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接种到氯化饮用水中后幽门螺杆菌的存活及活力

Survival and viability of Helicobacter pylori after inoculation into chlorinated drinking water.

作者信息

Moreno Yolanda, Piqueres Patricia, Alonso José L, Jiménez Ana, González Ana, Ferrús María A

机构信息

Departamento de Biotecnología, Universidad Politécnica, Camino de Vera 14, 46022 Valencia, Spain.

出版信息

Water Res. 2007 Aug;41(15):3490-6. doi: 10.1016/j.watres.2007.05.020. Epub 2007 May 18.

Abstract

The aim of this work was to assess the effect of chlorine water treatment on Helicobacter pylori and to study the succession of cellular alterations in response to chlorine exposure. H. pylori NCTC 11637 reference strain was used for inoculating water samples. The culturability, substrate responsiveness combined with fluorescent in situ hybridization detection (DVC-FISH assay), RNA content, DNA content, and mRNA changes of H. pylori cells were analyzed. Culturability was lost at 5 min in water with 0.96 mg/l of free chlorine. Viable cells were detected by DVC-FISH after 3h of exposure to chlorine but not after 24h. The percentage of coccoid forms was higher than spiral forms after 40s of chlorine exposure, but even after 24h, FISH detection revealed the presence of spiral cells. After 24h, amplification of the specific H. pylori 16S rDNA gene was achieved. Expression of the vacA gene was detected with the same intensity at all time points tested, demonstrating that these genes are expressed in non-culturable H. pylori cells. Levels of 16S rRNA were constant during the chlorine treatment, so killing of bacteria with chlorine probably does not involve ribosome degradation. According to our results, H. pylori could survive to disinfection practices normally used in drinking water treatment in the viable but non-culturable form, which would allow them to reach final consumption points and, at the same time, enable them to be undetectable by culture methods.

摘要

这项工作的目的是评估氯水处理对幽门螺杆菌的影响,并研究其对氯暴露的细胞变化过程。使用幽门螺杆菌NCTC 11637参考菌株接种水样,分析了幽门螺杆菌细胞的可培养性、底物反应性并结合荧光原位杂交检测(DVC-FISH测定法)、RNA含量、DNA含量和mRNA变化。在含有0.96mg/l游离氯的水中,5分钟后可培养性丧失。暴露于氯3小时后通过DVC-FISH检测到活细胞,但24小时后未检测到。氯暴露40秒后,球菌形态的百分比高于螺旋形态,但即使在24小时后,FISH检测仍显示存在螺旋细胞。24小时后,实现了幽门螺杆菌特异性16S rDNA基因的扩增。在所有测试时间点检测到vacA基因的表达强度相同,表明这些基因在不可培养的幽门螺杆菌细胞中表达。氯处理期间16S rRNA水平恒定,因此用氯杀死细菌可能不涉及核糖体降解。根据我们的结果,幽门螺杆菌可以以活的但不可培养的形式在饮用水处理中常用的消毒方法中存活,这将使它们能够到达最终消费点,同时使它们无法通过培养方法检测到。

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