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用于检测马来西亚本地人群中普通大肠杆菌和产志贺毒素大肠杆菌的环介导等温扩增检测法。

Loop-mediated isothermal amplification assay for detection of generic and verocytotoxin-producing Escherichia coli among indigenous individuals in Malaysia.

作者信息

Teh Cindy Shuan Ju, Chua Kek Heng, Lim Yvonne Ai Lian, Lee Soo Ching, Thong Kwai Lin

机构信息

Department of Medical Microbiology, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.

Department of Biomedical Science, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.

出版信息

ScientificWorldJournal. 2014;2014:457839. doi: 10.1155/2014/457839. Epub 2014 May 19.

DOI:10.1155/2014/457839
PMID:24967435
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4055146/
Abstract

We have successfully developed a Loop-mediated isothermal amplification (LAMP) assay that could specifically detect generic Escherichia coli (E. coli). This assay was tested on 85 bacterial strains and successfully identified 54 E. coli strains (average threshold time, Tt = 21.26). The sensitivity of this assay was evaluated on serial dilutions of bacterial cultures and spiked faeces. The assay could detect 10(2) CFU/mL for bacterial culture with Tt = 33.30 while the detection limit for spiked faeces was 10(3) CFU/mL (Tt = 31.12). We have also detected 46 generic E. coli from 50 faecal samples obtained from indigenous individuals with 16% of the positive samples being verocytotoxin-producing E. coli (VTEC) positive. VT1/VT2 allele was present in one faecal sample while the ratio of VT1 to VT2 was 6 : 1. Overall, our study had demonstrated high risk of VTEC infection among the indigenous community and most of the asymptomatic infection occurred among those aged below 15 years. The role of asymptomatic human carriers as a source of dissemination should not be underestimated. Large scale screening of the VTEC infection among indigenous populations and the potential contamination sources will be possible and easy with the aid of this newly developed rapid and simple LAMP assay.

摘要

我们成功开发了一种环介导等温扩增(LAMP)检测方法,该方法能够特异性检测普通大肠杆菌(E. coli)。此检测方法在85株细菌菌株上进行了测试,并成功鉴定出54株大肠杆菌菌株(平均阈值时间,Tt = 21.26)。该检测方法的灵敏度通过细菌培养物和加标粪便的系列稀释进行评估。对于细菌培养物,该检测方法能够检测到10(2)  CFU/mL,Tt = 33.30,而加标粪便的检测限为10(3)  CFU/mL(Tt = 31.12)。我们还从50份来自原住民个体的粪便样本中检测到46株普通大肠杆菌,其中16%的阳性样本产志贺毒素大肠杆菌(VTEC)呈阳性。在一份粪便样本中存在VT1/VT2等位基因,而VT1与VT2的比例为6 : 1。总体而言,我们的研究表明原住民社区中VTEC感染风险很高,且大多数无症状感染发生在15岁以下人群中。无症状人类携带者作为传播源的作用不应被低估。借助这种新开发的快速简便的LAMP检测方法,对原住民群体中的VTEC感染以及潜在污染源进行大规模筛查将变得可行且容易。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/243e/4055146/d97c2421258c/TSWJ2014-457839.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/243e/4055146/d97c2421258c/TSWJ2014-457839.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/243e/4055146/d97c2421258c/TSWJ2014-457839.001.jpg

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