Liu Yongjin, Kyle Steven, Straight Paul D
Biochemistry and Biophysics Department, Texas A&M University, College Station, Texas, USA.
Interdisciplinary Program in Genetics, Texas A&M University, College Station, Texas, USA.
mSphere. 2018 Feb 21;3(1). doi: 10.1128/mSphere.00586-17. eCollection 2018 Jan-Feb.
Competitive interactions between bacteria reveal physiological adaptations that benefit fitness. is a Gram-positive species with several adaptive mechanisms for competition and environmental stress. Biofilm formation, sporulation, and motility are the outcomes of widespread changes in a population of . These changes emerge from complex, regulated pathways for adapting to external stresses, including competition from other species. To identify competition-specific functions, we cultured with multiple species of and observed altered patterns of growth for each organism. In particular, when plated on agar medium near , initiates a robust and reproducible mobile response. To investigate the mechanistic basis for the interaction, we determined the type of motility used by and isolated inducing metabolites produced by . has three defined forms of motility: swimming, swarming, and sliding. induced sliding motility specifically in our experiments. The inducing agents produced by were identified as chloramphenicol and a brominated derivative at subinhibitory concentrations. Upon further characterization of the mobile response, our results demonstrated that subinhibitory concentrations of chloramphenicol, erythromycin, tetracycline, and spectinomycin all activate a sliding motility response by . Our data are consistent with sliding motility initiating under conditions of protein translation stress. This report underscores the importance of hormesis as an early warning system for potential bacterial competitors and antibiotic exposure. Antibiotic resistance is a major challenge for the effective treatment of infectious diseases. Identifying adaptive mechanisms that bacteria use to survive low levels of antibiotic stress is important for understanding pathways to antibiotic resistance. Furthermore, little is known about the effects of individual bacterial interactions on multispecies communities. This work demonstrates that subinhibitory amounts of some antibiotics produced by streptomycetes induce active motility in , which may alter species interaction dynamics among species-diverse bacterial communities in natural environments. The use of antibiotics at subinhibitory concentrations results in many changes in bacteria, including changes in biofilm formation, small-colony variants, formation of persisters, and motility. Identifying the mechanistic bases of these adaptations is crucial for understanding how bacterial communities are impacted by antibiotics.
细菌之间的竞争性相互作用揭示了有利于适应性的生理适应机制。[具体细菌名称]是一种革兰氏阳性菌,具有多种竞争和环境应激的适应机制。生物膜形成、孢子形成和运动性是[具体细菌名称]群体中广泛变化的结果。这些变化源自复杂的、受调控的适应外部应激的途径,包括来自其他物种的竞争。为了确定竞争特异性功能,我们将[具体细菌名称]与多种[其他细菌名称]共同培养,并观察到每种生物体生长模式的改变。特别是,当接种在靠近[具体细菌名称]的琼脂培养基上时,[具体细菌名称]会引发强烈且可重复的移动反应。为了研究这种相互作用的机制基础,我们确定了[具体细菌名称]所使用的运动类型,并分离出[具体细菌名称]产生的诱导代谢物。[具体细菌名称]有三种确定的运动形式:游泳、群体游动和滑动。在我们的实验中,[具体细菌名称]特异性地诱导了滑动运动。[具体细菌名称]产生的诱导剂被鉴定为亚抑制浓度的氯霉素和一种溴化衍生物。在对移动反应进行进一步表征后,我们的结果表明,亚抑制浓度的氯霉素、红霉素、四环素和壮观霉素都能激活[具体细菌名称]的滑动运动反应。我们的数据与在蛋白质翻译应激条件下启动滑动运动一致。本报告强调了兴奋效应作为潜在细菌竞争者和抗生素暴露早期预警系统的重要性。抗生素耐药性是有效治疗传染病的主要挑战。确定细菌用于在低水平抗生素应激下存活的适应机制对于理解抗生素耐药性途径很重要。此外,关于单个细菌相互作用对多物种群落的影响知之甚少。这项工作表明,链霉菌产生的某些抗生素的亚抑制量会诱导[具体细菌名称]的活跃运动,这可能会改变自然环境中物种多样的细菌群落之间的物种相互作用动态。使用亚抑制浓度的抗生素会导致细菌发生许多变化,包括生物膜形成的变化、小菌落变体、持留菌的形成和运动性。确定这些适应的机制基础对于理解细菌群落如何受到抗生素影响至关重要。