Parker Jennifer K, Feller Aaron L, Gu Richard, Sanchez-Paiva Simon, Perez Bethany C, O'Donnell Angela C, Deng Wendi, Ousterhout Rita M, Kim Sun-Young, Wilke Claus O, Davies Bryan W
Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA.
Department of Integrative Biology, The University of Texas at Austin, Austin, TX, USA.
Nat Commun. 2025 Jul 1;16(1):6048. doi: 10.1038/s41467-025-61151-z.
Bacteria produce antibacterials that drive competition and regulate community composition. While diverse examples have been found, few families of antibacterial agents appear to be widespread across phylogenetically divergent bacteria. Here, we show that what appeared to be a limited, niche class of Gram-negative bacteriocins, called class II microcins, is in fact a highly abundant, sequence- and function-diverse class of secreted bacteriocins. Based on systematic investigations in the Enterobacteriaceae and gut microbiomes, we demonstrate that class II microcins encompass diverse sequence space, bacterial strains of origin, spectra of activity, and mechanisms of action. Importantly, we show microcins discovered here are active against pathogenic E. coli during mouse gut colonization, supporting important roles for these unrecognized antibacterials in vivo. Our study reveals the overlooked abundance and diversity of microcins found dispersed throughout Bacteria and opens opportunities to uncover and exploit mechanisms of competition to modulate microbial communities.
细菌产生抗菌物质以驱动竞争并调节群落组成。虽然已发现多种实例,但抗菌剂家族中似乎很少有能广泛存在于系统发育上不同的细菌中的。在这里,我们表明,看似有限的、特定生态位的革兰氏阴性细菌素(称为II类微小菌素)实际上是一类高度丰富、序列和功能多样的分泌型细菌素。基于对肠杆菌科和肠道微生物群的系统研究,我们证明II类微小菌素涵盖了多样的序列空间、起源细菌菌株、活性谱和作用机制。重要的是,我们发现这里发现的微小菌素在小鼠肠道定殖过程中对致病性大肠杆菌具有活性,支持了这些未被认识的抗菌物质在体内发挥重要作用。我们的研究揭示了在整个细菌中广泛存在但被忽视的微小菌素的丰富性和多样性,并为揭示和利用竞争机制来调节微生物群落提供了机会。