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通过靶向16S rRNA开发一种基于DNA的无PCR检测方法,用于环境样本中弧菌属的特异性检测。

Development of a PCR-free DNA-based assay for the specific detection of Vibrio species in environmental samples by targeting the 16S rRNA.

作者信息

Da-Silva E, Barthelmebs L, Baudart J

机构信息

Biocapteurs Analyses Environment, Université Perpignan, Via Domitia, 66860, Perpignan, France.

CNRS, Laboratoire de Biodiversité et Biotechnologies Microbiennes (LBBM), Observatoire Océanologique, Sorbonne Universités, UPMC Univ. Paris 06, F-66650, Banyuls/Mer, France.

出版信息

Environ Sci Pollut Res Int. 2017 Feb;24(6):5690-5700. doi: 10.1007/s11356-016-8193-9. Epub 2016 Dec 30.

Abstract

A novel PCR-free DNA-based assay was developed for the detection of Vibrio spp. A sandwich hybridization format using an immobilized capture probe and a labeled signal probe was selected and combined with chemiluminescent method for the detection of the RNA target. In a first step, probes were validated using positive controls (PCs). A linearity was observed between 0.1 and 2.5 nM of PC, and detection limit was determined as 0.1 nM. In a second step, specificity was checked by using RNA extracted from a panel of 31 environmental bacterial strains. Detection limit of 5 ng μL of total fragmented RNA was obtained, and the assay allowed a good discrimination between the 21 Vibrio and the 10 non-Vibrio strains tested. Finally, the DNA-based assay was successfully applied to analysis of spiked and natural environmental samples. Stability and analysis time of the DNA-based assay were also investigated to optimize working conditions. We demonstrated that microplates can be coated beforehand with capture probe and stored at 4 °C without any buffer in wells for at least 30 days. The use of the pre-made plates enables the assay to be completed in 2 h. The developed assay appeared as an interesting tool to determine the presence of bacteria in environmental samples.

摘要

开发了一种新型的基于DNA的无PCR检测方法用于检测弧菌属。选择了一种使用固定化捕获探针和标记信号探针的夹心杂交形式,并与化学发光法相结合用于检测RNA靶标。第一步,使用阳性对照(PCs)验证探针。在0.1至2.5 nM的PC之间观察到线性关系,检测限确定为0.1 nM。第二步,通过使用从31株环境细菌菌株中提取的RNA检查特异性。获得了5 ng μL总片段化RNA的检测限,该检测方法能够很好地区分所测试的21株弧菌和10株非弧菌菌株。最后,基于DNA的检测方法成功应用于加标和天然环境样品的分析。还研究了基于DNA的检测方法的稳定性和分析时间以优化工作条件。我们证明微孔板可以预先用捕获探针包被,并在4°C下在孔中不添加任何缓冲液的情况下储存至少30天。使用预制板可使检测在2小时内完成。所开发的检测方法似乎是一种用于确定环境样品中细菌存在的有趣工具。

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