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通过选择性巢式聚合酶链反应鉴定结核分枝杆菌复合群、鸟分枝杆菌和胞内分枝杆菌。

Identification of Mycobacterium tuberculosis complex, Mycobacterium avium and Mycobacterium intracellulare by selective nested polymerase chain reaction.

作者信息

Oggioni M R, Fattorini L, Li B, De Milito A, Zazzi M, Pozzi G, Orefici G, Valensin P E

机构信息

Dipartimento di Biologia Molecolare, Università di Siena, Italy.

出版信息

Mol Cell Probes. 1995 Oct;9(5):321-6. doi: 10.1016/s0890-8508(95)91604-0.

Abstract

A nested polymerase chain reaction (PCR) procedure was devised for identification of mycobacteria. The outer reaction exploiting genus-specific sequences on the 16S rRNA gene was able to amplify specifically strains of the genus Mycobacterium. The identification of Mycobacterium tuberculosis complex, Mycobacterium avium and Mycobacterium intracellulare was accomplished by selective reamplification of the outer PCR product in three distinct inner amplifications exploiting species-specific primers mapping to a hypervariable region of mycobacterial 16S rRNA. Detection of mycobacteria, other than those for which species-specific primers were used, was accomplished by adding a supplementary genus-specific upper primer to one of the inner reactions. Specificity of amplification was confirmed for clinical isolates and reference strains of different mycobacterial species with the exception of a M. intracellulare type 7 strain which was recognized as M. avium. The amplification protocol presented thus provides a reliable and cost-effective way for identification of clinically relevant mycobacteria.

摘要

设计了一种巢式聚合酶链反应(PCR)方法用于鉴定分枝杆菌。利用16S rRNA基因上属特异性序列的外层反应能够特异性扩增分枝杆菌属的菌株。结核分枝杆菌复合群、鸟分枝杆菌和胞内分枝杆菌的鉴定是通过在三种不同的内层扩增中对外层PCR产物进行选择性再扩增来完成的,这三种内层扩增利用了与分枝杆菌16S rRNA高变区对应的种特异性引物。对于除使用种特异性引物鉴定的分枝杆菌之外的其他分枝杆菌的检测,是通过向其中一个内层反应中添加一条补充性的属特异性上游引物来实现的。除了一株被鉴定为鸟分枝杆菌的7型胞内分枝杆菌外,该扩增方法对不同分枝杆菌临床分离株和参考菌株的扩增特异性得到了证实。因此,所提出的扩增方案为鉴定临床相关分枝杆菌提供了一种可靠且经济高效的方法。

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