Lungu O, Crum C P, Silverstein S
Department of Microbiology, Columbia University, New York, New York 10032.
J Virol. 1991 Aug;65(8):4216-25. doi: 10.1128/JVI.65.8.4216-4225.1991.
Human papillomaviruses (HPVs) may be grouped according to the site from which they are isolated and the disease with which they are associated. We recently identified and cloned HPV type 51 (HPV-51) from a low-grade precancerous lesion (G. Nuovo, E. DeVilliers, R. Levine, S. Silverstein, and C. Crum. J. Virol. 62:1452-1455, 1988). Molecular epidemiologic analysis of cervical lesions, including condylomata and low- and high-grade precancers, revealed that HPV-51 was present in about 5% of the samples we examined. We have now determined the complete nucleotide sequence of this virus and compared it with other sequenced HPVs. Our analysis reveals that the 7,808-bp genome is composed of eight open reading frames which are encoded on the same strand and that this virus is most closely related to HPV-31. Sequence comparisons place this virus in the group of high-risk viruses (those with an increased risk of progressing to malignancy) along with HPV-16, -18, -31, and -33. Morphologic transformation experiments demonstrated that HPV-51 had transformation potential and that transformed cells contained RNAs homologous to E6 and E7.
人乳头瘤病毒(HPV)可根据其分离部位及相关疾病进行分类。我们最近从一个低度癌前病变中鉴定并克隆出了51型人乳头瘤病毒(HPV - 51)(G. 诺沃、E. 德维利尔斯、R. 莱文、S. 西尔弗斯坦和C. 克拉姆,《病毒学杂志》62:1452 - 1455, 1988年)。对包括湿疣以及低度和高度癌前病变在内的宫颈病变进行分子流行病学分析发现,HPV - 51存在于我们检测样本的约5%中。我们现已确定了该病毒的完整核苷酸序列,并将其与其他已测序的HPV进行了比较。我们的分析表明,该7808碱基对的基因组由八个开放阅读框组成,这些开放阅读框编码在同一条链上,且此病毒与HPV - 31关系最为密切。序列比较将该病毒与HPV - 16、 - 18、 - 31和 - 33一同归为高危病毒组(即进展为恶性肿瘤风险增加的病毒)。形态学转化实验表明,HPV - 51具有转化潜能,且转化细胞含有与E6和E7同源的RNA。