Department of Microbiology and Infectious Diseases, Royal Perth Hospital and PathWest Laboratory Medicine, WA. mcwehrhahn@hotmail
J Infect Dis. 2012 Jun 15;205(12):1840-8. doi: 10.1093/infdis/jis279. Epub 2012 Apr 5.
It is uncertain whether particular clones causing invasive community-onset methicillin-resistant and methicillin-sensitive Staphylococcus aureus (cMRSA/cMSSA) infection differ in virulence.
Invasive cMRSA and cMSSA cases were prospectively identified. Principal component analysis was used to derive an illness severity score (ISS) from clinical data, including 30-day mortality, requirement for intensive hospital support, the presence of bloodstream infection, and hospital length of stay. The mean ISS for each S. aureus clone (based on MLST) was compared with its DNA microarray-based genotype.
Fifty-seven cMRSA and 50 cMSSA infections were analyzed. Ten clones caused 82 (77%) of these infections and had an ISS calculated. The enterotoxin gene cluster (egc) and the collagen adhesin (cna) gene were found in 4 of the 5 highest-ranked clones (ST47-MSSA, ST30-MRSA-IV[2B], ST45-MSSA, and ST22-MRSA-IV[2B]) compared with none and 1 of the lowest 5 ranked clones, respectively. cMSSA clones caused more severe infection than cMRSA clones. The lukF/lukS Panton-Valentine leukocidin (PVL) genes did not directly correlate with the ISS, being present in the second, fourth, and 10th most virulent clones.
The clinical severity of invasive cMRSA and cMSSA infection is likely to be attributable to the isolates' entire genotype rather than a single putative virulence determinant such as PVL.
目前尚不清楚导致侵袭性社区获得性耐甲氧西林金黄色葡萄球菌(cMRSA/cMSSA)感染的特定克隆在毒力方面是否存在差异。
前瞻性地确定侵袭性 cMRSA 和 cMSSA 病例。主成分分析用于从临床数据中得出疾病严重程度评分(ISS),包括 30 天死亡率、需要强化医院支持、血流感染的存在以及住院时间。每个金黄色葡萄球菌克隆(基于 MLST)的平均 ISS 与其基于 DNA 微阵列的基因型进行比较。
分析了 57 例 cMRSA 和 50 例 cMSSA 感染。10 个克隆导致了 82 例(77%)感染,并计算了 ISS。肠毒素基因簇(egc)和胶原黏附素(cna)基因在排名前 4 位的克隆(ST47-MSSA、ST30-MRSA-IV[2B]、ST45-MSSA 和 ST22-MRSA-IV[2B])中发现,而在排名最低的 5 个克隆中则没有发现,分别为 1 个。cMSSA 克隆引起的感染比 cMRSA 克隆更严重。白细胞裂解素(PVL)基因与 ISS 没有直接相关性,存在于第二、第四和第十个最具毒力的克隆中。
侵袭性 cMRSA 和 cMSSA 感染的临床严重程度可能归因于分离株的整个基因型,而不是单个假定的毒力决定因素,如 PVL。