DEVELOPMENT OF A MULTIPLEX PCR ASSAY FOR THE SPECIFIC DETECTION OF SALMONELLA, CAMPYLOBACTER JEJUNI, ESCHERICHIA COLI O157:H7, AND LISTERIA MONOCYTOGENES

C. GILBERT, A. O'LEARY, D. WINTERS, M. SLAVIK
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引用次数: 8

Abstract

Abstract Detection of food-associated bacterial pathogens has become a major focus of the food industry, regulatory agencies, and researchers. Multiple pathogens need to be rapidly detected with high specificity and as cost efficient as possible. In this research, a multiplex PCR assay for the specific detection of Listeria monocytogenes, Escherichia coli O157:-H7, Salmonella, and Campylobacter jejuni was developed. The four bacteria were detectable at 104 CFU/PCR reaction. No cross-reactivity with other bacteria commonly found associated with the four target organisms was found. This assay would simplify detection procedures for the target pathogens, reduce the time and labor necessary to acquire food safety results, and might allow one protocol to be used for bacterial detection on a wide variety of food products.

建立沙门氏菌、空肠弯曲杆菌、大肠杆菌o157: h7和单核细胞增生李斯特菌特异性检测的多重PCR方法
食品相关病原菌的检测已成为食品行业、监管机构和研究人员关注的焦点。需要以高特异性和尽可能高的成本效益快速检测多种病原体。本研究建立了单增李斯特菌、大肠杆菌O157:-H7、沙门氏菌和空肠弯曲杆菌的多重PCR特异性检测方法。在104 CFU/PCR反应中检测到4种细菌。与其他常见的与四种目标生物相关的细菌没有交叉反应性。这种检测方法将简化目标病原体的检测程序,减少获得食品安全结果所需的时间和劳动力,并可能允许一种方案用于各种食品的细菌检测。
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来源期刊
Journal of Rapid Methods and Automation in Microbiology
Journal of Rapid Methods and Automation in Microbiology 生物-生物工程与应用微生物
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