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通过核糖体分型和随机扩增多态性DNA聚合酶链式反应对来自不同地理区域的环境、临床和患病鳗鱼创伤弧菌分离株进行遗传相关性分析

Genetic relatedness among environmental, clinical, and diseased-eel Vibrio vulnificus isolates from different geographic regions by ribotyping and randomly amplified polymorphic DNA PCR.

作者信息

Arias C R, Pujalte M J, Garay E, Aznar R

机构信息

Departamento de Microbiología, Universitat de València, Burjassot, E-46100 Valencia, Spain.

出版信息

Appl Environ Microbiol. 1998 Sep;64(9):3403-10. doi: 10.1128/AEM.64.9.3403-3410.1998.

Abstract

Genetic relationships among 132 strains of Vibrio vulnificus (clinical, environmental, and diseased-eel isolates from different geographic origins, as well as seawater and shellfish isolates from the western Mediterranean coast, including reference strains) were analyzed by random amplified polymorphic DNA (RAPD) PCR. Results were validated by ribotyping. For ribotyping, DNAs were digested with KpnI and hybridized with an oligonucleotide probe complementary to a highly conserved sequence in the 23S rRNA gene. Random amplification of DNA was performed with M13 and T3 universal primers. The comparison between ribotyping and RAPD PCR revealed an overall agreement regarding the high level of homogeneity of diseased-eel isolates in contrast to the genetic heterogeneity of Mediterranean isolates. The latter suggests the existence of autochthonous clones present in Mediterranean coastal waters. Both techniques have revealed a genetic proximity among Spanish fish farm isolates and a close relationship between four Spanish eel farm isolates and some Mediterranean isolates. Whereas the differentiation within diseased-eel isolates was only possible by ribotyping, RAPD PCR was able to differentiate phenotypically atypical isolates of V. vulnificus. On the basis of our results, RAPD PCR is proposed as a better technique than ribotyping for rapid typing in the routine analysis of new V. vulnificus isolates.

摘要

采用随机扩增多态性DNA(RAPD)PCR分析了132株创伤弧菌(包括来自不同地理区域的临床、环境和患病鳗鱼分离株,以及来自地中海西部海岸的海水和贝类分离株,还有参考菌株)之间的遗传关系。结果通过核糖体分型进行验证。对于核糖体分型,用KpnI消化DNA,并与与23S rRNA基因中高度保守序列互补的寡核苷酸探针杂交。用M13和T3通用引物进行DNA的随机扩增。核糖体分型和RAPD PCR之间的比较显示,患病鳗鱼分离株高度同质,而地中海分离株存在遗传异质性,二者总体一致。后者表明地中海沿海水域存在本地克隆。两种技术都揭示了西班牙养鱼场分离株之间的遗传亲缘关系,以及四个西班牙鳗鱼养殖场分离株与一些地中海分离株之间的密切关系。虽然患病鳗鱼分离株内部的分化只能通过核糖体分型实现,但RAPD PCR能够区分创伤弧菌表型非典型分离株。基于我们的结果,在对新的创伤弧菌分离株进行常规分析时,RAPD PCR被认为是一种比核糖体分型更好的快速分型技术。

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