Cameron David R, Mortin Lawrence I, Rubio Aileen, Mylonakis Eleftherios, Moellering Robert C, Eliopoulos George M, Peleg Anton Y
a Department of Microbiology ; School of Biomedical Sciences; Monash University ; Melbourne , Australia.
Virulence. 2015;6(2):127-31. doi: 10.1080/21505594.2015.1011532.
Daptomycin resistance (DAP(R)) in Staphylococcus aureus is associated with mutations in genes that are also implicated in staphylococcal pathogenesis. Using a laboratory-derived series of DAP exposed strains, we showed a relationship between increasing DAP MIC and reduced virulence in a Galleria mellonella infection model. Point mutations in walK and rpoC led to cumulative reductions in virulence and simultaneous increases in DAP MIC. A point mutation to mprF did not impact on S.aureus virulence; however deletion of mprF led to virulence attenuation and hyper-susceptibility to DAP. To validate our findings in G. mellonella, we confirmed the attenuated virulence of select isolates from the laboratory-derived series using a murine septicaemia model. As a corollary, we showed significant virulence reductions for clinically-derived DAP(R) isolates compared to their isogenic, DAP-susceptible progenitors (DAP(S)). Intriguingly, each clinical DAP(R) isolate was persistent in vivo. Taken together, it appears the genetic correlates underlying daptomycin resistance in S. aureus also alter pathogenicity.
金黄色葡萄球菌中的达托霉素耐药性(DAP(R))与也参与葡萄球菌致病机制的基因突变有关。使用实验室衍生的一系列暴露于达托霉素的菌株,我们在大蜡螟感染模型中显示了达托霉素最低抑菌浓度(MIC)增加与毒力降低之间的关系。walK和rpoC中的点突变导致毒力累积降低以及达托霉素MIC同时增加。mprF的点突变对金黄色葡萄球菌毒力没有影响;然而,mprF的缺失导致毒力减弱以及对达托霉素的超敏感性。为了在大蜡螟中验证我们的发现,我们使用小鼠败血症模型证实了来自实验室衍生系列的选定分离株的毒力减弱。作为一个推论,我们显示与它们的同基因、达托霉素敏感祖细胞(DAP(S))相比,临床来源的DAP(R)分离株的毒力显著降低。有趣的是,每个临床DAP(R)分离株在体内都具有持续性。综上所述,似乎金黄色葡萄球菌中达托霉素耐药性的潜在遗传关联也改变了致病性。