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Evaluating the potential of whole-genome sequencing for tracing transmission routes in experimental infections and natural outbreaks of bovine respiratory syncytial virus.
Johnson, Paul C D; Hägglund, Sara; Näslund, Katarina; Meyer, Gilles; Taylor, Geraldine; Orton, Richard J; Zohari, Siamak; Haydon, Daniel T; Valarcher, Jean François.
Affiliation
  • Johnson PCD; School of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Glasgow, UK. Paul.Johnson@glasgow.ac.uk.
  • Hägglund S; HPIG. Unit of Ruminant Medicine. Department of Clinical Sciences, Swedish University of Agricultural Sciences (SLU), Uppsala, Sweden.
  • Näslund K; Department of Microbiology, National Veterinary Institute, SVA, Uppsala, Sweden.
  • Meyer G; IHAP, Université de Toulouse, INRAE, ENVT, Toulouse, France.
  • Taylor G; The Pirbright Institute, Pirbright, Woking, UK.
  • Orton RJ; MRC-University of Glasgow Centre for Virus Research, Glasgow, UK.
  • Zohari S; Department of Microbiology, National Veterinary Institute, SVA, Uppsala, Sweden.
  • Haydon DT; School of Biodiversity, One Health and Veterinary Medicine, University of Glasgow, Glasgow, UK.
  • Valarcher JF; HPIG. Unit of Ruminant Medicine. Department of Clinical Sciences, Swedish University of Agricultural Sciences (SLU), Uppsala, Sweden.
Vet Res ; 53(1): 107, 2022 Dec 12.
Article in En | MEDLINE | ID: mdl-36510312
ABSTRACT
Bovine 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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cattle Diseases / Respiratory Syncytial Virus, Bovine / Respiratory Syncytial Virus Infections Limits: Animals Language: En Journal: Vet Res Journal subject: MEDICINA VETERINARIA Year: 2022 Type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cattle Diseases / Respiratory Syncytial Virus, Bovine / Respiratory Syncytial Virus Infections Limits: Animals Language: En Journal: Vet Res Journal subject: MEDICINA VETERINARIA Year: 2022 Type: Article Affiliation country: United kingdom