首页> 外文期刊>Canadian journal of microbiology >Denaturing gradient gel electrophoresis for nonlethal detection of Aeromonas salmonicida in salmonid mucus and its potential for other bacterial fish pathogens
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Denaturing gradient gel electrophoresis for nonlethal detection of Aeromonas salmonicida in salmonid mucus and its potential for other bacterial fish pathogens

机译:变性梯度凝胶电泳用于鲑鱼粘液中非致死性沙门氏菌的非致死检测及其在其他细菌鱼病原体中的潜力

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Denaturing gradient gel electrophoresis (DGGE) of 16S rDNA was used to nonlethally detect Aeromonas salmonicida and other bacteria in salmonid skin mucus. Mucus samples from wild spawning coho salmon (Oncorhynchus kisutch) with endemic A. salmonicida and from cultured lake trout (Salvelinus namaycush) were tested by PCR-DGGE and were compared with mucus culture on Coomassie brilliant blue agar and internal organ culture. PCR-DGGE gave a highly reproducible 4-band pattern for 9 strains of typical A. salmonicida, which was different from other Aeromonas spp. Aeromonas salmonicida presence in mucus was evident as a band that comigrated with the bottom band of the A. salmonicida 4-band pattern and was verified by sequencing. PCR-DGGE found 36 of 52 coho salmon positive for A. salmonicida, compared with 31 positive by mucus culture and 16 by organ culture. Numerous other bacteria were detected in salmonid mucus, including Pseudomonas spp., Shewanella putrefaciens, Aeromonas hydrophila and other aeromonads. However, Yersinia ruckeri was not detected in mucus from 27 lake trout, but 1 fish had a sorbitol-positive Y. ruckeri isolated from organ culture. Yersinia ruckeri seeded into a mucus sample suggested that PCR-DGGE detection of this bacterium from mucus was possible. PCR-DGGE allows nonlethal detection of A. salmonicida in mucus and differentiation of some Aeromonas spp. and has the potential to allow simultaneous detection of other pathogens present in fish mucus.
机译:16S rDNA的变性梯度凝胶电泳(DGGE)用于非致命性检测鲑鱼皮肤粘液中的鲑鱼气单胞菌和其他细菌。用PCR-DGGE对野生地方产鲑科鲑(Oncorhynchus kisutch)和地方性沙门氏菌和养殖的湖鳟(Salvelinus namaycush)的粘液样本进行了PCR-DGGE测试,并与考马斯亮蓝琼脂和内脏器官培养液中的粘液培养物进行了比较。 PCR-DGGE对9株典型的沙门氏菌进行了高度重现的4波段模式,这与其他气单胞菌不同。粘液中存在沙门氏菌气单胞菌,该条带与沙门氏菌沙门氏菌4带模式的底带相对应,并通过测序证实。 PCR-DGGE在52头鲑中检出了A. salicida阳性,而粘液培养为31例,器官培养为16例。在鲑鱼粘液中还检测到许多其他细菌,包括假单胞菌属,腐烂希瓦氏菌,嗜水气单胞菌和其他气单胞菌。但是,在27个湖鳟的粘液中未检出Rerseria ruckeri,但是有1条鱼的器官培养物中分离出的山梨醇阳性R. ruckeri。播种到粘液样本中的rucker yerinia ruckeri表明从粘液中PCR-DGGE检测该细菌是可能的。 PCR-DGGE可以非致死性检测粘液中的沙门氏菌并区分某些气单胞菌。并有可能同时检测鱼粘液中存在的其他病原体。

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