Queen's University Belfast, Centre for Infection & Immunity, 97 Lisburn Road, Belfast BT9 7BL, United Kingdom.
Int J Med Microbiol. 2010 Aug;300(6):380-6. doi: 10.1016/j.ijmm.2010.04.011. Epub 2010 May 6.
Staphylococcus epidermidis normally is a commensal inhabitant of the healthy human skin and mucosa, but also a common nosocomial pathogen in immunocompromised patients. Living at the edge between commensalism and pathogenicity, S. epidermidis has developed interesting strategies to conquer the hospital environment as a novel ecological niche and to transform into a notorious pathogen. Recent progress in genome analysis and molecular epidemiology gave interesting insights into the enormous flexibility by which these bacteria generate continuously novel phenotypic and genotypic variants. Recent multilocus sequence typing studies identified S. epidermidis as a highly diverse species that evolves mainly by recombination and acquires readily mobile genetic elements. With respect to healthcare-associated isolates, a limited number of epidemic clonal lineages were found to have emerged and established in hospital settings worldwide. These isolates are characterised by the carriage of various SCCmec gene cassettes, conferring methicillin resistance, and by a striking ability to form biofilms on medical devices. Moreover, nosocomial S. epidermidis strains typically harbour multiple copies of the insertion sequence element IS256 in their genomes. Nosocomial S. epidermidis strains vary virulence- and resistance-associated gene expression in the course of an infection to a remarkably high degree. Heterogenous gene expression in S. epidermidis is achieved, on the one hand, by complex regulatory pathways. On the other hand, it is associated with genetic mechanisms that were found to be mediated by the action of the IS256 element which obviously represents an important driving force for the flexibility of the S. epidermidis genome. The data accumulated so far suggest that recombination along with the frequent acquisition of mobile genetic elements are crucial factors for the success of S. epidermidis as a nosocomial pathogen.
表皮葡萄球菌通常是健康人体皮肤和黏膜的共生体,但也是免疫功能低下患者医院感染的常见病原体。作为一种新型生态位,表皮葡萄球菌生活在共生和致病性之间的边缘,它已经发展出了有趣的策略来征服医院环境,并转化为臭名昭著的病原体。最近在基因组分析和分子流行病学方面的进展,让人们对这些细菌通过不断产生新的表型和基因型变体的巨大灵活性有了有趣的了解。最近的多位点序列分型研究表明,表皮葡萄球菌是一个高度多样化的物种,主要通过重组和获得易移动的遗传元件来进化。就与医疗保健相关的分离株而言,发现少数流行克隆谱系已经在全球医院环境中出现并建立。这些分离株的特征是携带各种 SCCmec 基因盒,赋予耐甲氧西林性,并且具有在医疗器械上形成生物膜的惊人能力。此外,医院获得性表皮葡萄球菌株的基因组中通常携带多个插入序列元件 IS256。在感染过程中,医院获得性表皮葡萄球菌株的毒力和耐药相关基因表达差异极大。表皮葡萄球菌的异质性基因表达一方面是通过复杂的调控途径实现的,另一方面与遗传机制有关,这些机制被发现是由 IS256 元件介导的,显然这是表皮葡萄球菌基因组灵活性的重要驱动力。迄今为止积累的数据表明,重组和频繁获得移动遗传元件是表皮葡萄球菌作为医院病原体成功的关键因素。