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Environmental structure drives resistance to phages and antibiotics during phage therapy and to invading lysogens during colonisation

机译:环境结构在噬菌体治疗过程中驱动对噬菌体和抗生素的抗性在定居过程中驱动对溶原原的入侵

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摘要

Microbial communities are shaped by bacteriophages through predation and lysogeny. A better understanding of the interactions between these processes across different types of environments is key to elucidate how phages mediate microbial competition and to design efficient phage therapies. We introduce an individual-based model (eVIVALDI) to investigate the role of environmental structure in the elimination of a population with a combined treatment of antibiotics and virulent phages, and in the invasion of a population of phage-sensitive bacteria by lysogens. We show that structured environments facilitate the emergence of double resistance, to antibiotics and phages, due to limited diffusion of phage particles and increased nutrient availability from dead cells. They also hinder phage amplification, thus decreasing the generation of phage genetic diversity and increasing the unpredictability of phage-bacteria arms-races. We used a machine learning approach to determine the variables most important for the invasion of sensitive populations by lysogens. They revealed that phage-associated traits and environmental structure are the key drivers of the process. Structured environments hinder invasions, and accounting for their existence improves the fit of the model to published in vivo experimental data. Our results underline environmental structure as key to understand in vivo phage-bacteria interactions.
机译:细菌群落通过掠食和溶菌作用而形成微生物群落。更好地了解不同类型环境之间这些过程之间的相互作用是阐明噬菌体如何介导微生物竞争并设计有效噬菌体疗法的关键。我们引入了一个基于个体的模型(eVIVALDI),以研究环境结构在通过抗生素和强力噬菌体的联合治疗消除种群的过程中以及在溶菌原对噬菌体敏感细菌的入侵中的作用。我们显示结构化的环境促进了对抗生素和噬菌体的双重耐药性的出现,这是由于噬菌体颗粒的有限扩散和死细胞养分利用率的提高。它们还阻碍噬菌体扩增,从而减少了噬菌体遗传多样性的产生并增加了噬菌体细菌竞争的不可预测性。我们使用机器学习方法来确定对于溶原原入侵敏感人群最重要的变量。他们发现,噬菌体相关性状和环境结构是该过程的关键驱动力。结构化环境会阻止入侵,考虑其存在会改善模型与已发布的体内实验数据的拟合度。我们的结果强调了环境结构是理解体内噬菌体-细菌相互作用的关键。

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