High-resolution 3D spatial distribution of complex microbial colonies revealed by mass spectrometry imaging.

Yuting Shen, Yisu Wang, Jianing Wang, Peisi Xie, Chengyi Xie, Yanyan Chen, Niaz Banaei, Kangning Ren, Zongwei Cai
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Abstract

Introduction: Bacterial living states and the distribution of microbial colony signaling molecules are widely studied using mass spectrometry imaging (MSI). However, current approaches often treat 3D colonies as flat 2D disks, inadvertently omitting valuable details. The challenge of achieving 3D MSI in biofilms persists due to the unique properties of microbial samples.

Objectives: The study aimed to develop a new biofilm sample preparation method that can realize high-resolution 3D MSI of bacterial colonies to reveal the spatial organization of bacterial colonies.

Methods: This article introduces the moisture-assisted cryo-section (MACS) method, enabling embedding-free sectioning parallel to the growth plane. The MACS method secures intact sections by controlling ambient humidity and slice thickness, preventing molecular delocalization.

Results: Combined with matrix-assisted laser desorption ionization mass spectrometry (MALDI)-MSI, the MACS method provides high-resolution insights into endogenic and exogenous molecule distributions in Pseudomonas aeruginosa (P. aeruginosa) biofilms, including isomeric pairs. Moreover, analyzed colonies are revived into 3D models, vividly depicting molecular distribution from inner to outer layers. Additionally, we investigated metabolite spatiotemporal dynamics in multiple colonies, observing changes over time and distinct patterns in single versus merged colonies. These findings shed light on the repel-merge process for multi-colony formation. Furthermore, our study monitored chemical responses inside biofilms after antibiotic treatment, showing increased antibiotic levels in the outer biofilm layer over time while maintaining low levels in the inner region. Moreover, the MACS method demonstrated its universality and applicability to other bacterial strains.

Conclusion: These results unveil complex cell activities within biofilm colonies, offering insights into microbe communities. The MACS method is universally applicable to loosely packed microorganism colonies, overcoming the limitations of previously reported MSI methods. It has great potential for studying bacterial-infected cancer tissues and artificial organs, making it a valuable tool in microbiological research.

通过质谱成像揭示复杂微生物菌落的高分辨率三维空间分布。
导言:利用质谱成像技术(MSI)对细菌的生存状态和微生物菌落信号分子的分布进行了广泛研究。然而,目前的方法通常将三维菌落视为平面二维圆盘,无意中忽略了有价值的细节。由于微生物样本的独特性质,在生物膜中实现三维 MSI 的挑战依然存在:本研究旨在开发一种新的生物膜样品制备方法,该方法可实现细菌菌落的高分辨率三维 MSI,从而揭示细菌菌落的空间组织:本文介绍了湿气辅助低温切片(MACS)方法,该方法可实现平行于生长平面的无包埋切片。MACS方法通过控制环境湿度和切片厚度来确保切片完好无损,防止分子分散:结果:结合基质辅助激光解吸电离质谱(MALDI)-MSI,MACS 方法能高分辨率地揭示铜绿假单胞菌(P. aeruginosa)生物膜中的内源性和外源性分子分布,包括异构体对。此外,分析后的菌落被还原成三维模型,生动地描绘了分子从内层到外层的分布情况。此外,我们还研究了多个菌落中代谢物的时空动态,观察到单个菌落与合并菌落随时间的变化和不同的模式。这些发现揭示了多菌落形成的排斥-合并过程。此外,我们的研究还监测了抗生素治疗后生物膜内部的化学反应,结果显示随着时间的推移,生物膜外层的抗生素含量会增加,而内部区域的抗生素含量则保持在较低水平。此外,MACS 方法还证明了其普遍性和对其他细菌菌株的适用性:这些结果揭示了生物膜菌落内复杂的细胞活动,为了解微生物群落提供了线索。MACS 方法普遍适用于松散的微生物菌落,克服了之前报道的 MSI 方法的局限性。它在研究受细菌感染的癌症组织和人造器官方面具有巨大潜力,是微生物研究领域的重要工具。
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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