Integrating genotypes and phenotypes improves long-term forecasts of seasonal influenza A/H3N2 evolution

Author:

Huddleston John12ORCID,Barnes John R3,Rowe Thomas3,Xu Xiyan3,Kondor Rebecca3ORCID,Wentworth David E3ORCID,Whittaker Lynne4,Ermetal Burcu4,Daniels Rodney Stuart4,McCauley John W4ORCID,Fujisaki Seiichiro5,Nakamura Kazuya5,Kishida Noriko5,Watanabe Shinji5,Hasegawa Hideki5,Barr Ian6,Subbarao Kanta6ORCID,Barrat-Charlaix Pierre78ORCID,Neher Richard A78ORCID,Bedford Trevor1ORCID

Affiliation:

1. Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, United States

2. Molecular and Cell Biology Program, University of Washington, Seattle, United States

3. Virology Surveillance and Diagnosis Branch, Influenza Division, National Center for Immunization and Respiratory Diseases (NCIRD), Centers for Disease Control and Prevention (CDC), Atlanta, United States

4. WHO Collaborating Centre for Reference and Research on Influenza, Crick Worldwide Influenza Centre, The Francis Crick Institute, London, United Kingdom

5. Influenza Virus Research Center, National Institute of Infectious Diseases, Tokyo, Japan

6. The WHO Collaborating Centre for Reference and Research on Influenza, The Peter Doherty Institute for Infection and Immunity, Department of Microbiology and Immunology, The University of Melbourne, The Peter Doherty Institute for Infection and Immunity, Melbourne, Australia

7. Biozentrum, University of Basel, Basel, Switzerland

8. Swiss Institute of Bioinformatics, Basel, Switzerland

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.

Funder

Cancer Research UK

Medical Research Council

Wellcome

Ministry of Health, Labour and Welfare

Japan Agency for Medical Research and Development

Australian Government Department of Health

National Institute of Allergy and Infectious Diseases

National Institute of General Medical Sciences

Pew Charitable Trusts

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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