Senachai Pachara, Chomvarin Chariya, Namwat Wises, Wongboot Warawan, Wongwajana Suwin, Tangkanakul Waraluk
Department of Microbiology and Research and Diagnostic Center for Emerging Infectious Diseases, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Southeast Asian J Trop Med Public Health. 2013 Mar;44(2):249-58.
A tetraplex PCR method was developed for simultaneous detection of Vibrio cholerae, V. parahaemolyticus, V. vulnificus and V. mimicus in cockle samples in comparison with conventional culture method. Specific primers targeting ompW of V. cholerae, tl of V. parahaemolyticus, hsp60 of V. vulnificus and sodB of V. mimicus were employed in the same PCR. Detection limit of the tetraplex PCR assay was 104 cfu/ml (400 cfu/PCR reaction) for pure cultures of all four species of Vibrio. In Vibrio spiked cockle samples, the limit of detection after 6 hours enrichment in alkaline peptone water was 1 cfu/10 g of cockle tissue for three Vibrio spp, except for V. mimicus that was 102 cfu/10 g of cockle tissue. When the tetraplex PCR and culture methods were applied to 100 cockle samples, V. parahaemolyticus, V. vulnificus, V. cholerae and V. mimicus were detected in 100, 98, 80 and 9% of the samples by tetraplex PCR and in 76, 42, 0 and 0% by the culture method, respectively. This developed tetraplex PCR method should be suitable for simultaneous and rapid detection of Vibrio species in food samples and for food safety assessment.
开发了一种四重PCR方法,用于同时检测蛤仔样本中的霍乱弧菌、副溶血性弧菌、创伤弧菌和拟态弧菌,并与传统培养方法进行比较。在同一PCR中使用了针对霍乱弧菌ompW、副溶血性弧菌tl、创伤弧菌hsp60和拟态弧菌sodB的特异性引物。四重PCR检测对所有四种弧菌纯培养物的检测限为104 cfu/ml(400 cfu/PCR反应)。在添加弧菌的蛤仔样本中,在碱性蛋白胨水中富集6小时后的检测限,除拟态弧菌为102 cfu/10 g蛤仔组织外,其他三种弧菌均为1 cfu/10 g蛤仔组织。当将四重PCR和培养方法应用于100个蛤仔样本时,四重PCR分别在100%、98%、80%和9%的样本中检测到副溶血性弧菌、创伤弧菌、霍乱弧菌和拟态弧菌,而培养方法分别在76%、42%、0%和0%的样本中检测到。这种开发的四重PCR方法应适用于食品样本中弧菌的同时快速检测和食品安全评估。