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Updated: Dec 6, 2025

Isolation of Fidelity Variants of RNA Viruses and Characterization of Virus Mutation Frequency
Published on: June 16, 2011
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.
Abstract:
The low fidelity of foot-and-mouth disease virus (FMDV) RNA-dependent RNA polymerase allows FMDV to exhibit high genetic diversity. Previously, we showed that the genetic diversity of FMDV plays an important role in virulence in suckling mice. Here, we mutated the amino acid residue Phe257, located in the finger domain of FMDV polymerase and conserved across FMDV serotypes, to a cysteine (F257C) to study the relationship between viral genetic diversity, virulence, and transmissibility in natural hosts. The single amino acid substitution in FMDV polymerase resulted in a high-fidelity virus variant, rF257C, with growth kinetics indistinguishable from those of wild-type (WT) virus in cell culture, but it displayed smaller plaques and impaired fitness in direct competition assays. Furthermore, we found that rF257C was attenuated in vivo in both suckling mice and pigs (one of its natural hosts). Importantly, contact exposure experiments showed that the rF257C virus exhibited reduced transmissibility compared to that of wild-type FMDV in the porcine model. This study provides evidence that FMDV genetic diversity is important for viral virulence and transmissibility in susceptible animals. Given that type O FMDV exhibits the highest genetic diversity among all seven serotypes of FMDV, we propose that the lower polymerase fidelity of the type O FMDV could contribute to its dominance worldwide.IMPORTANCE Among the seven serotypes of FMDV, serotype O FMDV have the broadest distribution worldwide, which could be due to their high virulence and transmissibility induced by high genetic diversity. In this paper, we generated a single amino acid substitution FMDV variant with a high-fidelity polymerase associated with viral fitness, virulence, and transmissibility in a natural host. The results highlight that maintenance of viral population diversity is essential for interhost viral spread. This study provides evidence that higher genetic diversity of type O FMDV could increase both virulence and transmissibility, thus leading to their dominance in the global epidemic.
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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