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基于16S rRNA的夹心杂交分析法对军团菌进行灵敏的属特异性检测。

Sensitive genus-specific detection of Legionella by a 16S rRNA based sandwich hybridization assay.

作者信息

Leskelä Tarja, Tilsala-Timisjärvi Anu, Kusnetsov Jaana, Neubauer Peter, Breitenstein Antje

机构信息

Bioprocess Engineering Laboratory, Department of Process and Environmental Engineering and Biocenter Oulu, University of Oulu, PO Box 4300, FI-90014 University of Oulu, Finland.

出版信息

J Microbiol Methods. 2005 Aug;62(2):167-79. doi: 10.1016/j.mimet.2005.02.008. Epub 2005 Apr 7.

Abstract

The aim of this study was to develop a sensitive, cultivation-independent analytical method for Legionella in man-made water systems which can be performed within one day in crude sample extracts. The new assay for the genus Legionella is a paramagnetic bead based fluorescence sandwich hybridization assay (SHA) for the 16S rRNA based on two oligonucleotide probes which makes the method highly specific. An advantage over RT-PCR is the exclusive detection of viable cells and, due to the high number of 16S RNA molecules, the possibility to apply the method directly in crude cell extracts without prior purification of the nucleic acids. A high sensitivity was obtained by modifying the probe chemistry and hybridization conditions. The most sensitive assay uses a 3'-end biotin-labelled capture probe and a 3'-end DIG tailed detection probe and has a detection limit of 20 amol target molecules corresponding to 1.2x10(7) molecules of 16S rRNA and approximately 1800 Legionella cells. Using this assay type the number of Legionella cells was determined in Legionella contaminated water samples. The results show that the developed SHA can be applied for estimation of the approximate number of Legionella cells based on the number of 16S rRNA molecules in a water sample.

摘要

本研究的目的是开发一种灵敏的、无需培养的分析方法,用于检测人造水系统中的军团菌,该方法可在一天内对粗样品提取物进行检测。针对军团菌属的新检测方法是一种基于顺磁珠的荧光夹心杂交分析法(SHA),用于检测基于16S rRNA的两种寡核苷酸探针,这使得该方法具有高度特异性。与逆转录聚合酶链反应(RT-PCR)相比,该方法的优势在于仅检测活细胞,并且由于16S RNA分子数量众多,无需事先纯化核酸即可直接将该方法应用于粗细胞提取物。通过改进探针化学和杂交条件,获得了高灵敏度。最灵敏的检测方法使用3'-末端生物素标记的捕获探针和3'-末端地高辛标记的检测探针,检测限为20 amol目标分子,相当于1.2×10⁷个16S rRNA分子和约1800个军团菌细胞。使用这种检测类型,测定了军团菌污染水样中的军团菌细胞数量。结果表明,所开发的SHA可用于根据水样中16S rRNA分子的数量估算军团菌细胞的大致数量。

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