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Rapid Detection of Staphylococcus aureus Strains with Reduced Susceptibility to Vancomycin by Isothermal Microcalorimetry

机译:等温微量热法快速检测对万古霉素敏感性降低的金黄色葡萄球菌菌株

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Methicillin-resistant Staphylococcus aureus (MRSA) usually harbors a vancomycin-susceptible phenotype (VSSA) but can exhibit reduced vancomycin susceptibility phenotypes that can be heterogeneous-intermediate (hVISA), intermediate (VISA), or fully resistant (VRSA). Current detection techniques (e.g., Etest and population analysis profiles [PAPs]) are slow and time-consuming. We investigated the potential of microcalorimetry to detect reduced susceptibilities to vancomycin in MRSA strains. Representative MSSA, VSSA, hVISA, VISA, and VRSA reference strains, as well as clinical isolates, were used. PAPs were performed by standard methods. Microcalorimetry was performed by inoculating 5 × 107 CFU of overnight cultures into 3-ml vials of brain heart infusion broth supplemented with increasing concentrations of vancomycin, and growth-related heat production was measured at 37°C. For the reference strains, no heat production was detected in the VSSA isolates at vancomycin concentrations of >3 μg/ml during the 72 h of incubation. The hVISA and VISA strains showed heat production with concentration-proportional delays of up to 6 μg/ml in 48 h and up to 12 μg/ml in 72 h, respectively. The VRSA strain showed heat production at concentrations up to 16 μg/ml in 12 h. The testing of clinical strains indicated an excellent negative predictive value, allowing us to rule out a decreased vancomycin susceptibility phenotype in <8 h of incubation. Sequential isolates from a patient undergoing vancomycin therapy showed evolving microcalorimetric profiles up to a VISA phenotype. Microcalorimetry was able to detect strains with reduced susceptibilities to vancomycin in <8 h. The measurement of bacterial heat production might represent a simple and rapid method for the detection of reduced susceptibilities to vancomycin in MRSA strains.
机译:耐甲氧西林的金黄色葡萄球菌(MRSA)通常具有万古霉素敏感性表型(VSSA),但可以表现出降低的万古霉素敏感性表型,可以是异源-中间(hVISA),中度(VISA)或完全耐药(VRSA)。当前的检测技术(例如Etest和人口分析配置文件[PAP])缓慢且耗时。我们调查了微量量热法检测MRSA菌株对万古霉素敏感性降低的潜力。使用了代表性的MSSA,VSSA,hVISA,VISA和VRSA参考菌株以及临床分离株。 PAP通过标准方法进行。通过将5×10 7 CFU过夜培养物接种到3毫升小瓶的心脏输液肉汤中,并补充浓度升高的万古霉素,进行微量量热法,并在37°C下测量与生长相关的热量。对于参考菌株,在72小时的培养中,万古霉素浓度> 3μg/ ml时,在VSSA分离物中未检测到热量产生。 hVISA和VISA菌株显示出热量产生,浓度成比例的延迟在48小时内高达6μg/ ml,在72小时内高达12μg/ ml。 VRSA菌株在12小时内产生的热量高达16μg/ ml。对临床菌株的测试显示出极好的阴性预测值,使我们可以排除在孵育后8小时内万古霉素敏感性表型降低。来自接受万古霉素治疗的患者的顺序分离株显示出不断发展的微量量热特征,直至VISA表型。微量量热法能够在<8小时内检测出对万古霉素敏感性降低的菌株。细菌产热的测量可能代表了一种简单快速的方法,用于检测MRSA菌株对万古霉素敏感性降低。

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