Doern Christopher D, Park Jason Y, Gallegos Michael, Alspaugh Debbie, Burnham Carey-Ann D
Department of Pathology, Virginia Commonwealth University Medical Center, Richmond, Virginia, USA
Department of Pathology and the Eugene McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, Texas, USA Children's Medical Center, Dallas, Texas, USA.
J Clin Microbiol. 2016 May;54(5):1289-94. doi: 10.1128/JCM.01929-15. Epub 2016 Mar 2.
The objective of this study was to investigate an apparent increase in linezolid-nonsusceptible staphylococci and enterococci following a laboratory change in antimicrobial susceptibility testing from disk diffusion to an automated susceptibility testing system. Isolates with nonsusceptible results (n = 27) from Vitek2 were subjected to a battery of confirmatory testing which included disk diffusion, Microscan broth microdilution, Clinical and Laboratory Standards Institute (CLSI) reference broth microdilution, gradient diffusion (Etest), 23S rRNA gene sequencing, and cfr PCR. Our results show that there is poor correlation between methods and that only 70 to 75% of isolates were confirmed as linezolid resistant with alternative phenotypic testing methods (disk diffusion, Microscan broth microdilution, CLSI broth microdilution, and Etest). 23S rRNA gene sequencing identified mutations previously associated with linezolid resistance in 16 (59.3%) isolates, and the cfr gene was detected in 3 (11.1%) isolates. Mutations located at positions 2576 and 2534 of the 23S rRNA gene were most common. In addition, two previously undescribed variants (at positions 2083 and 2345 of the 23S rRNA gene) were also identified and may contribute to linezolid resistance.
本研究的目的是调查在抗菌药物敏感性试验从纸片扩散法改为自动化药敏试验系统后,耐利奈唑胺葡萄球菌和肠球菌明显增加的情况。对Vitek2检测结果为不敏感的菌株(n = 27)进行了一系列确证试验,包括纸片扩散法、Microscan肉汤微量稀释法、临床和实验室标准协会(CLSI)参考肉汤微量稀释法、梯度扩散法(Etest)、23S rRNA基因测序和cfr PCR。我们的结果表明,各方法之间相关性较差,采用其他表型检测方法(纸片扩散法、Microscan肉汤微量稀释法、CLSI肉汤微量稀释法和Etest)时,只有70%至75%的菌株被确认为耐利奈唑胺。23S rRNA基因测序在16株(59.3%)菌株中鉴定出先前与耐利奈唑胺相关的突变,在3株(11.1%)菌株中检测到cfr基因。位于23S rRNA基因2576和2534位点的突变最为常见。此外,还鉴定出两个先前未描述的变异体(位于23S rRNA基因的2083和2345位点),它们可能与耐利奈唑胺有关。