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首页> 外文期刊>Journal of applied microbiology >Simultaneous differential detection of human pathogenic and nonpathogenic Vibrio species using a multiplex PCR based on gyrB and pntA genes.
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Simultaneous differential detection of human pathogenic and nonpathogenic Vibrio species using a multiplex PCR based on gyrB and pntA genes.

机译:使用基于gyrB和pntA基因的多重PCR同时鉴别人类致病性和非致病性弧菌。

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Aims: To develop a multiplex PCR targeting the gyrB and pntA genes for Vibrio species differentiation. Methods and Results: Four pairs of primers targeting gyrB gene of Vibrios at genus level and pntA gene of Vibrio cholerae, Vibrio parahaemolyticus, Vibrio vulnificus were designed. This PCR method precisely identified 250 Vibrio species and demonstrated sensitivity in the range of 4 x 104 CFU ml-1 (c. 200 CFU per PCR) to 2 x 103 CFU ml-1 (c. 10 CFU per PCR). Overall, the gyrB gene marker showed a higher specificity than the dnaJ gene marker for Vibrio detection and was able to distinguish Aeromonas from Vibrio species. Conclusions: The multiplex PCR based on combined gyrB and pntA provides a high discriminatory power in the differentiation between Vibrio alginolyticus and V. parahaemolyticus, and between V. cholerae and Vibrio mimicus. Significance and Impact of the Study: This assay will be useful for rapid differentiation of various Vibrio species from clinical and environmental sources and significantly overcomes the limitations of the conventional methods.
机译:目的:开发针对gyrB和pntA基因的多重PCR,用于弧菌种分化。方法与结果:设计了四对以属水平为靶标的弧菌的gyrB基因和霍乱弧菌,副溶血性弧菌,创伤弧菌的pntA基因的引物。这种PCR方法精确地鉴定了250种弧菌,并显示了4 x 104 CFU ml-1(每个PCR约200 CFU)至2 x 103 CFU ml-1(每个PCR约10 CFU)的灵敏度。总体而言,gyrB基因标记在弧菌检测中显示出比dnaJ基因标记更高的特异性,并且能够区分弧菌和弧菌。结论:基于gyrB和pntA结合的多重PCR在溶藻弧菌和副溶血弧菌之间,霍乱弧菌和拟似弧菌之间的区分中具有很高的鉴别能力。研究的意义和影响:该测定法可用于从临床和环境来源快速区分各种弧菌,并大大克服了常规方法的局限性。

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