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A novel multiplex PCR for the simultaneous detection of Salmonella enterica and Shigella species

机译:同时检测肠炎沙门氏菌和志贺氏菌种的新型多重PCR

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摘要

Salmonella enterica and Shigella species are commonly associated with food and water borne infections leading to gastrointestinal diseases. The present work was undertaken to develop a sensitive and reliable PCR based detection system for simultaneous detection of Salmonella enterica and Shigella at species level. For this the conserved regions of specific genes namely ipaH1, ipaH, wbgZ, wzy and invA were targeted for detection of Shigella genus, S. flexneri, S. sonnei, S. boydii and Salmonella enterica respectively along with an internal amplification control (IAC). The results showed that twenty Salmonella and eleven Shigella spp., were accurately identified by the assay without showing non-specificity against closely related other Enterobacteriaceae organisms and also against other pathogens. Further evaluation of multiplex PCR was undertaken on 50 natural samples of chicken, eggs and poultry litter and results compared with conventional culture isolation and identification procedure. The multiplex PCR identified the presence of Salmonella and Shigella strains with a short pre-enrichment step of 5 h in peptone water and the same samples were processed by conventional procedures for comparison. Therefore, this reported multiplex PCR can serve as an alternative to the tedious time-consuming procedure of culture and identification in food safety laboratories.
机译:肠炎沙门氏菌和志贺氏菌属种通常与食物和水传播的感染有关,导致胃肠道疾病。当前的工作是为了开发一种灵敏且可靠的基于PCR的检测系统,用于在物种水平上同时检测肠沙门氏菌和志贺氏菌。为此,将特定基因的保守区域,即ipaH1,ipaH,wbgZ,wzy和invA定位为分别检测志贺氏菌属,弗氏志贺氏菌,松内链球菌,博伊氏菌和肠炎沙门氏菌以及内部扩增对照(IAC) 。结果表明,通过该测定法可以准确鉴定出二十种沙门氏菌和十一种志贺氏菌,而对紧密相关的其他肠杆菌科细菌以及其他病原体没有非特异性。对50个鸡,蛋和家禽垫料的天然样品进行了多重PCR的进一步评估,并将结果与​​常规培养物的分离和鉴定程序进行了比较。多重PCR鉴定了在蛋白ept水中预富集时间短至5小时的沙门氏菌和志贺氏菌菌株的存在,并且通过常规程序处理了相同的样品进行比较。因此,这种报道的多重PCR可以替代食品安全实验室中繁琐的培养和鉴定过程。

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