首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Detection of virulence factors in culturable Escherichia coli isolates from water samples by DNA probes and recovery of toxin-bearing strains in minimal o-nitrophenol-beta-D-galactopyranoside-4-methylumbelliferyl-beta-D-g luc uronide media.
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Detection of virulence factors in culturable Escherichia coli isolates from water samples by DNA probes and recovery of toxin-bearing strains in minimal o-nitrophenol-beta-D-galactopyranoside-4-methylumbelliferyl-beta-D-g luc uronide media.

机译:通过DNA探针检测水样本中可培养大肠杆菌分离物中的毒力因子并在最小的邻硝基苯酚β-D-吡喃半乳糖苷-4-甲基伞形酮-β-D-gluc uronide培养基中回收毒素菌株。

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摘要

A total of 449 Escherichia coli isolates in treated and raw water sources were submitted to DNA-DNA hybridization using seven different DNA probes to detect homology to sequences that code for Shiga-like toxins I and II; heat-stabile and heat-labile toxins, adherence factors EAF and eae, and the fimbrial antigen of entero-hemorrhagic E. coli. Fifty-nine (13%) of the isolates demonstrated homology with one or more specific DNA probes. More than 50% of the isolates in treated water were not recovered in MMO-4-methylumbelliferyl-beta-D-glucuronide media designed for detection of this indicator.
机译:使用七种不同的DNA探针,对经过处理和原水中的总共449株大肠杆菌进行DNA-DNA杂交,以检测与编码志贺氏样毒素I和II的序列的同源性。热稳定和不稳定的毒素,粘附因子EAF和eae以及肠出血性大肠杆菌的纤维抗原。分离物中有59个(13%)与一种或多种特异性DNA探针具有同源性。在设计用于检测该指标的MMO-4-甲基伞形基-β-D-葡糖醛酸苷培养基中,未回收处理水中超过50%的分离株。

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