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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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摘要

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的三十一种菌株的表型和分子特性进一步得到了表征。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16S rRNA基因,16S-23S rRNA基因间间隔区,CAMP因子编码基因cfg和sodA基因内部片段的其他鉴定与犬链球菌一致。通过脉冲场凝胶电泳对染色体DNA进行宏观限制性分析表明,犬链球菌分离株起源于单个克隆或密切相关。

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