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首页> 外文期刊>Letters in Applied Microbiology >Development of a real-time PCR assay with an internal amplification control for the screening of Shiga toxin-producing Escherichia coli in foods
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Development of a real-time PCR assay with an internal amplification control for the screening of Shiga toxin-producing Escherichia coli in foods

机译:开发具有内部扩增对照的实时PCR检测试剂盒,用于筛选食品中产生志贺毒素的大肠杆菌

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摘要

AIMS: To develop and evaluate a real-time PCR assay incorporating an internal amplification control (IAC) suitable for the screening of Shiga toxin (Stx)-producing Escherichia coli (STEC) in foods. METHODS AND RESULTS: A competitive IAC was constructed and included in an stx-specific real-time PCR assay. Coupled to 18-h enrichment and automated DNA extraction, the assay could reliably detect the presence of STEC in minced meats inoculated at 10 CFU per 25 g. Its performance was evaluated on 415 minced beef and 112 raw milk cheese samples and compared with that of a PCR-ELISA method. Fifty-three minced meats and 31 cheeses were found stx-positive, giving 98.3% and 93.75% concordance, respectively, with the PCR-ELISA reference method. CONCLUSIONS: A highly sensitive stx-specific real-time PCR method including an IAC was developed, facilitating monitoring of false-negative results due to PCR inhibitors. SIGNIFICANCE AND IMPACT OF THE STUDY: Combined with automated DNA extraction, the stx-IAC real-time PCR assay represents a suitable method for rapid screening of STEC in foods.
机译:目的:开发和评估包含内部扩增对照(IAC)的实时PCR分析方法,该方法适用于筛选食品中产生志贺毒素(Stx)的大肠杆菌(STEC)。方法和结果:构建了竞争性IAC,并将其包括在stx特异性实时PCR分析中。结合18小时富集和自动DNA提取,该测定法可以可靠地检测出以每10 g CFU / 25 g接种的碎肉中STEC的存在。在415切碎的牛肉和112份生乳奶酪样品上评估了其性能,并与PCR-ELISA方法进行了比较。用PCR-ELISA参考方法发现53种碎肉和31种奶酪的stx阳性,分别具有98.3%和93.75%的一致性。结论:开发了一种包括IAC在内的高灵敏stx特异性实时PCR方法,有助于监测由于PCR抑制剂引起的假阴性结果。研究的意义和影响:结合自动DNA提取,stx-IAC实时PCR分析代表了一种快速筛选食品中STEC的合适方法。

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