Zuerner R L, Alt D, Bolin C A
Leptospirosis and Mycobacteriosis Research Unit, U.S. Department of Agriculture, Ames, Iowa 50010, USA.
J Clin Microbiol. 1995 Dec;33(12):3284-9. doi: 10.1128/jcm.33.12.3284-3289.1995.
A PCR-based assay was developed for typing L. interrogans sensu lato serovars. The assay is designed to exploit the presence of many copies of the leptospiral insertion sequence IS1533 and IS1533-like sequences present in the genomes of most leptospiral serovars. The PCR primers were designed to amplify DNA of unknown sequence between closely placed IS1533 or IS1533-like sequences. Amplification reactions primed with IS1533-based primers generated products of different sizes. When few copies of IS1533 were present in the genome, amplification of a few products was still detected. These results suggest that IS1533 elements may be found close together. Analysis of DNA amplified from different serovars showed the presence of differently sized products, thus enabling the serovars to be identified. Genetic variation among isolates within the same serovar was also demonstrated with the IS1533-based primers. Amplification reactions using DNA extracted from the urine of infected animals generated specific products which were similar to the products generated from purified bacterial DNA. These results demonstrate that this assay is selective enough to be used for typing leptospiral serovars from clinical material and thus allows leptospiral typing without isolation of the bacteria in pure culture.
开发了一种基于聚合酶链反应(PCR)的检测方法用于钩端螺旋体狭义血清型分型。该检测方法旨在利用大多数钩端螺旋体血清型基因组中存在的许多拷贝的钩端螺旋体插入序列IS1533和类IS1533序列。PCR引物设计用于扩增紧密排列的IS1533或类IS1533序列之间未知序列的DNA。以基于IS1533的引物引发的扩增反应产生了不同大小的产物。当基因组中存在少量IS1533拷贝时,仍能检测到少量产物的扩增。这些结果表明IS1533元件可能紧密相邻。对不同血清型扩增的DNA分析显示存在不同大小的产物,从而能够鉴定血清型。基于IS1533的引物也证明了同一血清型内分离株之间的遗传变异。使用从感染动物尿液中提取的DNA进行的扩增反应产生了与从纯化细菌DNA产生的产物相似的特异性产物。这些结果表明该检测方法具有足够的选择性,可用于对临床材料中的钩端螺旋体血清型进行分型,从而无需在纯培养中分离细菌即可进行钩端螺旋体分型。