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利用寡核苷酸阵列鉴定具有临床重要性的非发酵革兰氏阴性菌。

Identification of non-fermenting Gram-negative bacteria of clinical importance by an oligonucleotide array.

作者信息

Su Siou Cing, Vaneechoutte Mario, Dijkshoorn Lenie, Wei Yu Fang, Chen Ya Lei, Chang Tsung Chain

机构信息

Department of Medical Laboratory Science and Biotechnology, College of Medicine, National Cheng Kung University, Tainan, Taiwan, ROC.

Laboratory Bacteriology Research (LBR), Department of Clinical Chemistry, Microbiology and Immunology, Blok A, Ghent University Hospital, Ghent, Belgium.

出版信息

J Med Microbiol. 2009 May;58(Pt 5):596-605. doi: 10.1099/jmm.0.004606-0.

Abstract

Many species of non-fermenting Gram-negative bacilli (non-fermenters) are important opportunistic and nosocomial pathogens. Identification of most species of non-fermenters by phenotypic characteristics can be difficult. In this study, an oligonucleotide array was developed to identify 38 species of clinically relevant non-fermenters. The method consisted of PCR-based amplification of 16S-23S rRNA gene intergenic spacer (ITS) regions using bacterial universal primers, followed by hybridization of the digoxigenin-labelled PCR products with oligonucleotide probes immobilized on a nylon membrane. A total of 398 strains, comprising 276 target strains (i.e. strains belonging to the 38 species to be identified) and 122 non-target strains (i.e. strains not included in the array), were analysed by the array. Four target strains (three reference strains and one clinical isolate) produced discrepant identification by array hybridization. Three of the four discordant strains were found to be correctly identified by the array, as confirmed by sequencing of the ITS and 16S rRNA genes, with the remaining one being an unidentified species. The sensitivity and specificity of the array for identification of non-fermenters were 100 and 96.7%, respectively. In summary, the oligonucleotide array described here offers a very reliable method for identification of clinically relevant non-fermenters, with results being available within one working day.

摘要

许多非发酵革兰氏阴性杆菌(非发酵菌)是重要的机会致病菌和医院感染病原体。通过表型特征鉴定大多数非发酵菌可能具有难度。在本研究中,开发了一种寡核苷酸阵列来鉴定38种临床相关的非发酵菌。该方法包括使用细菌通用引物基于PCR扩增16S - 23S rRNA基因间隔区(ITS),随后将地高辛标记的PCR产物与固定在尼龙膜上的寡核苷酸探针杂交。共有398株菌株,包括276株目标菌株(即属于待鉴定的38个物种的菌株)和122株非目标菌株(即阵列中未包含的菌株)通过该阵列进行分析。4株目标菌株(3株参考菌株和1株临床分离株)通过阵列杂交产生了不一致的鉴定结果。经ITS和16S rRNA基因测序证实,4株不一致菌株中的3株被该阵列正确鉴定,其余1株为未鉴定物种。该阵列鉴定非发酵菌的灵敏度和特异性分别为100%和96.7%。总之,本文所述的寡核苷酸阵列提供了一种非常可靠的方法来鉴定临床相关的非发酵菌,且在一个工作日内即可获得结果。

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