Modulation of lethal HPAIV H5N8 clade 2.3.4.4B infection in AIV pre-exposed mallards

References

• Lee D-H, Bertran K, Kwon J-H, et al. Evolution, global spread, and pathogenicity of highly pathogenic avian influenza H5Nx clade 2.3.4.4. J Vet Sci. 2017;18:269–280. doi: 10.4142/jvs.2017.18.S1.269
   PubMed Web of Science ®Google Scholar
• Zhong L, Zhao Q, Zhao K, et al. The antigenic drift molecular basis of the H5N1 influenza viruses in a novel branch of clade 2.3.4. Vet Microbiol. 2014;171:23–30. doi: 10.1016/j.vetmic.2014.02.033
   PubMed Web of Science ®Google Scholar
• Harder T, Maurer-Stroh S, Pohlmann A, et al. Influenza A(H5N8) virus similar to strain in Korea causing highly pathogenic avian influenza in Germany. Emerg Infect Dis. 2015;21:860–863. doi: 10.3201/eid2105.141897
   PubMed Web of Science ®Google Scholar
• Verhagen JH, Herfst S, Fouchier RAM. Infectious disease. How a virus travels the world. Science. 2015;347:616–617. doi: 10.1126/science.aaa6724
   PubMed Web of Science ®Google Scholar
• Pohlmann A, Starick E, Harder T, et al. Outbreaks among wild birds and domestic poultry caused by reassorted influenza A(H5N8) clade 2.3.4.4 viruses, Germany, 2016. Emerg Infect Dis. 2017;23:633–636. doi: 10.3201/eid2304.161949
   PubMed Web of Science ®Google Scholar
• Globig A, Starick E, Homeier T, et al. Epidemiological and molecular analysis of an outbreak of highly pathogenic avian influenza H5N8 clade 2.3.4.4 in a German Zoo: effective disease control with minimal culling. Transbound Emerg Dis. 2017;64:1813–1824. doi: 10.1111/tbed.12570
   PubMed Web of Science ®Google Scholar
• Krone O, Globig A, Ulrich R, et al. White-tailed sea eagle (Haliaeetus albicilla) die-off due to infection with highly pathogenic avian influenza virus, subtype H5N8, in Germany. Viruses. 2018;10:478. doi: 10.3390/v10090478
   PubMed Web of Science ®Google Scholar
• Pohlmann A, Starick E, Grund C, et al. Swarm incursions of reassortants of highly pathogenic avian influenza virus strains H5N8 and H5N5, clade 2.3.4.4b, Germany, winter 2016/17. Sci Rep. 2018;8:15. doi: 10.1038/s41598-017-16936-8
   PubMed Web of Science ®Google Scholar
• van den Brand JMA, Verhagen JH, Veldhuis Kroeze EJB, et al. Wild ducks excrete highly pathogenic avian influenza virus H5N8 (2014-2015) without clinical or pathological evidence of disease. Emerg Microbes Infect. 2018;7:67. doi: 10.1038/s41426-018-0070-9
   PubMed Web of Science ®Google Scholar
• Pantin-Jackwood MJ, Costa-Hurtado M, Shepherd E, et al. Swayne DE: pathogenicity and transmission of H5 and H7 highly pathogenic avian influenza viruses in mallards. J Virol. 2016;90:9967–9982. doi: 10.1128/JVI.01165-16
   PubMed Web of Science ®Google Scholar
• Spackman E, Prosser DJ, Pantin-Jackwood MJ, et al. The pathogenesis of clade 2.3.4.4 H5 highly pathogenic avian influenza viruses in ruddy duck(oxyura jamaicensis) and lesser scaup (aythya affinis). J Wildl Dis. 2017;53:832–842. doi: 10.7589/2017-01-003
   PubMed Web of Science ®Google Scholar
• Grund C, Hoffmann D, Ulrich R, et al. A novel European H5N8 influenza A virus has increased virulence in ducks but low zoonotic potential. Emerg Microbes Infect. 2018;7:132. doi: 10.1038/s41426-018-0130-1
   PubMed Web of Science ®Google Scholar
• Kleyheeg E, Slaterus R, Bodewes R, et al. Deaths among wild birds during highly pathogenic avian influenza A(H5N8) virus outbreak, the Netherlands. Emerg Infect Dis. 2017;23:2050–2054. doi: 10.3201/eid2312.171086
   PubMed Web of Science ®Google Scholar
• Phuong DQ, Dung NT, Jørgensen PH, et al. Susceptibility of Muscovy (Cairina Moschata) and mallard ducks (Anas Platyrhynchos) to experimental infections by different genotypes of H5N1 avian influenza viruses. Vet Microbiol. 2011;148:168–174. doi: 10.1016/j.vetmic.2010.09.007
   PubMed Web of Science ®Google Scholar
• Kang H-M, Lee E-K, Song B-M, et al. Experimental infection of mandarin duck with highly pathogenic avian influenza A (H5N8 and H5N1) viruses. Vet Microbiol. 2017;198:59–63. doi: 10.1016/j.vetmic.2016.12.005
   PubMed Web of Science ®Google Scholar
• Kang H-M, Lee E-K, Song B-M, et al. Novel reassortant influenza A(H5N8) viruses among inoculated domestic and wild ducks, South Korea, 2014. Emerg Infect Dis. 2015;21:298–304. doi: 10.3201/eid2102.141268
   PubMed Web of Science ®Google Scholar
• Kwon H-I, Kim E-H, Kim Y-I, et al. Comparison of the pathogenic potential of highly pathogenic avian influenza (HPAI) H5N6, and H5N8 viruses isolated in South Korea during the 2016–2017 winter season. Emerg Microbes Infect. 2018;7:29. doi: 10.1038/s41426-018-0029-x
   PubMed Web of Science ®Google Scholar
• Olsen B, Munster VJ, Wallensten A, et al. Global patterns of influenza a virus in wild birds. Science. 2006;312:384–388. doi: 10.1126/science.1122438
   PubMed Web of Science ®Google Scholar
• Knight-Jones TJD, Hauser R, Matthes D, et al. Evaluation of effectiveness and efficiency of wild bird surveillance for avian influenza. Vet Res. 2010;41:50. doi: 10.1051/vetres/2010023
   PubMed Web of Science ®Google Scholar
• Globig A, Baumer A, Revilla-Fernández S, et al. Ducks as sentinels for avian influenza in wild birds. Emerg Infect Dis. 2009;15:1633–1636. doi: 10.3201/eid1510.090439
   PubMed Web of Science ®Google Scholar
• Hoffmann B, Hoffmann D, Henritzi D, et al. Riems influenza a typing array (RITA): An RT-qPCR-based low density array for subtyping avian and mammalian influenza a viruses. Sci Rep. 2016;6:27211. doi: 10.1038/srep27211
   PubMed Web of Science ®Google Scholar
• Commission decision of 4 August 2006 approving a Diagnostic Manual for avian influenza as provided for in Council Directive 2005/94/EC.
   Google Scholar
• Graaf A, Ulrich R, Maksimov P, et al. A viral race for primacy: co-infection of a natural pair of low and highly pathogenic H7N7 avian influenza viruses in chickens and embryonated chicken eggs. Emerg Microbes Infect. 2018;7:204. doi: 10.1038/s41426-018-0204-0
   PubMed Web of Science ®Google Scholar
• Hirschberger J. Herstellung und Charakterisierung monoklonaler Antikörper gegen T-Lymphozyten des Huhnes [Dissertation Gießen]; 1987.
   Google Scholar
• Spackman E, Senne DA, Myers TJ, et al. Development of a real-time reverse transcriptase PCR assay for type A influenza virus and the avian H5 and H7 hemagglutinin subtypes. J Clin Microbiol. 2002;40:3256–3260. doi: 10.1128/JCM.40.9.3256-3260.2002
   PubMed Web of Science ®Google Scholar
• Henritzi D, Hoffmann B, Wacheck S, et al. A newly developed tetraplex real-time RT-PCR for simultaneous screening of influenza virus types A, B, C and D. Influenza Other Respir Viruses. 2019;13:71–82. doi: 10.1111/irv.12613
   PubMed Web of Science ®Google Scholar
• Slomka MJ, Pavlidis T, Banks J, et al. Validated H5 Eurasian real-time reverse transcriptase-polymerase chain reaction and its application in H5N1 outbreaks in 2005-2006. Avian Dis. 2007;51:373–377. doi: 10.1637/7664-060906R1.1
   PubMed Web of Science ®Google Scholar
• Animal & Plant Health Agency. Annual Report on surveillance for avian influenza in poultry and wild birds in Member States of the European Union in 2017. European Commission; 2018.
   Google Scholar
• Slomka MJ, Puranik A, Mahmood S, et al. Ducks are susceptible to infection with a range of doses of H5N8 highly pathogenic avian influenza virus (2016, clade 2.3.4.4b) and are largely resistant to virus-specific mortality, but efficiently transmit infection to contact Turkeys. Avian Dis. 2019;63:172–180. doi: 10.1637/11905-052518-Reg.1
   PubMed Web of Science ®Google Scholar
• Berhane Y, Leith M, Embury-Hyatt C, et al. Studying possible cross-protection of Canada geese preexposed to North American low pathogenicity avian influenza virus strains (H3N8, H4N6, and H5N2) against an H5N1 highly pathogenic avian influenza challenge. Avian Dis. 2010;54:548–554. doi: 10.1637/8841-040309-Reg.1
   PubMed Web of Science ®Google Scholar
• Fereidouni SR, Starick E, Beer M, et al. Highly pathogenic avian influenza virus infection of mallards with homo- and heterosubtypic immunity induced by low pathogenic avian influenza viruses. PLoS One. 2009;4:e6706. doi: 10.1371/journal.pone.0006706
   PubMed Web of Science ®Google Scholar
• Costa TP, Brown JD, Howerth EW, et al. Homo- and heterosubtypic low pathogenic avian influenza exposure on H5N1 highly pathogenic avian influenza virus infection in wood ducks (Aix sponsa). PLoS One. 2011;6:e15987. doi: 10.1371/journal.pone.0015987
   PubMed Web of Science ®Google Scholar
• Costa TP, Brown JD, Howerth EW, et al. Effect of a prior exposure to a low pathogenic avian influenza virus in the outcome of a heterosubtypic low pathogenic avian influenza infection in mallards (Anas platyrhynchos). Avian Dis. 2010;54:1286–1291. doi: 10.1637/9480-072210-Reg.1
   PubMed Web of Science ®Google Scholar
• Spivey TJ, Lindberg MS, Meixell BW, et al. Maintenance of influenza A viruses and antibody response in mallards (Anas platyrhynchos) sampled during the non-breeding season in Alaska. PLoS One. 2017;12:e0183505. doi: 10.1371/journal.pone.0183505
   PubMed Web of Science ®Google Scholar
• Fereidouni SR, Grund C, Häuslaigner R, et al. Dynamics of specific antibody responses induced in mallards after infection by or immunization with low pathogenicity avian influenza viruses. Avian Dis. 2010;54:79–85. doi: 10.1637/9005-073109-Reg.1
   PubMed Web of Science ®Google Scholar
• Latorre-Margalef N, Grosbois V, Wahlgren J, et al. Heterosubtypic immunity to influenza A virus infections in mallards may explain existence of multiple virus subtypes. PLoS Pathog. 2013;9:e1003443. doi: 10.1371/journal.ppat.1003443
   PubMed Web of Science ®Google Scholar
• Globig A, Fereidouni SR, Harder TC, et al. Consecutive natural influenza a virus infections in sentinel mallards in the evident absence of subtype-specific hemagglutination inhibiting antibodies. Transbound Emerg Dis. 2013;60:395–402. doi: 10.1111/j.1865-1682.2012.01357.x
   PubMed Web of Science ®Google Scholar
• Dirsmith KL, Jeffrey Root J, Bentler KT, et al. Persistence of maternal antibodies to influenza A virus among captive mallards (Anas platyrhynchos). Arch Virol. 2018;163:3235–3242. doi: 10.1007/s00705-018-3978-4
   PubMed Web of Science ®Google Scholar
• Kleyheeg E, van Dijk JGB, Tsopoglou-Gkina D, et al. Movement patterns of a keystone waterbird species are highly predictable from landscape configuration. Mov Ecol. 2017;5:2. doi: 10.1186/s40462-016-0092-7
   PubMed Web of Science ®Google Scholar
• Shin J-H, Lee K-S, Kim S-H, et al. Tracking mallards (Anas platyrhynchos) with GPS satellite transmitters along their migration route through Northeast Asia. Avian Dis. 2016;60:311–315. doi: 10.1637/11096-042015-Reg
   PubMed Web of Science ®Google Scholar
• Bengtsson D, Safi K, Avril A, et al. Does influenza A virus infection affect movement behaviour during stopover in its wild reservoir host? R Soc Open Sci. 2016;3:150633. doi: 10.1098/rsos.150633
   PubMed Web of Science ®Google Scholar
• Bengtsson D, Avril A, Gunnarsson G, et al. Movements, home-range size and habitat selection of mallards during autumn migration. PLoS One. 2014;9:e100764. doi: 10.1371/journal.pone.0100764
   PubMed Web of Science ®Google Scholar
• Hénaux V. Samuel MD: avian influenza shedding patterns in waterfowl: implications for surveillance, environmental transmission, and disease spread. J Wildl Dis. 2011;47:566–578. doi: 10.7589/0090-3558-47.3.566
   PubMed Web of Science ®Google Scholar
• van Dijk JG, Verhagen JH, Wille M, et al. Host and virus ecology as determinants of influenza A virus transmission in wild birds. Curr Opin Virol. 2018;28:26–36. doi: 10.1016/j.coviro.2017.10.006
   PubMed Web of Science ®Google Scholar
• The Global Consortium for H5N8 and Related Influenza Viruses. Role for migratory wild birds in the global spread of avian influenza H5N8. Science. 2016;354:213–217. doi: 10.1126/science.aaf8852
   PubMed Web of Science ®Google Scholar