Entry of Herpes Simplex Virus 1 and Other Alphaherpesviruses via the Paired Immunoglobulin-Like Type 2 Receptor α

Author:

Arii Jun12,Uema Masashi1,Morimoto Tomomi1,Sagara Hiroshi3,Akashi Hiroomi2,Ono Etsuro4,Arase Hisashi56,Kawaguchi Yasushi1

Affiliation:

1. Division of Viral Infection, Department of Infectious Disease Control, International Research Center for Infectious Diseases

2. Department of Veterinary Microbiology, Graduate School of Agricultural and Life Science, The University of Tokyo, Bunkyo-ku, Tokyo 113-8657

3. Department of Basic Medical Science, The Institute of Medical Science, The University of Tokyo, Minato-ku, Tokyo 108-8639

4. Laboratory of Biomedicine, Center of Biomedical Research, Graduate School of Medicine, Kyushu University, Fukuoka 812-8582

5. Department of Immunochemistry, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871

6. WPI Immunology Frontier Research Center, Osaka University, Suita, Osaka 565-0871, Japan

Abstract

ABSTRACT Herpes simplex virus 1 (HSV-1) enters cells either via fusion of the virion envelope and host cell plasma membrane or via endocytosis, depending on the cell type. In the study reported here, we investigated a viral entry pathway dependent on the paired immunoglobulin-like type 2 receptor α (PILRα), a recently identified entry coreceptor for HSV-1 that associates with viral envelope glycoprotein B (gB). Experiments using inhibitors of endocytic pathways and ultrastructural analyses of Chinese hamster ovary (CHO) cells transduced with PILRα showed that HSV-1 entry into these cells was via virus-cell fusion at the cell surface. Together with earlier observations that HSV-1 uptake into normal CHO cells and those transduced with a receptor for HSV-1 envelope gD is mediated by endocytosis, these results indicated that expression of PILRα produced an alternative HSV-1 entry pathway in CHO cells. We also showed that human and murine PILRα were able to mediate entry of pseudorabies virus, a porcine alphaherpesvirus, but not of HSV-2. These results indicated that viral entry via PILRα appears to be conserved but that there is a PILRα preference among alphaherpesviruses.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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