多重聚合酶链反应早期检测水产品中污染的副溶血性弧菌和大肠杆菌

N. Hasanah, P. E. Sudaryatma, Imanuddin Razaq, Ni Nyoman Eriawati, W. Nugraha, Hidayati Kumalasari, Ni Putu Arya Shintya Anggraeni, Ida Ayu Mirah Meliana Dewi
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引用次数: 0

摘要

渔业部门每年增加出口活动,对印度尼西亚经济作出重大贡献。出口的水产品包括活鱼、冷冻鱼、各种鱼类和甲壳类、软体动物的保鲜制品等。致病菌副溶血性弧菌和大肠杆菌污染,造成源自渔业部门的健康问题(海产疾病)。这两种细菌污染的水产品是由于加工过程中的处理和储存不当,从而引起急性腹泻、胃肠道感染和发烧。为了提高细菌污染检测过程的时间、精力和准确性,开发了多重聚合酶链反应(mPCR)方法。该方法首先对两种细菌基因靶点进行优化,进行敏感性试验、特异性试验,然后将其应用于水产品样品中。mPCR方法有两种机制,即从琼脂培养基上分离的菌落进行“一次运行”和直接从水产品中进行“一管”。该方法对副溶血性弧菌和大肠杆菌分别在DNA浓度为5.6 pg/ml和5.5 pg/ml时具有较高的敏感性。单管pcr检测得到副溶血性弧菌阳性菌落7个,大肠杆菌阳性菌落38个。同时,直接从虾类样品中提取的单管mPCR可以对这两种细菌进行鉴定。
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Early Detection of Contamination Vibrio parahaemolyticus and Escherichia coli in Fisheries Product Using Multiplex Polymerase Chain Reaction
The fisheries sector provided a significant contribution to the Indonesian economy by increasing export activities in every year. The exported fisheries product are categorized of live fish, frozen fish, preservation products from various types of fish, crustaceans, and molluscs. The contamination of pathogenic bacteria Vibrio parahaemolyticus and Escherichia coli causing healthy problems originating from the fishery sector (sea-food borne disease). These two bacteria contaminated fisheries product is due to mishandling and storaging in the processing, which causes acute diarrhea, gastrointestinal infections and fever. The multiplex polymerase chain reaction (mPCR) method was developed to increase the efficiency of time, effort and accuracy of the bacterial contamination testing process. The mPCR method begins with the optimization of the two bacterial gene targets, sensitivity test, specificity test and then applied to samples of fishery products. The mPCR method is carried out in two mechanisms, namely “one-run” conducted from bacterial colonies isolated on agar media and “one-tube” which is applied directly from fishery products. The results of the development of the mPCR method on V. parahaemolyticus and E. coli resulted in sensitivity at concentrations of DNA 5.6 pg/ml and DNA 5.5 pg/ml, respectively. One-tube mPCR application obtained 7 positive colonies of V. parahaemolyticus and 38 positive colonies of E. coli. Meanwhile, one-tube mPCR which was applied directly from shrimp samples could identify the two bacteria.
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