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首页> 外文期刊>Food Control >Towards the production of reliable quantitative microbiological data for risk assessment: Direct quantification of Campylobacter in naturally infected chicken fecal samples using selective culture and real-time PCR
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Towards the production of reliable quantitative microbiological data for risk assessment: Direct quantification of Campylobacter in naturally infected chicken fecal samples using selective culture and real-time PCR

机译:建立可靠的定量微生物数据进行风险评估:使用选择性培养和实时PCR对自然感染鸡粪样品中的弯曲杆菌进行直接定量

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摘要

Poultry has been identified as a significant source for human campylobacteriosis which constitutes an important zoonosis and public health problem in many areas of the world. Rapid, direct and accurate quantification of Campylobacter in poultry is essential for the assessment of public health risks and for the evaluation of control strategies implemented in poultry production. The aim of this study was to compare estimates of the numbers of Campylobacter spp. in naturally infected chicken fecal samples obtained using direct quantification by selective culture and by real-time PCR. Absolute quantification of Campylobacter by real-time PCR was performed using standard curves designed for two different DNA extraction methods: EasyDNA (TM) Kit from Invitrogen (Easy-DNA) and NucliSENS (R) MiniMAG (R) from bioMerieux (MiniMAG). Results indicated that the estimation of the numbers of Campylobacter present in chicken fecal samples was partly dependent on the methodologies used. In general, the numbers of Campylobacter obtained by real-time PCR when extracting DNA using the MiniMAG method were in most cases higher than the numbers of Campylobacter obtained by selective culture and by real-time PCR when using the Easy-DNA method. Although there were differences in terms of estimates of Campylobacter numbers between the methods and samples, the differences between culture and real-time PCR were not statistically significant for most of the samples used in this study. (C) 2015 Elsevier Ltd. All rights reserved.
机译:家禽已被确定为人类弯曲菌病的重要来源,在世界许多地区构成了重要的人畜共患病和公共卫生问题。快速,直接和准确地定量家禽中的弯曲杆菌对于评估公共卫生风险和评估在家禽生产中实施的控制策略至关重要。这项研究的目的是比较弯曲杆菌属的估计数。在自然感染的鸡粪样品中检测到的血样,这些样品是通过选择性培养和实时PCR直接定量获得的。使用为两种不同的DNA提取方法设计的标准曲线,通过实时PCR对弯曲杆菌进行绝对定量:来自Invitrogen(Easy-DNA)的EasyDNA(TM)Kit和来自bioMerieux(MiniMAG)的NucliSENS(R)MiniMAG(R)。结果表明,鸡粪便样品中弯曲杆菌数量的估计部分取决于所使用的方法。通常,在大多数情况下,使用MiniMAG方法提取DNA时通过实时PCR获得的弯曲杆菌数量要比使用Easy-DNA方法时通过选择性培养和实时PCR获得的弯曲杆菌数量更高。尽管方法和样品之间弯曲杆菌数量的估计值存在差异,但对于本研究中使用的大多数样品,培养液和实时PCR的差异在统计学上并不显着。 (C)2015 Elsevier Ltd.保留所有权利。

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