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将弓形杆菌人工接种到饮用水中后的存活与损伤情况。

Survival and injury of Arcobacter after artificial inoculation into drinking water.

作者信息

Moreno Yolanda, Alonso José Luis, Botella Salut, Ferrús M Antonia, Hernández Javier

机构信息

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

出版信息

Res Microbiol. 2004 Nov;155(9):726-30. doi: 10.1016/j.resmic.2004.05.011.

Abstract

The aim of this work was to assess the effect of chlorine water treatment on Arcobacter butzleri and to study the survival strategies of this organism in chlorinated and non-chlorinated drinking water. A. butzleri NCTC 12481 was inoculated into chlorinated and non-chlorinated water and samples were removed aseptically, immediately and periodically during the next 2 days (for chlorinated drinking water) or 35 days (for non-chlorinated drinking water). The membrane integrity (Live/Dead BacLight kit), 16S rRNA (FISH technique), DNA content (23S rRNA PCR-RFLPs) and culturability changes in A. butzleri cells were analyzed. Culturability of the cells was lost at 5 min in chlorinated drinking water. At that time the cells showed membrane damage, although fluorescent intensity of 16S rRNA hybridization was constant throughout the chlorine treatment. After 48 h the amplicon specific for the 23S rRNA gene was weakly detected. In non-chlorinated drinking water cells lost their culturability after 16 days but the other factors measured indicated that Arcobacter remained viable throughout the experiment.

摘要

这项工作的目的是评估氯水处理对布氏嗜冷杆菌的影响,并研究该菌在氯化和非氯化饮用水中的生存策略。将布氏嗜冷杆菌NCTC 12481接种到氯化水和非氯化水中,并在接下来的2天(对于氯化饮用水)或35天(对于非氯化饮用水)期间立即和定期无菌采集样本。分析了布氏嗜冷杆菌细胞的膜完整性(死活细菌荧光染色试剂盒)、16S rRNA(荧光原位杂交技术)、DNA含量(23S rRNA PCR-RFLP)和可培养性变化。在氯化饮用水中,细胞在5分钟时失去可培养性。此时细胞显示出膜损伤,尽管在整个氯处理过程中16S rRNA杂交的荧光强度保持不变。48小时后,微弱检测到23S rRNA基因特异性扩增子。在非氯化饮用水中,细胞在16天后失去可培养性,但所测量的其他因素表明,嗜冷杆菌在整个实验过程中仍保持存活。

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