The Hemagglutinin-Esterase Fusion Glycoprotein Is a Primary Determinant of the Exceptional Thermal and Acid Stability of Influenza D Virus

Author:

Yu Jieshi1,Hika Busha1,Liu Runxia1,Sheng Zizhang23,Hause Ben M.4,Li Feng156,Wang Dan16ORCID

Affiliation:

1. Department of Biology and Microbiology, South Dakota State University, Brookings, South Dakota, USA

2. Department of Biochemistry and Molecular Biophysics, Columbia University, New York, New York, USA

3. Department of Systems Biology, Columbia University, New York, New York, USA

4. Cambridge Technologies, Inc., Worthington, Minnesota, USA

5. Department of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, South Dakota, USA

6. BioSNTR, Brookings, South Dakota, USA

Abstract

Influenza D virus (IDV) utilizes cattle as a primary reservoir. Increased outbreaks in pigs and serological evidence of human infection have raised a concern about the potential of IDV adapting to humans. Here, we directly compared IDV’s stability to that of other influenza types (A, B, and C) following prolonged incubation at high temperatures or in a low-pH environment. We found that IDV is the most stable of the four types of influenza viruses. Importantly, we demonstrated that the hemagglutinin-esterase fusion (HEF) protein, which drives the fusion between viral and host cell membranes, is the primary determinant for the high thermal and acid stability of IDV. Considering that there is a link between the acid stability of the hemagglutinin protein of influenza A virus and its cross-species transmission, further investigation of the mechanism of HEF-directed viral tolerance may offer novel insights into tissue tropism and cross-species transmission of influenza viruses.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

National Science Foundation

South Dakota State University

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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