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用于快速同时检测水生动物中十种病原菌的集成在微流控盘芯片上的实时荧光环介导等温扩增检测方法(芯片上的环介导等温扩增法)的开发与评估

Development and evaluation of a real-time fluorogenic loop-mediated isothermal amplification assay integrated on a microfluidic disc chip (on-chip LAMP) for rapid and simultaneous detection of ten pathogenic bacteria in aquatic animals.

作者信息

Zhou Qian-Jin, Wang Lei, Chen Jiong, Wang Rui-Na, Shi Yu-Hong, Li Chang-Hong, Zhang De-Min, Yan Xiao-Jun, Zhang Yan-Jun

机构信息

Laboratory of Biochemistry and Molecular Biology, School of Marine Sciences, Ningbo University, Ningbo 315211, PR China; Ningbo Branch of National Engineering Research Center for Beijing Biochip Technology, Ningbo University, Ningbo 315211, PR China.

CapitalBio Corporation, 18 Life Science Parkway, Changping District, Beijing 102206, PR China.

出版信息

J Microbiol Methods. 2014 Sep;104:26-35. doi: 10.1016/j.mimet.2014.06.008. Epub 2014 Jun 20.

Abstract

Rapid, low-cost, and user-friendly strategies are urgently needed for early disease diagnosis and timely treatment, particularly for on-site screening of pathogens in aquaculture. In this study, we successfully developed a real-time fluorogenic loop-mediated isothermal amplification assay integrated on a microfluidic disc chip (on-chip LAMP), which was capable of simultaneously detecting 10 pathogenic bacteria in aquatic animals, i.e., Nocardia seriolae, Pseudomonas putida, Streptococcus iniae, Vibrio alginolyticus, Vibrio anguillarum, Vibrio fluvialis, Vibrio harveyi, Vibrio parahaemolyticus, Vibrio rotiferianus, and Vibrio vulnificus. The assay provided a nearly-automated approach, with only a single pipetting step per chip for sample dispensing. This technique could achieve limits of detection (LOD) ranging from 0.40 to 6.42pg per 1.414μL reaction in less than 30 min. The robust reproducibility was demonstrated by a little variation among duplications for each bacterium with the coefficient of variation (CV) for time to positive (Tp) value less than 0.10. The clinical sensitivity and specificity of this on-chip LAMP assay in detecting field samples were 96.2% and 93.8% by comparison with conventional microbiological methods. Compared with other well-known techniques, on-chip LAMP assay provides low sample and reagent consumption, ease-of-use, accelerated analysis, multiple bacteria and on-site detection, and high reproducibility, indicating that such a technique would be applicable for on-site detection and routine monitoring of multiple pathogens in aquaculture.

摘要

对于早期疾病诊断和及时治疗,尤其是水产养殖中病原体的现场筛查,迫切需要快速、低成本且用户友好的策略。在本研究中,我们成功开发了一种集成在微流控盘芯片上的实时荧光环介导等温扩增检测方法(芯片上的LAMP),该方法能够同时检测水生动物中的10种致病细菌,即嗜水气单胞菌、恶臭假单胞菌、海豚链球菌、溶藻弧菌、鳗弧菌、弗氏弧菌、哈维弧菌、副溶血性弧菌、轮虫弧菌和创伤弧菌。该检测方法提供了一种近乎自动化的方法,每个芯片仅需一个移液步骤用于样品分配。该技术在不到30分钟的时间内,每1.414μL反应的检测限(LOD)范围为0.40至6.42pg。每种细菌的重复检测之间变化很小,阳性时间(Tp)值的变异系数(CV)小于0.10,证明了其强大的重现性。与传统微生物学方法相比,这种芯片上的LAMP检测方法在检测现场样品时的临床敏感性和特异性分别为96.2%和93.8%。与其他知名技术相比,芯片上的LAMP检测方法具有低样品和试剂消耗、易于使用、分析加速、可同时检测多种细菌和现场检测以及高重现性等优点,表明该技术适用于水产养殖中多种病原体的现场检测和常规监测。

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