Duchossois Family Institute and Department of Microbiology, University of Chicago, Chicago, IL 60637, USA.
Duchossois Family Institute and Department of Microbiology, University of Chicago, Chicago, IL 60637, USA.
Cell Host Microbe. 2024 Jun 12;32(6):794-803. doi: 10.1016/j.chom.2024.05.006.
Most bacteria live in communities, often with closely related strains and species with whom they must compete for space and resources. Consequently, bacteria have acquired or evolved mechanisms to antagonize competitors through the production of antibacterial toxins. Similar to bacterial systems that combat phage infection and mechanisms to thwart antibiotics, bacteria have also acquired and evolved features to protect themselves from antibacterial toxins. Just as there is a large body of research identifying and characterizing antibacterial proteins and toxin delivery systems, studies of bacterial mechanisms to resist and survive assault from competitors' weapons have also expanded tremendously. Emerging data are beginning to reveal protective processes and mechanisms that are as diverse as the toxins themselves. Protection against antibacterial toxins can be acquired by horizontal gene transfer, receptor or target alteration, induction of protective functions, physical barriers, and other diverse processes. Here, we review recent studies in this rapidly expanding field.
大多数细菌生活在群落中,通常与密切相关的菌株和物种共存,它们必须为争夺空间和资源而竞争。因此,细菌已经获得或进化出通过产生抗菌毒素来对抗竞争者的机制。类似于细菌系统对抗噬菌体感染和阻止抗生素的机制,细菌也已经获得和进化出了保护自己免受抗菌毒素侵害的特征。正如有大量的研究确定和描述抗菌蛋白和毒素输送系统一样,研究细菌抵抗和生存来自竞争者武器攻击的机制也有了巨大的扩展。新出现的数据开始揭示出与毒素本身一样多样化的保护过程和机制。通过水平基因转移、受体或靶标改变、保护性功能的诱导、物理屏障和其他多样化的过程,可以获得对抗抗菌毒素的保护。在这里,我们综述了这一快速发展领域的最新研究进展。