OR14I1 is a receptor for the human cytomegalovirus pentameric complex and defines viral epithelial cell tropism
Authors
E, XiaofeiMeraner, Paul
Lu, Ping
Perreira, Jill M.
Aker, Aaron M.
McDougall, William M.
Zhuge, Ronghua
Chan, Gary C.
Gerstein, Rachel M.
Caposio, Patrizia
Yurochko, Andrew D.
Brass, Abraham L.
Kowalik, Timothy F.
UMass Chan Affiliations
Gastroenterology Division, Department of MedicineDepartment of Microbiology and Physiological Systems
Document Type
Journal ArticlePublication Date
2019-04-02Keywords
CRISPR screenOR14I1
human cytomegalovirus
pentameric glycoprotein complex
virus receptor
Amino Acids, Peptides, and Proteins
Computational Biology
Genetic Phenomena
Immunoprophylaxis and Therapy
Microbiology
Viruses
Metadata
Show full item recordAbstract
A human cytomegalovirus (HCMV) pentameric glycoprotein complex (PC), gH-gL-UL128-UL130-UL131A, is necessary for viral infection of clinically relevant cell types, including epithelial cells, which are important for interhost transmission and disease. We performed genome-wide CRISPR/Cas9 screens of different cell types in parallel to identify host genes specifically required for HCMV infection of epithelial cells. This effort identified a multipass membrane protein, OR14I1, as a receptor for HCMV infection. This olfactory receptor family member is required for HCMV attachment, entry, and infection of epithelial cells and is dependent on the presence of viral PC. OR14I1 is required for AKT activation and mediates endocytosis entry of HCMV. We further found that HCMV infection of epithelial cells is blocked by a synthetic OR14I1 peptide and inhibitors of adenylate cyclase and protein kinase A (PKA) signaling. Identification of OR14I1 as a PC-dependent HCMV host receptor associated with epithelial tropism and the role of the adenylate cyclase/PKA/AKT-mediated signaling pathway in HCMV infection reveal previously unappreciated targets for the development of vaccines and antiviral therapies.Source
Proc Natl Acad Sci U S A. 2019 Apr 2;116(14):7043-7052. doi: 10.1073/pnas.1814850116. Epub 2019 Mar 20. Link to article on publisher's site
DOI
10.1073/pnas.1814850116Permanent Link to this Item
http://hdl.handle.net/20.500.14038/41018PubMed ID
30894498Related Resources
Rights
Copyright © 2019 the Author(s). Published by PNAS. This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND).Distribution License
http://creativecommons.org/licenses/by-nc-nd/4.0/ae974a485f413a2113503eed53cd6c53
10.1073/pnas.1814850116
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Except where otherwise noted, this item's license is described as Copyright © 2019 the Author(s). Published by PNAS. This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND).