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一种用于检测沙眼衣原体的商业聚合酶链反应检测方法的评估。

Evaluation of a commercial polymerase chain reaction assay for the detection of Chlamydia trachomatis.

作者信息

Kay I D, Palladino S, Alexander R, Leahy B J, Pearman J W

机构信息

Department of Microbiology, Royal Perth Hospital, Australia.

出版信息

Diagn Microbiol Infect Dis. 1997 Jun;28(2):75-9. doi: 10.1016/s0732-8893(97)00003-5.

Abstract

Cell culture has traditionally been considered the most sensitive method for detecting Chlamydia trachomatis from clinical specimens, but depends upon the organisms being viable at the time of cell inoculation. Furthermore, cell culture is slow and labor intensive. Even when a special transport medium is used, there is a progressive loss of viability of C. trachomatis during transport. The detection of C. trachomatis by cell culture is more rapid when immunofluorescence is used to detect early antigen, but requires considerable experience to interpret. The Amplicor C. trachomatis system is a commercial polymerase chain reaction (PCR)-based assay combined with nucleic acid hybridization for the direct detection of C. trachomatis in urine and swabs of appropriate sites, with results available within 6 h. All specimens for C. trachomatis received by the Royal Perth Hospital Department of Microbiology during the period 1 July 1994 to 30 June 1995 that were suitable for culture and Amplicor PCR were tested by both methods (2029 specimens). Discordant results were obtained in nine cases and resolved by additional testing. Seventy-one specimens were confirmed as true positives, of these Amplicor PCR correctly detected 67 (sensitivity 94.4%) and culture correctly detected 62 (sensitivity 87.3%). The Amplicor PCR assay was found to be more sensitive and as specific as culture. It had the added advantages of ease of use, rapid availability of results, standardization and was more suited than culture to processing large number of specimens.

摘要

传统上,细胞培养一直被认为是从临床标本中检测沙眼衣原体最敏感的方法,但这取决于在细胞接种时病原体是否存活。此外,细胞培养耗时且劳动强度大。即使使用特殊的运输培养基,沙眼衣原体在运输过程中的活力也会逐渐丧失。当使用免疫荧光检测早期抗原时,通过细胞培养检测沙眼衣原体的速度更快,但需要相当多的经验来解读结果。Amplicor沙眼衣原体检测系统是一种基于商业聚合酶链反应(PCR)并结合核酸杂交的检测方法,用于直接检测尿液和合适部位拭子中的沙眼衣原体,6小时内可得到结果。1994年7月1日至1995年6月30日期间,珀斯皇家医院微生物科接收的所有适合培养和Amplicor PCR检测的沙眼衣原体标本均采用这两种方法进行检测(共2029份标本)。9例结果不一致,通过额外检测得以解决。71份标本被确认为真阳性,其中Amplicor PCR正确检测出67份(敏感性94.4%),培养正确检测出62份(敏感性87.3%)。结果发现,Amplicor PCR检测方法比培养更敏感,特异性相同。它还具有使用方便、结果快速可得、标准化等优点,并且比培养更适合处理大量标本。

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