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开发一种改进的聚合酶链反应-免疫层析杂交检测法,用于直接从冷却塔水样中检测军团菌和嗜肺军团菌。

Development of an improved PCR-ICT hybrid assay for direct detection of Legionellae and Legionella pneumophila from cooling tower water specimens.

作者信息

Horng Yu-Tze, Soo Po-Chi, Shen Bin-Jon, Hung Yu-Li, Lo Kai-Yin, Su Hsun-Pi, Wei Jun-Rong, Hsieh Shang-Chen, Hsueh Po-Ren, Lai Hsin-Chih

机构信息

Department of Clinical Laboratory Sciences and Medical Biotechnology, National Taiwan University College of Medicine, No. 1. Chan-Dar Street 100, Taipei, Taiwan, ROC.

出版信息

Water Res. 2006 Jun;40(11):2221-9. doi: 10.1016/j.watres.2006.03.033. Epub 2006 May 19.

Abstract

A novelly improved polymerase chian reaction and immunochromatography test (PCR-ICT) hybrid assay comprising traditional multiplex-nested PCR and ICT, (a lateral-flow device) was developed for direct detection of Legionella bacteria from environmental cooling tower samples. The partial 16S rDNA (specific for Legionella spp.) and dnaJ (specific for Legionella pneumophila) genes from Legionella chromosome were first specifically amplified by multiplex-nested PCR, respectively, followed by detection using ICT strip. Reading of results was based on presence or absence of the two test lines on the strips. Presence of test line 1 indicated existence of Legionella spp. specific 16S rDNA and identified Legionella spp. Presence of test line 2 further indicated existence of dnaJ and thus specifically identified L. pneumophila. In contrast, for non-Legionellae bacteria no test line formation was observed. Results of direct detection of Legionella bacteria and L. pneumophila from water tower specimens by this assay showed 100% sensitivity, and 96.6% and 100% specificity, respectively compared with traditional culture, biochemical and serological identification methods. The PCR-ICT hybrid assay does not require sophisticated equipment and was proved to be practically useful in rapid and direct Legionellae detection from environmental water samples.

摘要

一种新改进的聚合酶链反应和免疫层析检测(PCR-ICT)杂交检测方法,该方法包括传统的多重巢式PCR和ICT(一种侧向流动装置),用于直接从环境冷却塔样本中检测军团菌。首先通过多重巢式PCR分别特异性扩增军团菌染色体上的部分16S rDNA(军团菌属特异性)和dnaJ(嗜肺军团菌特异性)基因,然后使用ICT试纸条进行检测。结果读取基于试纸上两条检测线的有无。检测线1的出现表明存在军团菌属特异性16S rDNA并鉴定出军团菌属。检测线2的出现进一步表明存在dnaJ,从而特异性鉴定出嗜肺军团菌。相比之下,对于非军团菌细菌,未观察到检测线形成。通过该检测方法直接检测冷却塔样本中的军团菌和嗜肺军团菌的结果显示,与传统培养、生化和血清学鉴定方法相比,灵敏度分别为100%,特异性分别为96.6%和100%。PCR-ICT杂交检测方法不需要复杂的设备,并且被证明在从环境水样中快速直接检测军团菌方面具有实际应用价值。

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