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      Inventory of molecular markers affecting biological characteristics of avian influenza A viruses

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          Abstract

          Avian influenza viruses (AIVs) circulate globally, spilling over into domestic poultry and causing zoonotic infections in humans. Fortunately, AIVs are not yet capable of causing sustained human-to-human infection; however, AIVs are still a high risk as future pandemic strains, especially if they acquire further mutations that facilitate human infection and/or increase pathogenesis. Molecular characterization of sequencing data for known genetic markers associated with AIV adaptation, transmission, and antiviral resistance allows for fast, efficient assessment of AIV risk. Here we summarize and update the current knowledge on experimentally verified molecular markers involved in AIV pathogenicity, receptor binding, replicative capacity, and transmission in both poultry and mammals with a broad focus to include data available on other AIV subtypes outside of A/H5N1 and A/H7N9.

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          Most cited references268

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          Human Infection with a Novel Avian-Origin Influenza A (H7N9) Virus

          New England Journal of Medicine, 368(20), 1888-1897
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            Avian flu: influenza virus receptors in the human airway.

            Although more than 100 people have been infected by H5N1 influenza A viruses, human-to-human transmission is rare. What are the molecular barriers limiting human-to-human transmission? Here we demonstrate an anatomical difference in the distribution in the human airway of the different binding molecules preferred by the avian and human influenza viruses. The respective molecules are sialic acid linked to galactose by an alpha-2,3 linkage (SAalpha2,3Gal) and by an alpha-2,6 linkage (SAalpha2,6Gal). Our findings may provide a rational explanation for why H5N1 viruses at present rarely infect and spread between humans although they can replicate efficiently in the lungs.
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              Molecular basis for high virulence of Hong Kong H5N1 influenza A viruses.

              M Hatta (2001)
              In 1997, an H5N1 influenza A virus was transmitted from birds to humans in Hong Kong, killing 6 of the 18 people infected. When mice were infected with the human isolates, two virulence groups became apparent. Using reverse genetics, we showed that a mutation at position 627 in the PB2 protein influenced the outcome of infection in mice. Moreover, high cleavability of the hemagglutinin glycoprotein was an essential requirement for lethal infection.
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                Author and article information

                Contributors
                ekarlsson@pasteur-kh.org
                Journal
                Virus Genes
                Virus Genes
                Virus Genes
                Springer US (New York )
                0920-8569
                1572-994X
                19 August 2019
                19 August 2019
                2019
                : 55
                : 6
                : 739-768
                Affiliations
                [1 ]GRID grid.418537.c, Virology Unit, , Institut Pasteur du Cambodge, Institut Pasteur International Network, ; 5 Monivong Blvd, PO Box #983, Phnom Penh, Cambodia
                [2 ]GRID grid.1040.5, ISNI 0000 0001 1091 4859, School of Health and Life Sciences, , Federation University, ; Churchill, Australia
                [3 ]World Health Organization Collaborating Centre for Reference and Research on Influenza, Peter Doherty Institute for Infection and Immunity, Melbourne, Australia
                [4 ]GRID grid.1011.1, ISNI 0000 0004 0474 1797, College of Public Health, Medical and Veterinary Sciences, , James Cook University, ; Townsville, QLD Australia
                Author notes

                Edited by William Dundon.

                Author information
                http://orcid.org/0000-0001-6004-5671
                Article
                1700
                10.1007/s11262-019-01700-z
                6831541
                31428925
                9b54418a-cc6d-4aa1-9dd9-a7fca4c004f5
                © The Author(s) 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 9 June 2019
                : 9 August 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000016, U.S. Department of Health and Human Services;
                Award ID: IDSEP140020-01-00
                Categories
                Review Paper
                Custom metadata
                © Springer Science+Business Media, LLC, part of Springer Nature 2019

                Microbiology & Virology
                avian influenza,influenza virus,molecular marker,mutation,risk assessment,molecular inventory

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