首页> 外文期刊>Water Science and Technology >Detection of Vibrio cholerae and Vibrio parahaemolyticus by molecular and culture based methods from source water to household container-stored water at the point-of-use in South African rural communities.
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Detection of Vibrio cholerae and Vibrio parahaemolyticus by molecular and culture based methods from source water to household container-stored water at the point-of-use in South African rural communities.

机译:在南非农村社区使用时,通过分子和基于文化的方法从源水到家用容器存储的水,检测霍乱弧菌和副溶血弧菌。

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摘要

Detection methods for Vibrio cholerae and Vibrio parahaemolyticus which included the culture based approach with polymerase chain reaction (PCR) confirmation, PCR detection without enrichment and PCR with a pre-enrichment were developed and their performance evaluated. PCR assays targeted the SodB (V. cholerae species), Flae (V. parahaemolyticus species), 16S rRNA (Vibrio and Enterobacteriacea species) genes (Multiplex 1) and V. cholerae O1 and V. cholerae O139 rfb genes, ctxA (cholera toxin) gene and 16S rRNA gene (Multiplex 2). These methods were used to determine the occurrence of selected Vibrios in source water as well as in household container-stored water. The combination of filtration, enrichment and PCR method provided a sensitive and specific method for the detection of selected Vibrios in water samples. The PCR with a pre-enrichment method detected as few as 4-10 cfu/100 mL of selected Vibrios and PCR detection without the enrichment method detected as few as 40-100 cfu/100 mL of selected Vibrios. The inclusion of an enrichment period allows detection of culturable bacteria. As an application of the developed methods, V. cholerae and V. parahaemolyticus were detected in the source water used by the population and in the water-storage containers. The results indicate that Vibrio species in the containers could have originated from the source water and survive in biofilms inside the containers.
机译:霍乱弧菌和副溶血性弧菌的检测方法得到了发展,包括基于培养的方法和聚合酶链反应(PCR)确认,不富集的PCR检测以及预富集的PCR的检测方法,并对其性能进行了评估。 PCR检测针对SodB(霍乱弧菌),Flae(副溶血弧菌),16S rRNA(弧菌和肠杆菌科种)基因(复合体1)以及霍乱弧菌O1和霍乱弧菌O139 rfb基因,ctxA(霍乱毒素) )基因和16S rRNA基因(Multiplex 2)。这些方法用于确定源水以及家用容器存储水中选定弧菌的发生。过滤,富集和PCR方法的结合为检测水样中选定的弧菌提供了灵敏而特异的方法。采用预富集方法的PCR检测到的选定弧菌只有4-10 cfu / 100 mL,而没有富集方法的PCR检测则检测到的选定弧菌只有40-100 cfu / 100 mL。包含富集期允许检测可培养细菌。作为开发方法的应用,在人群使用的原水中和储水容器中检测到霍乱弧菌和副溶血弧菌。结果表明,容器中的弧菌物种可能起源于水源,并在容器内的生物膜中生存。

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