| Literature DB >> 25830650 |
David R Cameron1, Lawrence I Mortin, Aileen Rubio, Eleftherios Mylonakis, Robert C Moellering, George M Eliopoulos, Anton Y Peleg.
Abstract
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.Entities:
Keywords: Galleria mellonella; S. aureus; bacterial persistence; mprF; walK
Mesh:
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Year: 2015 PMID: 25830650 PMCID: PMC4601193 DOI: 10.1080/21505594.2015.1011532
Source DB: PubMed Journal: Virulence ISSN: 2150-5594 Impact factor: 5.882