Department of Biology, Duke University, Durham, United States.
Department of Molecular Genetics and Microbiology, Duke University, Durham, United States.
Elife. 2018 Jun 19;7:e35987. doi: 10.7554/eLife.35987.
How host and microbial factors combine to structure gut microbial communities remains incompletely understood. Redox potential is an important environmental feature affected by both host and microbial actions. We assessed how antibiotics, which can impact host and microbial function, change redox state and how this contributes to post-antibiotic succession. We showed gut redox potential increased within hours of an antibiotic dose in mice. Host and microbial functioning changed under treatment, but shifts in redox potentials could be attributed specifically to bacterial suppression in a host-free ex vivo human gut microbiota model. Redox dynamics were linked to blooms of the bacterial family Enterobacteriaceae. Ecological succession to pre-treatment composition was associated with recovery of gut redox, but also required dispersal from unaffected gut communities. As bacterial competition for electron acceptors can be a key ecological factor structuring gut communities, these results support the potential for manipulating gut microbiota through managing bacterial respiration.
宿主和微生物因素如何结合来构建肠道微生物群落仍不完全清楚。氧化还原电位是一个受宿主和微生物作用影响的重要环境特征。我们评估了抗生素(可以影响宿主和微生物功能)如何改变氧化还原状态,以及这如何促成抗生素治疗后的群落演替。我们发现,抗生素给药后几小时内,小鼠肠道的氧化还原电位就会升高。在治疗过程中,宿主和微生物的功能发生了变化,但氧化还原电位的变化可以专门归因于在无宿主的离体人类肠道微生物群模型中细菌的抑制。氧化还原动力学与肠杆菌科的细菌家族的大量繁殖有关。恢复肠道氧化还原与恢复到治疗前的群落组成有关,但也需要从未受影响的肠道群落中扩散。由于细菌对电子受体的竞争可能是影响肠道群落结构的关键生态因素,因此这些结果支持通过管理细菌呼吸来操纵肠道微生物群的潜力。