PSL Université Paris: EPHE-UPVD-CNRS, USR 3278 CRIOBE, Université de Perpignan, 52 Avenue Paul Alduy, 66860 Perpignan Cedex, France.
UFR Sciences Exactes et Expérimentales, Université de Perpignan Via Domitia, 52 Avenue Paul Alduy, 66860 Perpignan Cedex, France.
Rapid Commun Mass Spectrom. 2021 Jan 30;35(2):e8977. doi: 10.1002/rcm.8977.
Correct biomarker determination in metabolomics is crucial for unbiased conclusions and reliable applications. However, this determination is subject to several drifts, e.g. matrix effects and ion suppression in Liquid Chromatography/Mass Spectrometry (LC/MS)-based approaches. This phenomenon provokes critical issues for biomarker determination, particularly during comparative studies dealing with samples exhibiting heterogeneous complexities.
Occurrence of the issue was coincidentally noticed when studying the environmental impact of a complex bioinsecticide: Bacillus thuringiensis israelensis. The studied samples comprised insecticide-spiked sediments and untreated control sediments. QuEChERS extractions followed by LC/ESI-Q/ToF analyses were performed on sediments after 15 days of incubation. Meta-metabolomes containing pesticide xenometabolites and sediment endometabolites were analyzed in depth using XCMS-based computational data preprocessing. Multivariate statistical analyses (PCA, OPLS-DA) and raw data crosschecks were performed to search for environmental biomarkers.
Multivariate analyses and raw data crosschecks led to the selection of nine metabolites as biomarker candidates. However, when exploring the mass spectra, co-elutions were noticed between seven of these metabolites and multi-charged macromolecules originating from the pesticide. Provoked false positives were thus suspected due to a potential ion suppression exclusively occurring in the spiked samples. A dilution-based approach was then applied. It confirmed five metabolites as suppressed ions.
Ion suppression should be considered as a critical issue for biomarker determination when comparing heterogeneous metabolic profiles. Raw chromatograms and mass spectra crosschecks are mandatory to reveal potential ion suppressions in such cases. Dilution is a suitable approach to filter reliable biomarker candidates before their identification and absolute quantification.
在代谢组学中正确确定生物标志物对于得出无偏结论和可靠应用至关重要。然而,这种确定受到多种漂移的影响,例如基于液相色谱/质谱(LC/MS)的方法中的基质效应和离子抑制。这种现象给生物标志物的确定带来了严重的问题,特别是在涉及具有不同复杂性的样品的比较研究中。
在研究复杂生物杀虫剂苏云金芽孢杆菌以色列亚种对环境的影响时,偶然注意到了这个问题的发生。研究的样品包括杀虫剂污染的沉积物和未处理的对照沉积物。在 15 天的孵育后,对沉积物进行 QuEChERS 提取,然后进行 LC/ESI-Q/ToF 分析。使用基于 XCMS 的计算数据预处理方法对含有农药 xenometabolites 和沉积物内源性代谢物的元代谢组进行深入分析。进行多元统计分析(PCA、OPLS-DA)和原始数据交叉检查,以搜索环境生物标志物。
多元分析和原始数据交叉检查导致选择了 9 种代谢物作为生物标志物候选物。然而,当探索质谱时,注意到其中 7 种代谢物与源自杀虫剂的多电荷大分子发生共洗脱。因此,由于仅在污染样品中发生的潜在离子抑制,怀疑存在假阳性。然后应用了稀释法。它证实了五种代谢物是被抑制的离子。
当比较异质代谢谱时,应将离子抑制视为生物标志物确定的一个关键问题。在这种情况下,必须检查原始色谱图和质谱图的交叉检查,以揭示潜在的离子抑制。稀释是在鉴定和绝对定量之前筛选可靠生物标志物候选物的合适方法。