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Intraspecific characterization of Vibrio tapetis strains by use of pulsed-field gel electrophoresis ribotyping and plasmid profiling.

机译:通过使用脉冲场凝胶电泳核糖分型法和质粒分析法对Tapetis tapetis菌株进行种内表征。

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摘要

A total of twenty-two strains of Vibrio tapetis, the causative agent of brown ring disease affecting cultured clams, were compared and evaluated in an investigation of strain heterogeneity using pulsed-field gel electrophoresis (PFGE), ribotyping, and plasmid profile analysis. A total of 90.9% of V. tapetis strains tested by using NotI showed the same PFGE pattern, consisting of 15 bands. In contrast, the V. tapetis strains showed a low degree of similarity with six reference Vibrio species tested. All V. tapetis strains harbored a large plasmid of 74.5 kb. This plasmid was not detected in any of the other Vibrio species. In addition, endonuclease restriction analysis of the plasmid content of the strains using EcoRI and HindIII clearly showed that all the strains of V. tapetis possessed the same cleavage pattern. The three enzymes used for ribotyping, PvuII, SmaI, and SalI, yielded patterns with 8 to 12 bands ranging in size from 2 to 23 kb. The application of the SalI and SmaI endonuclease rendered the separation of the strains tested in two ribotypes, while all the V. tapetis strains belonged to the same ribotype when the enzyme PvuII was used.
机译:在使用脉冲场凝胶电泳(PFGE),核糖分型和质粒谱分析的菌株异质性研究中,比较并评估了总共22株巴斯德弧菌(棕色环病的病原体影响培养的蛤)。通过使用NotI测试的总共90.9%的V. tapetis菌株显示出相同的PFGE模式,由15个条带组成。相反,V。tapetis菌株与测试的六个参照弧菌属物种显示出较低的相似度。所有V. tapetis菌株都带有一个74.5 kb的大质粒。在任何其他弧菌物种中均未检测到该质粒。另外,使用EcoRI和HindIII对菌株的质粒含量进行核酸内切酶限制性分析清楚地表明,所有V. tapetis菌株均具有相同的切割模式。用于核糖分型的三种酶PvuII,SmaI和SalI产生的花样具有8至12条带,大小从2至23 kb不等。 SalI和SmaI核酸内切酶的应用分离了两种核糖型测试的菌株,而使用酶PvuII时,所有V. tapetis菌株均属于同一核糖型。

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