Polymerase Fidelity Contributes to Foot-and-Mouth Disease Virus Pathogenicity and Transmissibility In Vivo

Chen Li1, Jiabao Shi1, Haiwei Wang2

  • 1Division of Livestock Infectious Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, People's Republic of China.

Journal of Virology
|October 8, 2020
PubMed

Insights

Foot-and-mouth disease virus (FMDV) genetic diversity is crucial for its virulence and transmissibility. A high-fidelity FMDV variant showed reduced virulence and spread in pigs, highlighting the importance of viral diversity.

Area of Science:

  • Virology
  • Molecular Biology
  • Animal Health

Background:

  • Foot-and-mouth disease virus (FMDV) exhibits high genetic diversity due to its error-prone RNA polymerase.
  • Previous research linked FMDV genetic diversity to increased virulence in animal models.

Purpose of the Study:

  • To investigate the role of FMDV genetic diversity in virulence and transmissibility.
  • To create and characterize a high-fidelity FMDV variant by mutating a conserved polymerase residue.

Main Methods:

  • Site-directed mutagenesis of FMDV polymerase (Phe257 to Cysteine).
  • Characterization of the resulting high-fidelity variant (rF257C) in cell culture and animal models (mice and pigs).
  • Assessment of viral fitness, virulence, and transmissibility through plaque assays, competition assays, and contact exposure experiments.

Main Results:

  • The F257C mutation yielded a high-fidelity FMDV variant (rF257C) with attenuated virulence in suckling mice and pigs.
  • rF257C displayed reduced transmissibility in a porcine model compared to wild-type FMDV.
  • Impaired viral fitness was observed for rF257C in direct competition assays.

Conclusions:

  • FMDV genetic diversity is essential for maintaining viral virulence and efficient interhost transmission.
  • The high genetic diversity of FMDV serotype O may contribute to its global dominance due to enhanced virulence and transmissibility.
  • Targeting viral polymerase fidelity could be a strategy to control FMDV spread.

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