CD300LF Polymorphisms of Inbred Mouse Strains Confer Resistance to Murine Norovirus Infection in a Cell Type-Dependent Manner

Author:

Furlong Kevin1,Biering Scott B.1,Choi Jayoung2,Wilen Craig B.34,Orchard Robert C.5ORCID,Wobus Christiane E.6ORCID,Nelson Christopher A.789,Fremont Daved H.789,Baldridge Megan T.910,Randall Glenn11,Hwang Seungmin12ORCID

Affiliation:

1. Committee on Microbiology, The University of Chicago, Chicago, Illinois, USA

2. Department of Pathology, The University of Chicago, Chicago, Illinois, USA

3. Department of Laboratory Medicine, Yale University School of Medicine, New Haven, Connecticut, USA

4. Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut, USA

5. Department of Immunology, The University of Texas Southwestern Medical Center, Dallas, Texas, USA

6. Department of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan, USA

7. Department of Pathology & Immunology, Washington University, St. Louis, Missouri, USA

8. Department of Biochemistry & Molecular Biophysics, Washington University, St. Louis, Missouri, USA

9. Department of Molecular Microbiology, Washington University, St. Louis, Missouri, USA

10. Division of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA

11. Department of Microbiology, The University of Chicago, Chicago, Illinois, USA

Abstract

MNV is a prevalent model system for studying human norovirus, which is the leading cause of gastroenteritis worldwide and thus a sizeable public health burden. Elucidating mechanisms underlying susceptibility of host cells to MNV infection can lead to insights on the roles that specific cell types play during norovirus pathogenesis. Here, we show that different alleles of the proteinaceous receptor for MNV, CD300LF, function in a cell type-dependent manner. In contrast to the C57BL/6J allele, which functions as an MNV entry factor in all tested cell types, including human cells, I/LnJ CD300LF does not function as an MNV entry factor in macrophage-like cells but does allow MNV entry in other cell types. Together, these observations indicate the existence of cell type-specific modifiers of CD300LF-dependent MNV entry.

Funder

HHS | National Institutes of Health

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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