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Multiplex PCR Assay for Detection of Bacterial Pathogens Associated with Warm-Water Streptococcosis in Fish

机译:多重PCR检测鱼中温水链球菌病相关细菌病原体

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摘要

A multiplex PCR-based method was designed for the simultaneous detection of the main pathogens involved in warm-water streptococcosis in fish (Streptococcus iniae, Streptococcus difficilis, Streptococcus parauberis, and Lactococcus garvieae). Each of the four pairs of oligonucleotide primers exclusively amplified the targeted gene of the specific microorganism. The sensitivity of the multiplex PCR using purified DNA was 25 pg for S. iniae, 12.5 pg for S. difficilis, 50 pg for S. parauberis, and 30 pg for L. garvieae. The multiplex PCR assay was useful for the specific detection of the four species of bacteria not only in pure culture but also in inoculated fish tissue homogenates and naturally infected fish. Therefore, this method could be a useful alternative to the culture-based method for the routine diagnosis of warm-water streptococcal infections in fish.
机译:设计了一种基于多重PCR的方法,用于同时检测鱼类中温水链球菌病的主要病原体(猪链球菌,艰难链球菌,副猪链球菌和加尔乳杆菌)。四对寡核苷酸引物中的每对都专门扩增特定微生物的靶向基因。使用纯化的DNA进行的多重PCR的敏感性对海豚链球菌为25 pg,对艰难链球菌为12.5 pg,对伞形葡萄球菌为50 pg,对加维链球菌为30 pg。多重PCR分析不仅可用于纯培养中的四种细菌的特异性检测,而且可用于接种鱼的组织匀浆和自然感染鱼的特异性检测。因此,该方法对于常规诊断鱼类温水链球菌感染可能是一种替代基于培养的方法的有用方法。

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