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用于检测人乳头瘤病毒DNA的单管实时巢式聚合酶链反应

Single-tube real-time nested polymerase chain reaction for detecting human papillomavirus DNA.

作者信息

Strauss S, Jordens J Z, Desselberger U, Gray J J

机构信息

Clinical Microbiology and Public Health Laboratory, Addenbrooke's Hospital, Cambridge, United Kingdom.

出版信息

Diagn Mol Pathol. 2000 Sep;9(3):151-7. doi: 10.1097/00019606-200009000-00005.

Abstract

A single-tube real-time nested polymerase chain reaction (PCR) was developed to detect human Papillomavirus (HPV) DNA in a closed tube system. The oligonucleotide primers MY09/MY11 and GP5+/GP6+ were included in contiguous reactions, thus eliminating the need to transfer first round PCR product into a second tube. The sensitivity and specificity of the optimized single-tube nested PCR were comparable with that achieved by two separate reactions on a conventional thermal block system using serial dilutions derived from plasmids containing DNA of 20 HPV types. A minimum of 10 copies of HPV types 11 and 16 DNA could be detected by both systems. In clinical samples, HPV types 1A, 2, 3, 5, 6-8, 10, 11, 14, 16, 17, 18, 20, 31, 33, 35, 39, 45, 49, 50, 52-54, 57, 62, 66, 70, CP8304 and LVX82/MM7 could be detected by both PCR methods. A total of 145 samples collected from patients were tested for the presence of HPV DNA with the two PCR systems; 124 (86.1%) of 144 samples gave concordant results in both assays. The HPV DNA positive PCR amplicons were typed and concordant results were obtained in 47 of 67 positive samples tested in both amplicons. In samples containing multiple HPV types at least one type was common to both amplicons.

摘要

开发了一种单管实时巢式聚合酶链反应(PCR),用于在封闭管系统中检测人乳头瘤病毒(HPV)DNA。寡核苷酸引物MY09/MY11和GP5+/GP6+包含在连续反应中,从而无需将第一轮PCR产物转移到第二个管中。优化后的单管巢式PCR的灵敏度和特异性与在传统热块系统上使用来自包含20种HPV类型DNA的质粒的系列稀释液进行的两个单独反应所达到的灵敏度和特异性相当。两种系统均可检测到至少10份HPV 11型和16型DNA拷贝。在临床样本中,两种PCR方法均可检测到HPV 1A、2、3、5、6 - 8、10、11、14、16、17、18、20、31、33、35、39、45、49、50、52 - 54、57、62、66、70、CP8304和LVX82/MM7型。使用这两种PCR系统对从患者收集的总共145个样本进行HPV DNA检测;144个样本中的124个(86.1%)在两种检测中结果一致。对HPV DNA阳性PCR扩增子进行分型,在两种扩增子检测的67个阳性样本中有47个获得了一致结果。在含有多种HPV类型的样本中,两种扩增子至少有一种共同的类型。

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