Si Tong, Li Bin, Zhang Ke, Xu Yiran, Zhao Huimin, Sweedler Jonathan V
Department of Chemical and Biomolecular Engineering and Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign , Urbana, Illinois 61801, United States.
Department of Chemistry, University of Illinois at Urbana-Champaign , Urbana, Illinois 61801, United States.
J Proteome Res. 2016 Jun 3;15(6):1955-62. doi: 10.1021/acs.jproteome.6b00127. Epub 2016 May 11.
Colony biofilms of Bacillus subtilis are a widely used model for studying cellular differentiation. Here, we applied matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI) to examine cellular and molecular heterogeneity in B. subtilis colony biofilms. From B. subtilis cells cultivated on a biofilm-promoting medium, we detected two cannibalistic factors not found in previous MALDI MSI studies of the same strain under different culturing conditions. Given the importance of cannibalism in matrix formation of B. subtilis biofilms, we employed a transcriptional reporter to monitor matrix-producing cell subpopulations using fluorescence imaging. These two complementary imaging approaches were used to characterize three B. subtilis strains, the wild type isolate NCIB3610, and two mutants, Δspo0A and ΔabrB, with defective and enhanced biofilm phenotypes, respectively. Upon deletion of key transcriptional factors, correlated changes were observed in biofilm morphology, signaling, cannibalistic factor distribution, and matrix-related gene expression, providing new insights on cannibalism in biofilm development. This work underscores the advantages of using multimodal imaging to compare spatial patterns of selected molecules with the associated protein expression patterns, obtaining information on cellular heterogeneity and function not obtainable when using a single method to characterize biofilm formation.
枯草芽孢杆菌的菌落生物膜是研究细胞分化的一种广泛使用的模型。在此,我们应用基质辅助激光解吸/电离(MALDI)质谱成像(MSI)来检测枯草芽孢杆菌菌落生物膜中的细胞和分子异质性。从在促进生物膜形成的培养基上培养的枯草芽孢杆菌细胞中,我们检测到了在之前对同一菌株在不同培养条件下进行的MALDI MSI研究中未发现的两种自相残杀因子。鉴于自相残杀在枯草芽孢杆菌生物膜基质形成中的重要性,我们使用转录报告基因通过荧光成像来监测产生基质的细胞亚群。这两种互补的成像方法被用于表征三种枯草芽孢杆菌菌株,即野生型分离株NCIB3610以及两个突变体Δspo0A和ΔabrB,它们分别具有缺陷型和增强型生物膜表型。在关键转录因子缺失后,观察到生物膜形态、信号传导、自相残杀因子分布和基质相关基因表达的相关变化,为生物膜发育中的自相残杀提供了新的见解。这项工作强调了使用多模态成像将选定分子的空间模式与相关蛋白质表达模式进行比较的优势,能够获得使用单一方法表征生物膜形成时无法获得的细胞异质性和功能信息。