| Literature DB >> 32876050 |
John Huddleston1,2, John R Barnes3, Thomas Rowe3, Xiyan Xu3, Rebecca Kondor3, David E Wentworth3, Lynne Whittaker4, Burcu Ermetal4, Rodney Stuart Daniels4, John W McCauley4, Seiichiro Fujisaki5, Kazuya Nakamura5, Noriko Kishida5, Shinji Watanabe5, Hideki Hasegawa5, Ian Barr6, Kanta Subbarao6, Pierre Barrat-Charlaix7,8, Richard A Neher7,8, Trevor Bedford1.
Abstract
Seasonal influenza virus A/H3N2 is a major cause of death globally. Vaccination remains the most effective preventative. Rapid mutation of hemagglutinin allows viruses to escape adaptive immunity. This antigenic drift necessitates regular vaccine updates. Effective vaccine strains need to represent H3N2 populations circulating one year after strain selection. Experts select strains based on experimental measurements of antigenic drift and predictions made by models from hemagglutinin sequences. We developed a novel influenza forecasting framework that integrates phenotypic measures of antigenic drift and functional constraint with previously published sequence-only fitness estimates. Forecasts informed by phenotypic measures of antigenic drift consistently outperformed previous sequence-only estimates, while sequence-only estimates of functional constraint surpassed more comprehensive experimentally-informed estimates. Importantly, the best models integrated estimates of both functional constraint and either antigenic drift phenotypes or recent population growth.Entities:
Keywords: antigenic drift; evolution; evolutionary biology; infectious disease; influenza; microbiology; phenotypes; prediction; virus
Mesh:
Year: 2020 PMID: 32876050 PMCID: PMC7553778 DOI: 10.7554/eLife.60067
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140