HA stabilization promotes replication and transmission of swine H1N1 gamma influenza viruses in ferrets
Meng Hu,
Guohua Yang,
Jennifer DeBeauchamp,
Jeri Carol Crumpton,
Hyunsuh Kim,
Lei Li,
Xiu-Feng Wan,
Lisa Kercher,
Andrew S Bowman,
Robert G Webster,
Richard J Webby,
Charles J Russell
Affiliations
Meng Hu
Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, United States
Guohua Yang
Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, United States
Jennifer DeBeauchamp
Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, United States
Jeri Carol Crumpton
Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, United States
Hyunsuh Kim
Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, United States
Lei Li
Department of Basic Sciences, College of Veterinary Medicine, Mississippi State University, Mississippi State, United States
Xiu-Feng Wan
Department of Basic Sciences, College of Veterinary Medicine, Mississippi State University, Mississippi State, United States; Missouri University Center for Research on Influenza Systems Biology (CRISB), University of Missouri, Columbia, United States; Department of Molecular Microbiology and Immunology, School of Medicine, University of Missouri, Columbia, United States; Bond Life Sciences Center, University of Missouri, Columbia, United States; Department of Electrical Engineering Computer Science, College of Engineering, University of Missouri, Columbia, United States; MU Informatics Institute, University of Missouri, Columbia, United States
Lisa Kercher
Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, United States
Andrew S Bowman
Department of Veterinary Preventive Medicine, The Ohio State University, Columbus, United States
Robert G Webster
Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, United States
Richard J Webby
Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, United States; Department of Microbiology, Immunology & Biochemistry, College of Medicine, The University of Tennessee Health Science Center, Memphis, United States
Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, United States; Department of Microbiology, Immunology & Biochemistry, College of Medicine, The University of Tennessee Health Science Center, Memphis, United States
Pandemic influenza A viruses can emerge from swine, an intermediate host that supports adaptation of human-preferred receptor-binding specificity by the hemagglutinin (HA) surface antigen. Other HA traits necessary for pandemic potential are poorly understood. For swine influenza viruses isolated in 2009–2016, gamma-clade viruses had less stable HA proteins (activation pH 5.5–5.9) than pandemic clade (pH 5.0–5.5). Gamma-clade viruses replicated to higher levels in mammalian cells than pandemic clade. In ferrets, a model for human adaptation, a relatively stable HA protein (pH 5.5–5.6) was necessary for efficient replication and airborne transmission. The overall airborne transmission frequency in ferrets for four isolates tested was 42%, and isolate G15 airborne transmitted 100% after selection of a variant with a stabilized HA. The results suggest swine influenza viruses containing both a stabilized HA and alpha-2,6 receptor binding in tandem pose greater pandemic risk. Increasing evidence supports adding HA stability to pre-pandemic risk assessment algorithms.