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Characterizing Emerging Canine H3 Influenza Viruses.

Luis Martinez-SobridoPilar Blanco-LoboLaura RodriguezTheresa FitzgeraldHanyuan ZhangPhuong Quoc Thuc NguyenChristopher S AndersonJeanne Holden-WiltseSanjukta BandyopadhyayAitor NogalesMarta L DeDiegoBrian R WasikBenjamin L MillerCarole HenryPatrick C WilsonMark Y SangsterJohn J TreanorDavid J TophamLauren Byrd-LeotisDavid A SteinhauerRichard D CummingsJasmina M LuczoStephen Mark TompkinsKaori SakamotoCheryl A JonesJohn SteelAnice C LowenShamika DanzyHui TaoAshley L FinkSabra L KleinNicholas WohlgemuthKatherine Z J FenstermacherFarah El NajjarAndrew S PekoszLauren SauerMitra K LewisKathryn Shaw-SalibaRichard E RothmanZhen-Ying LiuKuan-Fu ChenColin R ParrishIan E H VoorheesYoshihiro KawaokaGabriele NeumannShiho ChibaShufang FanMasato HattaHuihui KongGongxun ZhongGuojun WangMelissa B UccelliniAdolfo García-SastreDaniel R PérezLucas M FerreriSander HerfstMathilde RichardRon FouchierDavid Francis BurkeDavid J PattinsonDerek J SmithVictoria MeliopoulosPamela FreidenBrandi LivingstonBridgett SharpSean CherryJuan Carlos DibGuohua YangCharles J RussellSubrata BarmanRichard J WebbyScott KraussAngela DannerKarlie WoodardJoseph S Malik PeirisR A P M PereraMichael Chi-Wai ChanElena A GovorkovaBindumadhav M MarathePhilippe Noriel Q PascuaGavin J D SmithYao-Tsun LiPaul G ThomasStacey Schultz-Cherry
Published in: PLoS pathogens (2020)
The continual emergence of novel influenza A strains from non-human hosts requires constant vigilance and the need for ongoing research to identify strains that may pose a human public health risk. Since 1999, canine H3 influenza A viruses (CIVs) have caused many thousands or millions of respiratory infections in dogs in the United States. While no human infections with CIVs have been reported to date, these viruses could pose a zoonotic risk. In these studies, the National Institutes of Allergy and Infectious Diseases (NIAID) Centers of Excellence for Influenza Research and Surveillance (CEIRS) network collaboratively demonstrated that CIVs replicated in some primary human cells and transmitted effectively in mammalian models. While people born after 1970 had little or no pre-existing humoral immunity against CIVs, the viruses were sensitive to existing antivirals and we identified a panel of H3 cross-reactive human monoclonal antibodies (hmAbs) that could have prophylactic and/or therapeutic value. Our data predict these CIVs posed a low risk to humans. Importantly, we showed that the CEIRS network could work together to provide basic research information important for characterizing emerging influenza viruses, although there were valuable lessons learned.
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