Darch Sophie E, Koley Dipankar
School of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA.
Emory-Children's Cystic Fibrosis Center, Atlanta, GA, USA.
Proc Math Phys Eng Sci. 2018 Dec;474(2220):20180405. doi: 10.1098/rspa.2018.0405. Epub 2018 Dec 12.
Bacteria are often found in their natural habitats as spatially organized biofilm communities. While it is clear from recent work that the ability to organize into precise spatial structures is important for fitness of microbial communities, a significant gap exists in our understanding regarding the mechanisms bacteria use to adopt such physical distributions. Bacteria are highly social organisms that interact, and it is these interactions that have been proposed to be critical for establishing spatially structured communities. A primary means by which bacteria interact is via small, diffusible molecules including dedicated signals and metabolic by-products; however, quantitatively monitoring the production of these molecules in time and space with the micron-scale resolution required has been challenging. In this perspective, scanning electrochemical microscopy (SECM) is discussed as a powerful tool to study microbe-microbe interactions through the detection of small redox-active molecules. We highlight SECM as a means to quantify and spatially resolve the chemical mediators of bacterial interactions and begin to elucidate the mechanisms used by bacteria to regulate the emergent properties of biofilms.
细菌在其自然栖息地中通常以空间组织化的生物膜群落形式存在。虽然近期的研究清楚地表明,组织成精确空间结构的能力对微生物群落的适应性很重要,但我们对细菌用于形成这种物理分布的机制的理解仍存在重大差距。细菌是高度社会性的相互作用生物,正是这些相互作用被认为对建立空间结构化群落至关重要。细菌相互作用的主要方式是通过小的、可扩散的分子,包括特定信号和代谢副产物;然而,以所需的微米级分辨率在时间和空间上定量监测这些分子的产生一直具有挑战性。从这个角度来看,扫描电化学显微镜(SECM)被作为一种通过检测小的氧化还原活性分子来研究微生物-微生物相互作用的强大工具进行讨论。我们强调SECM是一种量化和在空间上解析细菌相互作用化学介质的手段,并开始阐明细菌用于调节生物膜涌现特性的机制。