Willby Melisa, Sikes R David, Malik Seidu, Metchock Beverly, Posey James E
Laboratory Branch, Division of TB Elimination, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Laboratory Branch, Division of TB Elimination, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia, USA
Antimicrob Agents Chemother. 2015 Sep;59(9):5427-34. doi: 10.1128/AAC.00662-15. Epub 2015 Jun 22.
The newer fluoroquinolones moxifloxacin (MXF) and levofloxacin (LVX) are becoming more common components of tuberculosis (TB) treatment regimens. However, the critical concentrations for testing susceptibility of Mycobacterium tuberculosis to MXF and LVX are not yet well established. Additionally, the degree of cross-resistance between ofloxacin (OFX) and these newer fluoroquinolones has not been thoroughly investigated. In this study, the MICs for MXF and LVX and susceptibility to the critical concentration of OFX were determined using the agar proportion method for 133 isolates of M. tuberculosis. Most isolates resistant to OFX had LVX MICs of >1 μg/ml and MXF MICs of >0.5 μg/ml. The presence of mutations within the gyrA quinolone resistance-determining regions (QRDR) correlated well with increased MICs, and the level of LVX and MXF resistance was dependent on the specific gyrA mutation present. Substitutions Ala90Val, Asp94Ala, and Asp94Tyr resulted in low-level MXF resistance (MICs were >0.5 but ≤2 μg/ml), while other mutations led to MXF MICs of >2 μg/ml. Based on these results, a critical concentration of 1 μg/ml is suggested for LVX and 0.5 μg/ml for MXF drug susceptibility testing by agar proportion with reflex testing for MXF at 2 μg/ml.
新型氟喹诺酮类药物莫西沙星(MXF)和左氧氟沙星(LVX)正日益成为结核病(TB)治疗方案中更为常见的组成部分。然而,结核分枝杆菌对MXF和LVX药敏试验的临界浓度尚未完全确定。此外,氧氟沙星(OFX)与这些新型氟喹诺酮类药物之间的交叉耐药程度尚未得到充分研究。在本研究中,采用琼脂比例法对133株结核分枝杆菌分离株测定了MXF和LVX的最低抑菌浓度(MIC)以及对OFX临界浓度的敏感性。大多数对OFX耐药的分离株LVX的MIC>1μg/ml,MXF的MIC>0.5μg/ml。gyrA喹诺酮耐药决定区(QRDR)内突变的存在与MIC增加密切相关,LVX和MXF的耐药水平取决于存在的特定gyrA突变。Ala90Val、Asp94Ala和Asp94Tyr替代导致低水平的MXF耐药(MIC>0.5但≤2μg/ml),而其他突变导致MXF的MIC>2μg/ml。基于这些结果,对于通过琼脂比例法进行的LVX药敏试验,建议临界浓度为1μg/ml,对于MXF药敏试验,建议临界浓度为0.5μg/ml,对于MXF在2μg/ml时进行反射试验。