Novel influenza A viruses in pigs with zoonotic potential, Chile.

influenza A virus pigs zoonosis

Journal

Microbiology spectrum
ISSN: 2165-0497
Titre abrégé: Microbiol Spectr
Pays: United States
ID NLM: 101634614

Informations de publication

Date de publication:
06 Mar 2024
Historique:
medline: 6 3 2024
pubmed: 6 3 2024
entrez: 6 3 2024
Statut: aheadofprint

Résumé

Novel H1N2 and H3N2 swine influenza A viruses (IAVs) have recently been identified in Chile. The objective of this study was to evaluate their zoonotic potential. We perform phylogenetic analyses to determine the genetic origin and evolution of these viruses, and a serological analysis to determine the level of cross-protective antibodies in the human population. Eight genotypes were identified, all with pandemic H1N1 2009-like internal genes. H1N1 and H1N2 were the subtypes more commonly detected. Swine H1N2 and H3N2 IAVs had hemagglutinin and neuraminidase lineages genetically divergent from IAVs reported worldwide, including human vaccine strains. These genes originated from human seasonal viruses were introduced into the swine population since the mid-1980s. Serological data indicate that the general population is susceptible to the H3N2 virus and that elderly and young children also lack protective antibodies against the H1N2 strains, suggesting that these viruses could be potential zoonotic threats. Continuous IAV surveillance and monitoring of the swine and human populations is strongly recommended.IMPORTANCEIn the global context, where swine serve as crucial intermediate hosts for influenza A viruses (IAVs), this study addresses the pressing concern of the zoonotic potential of novel reassortant strains. Conducted on a large scale in Chile, it presents a comprehensive account of swine influenza A virus diversity, covering 93.8% of the country's industrialized swine farms. The findings reveal eight distinct swine IAV genotypes, all carrying a complete internal gene cassette of pandemic H1N1 2009 origin, emphasizing potential increased replication and transmission fitness. Genetic divergence of H1N2 and H3N2 IAVs from globally reported strains raises alarms, with evidence suggesting introductions from human seasonal viruses since the mid-1980s. A detailed serological analysis underscores the zoonotic threat, indicating susceptibility in the general population to swine H3N2 and a lack of protective antibodies in vulnerable demographics. These data highlight the importance of continuous surveillance, providing crucial insights for global health organizations.

Identifiants

pubmed: 38446039
doi: 10.1128/spectrum.02181-23
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0218123

Auteurs

Rodrigo Tapia (R)

Universidad de Chile, Santiago, Chile.

Bárbara Brito (B)

Universidad de Chile, Santiago, Chile.
Department of Pediatric Infectious Diseases and Immunology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
University of Technology Sydney, Sydney, New South Wales, Australia.

Marco Saavedra (M)

Department of Pediatric Infectious Diseases and Immunology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.

Juan Mena (J)

Universidad de Chile, Santiago, Chile.

Tamara García-Salum (T)

Department of Pediatric Infectious Diseases and Immunology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.

Raveen Rathnasinghe (R)

Department of Pediatric Infectious Diseases and Immunology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.

Gonzalo Barriga (G)

Department of Pediatric Infectious Diseases and Immunology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.

Karla Tapia (K)

Department of Pediatric Infectious Diseases and Immunology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.

Victoria García (V)

Universidad de Chile, Santiago, Chile.

Sergio Bucarey (S)

Universidad de Chile, Santiago, Chile.

Yunho Jang (Y)

Centers for Disease Control and Prevention (CDC), Atlanta, Georgia, USA.

David Wentworth (D)

Centers for Disease Control and Prevention (CDC), Atlanta, Georgia, USA.

Montserrat Torremorell (M)

University of Minnesota, St. Paul, Minnesota, USA.

Víctor Neira (V)

Universidad de Chile, Santiago, Chile.

Rafael A Medina (RA)

Department of Pediatric Infectious Diseases and Immunology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
Department of Pathology and Experimental Medicine, School of Medicine, Emory University, Atlanta, Georgia, USA.
Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Classifications MeSH