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通过共识和巢式型特异性聚合酶链反应(PCR)结合循环测序鉴定多种生殖道人乳头瘤病毒(HPV)类型和序列变异体。

Identification of multiple genital HPV types and sequence variants by consensus and nested type-specific PCR coupled with cycle sequencing.

作者信息

Chow V T, Loh E, Yeo W M, Tan S Y, Chan R

机构信息

Department of Microbiology, Faculty of Medicine, National University of Singapore, Singapore.

出版信息

Pathology. 2000 Aug;32(3):204-8.

Abstract

Consensus and type-specific HPV primers were employed for PCR and cycle sequencing of genital HPVs in scrapings and colposcopically directed biopsies of the cervix from a cohort of 188 female sex workers. A total of 27 individuals tested positive for a broad spectrum of HPV types, including HPVs 6b, 16, 18, 31, 33, 34, 35, 45, 56 and 58, as well as a new HPV type, with seven individuals displaying dual infections. Good correlation between the results of individually paired samples was observed. A HPV 16 primer biotinylated at the 5' end was also used as a probe, which could successfully detect amplified products of HPV 16 but not other HPV types tested by an automated ELISA detection system. DNA sequence analysis revealed several HPV sequence variants that harbored mutations, especially in the E6 gene, many of which culminated in non-conservative amino acid substitutions in the transforming E6 oncoprotein. Such an approach of coupling PCR with cycle sequencing permits the determination of many known and even novel HPV types associated with varying degrees of risk to cervical carcinogenesis, and enables the identification of HPV sequence variants of putative biological and clinical significance, thus justifying its utility as an adjunct tool to complement cervical cytology and colposcopy. This study also emphasises the need for educational, interventional and behavioral modification to minimise HPV transmission, such as through consistent condom usage among sex workers.

摘要

使用共识性和型特异性人乳头瘤病毒(HPV)引物,对188名女性性工作者宫颈刮片及阴道镜引导下活检组织中的生殖道HPV进行聚合酶链反应(PCR)和循环测序。共有27人检测出多种HPV类型呈阳性,包括HPV 6b、16、18、31、33、34、35、45、56和58,以及一种新的HPV类型,其中7人呈现双重感染。观察到单独配对样本的结果之间具有良好的相关性。5'端生物素化的HPV 16引物也用作探针,通过自动化酶联免疫吸附测定(ELISA)检测系统,该探针能够成功检测HPV 16的扩增产物,但不能检测其他检测的HPV类型。DNA序列分析揭示了几个携带突变的HPV序列变体,特别是在E6基因中,其中许多最终导致转化性E6癌蛋白中出现非保守氨基酸取代。这种将PCR与循环测序相结合的方法,能够确定许多与宫颈癌发生风险程度不同相关的已知甚至新型HPV类型,并能够识别具有假定生物学和临床意义的HPV序列变体,从而证明其作为补充宫颈细胞学和阴道镜检查的辅助工具的实用性。本研究还强调需要进行教育、干预和行为改变,以尽量减少HPV传播,例如性工作者始终坚持使用避孕套。

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