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基于重复序列的 PCR 对义齿佩戴者分离的白色念珠菌菌株进行分子分型。

Molecular typing of Candida albicans strains isolated from denture wearers by repetitive sequence-based PCR.

机构信息

Faculty of Science, Department of Biology, Basic & Industrial Microbiology Section, Ege University, Bornova-Izmir, Turkey.

出版信息

Eur J Clin Microbiol Infect Dis. 2011 Feb;30(2):141-9. doi: 10.1007/s10096-010-1062-4. Epub 2010 Sep 29.

Abstract

Long-term use of prosthesis is the most important risk factor for the colonization of Candida species on the mucosal surfaces, which can lead to the development of denture-related stomatitis (DRS). Some individuals wearing prosthesis develop DRS and others do not. C. albicans strains isolated from both groups were genotypically compared. The purpose of this study was to determine whether the strain causing prosthesis stomatitis was different from the other strains genotypically. The study included 90 individuals wearing different prostheses and 20 control individuals with natural teeth. In the study 109 C. albicans strains were used which were isolated from the saliva samples and the mucosal surfaces of the tongues and palates of 51 individuals and then defined phenotypically. Phenotypic diagnosis of the isolates was genotypically verified by using species-specific PCR. For molecular typing, repetitive extragenic palindromic sequence polymerase chain reaction (REP-PCR) was employed. The results of the study revealed that REP-PCR had the capability to separate 109 C. albicans strains and six reference strains into 44 genotypes. Whereas C. albicans strains showed heterogenic distribution, C. albicans strains isolated from the individuals suffering from prosthesis stomatitis showed no specific genotypes. REP-PCR is a simple, fast and low-cost method and helped work on a great number of samples.

摘要

长期使用义齿是假膜性念珠菌定植于口腔黏膜表面,进而引发义齿相关性口炎(DRS)的最重要危险因素。一些佩戴义齿的个体出现 DRS,而另一些则没有。本研究对两组个体分离出的白色念珠菌菌株进行了基因分型比较,目的是确定引起义齿性口炎的菌株在基因分型上是否与其他菌株不同。该研究纳入了 90 名佩戴不同义齿的个体和 20 名有天然牙的对照个体。本研究共使用了 109 株从 51 名个体的唾液样本和舌、腭黏膜表面分离出的白色念珠菌菌株,这些菌株首先进行了表型鉴定。采用种特异性 PCR 对分离株的表型诊断进行了基因分型验证。对于分子分型,采用重复回文外显子序列聚合酶链反应(REP-PCR)。研究结果表明,REP-PCR 可将 109 株白色念珠菌菌株和 6 株参考菌株分为 44 种基因型。虽然白色念珠菌菌株表现出异质性分布,但从患有义齿性口炎的个体中分离出的白色念珠菌菌株并未显示出特定的基因型。REP-PCR 是一种简单、快速且成本低廉的方法,有助于处理大量样本。

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