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Semi-nested polymerase chain reaction for detection of toxigenic Vibrio cholerae from environmental water samples

机译:半巢式聚合酶链反应用于检测环境水样中的产霍乱弧菌

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摘要

A rapid and sensitive direct cell semi-nested PCR assay was developed for the detection of viable toxigenic V. cholerae in environmental water samples. The semi-nested PCR assay amplified cholera toxin (ctxA2B) gene present in the toxigenic V. cholerae. The detection sensitivity of direct cell semi-nested PCR was 2 × 103 CFU of V. cholerae whereas direct cell single-step PCR could detect 2 × 104 CFU of V. cholerae. The performance of the assay was evaluated using environmental water samples after spiking with known number of Vibrio cholerae O1. The spiked water samples were filtered through a 0.22 micrometer membrane and the bacteria retained on filters were enriched in alkaline peptone water and then used directly in the PCR assay. The semi-nested PCR procedure coupled with enrichment could detect less than 1 CFU/ml in ground water and sea water whereas 2 CFU/ml and 20 CFU/ml could be detected in pond water and tap water, respectively. The proposed method is simple, faster than the conventional detection assays and can be used for screening of drinking water or environmental water samples for the presence of toxigenic V. cholerae.
机译:开发了一种快速灵敏的直接细胞半巢式PCR检测试剂盒,用于检测环境水样品中的有毒的霍乱弧菌。半巢式PCR检测扩增了产毒霍乱弧菌中存在的霍乱毒素(ctxA2B)基因。直接细胞半巢式PCR的检测灵敏度为霍乱弧菌的2×10 3 CFU,而直接细胞单步PCR可以检测V的2×10 4 CFU霍乱在掺入已知数量的霍乱弧菌O1后,使用环境水样品评估测定的性能。加标的水样品通过0.22微米的滤膜过滤,保留在滤膜上的细菌富含碱性蛋白ept水,然后直接用于PCR分析。半巢式PCR程序与富集相结合,在地下水和海水中可检测到低于1 CFU / ml,而在池塘水和自来水中则分别检测到2 CFU / ml和20 CFU / ml。所提出的方法比常规的检测方法简单,快速,并且可以用于筛查饮用水或环境水样品中是否存在产毒霍乱弧菌。

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