Rapid evolution of A(H5N1) influenza viruses after intercontinental spread to North America

Ahmed Kandeil(St. Jude Children's Research Hospital), Christopher Patton(St. Jude Children's Research Hospital), Jeremy C. Jones(St. Jude Children's Research Hospital), Trushar Jeevan(St. Jude Children's Research Hospital), Walter N. Harrington(St. Jude Children's Research Hospital), Sanja Trifkovic(St. Jude Children's Research Hospital), Jon P. Seiler(St. Jude Children's Research Hospital), Thomas Fabrizio(St. Jude Children's Research Hospital), Karlie Woodard(St. Jude Children's Research Hospital), Jasmine Turner(St. Jude Children's Research Hospital), Jeri‐Carol Crumpton(St. Jude Children's Research Hospital), Lance A. Miller(St. Jude Children's Research Hospital), Adam Rubrum(St. Jude Children's Research Hospital), Jennifer DeBeauchamp(St. Jude Children's Research Hospital), Charles J. Russell(St. Jude Children's Research Hospital), Elena A. Govorkova(St. Jude Children's Research Hospital), Peter Vogel(St. Jude Children's Research Hospital), Mia Kim-Torchetti(Animal and Plant Health Inspection Service), Yohannes Berhane(Canadian Science Centre for Human and Animal Health), David E. Stallknecht(University of Georgia), Rebecca L. Poulson(University of Georgia), Lisa Kercher(St. Jude Children's Research Hospital), Richard J. Webby(St. Jude Children's Research Hospital)
Nature Communications
May 29, 2023
Cited by 235Open Access
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Abstract

Highly pathogenic avian influenza A(H5N1) viruses of clade 2.3.4.4b underwent an explosive geographic expansion in 2021 among wild birds and domestic poultry across Asia, Europe, and Africa. By the end of 2021, 2.3.4.4b viruses were detected in North America, signifying further intercontinental spread. Here we show that the western movement of clade 2.3.4.4b was quickly followed by reassortment with viruses circulating in wild birds in North America, resulting in the acquisition of different combinations of ribonucleoprotein genes. These reassortant A(H5N1) viruses are genotypically and phenotypically diverse, with many causing severe disease with dramatic neurologic involvement in mammals. The proclivity of the current A(H5N1) 2.3.4.4b virus lineage to reassort and target the central nervous system warrants concerted planning to combat the spread and evolution of the virus within the continent and to mitigate the impact of a potential influenza pandemic that could originate from similar A(H5N1) reassortants.


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