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Simultaneous Detection of Streptococcus spp. and Aeromonas spp. from Diseased Tilapia (Oreochromis niloticus) using Multiplex-Polymerase Chain Reaction

机译:同时检测链球菌。和气单胞菌属。多重聚合酶链反应从患病罗非鱼(尼罗罗非鱼)中提取

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摘要

A multiplex Polymerase Chain Reaction (m-PCR) assay was developed for simultaneous detection of two major pathogens, Streptococcal and Aeromonad bacteria, in farmed tilapia. DNA fragments of Streptococcus spp. and Aeromonas spp. were amplified using genus specific primers, C1/C2 and AERF/AERR, which produced PCR of 207 bp and 953 bp, respectively. The lowest concentration of each Streptococcus and Aeromonas spp. extracted genomic DNA from a colony detected by m-PCR was 2 ng. The m-PCR assay was proven applicable for detection of bacterial genomic DNA in tissues (brain and posterior kidney) of infected fish. Specificity of the assay tested with other Gram-positive (Staphylococcus aureus) and Gram-negative water borne bacteria (Escherichia coli, Enterococcus faecalis, Pseudomonas aeruginosa, Salmonella enteritidis, Salmonella typhimurium, Vibrio harveyi and Vibrio parahemolyticus) showed no amplification. As Streptococcal and Aeromonad infections are common concurrent bacterial diseases, the m-PCR assay established in this study enabled effective simultaneous detection of these two major bacterial infections responsible for current economic losses in tilapia farming in Thailand.
机译:开发了一种多重聚合酶链反应(m-PCR)分析方法,用于同时检测养殖罗非鱼中的两种主要病原体,链球菌和Aeromonad细菌。链球菌属的DNA片段。和气单胞菌属。使用属特异性引物C1 / C2和AERF / AERR分别扩增,分别产生207 bp和953 bp的PCR。每种链球菌和气单胞菌的最低浓度。通过m-PCR检测到的从菌落中提取的基因组DNA为2ng。事实证明,m-PCR测定法可用于检测受感染鱼的组织(大脑和后肾)中的细菌基因组DNA。用其他革兰氏阳性(金黄色葡萄球菌)和革兰氏阴性水传播细菌(大肠杆菌,粪肠球菌,铜绿假单胞菌,肠炎沙门氏菌,鼠伤寒沙门氏菌,哈维氏弧菌和副溶血弧菌)测试的测定特异性未显示扩增。由于链球菌和Aeromonad感染是常见的并发细菌性疾病,因此本研究中建立的m-PCR分析能够有效地同时检测这两种主要的细菌感染,这些感染是泰国罗非鱼养殖目前造成的经济损失。

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