Franklin Hollyn C, Makhlouf Rita, Ha Anh D, Bataglioli Rogerio A, Baker Zachary R, Murphy Sydney A, Jirsa Hannah, Heuler Joshua, Southard Teresa, Aylward Frank O, Hsu Bryan B
Department of Biological Sciences, Fralin Life Sciences Institute, and Center for Emerging, Zoonotic, and Arthropod-borne Pathogens, Virginia Tech, Blacksburg, VA 24061, USA.
Department of Biomedical Sciences and Pathobiology, VA-MD College of Veterinary Medicine, Virginia Tech, Blacksburg, VA 24061, USA.
Cell Host Microbe. 2025 May 14;33(5):745-758.e6. doi: 10.1016/j.chom.2025.04.002. Epub 2025 Apr 28.
The significance of bacteriophages in the gut microbiota remains poorly understood due, in part, to an absence of an animal model that allows for comparative study of conditions with or without phages while retaining the microbial diversity attained by conventional colonization. We describe a mouse model that uses a broadly available chemical compound, acriflavine, to preferentially deplete virulent phages from the gut without significantly impacting gut bacteria. We then show that gut phage density can be reconstituted by oral gavage. Using this bacteriophage-conditional (BaCon) mouse model, we reveal that while phages have comparatively minimal impact during equilibrium conditions, they increase the potency of ampicillin against commensal gut bacteria. Collectively, our work presents an animal model that can be leveraged to conditionally study the role of phages in complex, physiologically relevant systems and further identifies virulent gut phages as potential sources of bacterial variability during major perturbations.
噬菌体在肠道微生物群中的重要性仍未得到充分理解,部分原因是缺乏一种动物模型,该模型能够在保留通过传统定殖获得的微生物多样性的同时,对有或没有噬菌体的条件进行比较研究。我们描述了一种小鼠模型,该模型使用一种广泛可用的化合物吖啶黄,优先从肠道中清除烈性噬菌体,而不会对肠道细菌产生显著影响。然后我们表明,可以通过口服灌胃来重建肠道噬菌体密度。使用这种噬菌体条件性(BaCon)小鼠模型,我们发现虽然噬菌体在平衡条件下的影响相对较小,但它们会增加氨苄青霉素对共生肠道细菌的效力。总的来说,我们的工作提出了一种动物模型,可用于有条件地研究噬菌体在复杂的、生理相关系统中的作用,并进一步确定烈性肠道噬菌体是重大扰动期间细菌变异性的潜在来源。