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首页> 外文期刊>Diseases of Aquatic Organisms >Phylogenetic analysis of Piscirickettsia salmonis by 16S, internal transcribed spacer (ITS) and 23S ribosomal DNA sequencing
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Phylogenetic analysis of Piscirickettsia salmonis by 16S, internal transcribed spacer (ITS) and 23S ribosomal DNA sequencing

机译:通过16S,内部转录间隔区(ITS)和23S核糖体DNA测序对鲑鱼立克次氏体进行系统发育分析

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ABSTRACT: Piscirickettsia salmonis, the etiologic agent of piscirickettsiosis, is a systemic disease of salmonid fish. Variations in virulence and mortality have been observed during epizootics at different geographical regions and in laboratory experiments with isolates from these different locations. This raises the possibility that biogeographical patterns of genetic variation might be a significant factor with this disease. To assess the genetic variability the 16S ribosomal DNA, the internal transcribed spacer (ITS) and the 23S ribosomal DNA of isolates from 3 different hosts and 3 geographic origins were amplified using the polymerase chain reaction (PCR). Results of this analysis confirm that P. salmonis is a member of the gamma subgroup of the Proteobacteria and show that the isolates form a tight monophyletic cluster with 16S rDNA similarities ranging from 99.7 to 98.5%. The ITS regions were 309 base pairs (bp), did not contain tRNA genes, and varied between isolates (95.2 to 99.7% similarity). Two-thirds of the 23S rRNA gene was sequenced from 5 of the isolates, yielding similarities ranging from 97.9 to 99.8%. Phylogenetic trees were constructed based on the 16S rDNA, ITS and 23S rDNA sequence data and compared. The trees were topologically similar, suggesting that the 3 types of molecules provided similar phylogenetic information. Five of the isolates are closely related (99.4% 16S rDNA similarity, 99.1 to 99.7% ITS and 99.3 to 99.8% 23S rDNA similarities). The sequence of one Chilean isolate, EM-90, was unique, with 16S rDNA similarities to the other isolates ranging from 98.5 to 98.9%, the ITS from 95.2 to 96.9% and the 23S rDNA from 97.6 to 98.5%. >
机译:摘要:立克次体病的病原体鲑鱼立克次体是鲑鱼的全身性疾病。在不同地理区域的流行病期间以及在实验室实验中,使用了来自这些不同位置的分离株,观察到毒力和死亡率的变化。这增加了遗传变异的生物地理模式可能是该疾病的重要因素的可能性。为了评估遗传变异性,使用聚合酶链反应(PCR)扩增了来自3个不同宿主和3个地理起源的分离株的16S核糖体DNA,内部转录间隔区(ITS)和23S核糖体DNA。该分析的结果证实了 P。鲑鱼是Proteobacteriaγ亚组的成员,表明分离株形成紧密的单系簇,其16S rDNA相似性范围为99.7至98.5%。 ITS区为309个碱基对(bp),不含tRNA基因,并且在分离株之间有所不同(相似性为95.2至99.7%)。 23S rRNA基因的三分之二是从5个分离物中进行测序的,其相似性在97.9%至99.8%之间。根据16S rDNA,ITS和23S rDNA序列数据构建系统发育树并进行比较。树木的拓扑相似,表明这三种分子提供了相似的系统发育信息。其中五个分离物密切相关(> 99.4%的16S rDNA相似性,99.1%至99.7%的ITS和99.3%至99.8%的23S rDNA相似性)。一个智利分离株EM-90的序列是唯一的,与其他分离株的16S rDNA相似性在98.5%至98.9%之间,ITS在95.2%至96.9%之间,而23S rDNA在97.6%至98.5%之间。 >

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