Multiparametric Optimization of Data-Dependent Acquisition Towards More Holistic Bacterial Metabolite Coverage Through Molecular Networking.

IF 3.2 Q3 MICROBIOLOGY
International Journal of Microbiology Pub Date : 2025-07-21 eCollection Date: 2025-01-01 DOI:10.1155/ijm/4388417
Adivhaho Khwathisi, Amidou Samie, Asfatou Ndama Traore, Ntakadzeni Edwin Madala
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引用次数: 0

Abstract

Prokaryotic organisms rely on a limited array of metabolites for survival, which varies according to their natural environment. For example, soil-borne bacteria produce diverse metabolites, such as antibiotics, to thrive in their competitive surroundings, inhibiting the growth of nearby competing bacteria. The structural diversity of these compounds offers great analytical challenges, since there is no universal acquisition setting that can be applied to achieve their comprehensive coverage. Therefore, the use of a single experimental setup inevitably hinders the comprehensive metabolite coverage, which would affect the outputs. To address this, we propose employing a design of experiment (DoE) approach through the central composite design (CCD) to enhance the metabolite detection and broaden the coverage of the data-dependent acquisition (DDA) mode of the UHPLC-qTOF-MS technique. Our study reveals that altering collision energy significantly enhances metabolite coverage compared to adjusting the DDA threshold of detection. Furthermore, the ability of global natural product social (GNPS)-based molecular network models to annotate metabolites is greatly influenced by data acquisition settings, particularly affecting MS2 data. Interestingly, molecular networks constructed from averaged spectral data obtained through randomly selected DDA settings outperform those generated using customized settings through DoE modeling. This study demonstrates that in untargeted LC-MS metabolomics, both collision energy and intensity threshold independently enhance metabolite coverage in untargeted metabolomics. However, their combined use results in even greater coverage. Consequently, we recommend adopting group-based optimization over single-point optimization for more comprehensive metabolite coverage and in-depth exploration. However, caution should be taken in order to balance between robust data and redundancy.

通过分子网络获取数据依赖的多参数优化,以实现更全面的细菌代谢物覆盖。
原核生物依靠有限的代谢物来生存,这些代谢物根据它们的自然环境而变化。例如,土壤传播的细菌产生多种代谢物,如抗生素,在竞争环境中茁壮成长,抑制附近竞争细菌的生长。这些化合物的结构多样性提供了巨大的分析挑战,因为没有通用的获取设置,可以应用于实现它们的全面覆盖。因此,使用单一的实验装置不可避免地阻碍了全面的代谢物覆盖,这将影响输出。为了解决这个问题,我们建议采用实验设计(DoE)方法,通过中心复合设计(CCD)来增强代谢物的检测,并扩大UHPLC-qTOF-MS技术的数据依赖采集(DDA)模式的覆盖范围。我们的研究表明,与调整DDA检测阈值相比,改变碰撞能量显著提高代谢物覆盖率。此外,基于全球天然产物社会(GNPS)的分子网络模型注释代谢物的能力受到数据采集设置的极大影响,尤其是对MS2数据的影响。有趣的是,通过随机选择的DDA设置获得的平均光谱数据构建的分子网络优于通过DoE建模使用定制设置生成的分子网络。本研究表明,在非靶向LC-MS代谢组学中,碰撞能量和强度阈值都独立增强了非靶向代谢组学中代谢物的覆盖率。然而,它们的结合使用会产生更大的覆盖范围。因此,我们建议采用基于群体的优化,而不是单点优化,以获得更全面的代谢物覆盖和更深入的探索。但是,为了在健壮数据和冗余之间取得平衡,应该谨慎。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.90
自引率
0.00%
发文量
57
审稿时长
13 weeks
期刊介绍: International Journal of Microbiology is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies on microorganisms and their interaction with hosts and the environment. The journal covers all microbes, including bacteria, fungi, viruses, archaea, and protozoa. Basic science will be considered, as well as medical and applied research.
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