Hemagglutinin Cleavability, Acid Stability, and Temperature Dependence Optimize Influenza B Virus for Replication in Human Airways

Author:

Laporte Manon1ORCID,Stevaert Annelies1ORCID,Raeymaekers Valerie1,Boogaerts Talitha1,Nehlmeier Inga2,Chiu Winston1,Benkheil Mohammed1ORCID,Vanaudenaerde Bart3,Pöhlmann Stefan24ORCID,Naesens Lieve1ORCID

Affiliation:

1. Katholieke Universiteit Leuven, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, Laboratory of Virology and Chemotherapy, Leuven, Belgium

2. Infection Biology Unit, German Primate Center–Leibniz Institute for Primate Research, Göttingen, Germany

3. Katholieke Universiteit Leuven, Department of Chronic Diseases, Metabolism and Ageing, Laboratory of Pneumology, University Hospital Leuven, Leuven, Belgium

4. Faculty of Biology and Psychology, University Göttingen, Göttingen, Germany

Abstract

Influenza epidemics are caused by influenza A and influenza B viruses (IAV and IBV, respectively). IBV causes substantial disease; however, it is far less studied than IAV. While IAV originates from animal reservoirs, IBV circulates in humans only. Virus spread requires that the viral hemagglutinin (HA) is active and sufficiently stable in human airways. We resolve here how these mechanisms differ between IBV and IAV. Whereas human IAVs rely on one particular protease for HA activation, this is not the case for IBV. Superior activation of IBV by several proteases should enhance shedding of infectious particles. IBV HA exhibits acid stability and a preference for 33°C, indicating pronounced adaptation to the human upper airways, where the pH is mildly acidic and a cooler temperature exists. These adaptive features are rationalized by the long existence of IBV in humans and may have broader relevance for understanding the biology and evolution of respiratory viruses.

Funder

Herculesstichting

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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