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      Emergence and Evolution of Novel Reassortant Influenza A Viruses in Canines in Southern China

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          ABSTRACT

          The capacity of influenza A viruses (IAVs) to host jump from animal reservoir species to humans presents an ongoing pandemic threat. Birds and swine are considered major reservoirs of viral genetic diversity, whereas equines and canines have historically been restricted to one or two stable IAV lineages with no transmission to humans. Here, by sequencing the complete genomes of 16 IAVs obtained from canines in southern China (Guangxi Zhuang Autonomous Region [Guangxi]) in 2013 to 2015, we demonstrate that the evolution of canine influenza viruses (CIVs) in Asian dogs is increasingly complex, presenting a potential threat to humans. First, two reassortant H1N1 virus genotypes were introduced independently from swine into canines in Guangxi, including one genotype associated with a zoonotic infection. The genomes contain segments from three lineages that circulate in swine in China: North American triple reassortant H3N2, Eurasian avian-like H1N1, and pandemic H1N1. Furthermore, the swine-origin H1N1 viruses have transmitted onward in canines and reassorted with the CIV-H3N2 viruses that circulate endemically in Asian dogs, producing three novel reassortant CIV genotypes (H1N1r, H1N2r, and H3N2r [r stands for reassortant]). CIVs from this study were collected primarily from pet dogs presenting with respiratory symptoms at veterinary clinics, but dogs in Guangxi are also raised for meat, and street dogs roam freely, creating a more complex ecosystem for CIV transmission. Further surveillance is greatly needed to understand the full genetic diversity of CIV in southern China, the nature of viral emergence and persistence in the region’s diverse canine populations, and the zoonotic risk as the viruses continue to evolve.

          IMPORTANCE

          Mammals have emerged as critically underrecognized sources of influenza virus diversity, including pigs that were the source of the 2009 pandemic and bats and bovines that harbor highly divergent viral lineages. Here, we identify two reassortant IAVs that recently host switched from swine to canines in southern China, including one virus with known zoonotic potential. Three additional genotypes were generated via reassortment events in canine hosts, demonstrating the capacity of dogs to serve as “mixing vessels.” The continued expansion of IAV diversity in canines with high human contact rates requires enhanced surveillance and ongoing evaluation of emerging pandemic threats.

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          Most cited references48

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          A single amino acid in the PB2 gene of influenza A virus is a determinant of host range.

          The single gene reassortant virus that derives its PB2 gene from the avian influenza A/Mallard/NY/78 virus and remaining genes from the human influenza A/Los Angeles/2/87 virus exhibits a host range restriction (hr) phenotype characterized by efficient replication in avian tissue and failure to produce plaques in mammalian Madin-Darby canine kidney cells. The hr phenotype is associated with restriction of viral replication in the respiratory tract of squirrel monkeys and humans. To identify the genetic basis of the hr phenotype, we isolated four phenotypic hr mutant viruses that acquired the ability to replicate efficiently in mammalian tissue. Segregational analysis indicated that the loss of the hr phenotype was due to a mutation in the PB2 gene itself. The nucleotide sequences of the PB2 gene of each of the four hr mutants revealed that a single amino acid substitution at position 627 (Glu-->Lys) was responsible for the restoration of the ability of the PB2 single gene reassortant to replicate in Madin-Darby canine kidney cells. Interestingly, the amino acid at position 627 in every avian influenza A virus PB2 protein analyzed to date is glutamic acid, and in every human influenza A virus PB2 protein, it is lysine. Thus, the amino acid at residue 627 of PB2 is an important determinant of host range of influenza A viruses.
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            Influenza A viruses: new research developments.

            Influenza A viruses are zoonotic pathogens that continuously circulate and change in several animal hosts, including birds, pigs, horses and humans. The emergence of novel virus strains that are capable of causing human epidemics or pandemics is a serious possibility. Here, we discuss the value of surveillance and characterization of naturally occurring influenza viruses, and review the impact that new developments in the laboratory have had on our understanding of the host tropism and virulence of viruses. We also revise the lessons that have been learnt from the pandemic viruses of the past 100 years.
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              Transmission of equine influenza virus to dogs.

              Molecular and antigenic analyses of three influenza viruses isolated from outbreaks of severe respiratory disease in racing greyhounds revealed that they are closely related to H3N8 equine influenza virus. Phylogenetic analysis indicated that the canine influenza virus genomes form a monophyletic group, consistent with a single interspecies virus transfer. Molecular changes in the hemagglutinin suggested adaptive evolution in the new host. The etiologic role of this virus in respiratory disease was supported by the temporal association of rising antibody titers with disease and by experimental inoculation studies. The geographic expansion of the infection and its persistence for several years indicate efficient transmission of canine influenza virus among greyhounds. Evidence of infection in pet dogs suggests that this infection may also become enzootic in this population.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                mBio
                MBio
                mbio
                mbio
                mBio
                mBio
                American Society for Microbiology (1752 N St., N.W., Washington, DC )
                2150-7511
                5 June 2018
                May-Jun 2018
                : 9
                : 3
                : e00909-18
                Affiliations
                [a ]College of Animal Science and Technology, Guangxi University, Nanning, Guangxi, China
                [b ]Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA
                [c ]Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York, New York, USA
                [d ]Division of International Epidemiology and Population Studies, Fogarty International Center, National Institutes of Health, Bethesda, Maryland, USA
                [e ]Huabo Pet Hospital, Nanning, Guangxi, China
                [f ]Department of Medicine, Division of Infectious Diseases, Icahn School of Medicine at Mount Sinai, New York, New York, USA
                St. Jude Children's Research Hospital
                Author notes
                Address correspondence to Adolfo García-Sastre, Adolfo.Garcia-Sastre@ 123456mssm.edu .

                Y.C., N.S.T., and G.W. equally contributed to this work.

                This article is a direct contribution from a Fellow of the American Academy of Microbiology. Solicited external reviewers: Philippe Lemey, Rega Institute, KU Leuven; Colin Parrish, Cornell University.

                Article
                mBio00909-18
                10.1128/mBio.00909-18
                5989073
                29871917
                2cf2e8ce-bde7-4ec4-b915-3c84068b8d11
                Copyright © 2018 Chen et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

                History
                : 30 April 2018
                : 3 May 2018
                Page count
                supplementary-material: 6, Figures: 8, Tables: 3, Equations: 0, References: 65, Pages: 18, Words: 10601
                Funding
                Funded by: Doctor startup funds of Guangxi University;
                Award ID: XBZ160123
                Award Recipient :
                Funded by: HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID), https://doi.org/10.13039/100000060;
                Award ID: HHSN272201400008C
                Award Recipient :
                Funded by: HHS | NIH | Fogarty International Center (FIC), https://doi.org/10.13039/100000061;
                Award ID: MISMS project
                Award Recipient :
                Funded by: Natural Science Foundation of Guangxi Province (Guangxi Natural Science Foundation), https://doi.org/10.13039/501100004607;
                Award ID: 2015GXNSFCA139002
                Award Recipient :
                Funded by: Natural Science Foundation of Guangxi Province (Guangxi Natural Science Foundation), https://doi.org/10.13039/501100004607;
                Award ID: 2016GXNSFBA380219
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                May/June 2018

                Life sciences
                canine,influenza,virus emergence,virus evolution
                Life sciences
                canine, influenza, virus emergence, virus evolution

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