首页> 外文期刊>Anaerobe >Development of a triplex real-time PCR assay for the simultaneous detection of Clostridium beijerinckii, Clostridium sporogenes and Clostridium tyrobutyricum in milk
【24h】

Development of a triplex real-time PCR assay for the simultaneous detection of Clostridium beijerinckii, Clostridium sporogenes and Clostridium tyrobutyricum in milk

机译:用于同时检测牛奶中梭菌孢子苷和梭菌梭菌梭菌梭菌梭菌和梭菌梭菌的三重实时PCR测定

获取原文
获取原文并翻译 | 示例
           

摘要

Clostridium beijerinckii, Clostridium sporogenes and Clostridium tyrobutyricum are considered the leading bacteria implicated in late blowing defects affecting semi-hard and hard cheese production. The aim of this study was to develop a multiplex Real-Time PCR (qPCR) analysis for a rapid and simultaneous detection of C. beijerinckii, C. sporogenes and C. tyrobutyricum, using specific primers respectively targeting the nifH, gerAA and enr genes. The limits of detection in raw milk were 300 CFU/50 mL in the case of C. beijerinckii, 2 CFU/50 mL for C. sporogenes and 5 CFU/50 mL for C. tyrobutyricum spores. The qPCR method was applied to artificially contaminated raw milk samples, and molecular quantification showed good correlation (R-2 = 0.978) with microbiological counting. Our results demonstrate that this method, combined with a DNA extraction protocol optimized for spore lysis, could be a useful tool for the direct quantification of the considered clostridia species. (C) 2015 Elsevier Ltd. All rights reserved.
机译:Clostridium Beijerinckii,Clostridium Sporogenes和Tyrobutyricum患者被认为是影响半硬质和硬奶酪生产的晚期吹缺陷的前导细菌。本研究的目的是利用分别靶向NiFH,Geraa和EnR基因的特异性引物,开发多重的实时PCR(QPCR)分析。在C.Beijerinckii,2个C.CFU / 50ml的C.孢子蛋白和5℃/ 50ml的C. TyroButricum孢子的情况下,原料牛奶中的检测极限为300cu / 50ml。将QPCR方法应用于人工污染的原汁样品,分子定量显示出微生物计数的良好相关性(R-2 = 0.978)。我们的结果表明,该方法与针对孢子裂解的DNA提取方案组合,可以是用于直接定量所考虑的梭菌种类的有用工具。 (c)2015 Elsevier Ltd.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号