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首页> 外文期刊>Journal of Microbiological Methods >Comparative evaluation of Polymerase Chain Reaction-Restriction Enzyme Analysis (PRA) and sequencing of heat shock protein 65 (hsp65) gene for identification of aquatic mycobacteria
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Comparative evaluation of Polymerase Chain Reaction-Restriction Enzyme Analysis (PRA) and sequencing of heat shock protein 65 (hsp65) gene for identification of aquatic mycobacteria

机译:聚合酶链反应限制性酶分析(PRA)和热休克蛋白65(hsp65)基因测序的比较评估,以鉴定水生分枝杆菌

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摘要

Traditional identification of mycobacteria based on cultural and biochemical tests can take several weeks and may fail to provide a precise identification. Polymerase Chain Reaction-Restriction Enzyme Analysis (PRA) of the gene encoding heat shock protein 65 kDa (hsp65) gene has been proposed as a rapid and inexpensive alternative approach. Despite being widely used for differentiation of mammalian mycobacteria, this method has only been applied in the identification of a small number of aquatic mycobacteria. The present study aimed to evaluate the potential use of PRA of hsp65 for the identification of aquatic mycobacteria compared with sequence analysis. Seventy one mycobacterial isolates including, 10 type/reference strains and the remainder field isolates, were subjected to PRA of a 441 bp fragment of this gene. For 68 representative isolates, sequence analysis was performed. All rapidly and slowly growing mycobacteria had best matches with 99.3% to 100% similarity with their corresponding species in the databanks. PRA proved to be a simple and rapid method for identifying aquatic mycobacteria. However, the incidence of similar or identical restriction patterns for some species of mycobacteria, and in particular, identification of new species of mycobacteria is a major problem using such a method. In contrast, the nucleic acid sequencing of the hsp65 gene yielded unambiguous results.
机译:基于文化和生化测试的传统分枝杆菌鉴定可能需要数周时间,并且可能无法提供准确的鉴定结果。已经提出了编码热激蛋白65kDa(hsp65)基因的基因的聚合酶链反应-限制酶分析(PRA),作为一种快速且廉价的替代方法。尽管已广泛用于区分哺乳动物分枝杆菌,但该方法仅用于鉴定少量水生分枝杆菌。本研究旨在评估与序列分析相比,hsp65 PRA在鉴定水生分枝杆菌中的潜在用途。对包括10个类型/参考菌株和其余野外分离株在内的71个分枝杆菌分离株进行了该基因441 bp片段的PRA分析。对于68个代表性分离株,进行了序列分析。所有快速且缓慢生长的分枝杆菌与数据库中其对应物种的相似性最佳,达到99.3%至100%。 PRA被证明是一种鉴定水生分枝杆菌的简单而快速的方法。但是,对于某些分枝杆菌属而言,相似或相同的限制性模式的发生,特别是新分枝杆菌属的鉴定是使用这种方法的主要问题。相反,hsp65基因的核酸测序产生了明确的结果。

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