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噬菌体扩增与环介导等温扩增(PA-LAMP)相结合,可用于当天检测生禽肉中存活的肠炎沙门氏菌。

Phage amplification coupled with loop-mediated isothermal amplification (PA-LAMP) for same-day detection of viable Salmonella Enteritidis in raw poultry meat.

机构信息

Food Hygiene, Inspection and Control Laboratory, Department of Analytical Chemistry, Nutrition and Bromatology, University of Santiago de Compostela, Spain.

Centre of Biological Engineering, University of Minho, 4710-057, Braga, Portugal; LABBELS - Associate Laboratory, 4800-122, Braga, Guimarães, Portugal.

出版信息

Food Microbiol. 2023 Oct;115:104341. doi: 10.1016/j.fm.2023.104341. Epub 2023 Jul 11.

Abstract

Salmonella Enteritidis is the main serotype responsible for human salmonellosis in the European Union. One of the main sources of Salmonella spp. in the food chain are poultry products, such as eggs or chicken meat. In recent years, molecular methods have become an alternative to culture dependent methods for the rapid screening of Salmonella spp. In this work, the strain S. Enteritidis S1400, and previously isolated and characterized bacteriophage PVP-SE2, were used to develop and evaluate a same-day detection method combining Phage Amplification and Loop-mediated isothermal amplification (PA-LAMP) to specifically detect viable S. Enteritidis in chicken breast. This method is based on the detection of the phage DNA rather than bacterial DNA. The virus is added to the sample during pre-enrichment in buffered peptone water, where it replicates in the presence of viable S. Enteritidis. The detection of phage DNA allows, on the one hand to detect viable bacteria, since viruses only replicate in them, and on the other hand to increase the sensitivity of the method since for each infected S. Enteritidis cell, hundreds of new viruses are produced. Two different PA-LAMP detection strategies were evaluated, a real time fluorescence and a naked-eye detection. The present method could down to 0.2 fg/μL of pure phage DNA and a concentration of viral particles of 2.2 log PFU/mL. After a short Salmonella recovery step of 3 h and a co-culture of 4 h of the samples with phage particles, both real-time fluorescence and naked-eye method showed a LoD of 6.6 CFU/25 g and a LoD of 1.5/25 g in spiked chicken breast samples. The entire detection process, including DNA extraction and LAMP analysis, can be completed in around 8 h. In the current proof-of-concept, the novel PA-LAMP obtained comparable results to those of the reference method ISO 6579, to detect Salmonella Enteritidis in poultry meat.

摘要

肠炎沙门氏菌是欧盟人类沙门氏菌病的主要血清型。食物链中沙门氏菌的主要来源之一是家禽产品,如鸡蛋或鸡肉。近年来,分子方法已成为依赖于文化的方法的替代方法,用于快速筛选沙门氏菌。在这项工作中,使用肠炎沙门氏菌 S1400 菌株和先前分离和表征的噬菌体 PVP-SE2 来开发和评估一种结合噬菌体扩增和环介导等温扩增(PA-LAMP)的同日检测方法,以特异性检测鸡肉中的存活肠炎沙门氏菌。该方法基于噬菌体 DNA 的检测,而不是细菌 DNA 的检测。病毒在缓冲蛋白胨水中进行预富集时添加到样品中,在存在存活肠炎沙门氏菌的情况下,病毒在其中复制。噬菌体 DNA 的检测一方面可以检测到存活的细菌,因为病毒只能在其中复制,另一方面可以提高方法的灵敏度,因为每个感染的肠炎沙门氏菌细胞都会产生数百个新病毒。评估了两种不同的 PA-LAMP 检测策略,一种是实时荧光检测,另一种是肉眼检测。本方法可以检测到 0.2 fg/μL 的纯噬菌体 DNA 和 2.2 log PFU/mL 的病毒颗粒浓度。经过 3 小时的短时间沙门氏菌回收步骤和样品与噬菌体颗粒共培养 4 小时后,实时荧光和肉眼方法均显示出 6.6 CFU/25 g 的 LoD 和 1.5/25 g 的 LoD 在加标鸡肉样品中。整个检测过程,包括 DNA 提取和 LAMP 分析,大约可以在 8 小时内完成。在目前的概念验证中,新型 PA-LAMP 获得的结果与 ISO 6579 参考方法相当,可用于检测禽肉中的肠炎沙门氏菌。

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