Discovery of a proteinaceous cellular receptor for a norovirus
Author(s) -
Robert C. Orchard,
Craig B. Wilen,
John G. Doench,
Megan T. Baldridge,
Broc T. McCune,
YingChiang J. Lee,
Sanghyun Lee,
Shondra M. PruettMiller,
Christopher A. Nelson,
Daved H. Fremont,
Herbert W. Virgin
Publication year - 2016
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aaf1220
Subject(s) - norovirus , infectivity , murine norovirus , virology , biology , virus , viral entry , host (biology) , receptor , microbiology and biotechnology , viral replication , genetics
Noroviruses (NoVs) are a leading cause of gastroenteritis globally, yet the host factors required for NoV infection are poorly understood. We identified host molecules that are essential for murine NoV (MNoV)-induced cell death, including CD300lf as a proteinaceous receptor. We found that CD300lf is essential for MNoV binding and replication in cell lines and primary cells. Additionally, Cd300lf(-/-) mice are resistant to MNoV infection. Expression of CD300lf in human cells breaks the species barrier that would otherwise restrict MNoV replication. The crystal structure of the CD300lf ectodomain reveals a potential ligand-binding cleft composed of residues that are critical for MNoV infection. Therefore, the presence of a proteinaceous receptor is the primary determinant of MNoV species tropism, whereas other components of cellular machinery required for NoV replication are conserved between humans and mice.
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