Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA.
Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA; John Ring LaMontagne Center for Infectious Diseases, The University of Texas at Austin, Austin, TX, USA.
Cell Host Microbe. 2024 Nov 13;32(11):1959-1971.e6. doi: 10.1016/j.chom.2024.08.012. Epub 2024 Sep 10.
Microcins are small antibacterial proteins that mediate interbacterial competition. Their narrow-spectrum activity provides opportunities to discover microbiome-sparing treatments. However, microcins have been found almost exclusively in Enterobacteriaceae. Their broader existence and potential implications in other pathogens remain unclear. Here, we identify and characterize a microcin active against pathogenic Vibrio cholerae: MvcC. We show that MvcC is reliant on the outer membrane porin OmpT to cross the outer membrane. MvcC then binds the periplasmic protein OppA to reach and disrupt the cytoplasmic membrane. We demonstrate that MvcC's cognate immunity protein is a protease, which precisely cleaves MvcC to neutralize its activity. Importantly, we show that MvcC is active against diverse cholera isolates and in a mouse model of V. cholerae colonization. Our results provide a detailed analysis of a microcin outside of Enterobacteriaceae and its potential to influence V. cholerae infection.
微菌素是一类介导细菌间竞争的小型抗菌蛋白。它们的窄谱活性为发现不影响微生物组的治疗方法提供了机会。然而,微菌素几乎只存在于肠杆菌科中。它们在其他病原体中的更广泛存在和潜在影响尚不清楚。在这里,我们鉴定并表征了一种针对致病性霍乱弧菌的微菌素:MvcC。我们表明,MvcC 依赖于外膜孔蛋白 OmpT 穿过外膜。MvcC 然后结合周质蛋白 OppA 以到达并破坏细胞质膜。我们证明 MvcC 的同源免疫蛋白是一种蛋白酶,它能精确切割 MvcC 以中和其活性。重要的是,我们表明 MvcC 对不同的霍乱分离株有效,并且在 V. cholerae 定植的小鼠模型中有效。我们的研究结果提供了肠杆菌科以外的微菌素及其影响霍乱弧菌感染潜力的详细分析。