| Literature DB >> 28477235 |
Y Iwata1,2, K Satou3, H Tsuzuku4, K Furuichi2,5, Y Senda4, Y Sakai-Takemori4, T Wada7,8, S Fujita1, T Miyake2,6, H Yasuda4, N Sakai2,5, S Kitajima2,6, T Toyama2,6, Y Shinozaki2,6, A Sagara2,6, T Miyagawa2,6, A Hara2,6, M Shimizu2,6, Y Kamikawa2,6, S Kaneko6, T Wada7,8.
Abstract
Daptomycin (DAP) is widely used in the treatment of methicillin-resistant Staphylococcus aureus (MRSA) infection. The emergence of DAP non-susceptible MRSA strains during therapy is a major concern in clinical settings. Recent studies revealed that MRSA spontaneously reverts to a subsequent methicillin-susceptible S. aureus (MSSA) strain. However, it is not clear whether DAP non-susceptible MRSA has the ability to revert to a susceptible strain. We obtained an MRSA strain pair, DAP non-susceptible strain and subsequent DAP susceptible strain, from a patient. To understand the underlying mechanism by which DAP non-susceptible MRSA reverts to a susceptible strain, we performed genetic and phenotypic analysis in the strain pair. Although whole-genome analysis revealed four missense mutations, including L826F in mprF, in both strains, the net cell-surface charge was similar between the DAP non-susceptible and susceptible strains. However, the thickness of the cell wall was higher in the DAP non-susceptible strain, which was decreased to the same level as the control after reversion to the DAP susceptible strain. Moreover, the non-susceptible strain showed higher mRNA expression of the two-component system (TCS), such as VraSR, yycG and GraS, with the up-regulated transcription levels of cell-wall biosynthesis-related genes. The expression levels of those genes were decreased after reversion to the susceptible strain. These results indicated that DAP non-susceptibility due to up-regulation of the TCS and cell-wall biosynthesis-related genes may be reversible by the discontinuation of DAP, leading to reversion to the DAP susceptible phenotype.Entities:
Keywords: Caseinolytic Protease; Daptomycin; Pleural Fluid Drainage; Strain Pair; Susceptible Strain
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Year: 2017 PMID: 28477235 DOI: 10.1007/s10096-017-2999-3
Source DB: PubMed Journal: Eur J Clin Microbiol Infect Dis ISSN: 0934-9723 Impact factor: 3.267