Filovirus receptor NPC1 contributes to species-specific patterns of ebolavirus susceptibility in bats

Author:

Ng Melinda1,Ndungo Esther1,Kaczmarek Maria E2,Herbert Andrew S3,Binger Tabea4,Kuehne Ana I3,Jangra Rohit K1,Hawkins John A5,Gifford Robert J6,Biswas Rohan1,Demogines Ann7,James Rebekah M3,Yu Meng8,Brummelkamp Thijn R9,Drosten Christian410,Wang Lin-Fa8,Kuhn Jens H11ORCID,Müller Marcel A4,Dye John M3,Sawyer Sara L71213,Chandran Kartik1ORCID

Affiliation:

1. Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, United States

2. Department of Integrative Biology, University of Texas at Austin, Austin, United States

3. United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, United States

4. Institute of Virology, University of Bonn Medical Center, Bonn, Germany

5. Institute for Computational Engineering and Sciences, University of Texas at Austin, Austin, United States

6. University of Glasgow MRC Virology Unit, Glasgow, United Kingdom

7. Department of Molecular Biosciences, University of Texas at Austin, Austin, United States

8. Program in Emerging Infectious Diseases, Duke-NUS Graduate Medical School, Singapore

9. Netherlands Cancer Institute, Plesmanlaan, The Netherlands

10. German Centre for Infectious Diseases Research, Bonn, Germany

11. Integrated Research Facility at Fort Detrick, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Fort Detrick, Frederick, United States

12. BioFrontiers Institute, University of Colorado Boulder, Boulder, United States

13. Department of Molecular, Cellular and Developmental Biology, University of Colorado Boulder, Boulder, United States

Abstract

Biological factors that influence the host range and spillover of Ebola virus (EBOV) and other filoviruses remain enigmatic. While filoviruses infect diverse mammalian cell lines, we report that cells from African straw-colored fruit bats (Eidolon helvum) are refractory to EBOV infection. This could be explained by a single amino acid change in the filovirus receptor, NPC1, which greatly reduces the affinity of EBOV-NPC1 interaction. We found signatures of positive selection in bat NPC1 concentrated at the virus-receptor interface, with the strongest signal at the same residue that controls EBOV infection in Eidolon helvum cells. Our work identifies NPC1 as a genetic determinant of filovirus susceptibility in bats, and suggests that some NPC1 variations reflect host adaptations to reduce filovirus replication and virulence. A single viral mutation afforded escape from receptor control, revealing a pathway for compensatory viral evolution and a potential avenue for expansion of filovirus host range in nature.

Funder

National Institutes of Health

Defense Threat Reduction Agency

European Commission

Bundesministerium für Bildung und Forschung

National Research Foundation-Prime Minister's office, Republic of Singapore

Publisher

eLife Sciences Publications, Ltd

Subject

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

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