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Updated: Apr 17, 2026

Merkel Cell Polyomavirus Infection and Detection
Published on: February 7, 2019
Characterization of self-assembled virus-like particles of Merkel cell polyomavirus
Tian-Cheng Li1, Kenji Iwasaki2, Harutaka Katano3
1Department of Virology II, National Institute of Infectious Diseases, Tokyo, Japan.
Abstract:
In our recombinant baculovirus system, VP1 protein of merkel cell polyomavirus (MCPyV), which is implicated as a causative agent in Merkel cell carcinoma, was self-assembled into MCPyV-like particles (MCPyV-LP) with two different sizes in insect cells, followed by being released into the culture medium. DNA molecules of 1.5- to 5-kb, which were derived from host insect cells, were packaged in large, ~50-nm spherical particles but not in small, ~25-nm particles. Structure reconstruction using cryo-electron microscopy showed that large MCPyV-LPs are composed of 72 pentameric capsomeres arranged in a T = 7 icosahedral surface lattice and are 48 nm in diameter. The MCPyV-LPs did not share antigenic determinants with BK- and JC viruses (BKPyV and JCPyV). The VLP-based enzyme immunoassay was applied to investigate age-specific prevalence of MCPyV infection in the general Japanese population aged 1-70 years. While seroprevalence of MCPyV increased with age in children and young individuals, its seropositivity in each age group was lower compared with BKPyV and JCPyV.
Insights
Merkel cell polyomavirus (MCPyV) VP1 protein self-assembles into virus-like particles (MCPyV-LPs) in insect cells. These particles package host DNA and show age-specific seroprevalence in Japan.
Area of Science:
- Virology
- Structural Biology
- Epidemiology
Background:
- Merkel cell polyomavirus (MCPyV) is linked to Merkel cell carcinoma.
- MCPyV VP1 protein self-assembly into virus-like particles (VLPs) is crucial for understanding viral structure and infection.
- Investigating MCPyV seroprevalence provides insights into population-level exposure and immune responses.
Purpose of the Study:
- To characterize MCPyV-like particles (MCPyV-LPs) produced in a recombinant baculovirus system.
- To determine the structural features and DNA packaging capabilities of MCPyV-LPs.
- To assess the age-specific seroprevalence of MCPyV infection in the Japanese population.
Main Methods:
- Recombinant baculovirus expression system for MCPyV VP1 protein production.
- Cryo-electron microscopy for structural analysis of MCPyV-LPs.
- Enzyme immunoassay (EIA) for serological detection of MCPyV antibodies.
Main Results:
- MCPyV VP1 self-assembled into two sizes of MCPyV-LPs (~25 nm and ~50 nm) in insect cells.
- Large MCPyV-LPs (~48 nm) packaged host DNA and exhibited a T=7 icosahedral structure with 72 pentameric capsomeres.
- MCPyV-LPs did not share antigenic determinants with BKPyV and JCPyV.
- Seroprevalence of MCPyV increased with age in Japanese individuals aged 1-70 years, but was lower than for BKPyV and JCPyV.
Conclusions:
- MCPyV-LPs can be successfully produced and characterized using a baculovirus system.
- The structural and antigenic properties of MCPyV-LPs were elucidated.
- Age-specific seroprevalence data suggest varying exposure patterns of MCPyV compared to other polyomaviruses in Japan.
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