Hassan Abdulwahed Ahmed, Akineden Omer, Usleber Ewald
Institut für Tierärztliche Nahrungsmittelkunde, Justus-Liebig-Universität Giessen, Ludwigstrasse 21, D-35390 Giessen, Germany.
J Clin Microbiol. 2005 Mar;43(3):1234-8. doi: 10.1128/JCM.43.3.1234-1238.2005.
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 alpha-galactosidase, and all were negative for beta-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.
在德国北莱茵-威斯特法伦州一个受亚临床乳腺炎影响的奶牛场(有49头泌乳奶牛)中,从11头奶牛的31份牛奶样本中分离出犬链球菌。对从受感染乳房区域分离出的31株菌株进一步进行表型和分子特性鉴定。大多数菌株(83.9%)产生α-半乳糖苷酶,所有菌株的β-d-葡萄糖醛酸酶均为阴性。通过PCR方法扩增16S rRNA基因并用限制性内切酶RsaI、MspI和AvaII进行消化,产生了物种特异性图谱。通过对16S rRNA基因、16S-23S rRNA基因间隔区、CAMP因子编码基因cfg和sodA基因内部片段进行物种特异性扩增进行的额外鉴定与犬链球菌一致。通过脉冲场凝胶电泳对染色体DNA进行的宏观限制性分析表明,犬链球菌分离株源自单个克隆或密切相关。