Department of Microbiology and Infection, Kochi Medical School, Kochi University, Kochi, Japan.
Clinical Laboratory Science, Nitobe Bunka College, Tokyo, Japan.
J Infect Dis. 2018 Apr 23;217(10):1601-1611. doi: 10.1093/infdis/jiy070.
Merkel cell polyomavirus (MCPyV) is a ubiquitous cutaneous virus that causes Merkel cell carcinoma, which develops preferentially in white populations from Europe and North America. However, the genomic variations of MCPyV among ethnic groups have not been well delineated, and even less is known regarding alterations in the noncoding control region (NCCR) in the general population.
MCPyV strains recovered from skin swab specimens from 250 healthy participants with distinct ethnicities and geographic origins were subjected to sequencing analysis of the NCCR.
A 25-base pair tandem repeat caused by a 25-base pair insertion within the NCCR was found predominantly in Japanese and East Asian individuals. Based on the presence of 2 other insertions and a deletion, the NCCR could be classified further into 5 genotypes. This tandem repeat was also found exclusively in the NCCR from Japanese patients with Merkel cell carcinoma, while other genotypes were detected in white patients from Europe and North America.
Our results suggest that the MCPyV NCCR varies according to ethnicity and that assessing the short NCCR sequence provides a rapid and simple means for identification of the Japanese and East Asian variant genotype. It remains to be established whether these NCCR variations are associated differentially with the pathogenesis of MCPyV-driven Merkel cell carcinoma between regions with varying endemicity.
默克尔细胞多瘤病毒(MCPyV)是一种普遍存在的皮肤病毒,可导致默克尔细胞癌,这种癌症主要发生在欧洲和北美的白种人群中。然而,不同种族间 MCPyV 的基因组变异尚未得到很好的描述,关于普通人群中非编码控制区(NCCR)的改变,人们知之甚少。
对来自 250 名具有不同种族和地理起源的健康参与者的皮肤拭子标本中回收的 MCPyV 株进行 NCCR 测序分析。
在 NCCR 内发现了一个 25 个碱基对的插入引起的 25 个碱基对串联重复,主要存在于日本和东亚人群中。根据另外 2 个插入和 1 个缺失的存在,可以将 NCCR 进一步分为 5 种基因型。这种串联重复也仅在日本 Merkel 细胞癌患者的 NCCR 中发现,而其他基因型则在来自欧洲和北美的白种患者中检测到。
我们的研究结果表明,MCPyV 的 NCCR 随种族而变化,评估短 NCCR 序列为鉴定日本和东亚变异基因型提供了一种快速简便的方法。这些 NCCR 变异是否与不同流行地区 MCPyV 驱动的 Merkel 细胞癌的发病机制存在差异仍有待确定。