Institute of Medical Microbiology, University Hospital Münster, Münster, Germany.
Bruker Daltonik GmbH, Bremen, Germany.
Int J Med Microbiol. 2020 Apr;310(3):151413. doi: 10.1016/j.ijmm.2020.151413. Epub 2020 Feb 14.
Differentiation of Streptococcus pneumoniae from other Streptococcus mitis group streptococci (SMGS) remains challenging despite the introduction of matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). While the bile solubility test (BST) provides most reliable discrimination of pneumococci, its practical implementation is limited by subjective visual interpretation and frequent inconclusive results. We aimed to develop a rapid confirmation BST based on direct-on-target MALDI-TOF MS assay. After establishment of optimal test conditions, test performance was evaluated on 36 consecutive clinical SMGS isolates. Colony material was suspended and pipetted onto a MALDI target. After drying, sodium deoxycholate in different concentrations (2%, 5%, and 10 %) was added. Incubation for 30 min (at room temperature or 35 °C) was followed by liquid removal and spot washing. After adding 70 % formic acid, spots were overlaid with matrix and measured (MALDI Biotyper smart, Bruker). The absence of microbial spectra (Biotyper score <1.7) in samples with sodium deoxycholate indicated efficient removal of bacterial biomass due to bile solubility, thus, identifying pneumococci. In contrast, scores ≥1.7 were interpreted as lack of bile solubility and confirmation as viridans streptococci other than S. pneumoniae. Highest test accuracy was achieved applying 5% sodium deoxycholate at 35 °C and 10 % sodium deoxycholate at room temperature. These test conditions provided 100 % sensitivity and 100 % specificity for discrimination of S. pneumoniae. The developed MALDI-TOF MS-based BST is an easy-to-perform assay with minimum hands-on time and objective readout. The promising results of this proof-of-principle study warrant confirmation with large collections of epidemiologically diverse strains.
尽管已经引入基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS),但将肺炎链球菌与其他口腔链球菌属链球菌(SMGS)区分开来仍然具有挑战性。虽然胆盐溶解度试验(BST)可提供最可靠的肺炎球菌鉴别,但由于其主观的视觉解释和频繁的不确定结果,其实用性受到限制。我们旨在开发一种基于直接靶标 MALDI-TOF MS 测定的快速确认 BST。在建立最佳测试条件后,我们在 36 个连续的临床 SMGS 分离株上评估了测试性能。将菌落材料悬浮并吸移到 MALDI 靶标上。干燥后,加入不同浓度(2%、5%和 10%)的脱氧胆酸钠。孵育 30 分钟(室温或 35°C)后,去除液体并用点冲洗。加入 70%甲酸后,用基质覆盖斑点并进行测量(MALDI Biotyper smart,Bruker)。如果样本中没有微生物谱(Biotyper 评分 <1.7),则表明由于胆盐溶解度而有效地去除了细菌生物量,从而鉴定出肺炎链球菌。相反,评分≥1.7 被解释为缺乏胆盐溶解度,并确认为除肺炎链球菌外的草绿色链球菌。在 35°C 下应用 5%脱氧胆酸钠和在室温下应用 10%脱氧胆酸钠时,测试的准确性最高。这些测试条件为区分肺炎链球菌提供了 100%的灵敏度和 100%的特异性。开发的基于 MALDI-TOF MS 的 BST 是一种易于操作的测定方法,操作时间最短,结果客观。这项初步研究的有希望结果需要用具有不同流行病学的大量菌株进行验证。