Mazzoni Elisa, Rotondo John C, Marracino Luisa, Selvatici Rita, Bononi Ilaria, Torreggiani Elena, Touzé Antoine, Martini Fernanda, Tognon Mauro G
Laboratories of Cell Biology and Molecular Genetics, Department of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, University of Ferrara, Ferrara, Italy.
Department of Medical Sciences, Section of Microbiology and Medical Genetics, University of Ferrara, Ferrara, Italy.
Front Oncol. 2017 Nov 29;7:294. doi: 10.3389/fonc.2017.00294. eCollection 2017.
Merkel cell polyomavirus (MCPyV) has been detected in 80% of Merkel cell carcinomas (MCC). In the host, the MCPyV reservoir remains elusive. MCPyV DNA sequences were revealed in blood donor buffy coats. In this study, MCPyV DNA sequences were investigated in the sera ( = 190) of healthy blood donors. Two MCPyV DNA sequences, coding for the viral oncoprotein large T antigen (LT), were investigated using polymerase chain reaction (PCR) methods and DNA sequencing. Circulating MCPyV sequences were detected in sera with a prevalence of 2.6% (5/190), at low-DNA viral load, which is in the range of 1-4 and 1-5 copies/μl by real-time PCR and droplet digital PCR, respectively. DNA sequencing carried out in the five MCPyV-positive samples indicated that the two MCPyV LT sequences which were analyzed belong to the MKL-1 strain. Circulating MCPyV LT sequences are present in blood donor sera. MCPyV-positive samples from blood donors could represent a potential vehicle for MCPyV infection in receivers, whereas an increase in viral load may occur with multiple blood transfusions. In certain patient conditions, such as immune-depression/suppression, additional disease or old age, transfusion of MCPyV-positive samples could be an additional risk factor for MCC onset.
在80%的默克尔细胞癌(MCC)中检测到默克尔细胞多瘤病毒(MCPyV)。在宿主体内,MCPyV的储存库仍不清楚。在献血者的血沉棕黄层中发现了MCPyV DNA序列。在本研究中,对健康献血者的血清(n = 190)中的MCPyV DNA序列进行了研究。使用聚合酶链反应(PCR)方法和DNA测序对编码病毒癌蛋白大T抗原(LT)的两个MCPyV DNA序列进行了研究。在血清中检测到循环MCPyV序列,其流行率为2.6%(5/190),DNA病毒载量较低,通过实时PCR和液滴数字PCR分别为1-4和1-5拷贝/μl。对五个MCPyV阳性样本进行的DNA测序表明,所分析的两个MCPyV LT序列属于MKL-1菌株。循环MCPyV LT序列存在于献血者血清中。来自献血者的MCPyV阳性样本可能是受血者感染MCPyV的潜在载体,而多次输血可能会导致病毒载量增加。在某些患者情况下,如免疫抑制/抑制、其他疾病或老年,输注MCPyV阳性样本可能是MCC发病的另一个危险因素。