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[聚合酶链反应用于检测伯氏疏螺旋体DNA]

[Polymerase chain reaction in the demonstration of Borrelia burgdorferi DNA].

作者信息

Kramer M D, Moter S E, Simon M M, Ebnet K, Wallich R

机构信息

Universitäts-Hautklinik Heidelberg.

出版信息

Hautarzt. 1990 Nov;41(11):587-90.

PMID:2276912
Abstract

Borrelia burgdorferi is the etiological agent of Lyme disease. Certain diagnostic problems associated with Lyme disease could be solved if a sensitive detection method were available for the pathogen: the polymerase chain reaction for the sensitive detection of Borrelia burgdorferi is a possible candidate. The latest methods for the amplification of Borrelia burgdorferi DNA are discussed. In particular, a method for the amplification of a Borrelia burgdorferi flagellin (41 kDa antigen) gene segment by the polymerase chain reaction is presented. Owing to its high degree of conservation between different Borrelia burgdorferi isolates, the flagellin gene is a suitable target sequence for gene amplification. In conclusion, the polymerase chain reaction is now ready to be used on clinical specimens. This technique will allow investigation of aspects concerning latency and recurrency of Borrelia burgdorferi in infected individuals.

摘要

伯氏疏螺旋体是莱姆病的病原体。如果能有一种针对该病原体的灵敏检测方法,那么与莱姆病相关的某些诊断问题就能得到解决:用于灵敏检测伯氏疏螺旋体的聚合酶链反应可能是一个选择。本文讨论了伯氏疏螺旋体DNA扩增的最新方法。特别介绍了一种通过聚合酶链反应扩增伯氏疏螺旋体鞭毛蛋白(41 kDa抗原)基因片段的方法。由于鞭毛蛋白基因在不同伯氏疏螺旋体分离株之间具有高度保守性,所以它是基因扩增的合适靶序列。总之,聚合酶链反应现已可用于临床标本检测。这项技术将有助于研究感染个体中伯氏疏螺旋体的潜伏和复发情况。

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