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用于鉴别中间普氏菌和变黑普氏菌的优化寡核苷酸。

Optimized oligonucleotides for the differentiation of Prevotella intermedia and Prevotella nigrescens.

作者信息

Conrads G, Pelz K, Hughes B, Seyfarth I, Devine D A

机构信息

Klinik für Zahnerheltung, Parodontologie und Präventive Zahnhelkunde der Universitätklinik Aachen, Germany.

出版信息

Oral Microbiol Immunol. 1997 Apr;12(2):117-20. doi: 10.1111/j.1399-302x.1997.tb00627.x.

Abstract

The gram-negative, anaerobic bacterium Prevotella intermedia plays an important role in the progression of periodontitis, whereas the etiological role of the closely related but phenotypically indistinguishable species Prevotella nigrescens is controversial. To differentiate between these species properly, 16S rDNA/RNA directed, computer-optimized oligonucleotides were designed and tested with 26 P. intermedia, 26 P. nigrescens and a number of closely and more distantly related strains. The oligonucleotides were used as primers in a polymerase chain reaction and could be demonstrated to be species specific with a detection limit of 50 bacterial cells, which could also be detected when diluted 1:10(5) with different plaque bacteria. In addition, the described oligonucleotides were digoxigenin-labeled at the 3' end and used as DNA probes in a dot blot hybridization assay. This assay, although slightly less sensitive than the polymerase chain reaction-based method, gave species-specific reactions and also allowed (semi-)quantification of bacterial cells in clinical specimens.

摘要

革兰氏阴性厌氧菌中间普氏菌在牙周炎进展中起重要作用,而与之密切相关但表型难以区分的变黑普氏菌的病因学作用存在争议。为了正确区分这些菌种,设计了针对16S rDNA/RNA的计算机优化寡核苷酸,并对26株中间普氏菌、26株变黑普氏菌以及一些近缘和远缘相关菌株进行了测试。这些寡核苷酸用作聚合酶链反应的引物,可证明具有种特异性,检测限为50个细菌细胞,当与不同的菌斑细菌按1:10(5)稀释时也能检测到。此外,所描述的寡核苷酸在3'端用洋地黄毒苷标记,并用作斑点印迹杂交试验中的DNA探针。该试验虽然比基于聚合酶链反应的方法灵敏度略低,但能产生种特异性反应,还能对临床标本中的细菌细胞进行(半)定量。

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