High load of Merkel cell polyomavirus DNA detected in the normal skin of Japanese patients with Merkel cell carcinoma

被引:16
作者
Hashida, Yumiko [1 ]
Nakajima, Kimiko [2 ]
Nakajima, Hideki [2 ]
Shiga, Takeo [2 ]
Tanaka, Moe [1 ]
Murakami, Masanao [1 ]
Matsuzaki, Shigenobu [1 ]
Naganuma, Seiji [3 ]
Kuroda, Naoki [4 ]
Seki, Yasutaka [5 ]
Katano, Harutaka [6 ]
Sano, Shigetoshi [2 ]
Daibata, Masanori [1 ]
机构
[1] Kochi Univ, Kochi Med Sch, Dept Microbiol & Infect, Kochi 7838505, Japan
[2] Kochi Univ, Kochi Med Sch, Dept Dermatol, Kochi, Japan
[3] Kochi Univ, Kochi Med Sch, Dept Pathol, Kochi, Japan
[4] Kochi Red Cross Hosp, Dept Pathol, Kochi, Japan
[5] Kochi Univ, Kochi Med Sch, Dept Mol Biophys, Kochi, Japan
[6] Natl Inst Infect Dis, Dept Pathol, Tokyo, Japan
关键词
Merkel cell polyomavirus; Merkel cell carcinoma; Human skin virome; MCPyV genotype; TUMOR-SPECIFIC SIGNATURE; FREQUENT DETECTION; T-ANTIGEN; VP1; GENE; EPIDEMIOLOGY; INTEGRATION;
D O I
10.1016/j.jcv.2016.07.011
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Although Merkel cell polyomavirus (MCPyV) has the potential to cause Merkel cell carcinoma (MCC), it is also found in the normal skin of healthy individuals. However, the mechanism for transformation of MCPyV to an oncogenic form is unknown. Objectives: To investigate the levels of MCPyV infection in the normal skin patients with MCC compared with those in a control cohort. Study design: We studied a total of six Japanese patients with cutaneous MCC. Sun-exposed and sun unexposed skin swabs were obtained and analyzed for MCPyV loads using quantitative real-time polymerase chain reaction. Results: At first, we found a patient with MCC carrying an extremely high load of MCPyV DNA in normal skin. This unique case prompted us to further explore the levels of MCPyV as skin microbiota in patients with MCC. We showed that MCPyV DNA levels were significantly higher in swabs obtained from normal skin samples of six patients with MCC compared with those from 30 age-matched healthy individuals and 19 patients with other cutaneous cancers. Whereas MCPyV strains obtained from the normal skin of patients with MCC had gene sequences without structural alterations, sequences of the tumor-derived strains showed truncating mutations or deletions. Conclusions: Although the number of patients with MCC studied was small, our findings suggest that MCC may occur with a background of high MCPyV load in the skin, and are expected to stimulate further studies on whether such skin virome levels could be one of predictive markers for the development of MCC. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:101 / 107
页数:7
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