Your browser doesn't support javascript.
loading
Ancestral sequence reconstruction pinpoints adaptations that enable avian influenza virus transmission in pigs.
Su, Wen; Harfoot, Rhodri; Su, Yvonne C F; DeBeauchamp, Jennifer; Joseph, Udayan; Jayakumar, Jayanthi; Crumpton, Jeri-Carol; Jeevan, Trushar; Rubrum, Adam; Franks, John; Pascua, Philippe Noriel Q; Kackos, Christina; Zhang, Yuqin; Zhang, Mengting; Ji, Yue; Bui, Huyen Trang; Jones, Jeremy C; Kercher, Lisa; Krauss, Scott; Pleschka, Stephan; Chan, Michael C W; Webster, Robert G; Wu, Chung-Yi; Van Reeth, Kristien; Peiris, Malik; Webby, Richard J; Smith, Gavin J D; Yen, Hui-Ling.
Affiliation
  • Su W; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
  • Harfoot R; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Su YCF; Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
  • DeBeauchamp J; Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore.
  • Joseph U; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Jayakumar J; Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore.
  • Crumpton JC; Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore.
  • Jeevan T; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Rubrum A; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Franks J; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Pascua PNQ; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Kackos C; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Zhang Y; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Zhang M; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
  • Ji Y; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
  • Bui HT; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
  • Jones JC; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
  • Kercher L; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Krauss S; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Pleschka S; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Chan MCW; Institute of Medical Virology, Justus Liebig University Giessen, Giessen, Germany.
  • Webster RG; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
  • Wu CY; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Van Reeth K; Genomics Research Center, Academia Sinica, Taipei, Taiwan, Republic of China.
  • Peiris M; Laboratory of Virology, Faculty of Veterinary Medicine, Department of Virology, Parasitology and Immunology, Ghent University, Merelbeke, Belgium.
  • Webby RJ; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
  • Smith GJD; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN, USA. Richard.Webby@stjude.org.
  • Yen HL; Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore. gavin.smith@duke-nus.edu.sg.
Nat Microbiol ; 6(11): 1455-1465, 2021 11.
Article in En | MEDLINE | ID: mdl-34702977
ABSTRACT
Understanding the evolutionary adaptations that enable avian influenza viruses to transmit in mammalian hosts could allow better detection of zoonotic viruses with pandemic potential. We applied ancestral sequence reconstruction to gain viruses representing different adaptive stages of the European avian-like (EA) H1N1 swine influenza virus as it transitioned from avian to swine hosts since 1979. Ancestral viruses representing the avian-like precursor virus and EA swine influenza viruses from 1979-1983, 1984-1987 and 1988-1992 were reconstructed and characterized. Glycan-binding analyses showed stepwise changes in the haemagglutinin receptor-binding specificity of the EA swine influenza viruses-that is, from recognition of both α2,3- and α2,6-linked sialosides to recognition of α2,6-linked sialosides only; however, efficient transmission in piglets was enabled by adaptive changes in the viral polymerase protein and nucleoprotein, which have been fixed since 1983. PB1-Q621R and NP-R351K increased viral replication and transmission in piglets when introduced into the 1979-1983 ancestral virus that lacked efficient transmissibility. The stepwise adaptation of an avian influenza virus to a mammalian host suggests that there may be opportunities to intervene and prevent interspecies jumps through strategic coordination of surveillance and risk assessment activities.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Swine Diseases / Adaptation, Physiological / Orthomyxoviridae Infections / Influenza A Virus, H1N1 Subtype / Influenza in Birds Type of study: Risk_factors_studies Limits: Animals Language: En Year: 2021 Type: Article

Full text: 1 Database: MEDLINE Main subject: Swine Diseases / Adaptation, Physiological / Orthomyxoviridae Infections / Influenza A Virus, H1N1 Subtype / Influenza in Birds Type of study: Risk_factors_studies Limits: Animals Language: En Year: 2021 Type: Article