MRC Centre for Molecular Bacteriology and Infection, Department of Life Sciences, Faculty of Natural Sciences, Imperial College London, London, United Kingdom.
Department of Bacteriology-Hygiene, Bicêtre Hospital, Assistance Publique-Hôpitaux de Paris, Le Kremlin-Bicêtre, France.
J Clin Microbiol. 2019 Nov 22;57(12). doi: 10.1128/JCM.01427-19. Print 2019 Dec.
Polymyxin antibiotics are a last-line treatment for multidrug-resistant Gram-negative bacteria. However, the emergence of colistin resistance, including the spread of mobile genes, necessitates the development of improved diagnostics for the detection of colistin-resistant organisms in hospital settings. The recently developed MALDIxin test enables detection of colistin resistance by matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) in less than 15 min but is not optimized for the mass spectrometers commonly found in clinical microbiology laboratories. In this study, we adapted the MALDIxin test for the MALDI Biotyper Sirius MALDI-TOF MS system (Bruker Daltonics). We optimized the sample preparation protocol by using a set of 6 mobile colistin resistance (MCR) protein-expressing clones and validated the assay with a collection of 40 clinical isolates, including 19 confirmed MCR protein producers, 12 colistin-resistant isolates that tested negative for commonly encountered genes (i.e., likely chromosomally resistant isolates), and 9 polymyxin-susceptible isolates. We calculated polymyxin resistance ratio (PRR) values from the acquired spectra; PRR values of 0, indicating polymyxin susceptibility, were obtained for all colistin-susceptible isolates, whereas positive PRR values, indicating resistance to polymyxins, were obtained for all resistant strains, independent of the genetic basis of resistance. Thus, we report a preliminary feasibility study showing that an optimized version of the MALDIxin test adapted for the routine MALDI Biotyper Sirius system provides an unbiased, fast, reliable, cost-effective, and high-throughput way of detecting colistin resistance in clinical isolates.
多黏菌素类抗生素是治疗多重耐药革兰氏阴性菌的最后手段。然而,由于黏菌素耐药性的出现,包括移动基因的传播,需要开发改进的诊断方法来检测医院环境中耐黏菌素的生物体。最近开发的 MALDIxin 测试通过基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)在不到 15 分钟的时间内实现了对黏菌素耐药性的检测,但该测试未针对临床微生物学实验室中常见的质谱仪进行优化。在这项研究中,我们针对 MALDI Biotyper Sirius MALDI-TOF MS 系统(布鲁克·道尔顿公司)对 MALDIxin 测试进行了改编。我们通过使用一组 6 个移动黏菌素耐药性(MCR)蛋白表达克隆对样品制备方案进行了优化,并使用 40 个临床分离株对该检测进行了验证,包括 19 个确认的 MCR 蛋白产生菌、12 个对常见基因检测呈阴性的黏菌素耐药分离株(即可能为染色体耐药的分离株)和 9 个多黏菌素敏感的分离株。我们从获得的光谱中计算了多黏菌素耐药比(PRR)值;所有黏菌素敏感的分离株的 PRR 值均为 0,表明多黏菌素敏感,而所有耐药株的 PRR 值均为阳性,表明对多黏菌素耐药,而与耐药的遗传基础无关。因此,我们报告了一项初步的可行性研究,表明针对常规 MALDI Biotyper Sirius 系统优化的 MALDIxin 测试版本提供了一种公正、快速、可靠、具有成本效益且高通量的方法来检测临床分离株中的黏菌素耐药性。