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Mutations in the H7 HA and PB1 genes of avian influenza a viruses increase viral pathogenicity and contact transmission in guinea pigs

Affiliation
Viral Zoonosis -One Health, Heinrich Pette Institute, Leibniz Institute for Experimental Virology, Germany
Dreier, Carola;
Affiliation
Institute of Virology, University of Veterinary Medicine, Hannover, Germany
Resa-Infante, Patricia;
Affiliation
Viral Zoonosis -One Health, Heinrich Pette Institute, Leibniz Institute for Experimental Virology, Germany
Thiele, Swantje;
Affiliation
Viral Zoonosis -One Health, Heinrich Pette Institute, Leibniz Institute for Experimental Virology, Germany
Stanelle-Bertram, Stephanie;
Affiliation
Viral Zoonosis -One Health, Heinrich Pette Institute, Leibniz Institute for Experimental Virology, Germany
Walendy-Gnirß, Kerstin;
Affiliation
Viral Zoonosis -One Health, Heinrich Pette Institute, Leibniz Institute for Experimental Virology, Germany
Speiseder, Thomas;
Affiliation
Viral Zoonosis -One Health, Heinrich Pette Institute, Leibniz Institute for Experimental Virology, Germany
Preuss, Annette;
Affiliation
Viral Zoonosis -One Health, Heinrich Pette Institute, Leibniz Institute for Experimental Virology, Germany
Müller, Zacharias;
Affiliation
Institute for Virology, Philipps University of Marburg, Marburg, Germany
Klenk, Hans-Dieter;
GND
1019542209
Affiliation
Institute for Molecular Virology and Cell Biology, Friedrich-Loeffler-Institute, Greifswald, Germany
Stech, Jürgen;
Affiliation
Viral Zoonosis -One Health, Heinrich Pette Institute, Leibniz Institute for Experimental Virology, Germany
Gabriel, Gülsah

Avian influenza A viruses (AIV) of the H7 subtype continue to evolve posing a pandemic threat. However, molecular markers of H7N7 AIV pathogenicity and transmission in mammals remain poorly understood. In this study, we performed a systematic in vitro and in vivo analysis by comparing an H7N7 highly pathogenic AIV and its ferret adapted variant. Passaging an H7N7 AIV in ferrets led to six mutations in genes encoding the viral polymerase complex and the viral surface proteins. Here, we show that mutations in the H7 hemagglutinin gene cause increased pathogenicity in mice. Contact transmission between guinea pigs required additional mutations in the gene encoding the polymerase subunit PB1. Thus, particular vigilance is required with respect to HA and PB1 mutations as predictive molecular markers to assess the pandemic risk posed by emerging H7 avian influenza viruses.

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