Interfaculty Institute of Microbiology and Infection Medicine, Microbial Bioactive Compounds, University of Tübingen, Tübingen, Germany.
Methods Mol Biol. 2023;2601:171-190. doi: 10.1007/978-1-0716-2855-3_9.
The urgent need of new antimicrobial agents to combat life-threatening bacterial infections demands the identification and characterization of novel compounds that interfere with new and unprecedented target pathways or structures in multiresistant bacteria. Here, bacterial cell division has emerged as a new and promising target pathway for antibiotic intervention. Compounds, which inhibit division, commonly induce a characteristic filamentation phenotype of rod-shaped bacteria, such as Bacillus subtilis. Hence, this filamentation phenotype can be used to identify and characterize novel compounds that primarily target bacterial cell division. Since novel compounds of both synthetic and natural product origin are often available in small amounts only, thereby limiting the number of assays during mode of action studies, we here describe a semiautomated, microscopy-based approach that requires only small volumes of compounds to allow for the real-time observation of their effects on living bacteria, such as filamentation or cell lysis, in high-throughput 96-well-based formats. We provide a detailed workflow for the initial characterization of multiple compounds at once and further tools for the initial, microscopy-based characterization of their antibacterial mode of action.
对抗危及生命的细菌感染,我们急需新的抗菌药物,这就要求我们识别和鉴定新型化合物,这些化合物能够干扰多耐药菌中新的、前所未有的靶标途径或结构。目前,细菌细胞分裂已成为抗生素干预的一个新的、有前途的靶标途径。通常,抑制细胞分裂的化合物会诱导杆状细菌(如枯草芽孢杆菌)产生特征性的丝状表型。因此,这种丝状表型可用于鉴定和表征主要靶向细菌细胞分裂的新型化合物。由于新型化合物通常来源于合成和天然产物,其数量通常较少,这限制了作用机制研究中测定的数量,因此,我们在此描述了一种基于半自动化显微镜的方法,该方法只需少量化合物即可实时观察化合物对活细菌(如丝状化或细胞裂解)的影响,并且能够在高通量 96 孔板格式中进行。我们提供了一种用于一次性初始鉴定多种化合物的详细工作流程,并进一步提供了用于基于显微镜的初始鉴定其抗菌作用机制的工具。