Mahbubani M H, Bej A K, Miller R, Haff L, DiCesare J, Atlas R M
Department of Microbiology and Immunology, University of Louisville, KY 40292.
Mol Cell Probes. 1990 Jun;4(3):175-87. doi: 10.1016/0890-8508(90)90051-z.
Methods were developed for the detection of Legionella in environmental water sources, based upon the polymerase chain reaction (PCR) and gene probes. All species of Legionella, including all 15 serogroups of L. pneumophila tested, were detected by PCR amplification of a 104 bp DNA sequence that codes for a region of 5S rRNA followed by radiolabelled oligoprobe hybridization to an internal region of the amplified DNA. Strains of L. pneumophila (all serogroups) were specifically detected based upon amplification of a portion of the coding region of the macrophage infectivity potentiator (mip) gene. Pseudomonas spp. that exhibit antigenic cross-reactivity in serological detection methods did not produce positive signals in the PCR-gene probe method using Southern blot analyses. Single cell, single gene Legionella detection was achieved with the PCR-gene probe methods.
基于聚合酶链反应(PCR)和基因探针,开发了用于检测环境水源中军团菌的方法。通过对编码5S rRNA区域的104 bp DNA序列进行PCR扩增,随后用放射性标记的寡核苷酸探针与扩增DNA的内部区域杂交,检测了所有军团菌属物种,包括所测试的嗜肺军团菌的所有15个血清群。基于巨噬细胞感染增强剂(mip)基因编码区一部分的扩增,特异性检测了嗜肺军团菌(所有血清群)菌株。在血清学检测方法中表现出抗原交叉反应的假单胞菌属在使用Southern印迹分析的PCR-基因探针方法中未产生阳性信号。通过PCR-基因探针方法实现了单细胞、单基因军团菌检测。