Mapping person-to-person variation in viral mutations that escape polyclonal serum targeting influenza hemagglutinin

Juhye Lee(University of Washington), Rachel Eguia(Fred Hutch Cancer Center), Seth J. Zost(University of Pennsylvania), Saket Choudhary(University of Southern California), Patrick C. Wilson(University of Chicago), Trevor Bedford(Fred Hutch Cancer Center), Terry Stevens‐Ayers(Fred Hutch Cancer Center), Michael Boeckh(Fred Hutch Cancer Center), Aeron C. Hurt(Peter Doherty Institute), Seema S. Lakdawala(University of Pittsburgh), Scott E. Hensley(University of Pennsylvania), Jesse D. Bloom(Howard Hughes Medical Institute)
eLife
August 26, 2019
Cited by 139Open Access
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Abstract

A longstanding question is how influenza virus evolves to escape human immunity, which is polyclonal and can target many distinct epitopes. Here, we map how all amino-acid mutations to influenza’s major surface protein affect viral neutralization by polyclonal human sera. The serum of some individuals is so focused that it selects single mutations that reduce viral neutralization by over an order of magnitude. However, different viral mutations escape the sera of different individuals. This individual-to-individual variation in viral escape mutations is not present among ferrets that have been infected just once with a defined viral strain. Our results show how different single mutations help influenza virus escape the immunity of different members of the human population, a phenomenon that could shape viral evolution and disease susceptibility.


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