Abstract
Daptomycin resistance (DAPR) 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 DAPRisolates compared to their isogenic, DAP-susceptible progenitors (DAPS). Intriguingly, each clinical DAPRisolate was persistent in vivo. Taken together, it appears the genetic correlates underlying daptomycin resistance in S. aureus also alter pathogenicity.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 127-131 |
| Number of pages | 5 |
| Journal | Virulence |
| Volume | 6 |
| Issue number | 2 |
| DOIs | |
| State | Published - Apr 1 2015 |
Keywords
- Bacterial persistence
- Galleria mellonella
- MprF
- S. aureus
- Walk
ASJC Scopus subject areas
- Parasitology
- Microbiology
- Immunology
- Microbiology (medical)
- Infectious Diseases
Divisions
- Infectious Disease
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