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Identification of Streptococcus canis Isolated from Milk of Dairy Cows with Subclinical Mastitis

机译:从亚临床乳腺炎的奶牛牛奶中分离出犬链球菌的鉴定

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Streptococcus canis was isolated from 31 milk samples from 11 cows in a dairy herd (with 49 lactating cows) affected by subclinical mastitis in north Rhine-Westphalia, Germany. Thirty-one isolates from the infected udder quarters were further characterized for their phenotypic and molecular properties. Most isolates (83.9%) produced α-galactosidase, and all were negative for β-d-glucuronidase. Amplification of the 16S rRNA gene by the PCR method and digestion with the restriction enzymes RsaI, MspI, and AvaII yielded species-specific patterns. Additional identification by species-specific amplification of the 16S rRNA gene, the 16S-23S rRNA gene intergenic spacer region, the CAMP factor-encoding gene cfg, and the internal fragments of the sodA gene was consistent with S. canis. Macrorestriction analysis of the chromosomal DNA by pulsed-field gel electrophoresis showed that the S. canis isolates originated from a single clone or were very closely related.
机译:从德国北莱茵-威斯特法伦州受亚临床乳腺炎影响的奶牛群(有49头泌乳母牛)的11头母牛的31份牛奶样本中分离出犬链球菌。从被感染的乳房区中分离出三十一个分离株,进一步表征其表型和分子特性。大多数分离株(83.9%)产生α-半乳糖苷酶,而所有β-d-葡萄糖醛酸苷酶均为阴性。通过PCR方法扩增16S rRNA基因,并用限制酶RsaI,MspI和AvaII消化,可产生物种特异性模式。通过物种特异性扩增进一步鉴定16S rRNA基因,16S-23S rRNA基因间间隔区,CAMP因子编码基因 cfg sodA 的内部片段em>基因与 S一致。犬。通过脉冲场凝胶电泳对染色体DNA进行宏观限制性分析,结果显示 S。 canis 分离株起源于单个克隆或密切相关。

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