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氯胺化水和河水诱导大肠杆菌 O157:H7 进入存活但非可培养状态,以及随后的复苏。

Induction of Escherichia coli O157:H7 into the viable but non-culturable state by chloraminated water and river water, and subsequent resuscitation.

机构信息

Division of Analytical and Environmental Toxicology, Department of Laboratory Medicine and Pathology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.

出版信息

Environ Microbiol Rep. 2009 Apr;1(2):155-61. doi: 10.1111/j.1758-2229.2009.00024.x. Epub 2009 Mar 6.

Abstract

Induction of culturable Escherichia coli O157:H7 cells into a viable but non-culturable (VBNC) state by chloraminated tap water was carefully investigated; as many as 90% of initial cells entered into a VBNC state within 15 min, compared with 14% in river water within 14 weeks. To understand what specific stresses may induce E. coli O157:H7 into a VBNC state, chloraminated tap water, autoclaved river water, and media with known ingredients (PBS buffer and deionized water) at 4°C or 25°C were used to examine induction efficiency. Chloramination alone, or the combination of starvation with either low temperature or osmotic pressure, induced E. coli O157:H7 into a VBNC state, while starvation alone did not induce the bacteria into a VBNC state within 1.5 years. The mRNA of the rfbE and fliC genes was detected in the 10-month-old VBNC cells induced by river water, confirming the viability of E. coli O157:H7 VBNC cells. The VBNC cells induced by chloraminated water and the 10-month-old VBNC cells induced by river water were first resuscitated using autoinducers produced by E. coli O157:H7 itself in a serum-based medium; the VBNC cells of bovine isolates recovered more efficiently compared with those of clinical isolates. These results demonstrate a potential health risk of VBNC E. coli O157:H7 in environmental water and the utility of monitoring viable E. coli O157:H7 including VBNC cells based on the mRNA of the rfbE and fliC genes.

摘要

采用加氯自来水诱导可培养大肠杆菌 O157:H7 进入活但非可培养(VBNC)状态的情况进行了仔细研究;与 14 周内在河水中仅有 14%的初始细胞进入 VBNC 状态相比,多达 90%的初始细胞在 15 分钟内进入 VBNC 状态。为了了解哪些特定的应激因素可能会导致大肠杆菌 O157:H7 进入 VBNC 状态,使用加氯自来水、巴氏消毒河水以及在 4°C 或 25°C 下具有已知成分的培养基(PBS 缓冲液和去离子水)来检查诱导效率。单独加氯,或饥饿与低温或渗透压相结合,会诱导大肠杆菌 O157:H7 进入 VBNC 状态,而单独饥饿在 1.5 年内不会诱导细菌进入 VBNC 状态。在由河水诱导的 10 个月龄 VBNC 细胞中检测到 rfbE 和 fliC 基因的 mRNA,证实了大肠杆菌 O157:H7 VBNC 细胞的活力。首先使用大肠杆菌 O157:H7 自身产生的自动诱导剂使加氯水诱导的 VBNC 细胞和河水中诱导的 10 个月龄 VBNC 细胞复苏;与临床分离株相比,牛分离株的 VBNC 细胞恢复得更有效。这些结果表明,环境水中 VBNC 大肠杆菌 O157:H7 存在潜在的健康风险,并且基于 rfbE 和 fliC 基因的 mRNA 监测包括 VBNC 细胞在内的可存活大肠杆菌 O157:H7 是有用的。

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