Infectious Entry of Merkel Cell Polyomavirus

Author:

Becker Miriam12,Dominguez Melissa12,Greune Lilo23,Soria-Martinez Laura124,Pfleiderer Moritz M.45,Schowalter Rachel6,Buck Christopher B.6ORCID,Blaum Bärbel S.45,Schmidt M. Alexander23,Schelhaas Mario124

Affiliation:

1. Institute of Cellular Virology, ZMBE, University of Münster, Münster, Germany

2. Cluster of Excellence EXC1003, Cells in Motion, Münster, Germany

3. Institute of Infectiology, ZMBE, University of Münster, Münster, Germany

4. Research Group, FOR2327 ViroCarb, Coordinating University of Tübingen, Tübingen, Germany

5. Interfaculty Institute of Biochemistry, University of Tübingen, Tübingen, Germany

6. Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA

Abstract

MCPyV is the first polyomavirus directly implicated in the development of an aggressive human cancer, Merkel cell carcinoma (MCC). Although MCPyV is constantly shed from healthy skin, the MCC incidence increases among aging and immunocompromised individuals. To date, the events connecting initial MCPyV infection and subsequent transformation still remain elusive. MCPyV differs from other known polyomaviruses concerning its cell tropism, entry receptor requirements, and infection kinetics. In this study, we examined the cellular requirements for endocytic entry as well as the subcellular localization of incoming virus particles. A thorough understanding of the determinants of the infectious entry pathway and the specific biological niche will benefit prevention of virus-derived cancers such as MCC.

Funder

Deutsche Forschungsgemeinschaft

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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