犬假中间葡萄球菌三种常用技术的分子分型

G. Meroni, S. Morandi, M. Brasca, P. Martino
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摘要

假中间葡萄球菌(Staphylococcus pseudointermedius)是一种新发现的葡萄球菌,是犬脓皮病的主要病原体[1]。最近在人类中发现了假中间假葡萄球菌感染。该病原体的一个重要特征是与另外两种葡萄球菌(即中间葡萄球菌和德尔菲尼葡萄球菌)具有高度的遗传同一性,这两种葡萄球菌都被纳入中间葡萄球菌群(SIG)[2]。这种情况严重阻碍了这三种病原体的表型分化。尽管如此,直到2008年才出现了第一个假中间假葡萄球菌诊断鉴定的分子方案[3]。本研究的目的是利用核糖体间隔扩增(RSA)、多态性DNA随机扩增(RAPD)和限制性片段长度多态性(RFLP)三种常用的细菌分型方法,从临床相关犬脓皮病病例中获得不同生物型的假中芽孢杆菌。本研究共纳入46个不同菌株。本研究首次应用RSA技术鉴定了假中间假葡萄球菌的存在,尽管它不能区分不同的生物型。RAPD检测显示,所有感兴趣的菌株被分为三个不同的子簇(图1)。RFLP技术表现出最大的鉴别能力,为清楚地识别这种细菌提供了机会。总之,使用这三种不同的技术可以清楚地识别假中间球菌,并观察到不同生物型的存在。在未来,将这些结果与抗生素耐药性的测定结合起来,以验证某些多重耐药菌株是否具有特定的RSA和RAPD谱,可能是有趣的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular typing of Staphylococcus pseudintermedius canine strains by three commonly used techniques
Staphylococcus pseudintermedius is a newly described species of Staphylococcus regarded as the main causative agent of canine pyoderma [1]. S. pseudintermedius infection was recently described in humans. An important feature of this pathogen is the high genetic identity with two other species of staphylococci, namely S. intermedius and S. delphini , which are included all together in the Staphylococcus Intermedius Group (SIG) [2]. This scenario seriously hampers phenotypic differentiation of these three pathogens. Despite this, only in 2008 was described the first molecular protocol for diagnostic identification of S. pseudintermedius [3]. The aim of this work was to investigate the presence of different biotypes of S. pseudintermedius obtained from clinically relevant cases of pyoderma in dogs using three molecular methods commonly used to type bacteria: the Ribosomal Spacers Amplification (RSA), the Random Amplification of Polymorphic DNA (RAPD) and the Restriction Fragment Length Polymorphism (RFLP). A total of 46 different strains were included in this work. The application of the RSA technique, which was applied here for the first time, identified the presence of S. pseudintermedius , although it did not allow any differentiation between biotypes. The RAPD assay showed a single cluster that assembles all the interested strains that are grouped in three different sub-clusters ( Fig. 1 ). The RFLP technique showed the most discriminative power, providing the opportunity to clearly identify this bacterium. In conclusion, the use of these three different techniques allows to clearly identify S. pseudintermedius and to observe the presence of different biotypes. In future it could be interesting to couple these results with the determination of the antibiotic resistance in order to verify if certain Multi Drug Resistant strains have particular RSA and RAPD profiles.
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