Department of Chemistry and Biochemistry, University of California, Santa Cruz, Santa Cruz, California 95064, United States.
Department of Microbiology and Environmental Toxicology, University of California, Santa Cruz, Santa Cruz, California 95064, United States.
Anal Chem. 2024 May 28;96(21):8308-8316. doi: 10.1021/acs.analchem.3c04687. Epub 2024 May 16.
Microbial biofilms represent an important lifestyle for bacteria and are dynamic three-dimensional structures. Cyclic dimeric guanosine monophosphate (c-di-GMP) is a ubiquitous signaling molecule that is known to be tightly regulated with biofilm processes. While measurements of global levels of c-di-GMP have proven valuable toward understanding the genetic control of c-di-GMP production, there is a need for tools to observe the local changes of c-di-GMP production in biofilm processes. We have developed a label-free method for the direct detection of c-di-GMP in microbial colony biofilms using matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI). We applied this method to the enteric pathogen , the marine symbiont , and the opportunistic pathogen PA14 and detected spatial and temporal changes in c-di-GMP signal that accompanied genetic alterations in factors that synthesize and degrade the compound. We further demonstrated how this method can be simultaneously applied to detect additional metabolites of interest from a single sample.
微生物生物膜代表了细菌的一种重要生活方式,是动态的三维结构。环二鸟苷酸(c-di-GMP)是一种普遍存在的信号分子,其生物膜过程的调控非常紧密。虽然测量 c-di-GMP 的全局水平对于理解 c-di-GMP 产生的遗传控制非常有价值,但需要有工具来观察生物膜过程中 c-di-GMP 产生的局部变化。我们开发了一种无标记方法,用于使用基质辅助激光解吸/电离质谱成像(MALDI-MSI)直接检测微生物菌落生物膜中的 c-di-GMP。我们将该方法应用于肠道病原体、海洋共生菌和机会性病原体 PA14,并检测了伴随合成和降解该化合物的因子遗传改变的 c-di-GMP 信号的时空变化。我们进一步证明了如何从单个样本中同时应用该方法来检测其他感兴趣的代谢物。