Department of Cell and Developmental Biology, University College London, London, UK.
Centre for Bacterial Resistance Biology, Department of Life Sciences, Imperial College London, London, UK.
Nat Commun. 2024 Jul 27;15(1):6332. doi: 10.1038/s41467-024-50591-8.
Bacteriocins are antimicrobial peptides that are naturally produced by many bacteria. They hold great potential in the fight against antibiotic resistant bacteria, including ESKAPE pathogens. Engineered live biotherapeutic products (eLBPs) that secrete bacteriocins can be created to deliver targeted bacteriocin production. Here we develop a modular bacteriocin secretion platform that can be used to express and secrete multiple bacteriocins from non-pathogenic Escherichia coli host strains. As a proof of concept we create Enterocin A (EntA) and Enterocin B (EntB) secreting strains that show strong antimicrobial activity against Enterococcus faecalis and Enterococcus faecium in vitro, and characterise this activity in both solid culture and liquid co-culture. We then develop a Lotka-Volterra model that can be used to capture the interactions of these competitor strains. We show that simultaneous exposure to EntA and EntB can delay Enterococcus growth. Our system has the potential to be used as an eLBP to secrete additional bacteriocins for the targeted killing of pathogenic bacteria.
细菌素是许多细菌自然产生的抗菌肽。它们在对抗抗生素耐药菌方面具有巨大的潜力,包括 ESKAPE 病原体。可以设计分泌细菌素的工程活生物治疗产品 (eLBP) 来进行靶向细菌素生产。在这里,我们开发了一个模块化的细菌素分泌平台,可用于从非致病性大肠杆菌宿主菌株中表达和分泌多种细菌素。作为概念验证,我们创建了分泌肠球菌素 A (EntA) 和肠球菌素 B (EntB) 的菌株,这些菌株在体外对粪肠球菌和屎肠球菌表现出很强的抗菌活性,并在固体培养和液体共培养中对这种活性进行了表征。然后,我们开发了一个可以用来捕捉这些竞争菌株相互作用的 Lotka-Volterra 模型。我们表明,同时暴露于 EntA 和 EntB 可以延迟肠球菌的生长。我们的系统有可能被用作 eLBP 来分泌其他细菌素,以靶向杀死致病菌。