Key result
Analysis of full open reading frame sequences of foot-and-mouth disease viruses in Southeast Asia revealed frequent inter- and intra-lineage recombination, challenging traditional capsid-based evolutionary histories.
Observational (n=96)
Analysis of non-structural protein coding sequences provides new insights into FMDV recombination patterns and evolutionary interdependence, challenging traditional capsid-based phylogeny.
Frequent recombination may confound FMDV strain tracking; leaves open whether full-genome surveillance should replace capsid phylogenies.
Recombination of rapidly evolving RNA-viruses provides an important mechanism for diversification, spread, and emergence of new variants with enhanced fitness. Foot-and-mouth disease virus (FMDV) causes an important transboundary disease of livestock that is endemic to most countries in Asia and Africa. Maintenance and spread of FMDV are driven by periods of dominance of specific viral lineages. Current understanding of the molecular epidemiology of FMDV lineages is generally based on the phylogenetic relationship of the capsid-encoding genes, with less attention to the process of recombination and evolution of non-structural proteins. In this study, the putative recombination breakpoints of FMDVs endemic to Southeast Asia were determined using full-open reading frame sequences. Subsequently, the lineages' divergence times of recombination-free genome regions were estimated. These analyses revealed a close relationship between two of the earliest endemic viral lineages that appear unrelated when only considering the phylogeny of their capsid proteins. Contrastingly, one lineage, named O/CATHAY, known for having a particular host predilection (pigs) has evolved independently. Additionally, intra-lineage recombination occurred at different breakpoints compared to the inter-lineage process. These results provide new insights about FMDV recombination patterns and the evolutionary interdependence of FMDV serotypes and lineages.
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Brito et al. (2018) conducted an observational in Foot-and-mouth disease virus (FMDV) evolution (n=96). Full open reading frame sequence analysis was evaluated on Recombination breakpoints and divergence times of recombination-free genome regions. Analysis of full open reading frame sequences of foot-and-mouth disease viruses in Southeast Asia revealed frequent inter- and intra-lineage recombination, challenging traditional capsid-based evolutionary histories.
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