Abstract
AbstractBovine respiratory syncytial virus (BRSV) is a major cause of respiratory disease in cattle. Genomic sequencing can resolve phylogenetic relationships between virus populations, which can be used to infer transmission routes and potentially inform the design of biosecurity measures. Sequencing of short (<2000 nt) segments of the 15 000-nt BRSV genome has revealed geographic and temporal clustering of BRSV populations, but insufficient variation to distinguish viruses collected from herds infected close together in space and time. This study investigated the potential for whole-genome sequencing to reveal sufficient genomic variation for inferring transmission routes between herds. Next-generation sequencing (NGS) data were generated from experimental infections and from natural outbreaks in Jämtland and Uppsala counties in Sweden. Sufficient depth of coverage for analysis of consensus and sub-consensus sequence diversity was obtained from 47 to 20 samples respectively. Few (range: 0–6 polymorphisms across the six experiments) consensus-level polymorphisms were observed along experimental transmissions. A much higher level of diversity (146 polymorphic sites) was found among the consensus sequences from the outbreak samples. The majority (144/146) of polymorphisms were between rather than within counties, suggesting that consensus whole-genome sequences show insufficient spatial resolution for inferring direct transmission routes, but might allow identification of outbreak sources at the regional scale. By contrast, within-sample diversity was generally higher in the experimental than the outbreak samples. Analyses to infer known (experimental) and suspected (outbreak) transmission links from within-sample diversity data were uninformative. In conclusion, analysis of the whole-genome sequence of BRSV from experimental samples discriminated between circulating isolates from distant areas, but insufficient diversity was observed between closely related isolates to aid local transmission route inference.
Funder
Vetenskapsrådet
HORIZON EUROPE Framework Programme
Publisher
Springer Science and Business Media LLC
Reference63 articles.
1. Valarcher JF, Taylor G (2007) Bovine respiratory syncytial virus infection. Vet Res 38:153–180
2. Stokstad M, Klem TB, Myrmel M, Oma VS, Toftaker I, Osteras O, Nodtvedt A (2020) Using biosecurity measures to combat respiratory disease in cattle: the Norwegian control program for bovine respiratory syncytial virus and bovine coronavirus. Front Vet Sci 7:167
3. De Jong MC, van der Poel WH, Kramps JA, Brand A, van Oirschot JT, Mourits MC, Nielen M, Frankena K, Schukken YH (1996) Quantitative investigation of population persistence and recurrent outbreaks of bovine respiratory syncytial virus on dairy farms. Am J Vet Res 57:628–633
4. Thomas LH, Stott EJ, Jones PW, Jebbett NJ, Collins AP (1980) The possible role of respiratory syncytial virus and Pasteurella spp in calf respiratory disease. Vet Rec 107:304–307
5. Valarcher JF, Bourhy H, Lavenu A, Bourges-Abella N, Roth M, Andreoletti O, Ave P, Schelcher F (2001) Persistent infection of B lymphocytes by bovine respiratory syncytial virus. Virology 291:55–67
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