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水中 STEC 的无培养检测和计数。

Culture-free detection and enumeration of STEC in water.

机构信息

Environmental Microbiology, Indian Institute of Toxicology Research (C.S.I.R), Post Box 80, Mahatma Gandhi Marg, Lucknow 226001, UP, India.

出版信息

Ecotoxicol Environ Saf. 2011 May;74(4):551-7. doi: 10.1016/j.ecoenv.2011.01.019. Epub 2011 Apr 3.

Abstract

Shiga toxin-producing Escherichia coli (STEC) causes worldwide outbreaks of food and waterborne diseases. Rapid identification of causative agents is critical for early intervention in the case of widespread diarrheal epidemics to prevent mortality. In this study, a Molecular-Beacon targeting stx2 gene (highly associated with human illness) was designed to develop a culture-independent real-time PCR assay for detection and quantification of STEC in water samples. The assay could detect lowest 10 genomic equivalent (GE) of the reference strain (E. coli I.T.R.C.-18) per PCR or 100 GE/mL. The presence of 10(6)CFU/mL of non-pathogenic E. coli DH5α has no impact on sensitivity of the assay. The assay could successfully enumerate STEC in surface water (collected from a sewage impacted river) and potable water samples collected from Lucknow city without prior enrichment. The assay will be useful in pre-emptive monitoring of surface/potable waters to prevent waterborne outbreaks caused by STEC.

摘要

产志贺毒素大肠杆菌(STEC)可引起全球范围内的食源性和水源性疾病暴发。在广泛的腹泻性流行疫情中,快速鉴定病原体对于早期干预和防止死亡至关重要。本研究设计了一种针对stx2 基因(与人类疾病高度相关)的分子信标,以开发一种无需培养的实时 PCR 检测方法,用于检测和定量水样中的 STEC。该检测方法可检测到参考菌株(大肠杆菌 I.T.R.C.-18)每 PCR 最低 10 个基因组当量(GE)或 100 GE/mL。10(6)CFU/mL 的非致病性大肠杆菌 DH5α 的存在对检测方法的灵敏度没有影响。该检测方法可成功地对地表水(取自受污水影响的河流)和从勒克瑙市采集的饮用水样本进行 STEC 计数,无需事先富集。该检测方法将有助于对地表水/饮用水进行主动监测,以防止由 STEC 引起的水源性暴发。

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