution. This study investigated the genetic dynamics of FMDV during persistent infections of naturally infected Asian buffalo. Using next-generation sequencing (NGS) we obtained 21 near complete FMDV genome sequences from 12 sub-clinically infected buffalo over a period of one year. Four animals yielded only one virus isolate and one yielded two isolates of different serotype suggesting a serial infection. Seven persistently infected animals yielded more than one virus of the same serotype showing a long-term intra-host viral genetic divergence at the consensus level of less than 2.5%. Quasi-species analysis showed few nucleotide variants and non-synonymous substitutions of progeny virus despite intra-host persistence of up to 152 days. Phylogenetic analyses of serotype Asia-1 VP1 sequences clustered all viruses from persistent animals with Group VII viruses circulating in Pakistan in 2011, but distinct from those circulating on 2008-2009. Furthermore, signature amino acid (aa) substitutions were found in the antigenically relevant VP1 of persistent viruses compared with viruses from 2008-2009. Intra-host purifying selective pressure was observed, with few codons in structural proteins undergoing positive selection. However, FMD persistent viruses did not show a clear pattern of antigenic selection. Our findings provide insight into the evolutionary dynamics of FMDV populations within naturally occurring subclinical and persistent infections that may have implications to vaccination strategies in the region.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Buffaloes*
  • Cattle
  • Foot-and-Mouth Disease / epidemiology
  • Foot-and-Mouth Disease / transmission
  • Foot-and-Mouth Disease / virology*
  • Foot-and-Mouth Disease Virus / genetics*
  • Foot-and-Mouth Disease Virus / isolation & purification
  • Foot-and-Mouth Disease Virus / pathogenicity
  • Genome, Viral*
  • Phylogeny
  • RNA, Viral / genetics
  • Sequence Alignment

Substances

  • RNA, Viral

Grants and funding

This research was funded in part by ARS-USDA CRIS Project 1940-32000-061-00D. Additional funding came from the US Department of State, BEP program, under agreement 58-1940-7-161-F to the NARC in Pakistan. Part of the work was also funded through an interagency agreement between USDA-ARS and the Science and Technology Directorate of the U.S. Department of Homeland Security under Award Number HSHQDC-12-X-00060. ZA and LR were recipients of a Plum Island Animal Disease Center Research Participation Program fellowship, administered by the Oak Ridge Institute for Science and Education (ORISE) through an interagency agreement between the U.S. Department of Energy (DOE) and the U.S. Department of Agriculture (USDA). All opinions expressed in this paper are the authors’ and do not necessarily reflect the policies and views of the USDA, DOE, ORAU/ORISE.