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首页> 外文期刊>BMC Microbiology >Multiplex PCR for detection of the Vibrio genus and five pathogenic Vibrio species with primer sets designed using comparative genomics
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Multiplex PCR for detection of the Vibrio genus and five pathogenic Vibrio species with primer sets designed using comparative genomics

机译:使用比较基因组学设计的引物组进行多重PCR检测弧菌属和5种致病性弧菌

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Background The genus Vibrio is clinically significant and major pathogenic Vibrio species causing human Vibrio infections are V. cholerae, V. parahaemolyticus, V. vulnificus, V. alginolyticus and V. mimicus. In this study, we screened for novel genetic markers using comparative genomics and developed a Vibrio multiplex PCR for the reliable diagnosis of the Vibrio genus and the associated major pathogenic Vibrio species. Methods A total of 30 Vibrio genome sequences were subjected to comparative genomics, and specific genes of the Vibrio genus and five major pathogenic Vibrio species were screened. The designed primer sets from the screened genes were evaluated by single PCR using DNAs from various Vibrio spp. and other non-Vibrio bacterial strains. A sextuplet multiplex PCR using six primer sets was developed to enable detection of the Vibrio genus and five pathogenic Vibrio species. Results The designed primer sets from the screened genes yielded specific diagnostic results for target the Vibrio genus and Vibrio species. The specificity of the developed multiplex PCR was confirmed with various Vibrio and non-Vibrio strains. This Vibrio multiplex PCR was evaluated using 117 Vibrio strains isolated from the south seashore areas in Korea and Vibrio isolates were identified as Vibrio spp., V. parahaemolyticus, V. vulnificus and V. alginolyticus, demonstrating the specificity and discriminative ability of the assay towards Vibrio species. Conclusions This novel multiplex PCR method could provide reliable and informative identification of the Vibrio genus and major pathogenic Vibrio species in the food safety industry and in early clinical treatment, thereby protecting humans against Vibrio infection.
机译:背景技术弧菌属在临床上具有重要意义,引起人弧菌感染的主要病原性弧菌是霍乱弧菌,副溶血弧菌,创伤弧菌,溶藻弧菌和模拟弧菌。在这项研究中,我们使用比较基因组学筛选了新的遗传标记,并开发了弧菌多重PCR技术来可靠地诊断弧菌属和相关的主要致病性弧菌。方法对30个弧菌基因组序列进行比较基因组学,筛选弧菌属的特异基因和5种主要致病弧菌。使用来自各种弧菌属物种的DNA,通过单次PCR对筛选出的基因设计的引物进行评估。和其他非弧菌细菌菌株。开发了使用六个引物对的六联体多重PCR,以能够检测弧菌属和五个病原性弧菌。结果从筛选的基因中设计出的引物对针对弧菌属和弧菌属物种产生了特定的诊断结果。用多种弧菌和非弧菌菌株证实了开发的多重PCR的特异性。使用从韩国南海岸地区分离出的117株弧菌对这种弧菌多重PCR进行了评估,并将弧菌分离物鉴定为弧菌属,副溶血弧菌,vulnificus弧菌和溶藻弧菌,证明了该检测方法对检测的特异性和区分能力弧菌种。结论这种新颖的多重PCR方法可为食品安全行业和早期临床治疗中的弧菌属和主要致病性弧菌提供可靠而丰富的信息,从而保护人类免受弧菌感染。

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