首页> 外文期刊>Veterinary Microbiology >Genotypic versus phenotypic identification of staphylococcal species of canine origin with special reference to Staphylococcus schleiferi subsp. coagulans
【24h】

Genotypic versus phenotypic identification of staphylococcal species of canine origin with special reference to Staphylococcus schleiferi subsp. coagulans

机译:犬源性葡萄球菌物种的基因型和表型鉴定,特别参考施氏葡萄球菌亚种。凝结物

获取原文
获取原文并翻译 | 示例
           

摘要

A comparative study was performed to examine the respective accuracy of 16S rDNA sequencing and of the commercial biochemical assay ID32 STAPH (bioMerieux, Marcy l'Etoile, France) in the identification of 232 staphylococcal samples representing 20 species and subspecies isolated from 367 dogs. Notable differences in species distribution were observed by comparing genotypic and phenotypic data. Partial sequencing of 16S rDNA resulted in an unambiguous identification of 226 (97.4%) of the isolates, whereas the phenotypic approach resulted in a correct diagnosis of 162 (69.8%) of the isolates. Statistical agreement between genotypic and phenotypic identification of staphylococci was substantial (Kappa coefficient of 0.6-0.8) for Staphylococcus aureus, S. hominis, S. warneri, S. cohnii subsp. urealyticus, and S. simulans, and "almost perfect" (Kappa coefficient of 0.8-1) for S. intermedius, S. epidermidis, S. equorum, S. haemolyticus, S. sciuri, and S. kloosi. No agreement above that expected by chance (Kappa coefficient=0) was observed for S. schleiferi subsp. coagulans, which was either confounded with S. intermedius and S. capitis, or categorized as unacceptable by the biochemical assay. Given the growing importance of this pathogen in veterinary medicine and its frequent misidentification with related staphylococci, a PCR-RFLP approach producing a S. schleiferi-specific restriction profile was developed. This fast and reliable assay represents a valuable tool in assisting in the monitoring of this pathogen.
机译:进行了一项比较研究,以检查16S rDNA测序和商业生化测定法ID32 STAPH(bioMerieux,Marcy l'Etoile,法国)在鉴定代表从367只狗中分离出的20个物种和亚种的232个葡萄球菌样品的准确性。通过比较基因型和表型数据观察到物种分布的显着差异。通过对16S rDNA进行部分测序,可以明确鉴定出226个(97.4%)分离株,而通过表型分析可以正确诊断出162个(69.8%)分离株。葡萄球菌的基因型和表型鉴定之间的统计一致性很高(Kappa系数为0.6-0.8),对于金黄色葡萄球菌,人沙门氏菌,华氏链球菌,科氏链球菌亚种。溶脲酶和链球菌,中间链球菌,表皮葡萄球菌,马刺链球菌,溶血链球菌,s。sciuri和链球菌“几乎完美”(卡帕系数为0.8-1)。对于S. schleiferi亚种,未观察到高于偶然预期的一致性(Kappa系数= 0)。凝集素,或者与中间链球菌和Cap。capitis混杂在一起,或者被生化分析归类为不可接受。鉴于这种病原体在兽医学中的重要性日益增加,并且经常将其与相关葡萄球菌错误识别,因此开发了一种PCR-RFLP方法,该方法产生了猪链球菌特异性限制性内切酶谱。这种快速而可靠的分析方法是协助监测这种病原体的宝贵工具。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号