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采用培养法和聚合酶链反应法检测食品样本中的大肠杆菌

Detection of Escherichia coli in Food Samples Using Culture and Polymerase Chain Reaction Methods.

作者信息

Hariri Sumyya

机构信息

Department of Microbiology, Umm Al-Qura University, Mecca, SAU.

出版信息

Cureus. 2022 Dec 21;14(12):e32808. doi: 10.7759/cureus.32808. eCollection 2022 Dec.

Abstract

Methods for the rapid detection of and its related toxins are key to minimizing the risk of exposure to foodborne pathogens. The present study aimed to detect in food specimens using culture and polymerase chain reaction (PCR) techniques. One hundred and fifty samples from different types of food, comprising beef (n=60), chicken (n=72), and fish (n=18), were analyzed for the identification of by conventional and PCR methods. The results showed that out of 150 food samples, 44 (29.3%) were positive by culture, and 50 (33.3%) were positive by PCR. Significant differences were detected between sample types with culture (p-value < 0.005). When culture was considered the gold standard, the sensitivity of PCR was 100%, while the specificity was 94.34%. The six-hour pre-enrichment and PCR analysis are reliable in fast detection of in food samples. Hence, the identification of food pathogens using molecular-based methods would become more useful in routine diagnostic laboratories.

摘要

快速检测[病原体名称]及其相关毒素的方法是将食源性病原体暴露风险降至最低的关键。本研究旨在使用培养和聚合酶链反应(PCR)技术检测食品样本中的[病原体名称]。对来自不同类型食品的150个样本进行了分析,这些食品包括牛肉(n = 60)、鸡肉(n = 72)和鱼肉(n = 18),采用传统方法和PCR方法鉴定[病原体名称]。结果显示,在150个食品样本中,培养法检测出44个(29.3%)呈阳性,PCR法检测出50个(33.3%)呈阳性。不同样本类型在培养法检测中存在显著差异(p值<0.005)。以培养法为金标准时,PCR的灵敏度为100%,特异性为94.34%。六小时的预富集和PCR分析在快速检测食品样本中的[病原体名称]方面是可靠的。因此,在常规诊断实验室中,使用基于分子的方法鉴定食品病原体将变得更有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6ff/9860202/b6115d7ad1ac/cureus-0014-00000032808-i01.jpg

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