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基于脂质指纹的 MALDI-TOF 在分枝杆菌感染诊断中的性能。

Performance of lipid fingerprint-based MALDI-ToF for the diagnosis of mycobacterial infections.

机构信息

Department of Infectious Diseases, Faculty of Medicine, Imperial College London, London, W12 ONN, UK.

Department of Infectious Diseases, Faculty of Medicine, Imperial College London, London, W12 ONN, UK.

出版信息

Clin Microbiol Infect. 2021 Jun;27(6):912.e1-912.e5. doi: 10.1016/j.cmi.2020.08.027. Epub 2020 Aug 27.

Abstract

OBJECTIVES

Bacterial diagnosis of mycobacteria is often challenging because of the variability of the sensitivity and specificity of the assay used, and it can be expensive to perform accurately. Although matrix-assisted laser desorption/ionization mass spectrometry (MALDI MS) has become the workhorse of clinical laboratories, the current MALDI methodology (which is based on cytosolic protein profiling) for mycobacteria is still challenging due to the number of steps involved (up to seven) and potential biosafety concerns. Knowing that mycobacteria produce surface-exposed species-specific lipids, we here hypothesized that the detection of those molecules could offer a rapid, reproducible and robust method for mycobacterial identification.

METHODS

We evaluated the performance of an alternative methodology based on characterized species-specific lipid profiling of intact bacteria, without any sample preparation, by MALDI MS; it uses MALDI-time-of-flight (ToF) MS combined with a specific matrix (super-2,5-dihydroxybenzoic acid solubilized in an apolar solvent system) to analyse lipids of intact heat-inactivated mycobacteria. Cultured mycobacteria are heat-inactivated and loaded directly onto the MALDI target followed by addition of the matrix. Acquisition of the data is done in both positive and negative ion modes. Blinded studies were performed using 273 mycobacterial strains comprising both the Mycobacterium tuberculosis (Mtb) complex and non-tuberculous mycobacteria (NTMs) subcultured in Middlebrook 7H9 media supplemented with 10% OADC (oleic acid/dextrose/catalase) growth supplement and incubated for up to 2 weeks at 37°C.

RESULTS

The method we have developed is fast (<10 mins) and highly sensitive (<1000 bacteria required); 96.7% of the Mtb complex strains (204/211) were correctly assigned as MTB complex and 91.7% (22/24) NTM species were correctly assigned based only on intact bacteria species-specific lipid profiling by MALDI-ToF MS.

CONCLUSIONS

Intact bacterial lipid profiling provides a biosafe and unique route for rapid and accurate mycobacterial identification.

摘要

目的

由于所用检测方法的灵敏度和特异性存在差异,分枝杆菌的细菌诊断常常具有挑战性,并且准确进行检测的成本可能很高。尽管基质辅助激光解吸/电离质谱(MALDI MS)已成为临床实验室的主力,但目前基于细胞质蛋白分析的 MALDI 方法(分枝杆菌)仍然具有挑战性,因为它涉及的步骤较多(多达 7 个),并且存在潜在的生物安全问题。由于分枝杆菌会产生表面暴露的种特异性脂质,因此我们假设这些分子的检测可以提供一种快速、可重复且稳健的分枝杆菌鉴定方法。

方法

我们评估了一种替代方法的性能,该方法基于完整细菌的特征种特异性脂质分析,无需任何样品制备,通过 MALDI MS 实现;它使用 MALDI-飞行时间(ToF)MS 与特定基质(超 2,5-二羟基苯甲酸溶解在非极性溶剂系统中)相结合,分析热灭活分枝杆菌的脂质。将培养的分枝杆菌热灭活后直接加载到 MALDI 靶标上,然后添加基质。在正离子和负离子模式下都可以进行数据采集。使用包含结核分枝杆菌(Mtb)复合体和非结核分枝杆菌(NTM)的 273 株分枝杆菌菌株进行了盲法研究,这些菌株均在含有 10% OADC(油酸/葡萄糖/过氧化氢酶)生长补充剂的 Middlebrook 7H9 培养基中进行亚培养,并在 37°C 下培养长达 2 周。

结果

我们开发的方法快速(<10 分钟)且高度敏感(<1000 个细菌即可);根据 MALDI-ToF MS 对完整细菌种特异性脂质的分析,96.7%(204/211)的 Mtb 复合体菌株被正确归为 MTB 复合体,91.7%(22/24)的 NTM 种被正确归为 NTM。

结论

完整细菌脂质分析为快速准确地鉴定分枝杆菌提供了一种安全且独特的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9292/8186428/9ee6bed9b7c9/fx1.jpg

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