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The use of genome wide association methods to investigate pathogenicity, population structure and serovar in Haemophilus parasuis.
Howell, Kate J; Weinert, Lucy A; Chaudhuri, Roy R; Luan, Shi-Lu; Peters, Sarah E; Corander, Jukka; Harris, David; Angen, Øystein; Aragon, Virginia; Bensaid, Albert; Williamson, Susanna M; Parkhill, Julian; Langford, Paul R; Rycroft, Andrew N; Wren, Brendan W; Holden, Matthew T G; Tucker, Alexander W; Maskell, Duncan J.
Afiliação
  • Howell KJ; Department of Veterinary Medicine, University of Cambridge, Madingley Road, Cambridge, CB3 0ES, UK. kjh52@cam.ac.uk.
  • Weinert LA; Department of Veterinary Medicine, University of Cambridge, Madingley Road, Cambridge, CB3 0ES, UK. lucy.weinert@gmail.com.
  • Chaudhuri RR; Department of Molecular Biology and Biotechnology, University of Sheffield, Firth Court, Western Bank, Sheffield, S10 2TN, UK. r.chaudhuri@sheffield.ac.uk.
  • Luan SL; Department of Veterinary Medicine, University of Cambridge, Madingley Road, Cambridge, CB3 0ES, UK. sl470@cam.ac.uk.
  • Peters SE; Department of Veterinary Medicine, University of Cambridge, Madingley Road, Cambridge, CB3 0ES, UK. sep34@cam.ac.uk.
  • Corander J; Department of Mathematics and Statistics, University of Helsinki, Helsinki, 00100, Finland. jukka.corander@helsinki.fi.
  • Harris D; The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK. deh@sanger.ac.uk.
  • Angen Ø; Norwegian Veterinary Institute, N-0106, Oslo, Norway. Oystein.Angen@vetinst.no.
  • Aragon V; Centre de Recerca en Sanitat Animal (CReSA), UAB-IRTA, Campus de la Universitat Autònoma de Barcelona, 08193, Bellaterra, and, Institut de Recerca i Tecnologia Agroalimentàries (IRTA), Barcelona, Spain. Virginia.Aragon@cresa.uab.cat.
  • Bensaid A; Centre de Recerca en Sanitat Animal (CReSA), UAB-IRTA, Campus de la Universitat Autònoma de Barcelona, 08193, Bellaterra, and, Institut de Recerca i Tecnologia Agroalimentàries (IRTA), Barcelona, Spain. albert.bensaid@cresa.uab.es.
  • Williamson SM; Animal Health and Veterinary Laboratories Agency (AHVLA), Rougham Hill, Bury St Edmunds, Suffolk, IP33 2RX, UK. Susanna.Williamson@ahvla.gsi.gov.uk.
  • Parkhill J; The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK. parkhill@sanger.ac.uk.
  • Langford PR; Department of Medicine, Section of Paediatrics, Imperial College London, St. Mary's Campus, London, W2 1PG, UK. p.langford@imperial.ac.uk.
  • Rycroft AN; The Royal Veterinary College, Hawkshead Campus, Hatfield, AL9 7TA, Hertfordshire, UK. ARycroft@rvc.ac.uk.
  • Wren BW; Faculty of Infectious & Tropical Diseases, London School of Hygiene & Tropical Medicine, Keppel Street, London, WC1E 7HT, UK. brendan.wren@lshtm.ac.uk.
  • Holden MT; School of Medicine, University of St. Andrews, St Andrews, KY16 9TF, UK. mh3@sanger.ac.uk.
  • Tucker AW; Department of Veterinary Medicine, University of Cambridge, Madingley Road, Cambridge, CB3 0ES, UK. awt1000@cam.ac.uk.
  • Maskell DJ; Department of Veterinary Medicine, University of Cambridge, Madingley Road, Cambridge, CB3 0ES, UK. djm47@cam.ac.uk.
BMC Genomics ; 15: 1179, 2014 Dec 24.
Article em En | MEDLINE | ID: mdl-25539682
BACKGROUND: Haemophilus parasuis is the etiologic agent of Glässer's disease in pigs and causes devastating losses to the farming industry. Whilst some hyper-virulent isolates have been described, the relationship between genetics and disease outcome has been only partially established. In particular, there is weak correlation between serovar and disease phenotype. We sequenced the genomes of 212 isolates of H. parasuis and have used this to describe the pan-genome and to correlate this with clinical and carrier status, as well as with serotype. RESULTS: Recombination and population structure analyses identified five groups with very high rates of recombination, separated into two clades of H. parasuis with no signs of recombination between them. We used genome-wide association methods including discriminant analysis of principal components (DAPC) and generalised linear modelling (glm) to look for genetic determinants of this population partition, serovar and pathogenicity. We were able to identify genes from the accessory genome that were significantly associated with phenotypes such as potential serovar specific genes including capsule genes, and 48 putative virulence factors that were significantly different between the clinical and non-clinical isolates. We also show that the presence of many previously suggested virulence factors is not an appropriate marker of virulence. CONCLUSIONS: These genes will inform the generation of new molecular diagnostics and vaccines, and refinement of existing typing schemes and show the importance of the accessory genome of a diverse species when investigating the relationship between genotypes and phenotypes.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Haemophilus parasuis / Estudo de Associação Genômica Ampla Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Haemophilus parasuis / Estudo de Associação Genômica Ampla Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals Idioma: En Ano de publicação: 2014 Tipo de documento: Article