Marfil Eduardo, Ruiz Pilar, Martínez-Martínez Luis, Causse Manuel
Microbiology Unit, University Hospital Reina Sofía, Cordoba, Spain; Maimonides Biomedical Research Institute of Cordoba (IMIBIC), Cordoba, Spain.
Department of Agricultural Chemistry, Soil Science and Microbiology, University of Córdoba, Córdoba, Spain.
J Glob Antimicrob Resist. 2022 Sep;30:395-398. doi: 10.1016/j.jgar.2022.07.012. Epub 2022 Jul 18.
The aim of this study is to compare the in vitro activity and minimal inhibitory concentration (MIC) distributions of tedizolid and linezolid against Mycobacterium avium complex (MAC) strains using a reference broth microdilution assay and a macrodilution assay with the Bactec-MGIT-960.
A total of 37 clinical isolates of MAC were included in the study. Reference broth microdilution was performed according to CLSI guidelines in a range of concentrations from 64 to 0.064 mg/L. Macrodilution was performed with the Bactec-MGIT-960 system. The cut-off points defined by CLSI for linezolid (resistant: > 16 mg/L, intermediate: 16 mg/L, susceptible: <16 mg/L) were used to define clinical categories of this drug. Essential agreement for both linezolid and tedizolid and categorical agreement for linezolid were defined following FDA criteria.
The MIC (16mg/L) and MIC (32mg/L) values for linezolid were identical with both methods. However, the MIC and MIC of tedizolid by microdilution (4 mg/L and 8 mg/L, respectively) were one twofold dilution higher than by macrodilution (2 mg/L and 4 mg/L, respectively). Ninety-four percent and 2.7% of the strains had MICs of tedizolid ≤4 mg/L and ≤ 0.5 mg/L, respectively, by the reference method. The linezolid macrodilution assay showed a categorical agreement of 40.5%, a minor error rate of 56.7% and a major error rate of 2.7% with respect to the reference method.
Tedizolid showed higher in vitro activity than linezolid against the tested MAC isolates. Macrodilution using the BD Bactec-MGIT-960 system is a practical approach to determine the susceptibility of MAC strains to tedizolid.
本研究旨在使用参考肉汤微量稀释法和Bactec-MGIT-960宏量稀释法,比较替加环素和利奈唑胺对鸟分枝杆菌复合群(MAC)菌株的体外活性及最低抑菌浓度(MIC)分布。
本研究共纳入37株MAC临床分离株。参考肉汤微量稀释法按照CLSI指南在64至0.064mg/L浓度范围内进行。宏量稀释法采用Bactec-MGIT-960系统进行。CLSI定义的利奈唑胺的截断值(耐药:>16mg/L,中介:16mg/L,敏感:<16mg/L)用于定义该药物的临床分类。按照FDA标准定义利奈唑胺和替加环素的基本一致性以及利奈唑胺的分类一致性。
两种方法测得的利奈唑胺的MIC(16mg/L)和MIC(32mg/L)值相同。然而,微量稀释法测得的替加环素的MIC和MIC(分别为4mg/L和8mg/L)比宏量稀释法测得的值(分别为2mg/L和4mg/L)高一个两倍稀释度。通过参考方法,分别有94%和2.7%的菌株替加环素的MIC≤4mg/L和≤0.5mg/L。利奈唑胺宏量稀释法与参考方法相比,分类一致性为40.5%,小错误率为56.7%,大错误率为2.7%。
在测试的MAC分离株中,替加环素显示出比利奈唑胺更高的体外活性。使用BD Bactec-MGIT-960系统进行宏量稀释是确定MAC菌株对替加环素敏感性的一种实用方法。