Institute of Medical Microbiology, University Hospital Münster, Münster, Germany.
Bruker Daltonik GmbH, Bremen, Germany.
Clin Microbiol Infect. 2018 Jul;24(7):738-743. doi: 10.1016/j.cmi.2017.10.016. Epub 2017 Oct 24.
We aimed to develop a universal phenotypic method, which allows easy and rapid antimicrobial susceptibility testing independently of underlying resistance mechanisms.
We established a novel direct-on-target microdroplet growth assay for the detection of antibiotic resistance within a few hours, which is based on matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). The microorganisms were incubated with and without meropenem in nutrient broth as microdroplets directly on MALDI-TOF MS target. Subsequently, broth was separated from microbial cells by contacting the microdroplets with an absorptive material. The microorganisms grown in the presence of antibiotic were detected by MALDI-TOF MS. A total of 24 Klebsiella pneumoniae and 24 Pseudomonas aeruginosa isolates were used to assess performance for detection of meropenem resistance. The microdroplet volumes investigated were 2, 4, 6, 8 and 10 μL.
The best performance was achieved using 6-μL microdroplets. Applying this volume, all growth controls were successfully detected (definition of valid test), and all isolates were correctly categorized as susceptible or non-susceptible after an 18-h incubation. For K. pneumoniae, rate of valid tests, sensitivity and specificity all reached 100% after a 4-h incubation of 6-μL microdroplets. Using the same microdroplet volume for P. aeruginosa, incubation for 5 h resulted in 83.3% of valid tests with 100% sensitivity and 100% specificity.
We demonstrated easy, rapid and accurate resistance detection using carbapenem-resistant Gram-negative bacteria as an example. Our technology is suitable for automatization and expandable to further applications, e.g. simultaneous testing of multiple antibiotics as well as resistance determination directly from clinical samples.
我们旨在开发一种通用表型方法,该方法可独立于潜在的耐药机制,轻松、快速地进行抗菌药物敏感性测试。
我们建立了一种新的基于基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)的直接靶标微滴生长检测法,用于在数小时内检测抗生素耐药性,该方法基于在营养肉汤中孵育微生物并在有无美罗培南的情况下将其直接作为 MALDI-TOF MS 靶标进行微滴化。随后,通过将微滴与吸收性材料接触,将肉汤与微生物细胞分离。通过 MALDI-TOF MS 检测在存在抗生素的情况下生长的微生物。使用 24 株肺炎克雷伯菌和 24 株铜绿假单胞菌分离株评估检测美罗培南耐药性的性能。研究了 2、4、6、8 和 10 μL 的微滴体积。
使用 6 μL 的微滴体积可获得最佳性能。使用该体积,所有生长对照均成功检测到(定义为有效测试),并且在孵育 18 小时后,所有分离株均正确分类为敏感或耐药。对于肺炎克雷伯菌,在孵育 4 小时后,使用 6 μL 微滴的有效测试率、敏感性和特异性均达到 100%。对于铜绿假单胞菌,使用相同的微滴体积,孵育 5 小时可使 83.3%的有效测试具有 100%的敏感性和 100%的特异性。
我们使用耐碳青霉烯类革兰氏阴性菌作为示例,证明了使用简单、快速、准确的方法检测耐药性。我们的技术适合自动化,并可扩展到其他应用,例如同时测试多种抗生素以及直接从临床样本中确定耐药性。