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首页> 外文期刊>Molecular and Cellular Probes: The Location, Diagnosis and Monitoring of Disease by Specific Molecules and Cell Lines >Direct detection of Shiga-like toxin-producing Escherichia coli in ground beef using the polymerase chain reaction.
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Direct detection of Shiga-like toxin-producing Escherichia coli in ground beef using the polymerase chain reaction.

机译:使用聚合酶链反应直接检测绞碎牛肉中产生志贺样毒素的大肠杆菌。

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摘要

We recently reported the development and assessment of a technique for the detection of Shiga-like toxin-producing Escherichia coli (SLTEC) using the polymerase chain reaction (PCR) and a digoxigenin-11-dUTP-labelled DNA probe. This technique has now been adapted for the direct identification of SLTEC in ground beef. Ground beef homogenates were diluted 1000-fold to reduce the concentration of components which inhibit the thermostable polymerase. Assessment of four different ground beef samples using the PCR detection technique revealed that fat content was a major inhibitory component. As few as 30 SLTEC ml-1 of a ground beef homogenate were detected using the PCR technique, although it was necessary to enrich six of the samples for positive detection. These findings indicate that the PCR detection technique is suitable for the identification of SLTEC directly from contaminated ground beef without isolation of the bacterium or purification of its DNA.
机译:我们最近报道了使用聚合酶链反应(PCR)和地高辛配基11-dUTP标记的DNA探针检测志贺样毒素的大肠杆菌(SLTEC)的技术的开发和评估。该技术现已适用于直接鉴定碎牛肉中的SLTEC。将绞碎的牛肉匀浆稀释1000倍,以减少抑制热稳定聚合酶的成分的浓度。使用PCR检测技术对四种不同的碎牛肉样品进行评估后发现,脂肪含量是主要的抑制成分。使用PCR技术只能检测到30份SLTEC ml-1的碎牛肉匀浆,尽管必须富集六个样品才能进行阳性检测。这些发现表明,PCR检测技术适合直接从受污染的碎牛肉中鉴定SLTEC,而无需分离细菌或纯化其DNA。

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