Heterogeneous vancomycin resistance in Staphylococcus aureus does not predict development of vancomycin resistance upon vancomycin pressure

被引:3
|
作者
Gaillard, Tiphaine [1 ]
Dupieux-Chabert, Celine [1 ,2 ]
Butin, Marine [2 ]
Dumitrescu, Oana [1 ,2 ]
Naceur, Oilida [2 ]
Bouveyron, Caroline [1 ]
Martra, Annie [1 ]
Bes, Michele [1 ,2 ]
Tristan, Anne [1 ,2 ]
Vandenesch, Francois [1 ,2 ]
Lina, Gerard [1 ,2 ]
Laurent, Frederic [1 ,2 ]
Rasigade, Jean-Philippe [1 ,2 ]
机构
[1] Hosp Civils Lyon, Ctr Natl Reference Staphylocoques, Lyon, France
[2] Univ Lyon 1, Ctr Int Rech Infectiol, CNRS UMR5308, ENS Lyon,INSERM U1111, Lyon, France
关键词
MINIMUM INHIBITORY CONCENTRATION; CLINICAL-OUTCOMES; INFECTIONS;
D O I
10.1093/jac/dkab488
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background It is unclear whether Staphylococcus aureus with heterogeneous intermediate vancomycin resistance (hVISA) can develop vancomycin resistance faster than vancomycin-susceptible S. aureus (VSSA) strains. Methods We compared the kinetics of vancomycin MIC increase for 15 days of sustained in vitro vancomycin exposure for clinical hVISA (n = 12) and VSSA (n = 24) isolates, as well as for reference strains Mu3 (hVISA) and ATCC 29213 (VSSA). Clinical isolates were categorized as hVISA using the population analysis profile method. MICs were monitored for 15 days and the rate of MIC increase under exposure, for each strain, was evaluated in a linear regression model relative to time. Results All isolates acquired vancomycin resistance upon exposure. Vancomycin MICs increased faster for VSSA compared with hVISA isolates (P < 0.01). Conclusions The hVISA phenotype does not correspond to an enhanced adaptation potential to in vitro vancomycin pressure.
引用
收藏
页码:1032 / 1035
页数:4
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