Redkar R J, Dubé M P, McCleskey F K, Rinaldi M G, Del Vecchio V G
Molecular Biology Institute, University of Scranton, Pennsylvania 18510, USA.
J Clin Microbiol. 1996 Jul;34(7):1677-81. doi: 10.1128/JCM.34.7.1677-1681.1996.
A repetitive sequence-based PCR (rep-PCR) technique was developed to characterize the genotypic relatedness among Candida rugosa isolates. Two repetitive sequences, viz., Care-2 and Com29 from Candida albicans, were used to design primers Ca-21, Ca-22, and Com-21, respectively. When used alone or in combination, these primers generated discriminatory fingerprints by amplifying the adjacent variable regions of the genome. Twenty-three isolates from burn patients, eight from other human sources, and four C. rugosa isolates pathogenic in animals were placed into nine fingerprinting groups. Different primers placed these isolates into identical groups, indicating that rep-PCR is a specific and reproducible technique for molecular characterization of C. rugosa. Moreover, these primers unequivocally discriminated among other important Candida species such as C. albicans, C. glabrata, C. tropicalis, C. krusei, C. parapsilosis, C. kefyr, and C. lusitaniae. These data confirm the conservation of repetitive sequences in Candida species. Because of its ease and sensitivity, rep-PCR offers a relatively rapid and discriminatory method for molecular typing of C. rugosa in outbreaks.
开发了一种基于重复序列的PCR(rep-PCR)技术,以表征皱落假丝酵母分离株之间的基因型相关性。使用来自白色念珠菌的两个重复序列,即Care-2和Com29,分别设计引物Ca-21、Ca-22和Com-21。当单独使用或组合使用时,这些引物通过扩增基因组的相邻可变区产生可区分的指纹图谱。来自烧伤患者的23株分离株、来自其他人类来源的8株分离株以及4株对动物致病的皱落假丝酵母分离株被分为9个指纹图谱组。不同的引物将这些分离株归入相同的组,表明rep-PCR是一种用于皱落假丝酵母分子表征的特异性和可重复技术。此外,这些引物能够明确区分其他重要的念珠菌物种,如白色念珠菌、光滑念珠菌、热带念珠菌、克柔念珠菌、近平滑念珠菌、凯菲念珠菌和葡萄牙念珠菌。这些数据证实了念珠菌物种中重复序列的保守性。由于其简便性和敏感性,rep-PCR为爆发中皱落假丝酵母的分子分型提供了一种相对快速且具有区分性的方法。