Hernandez-Leyva Ariel J, Berna Amalia Z, Liu Yang, Rosen Anne L, Lint Michael A, Whiteside Samantha A, Jaeger Natalia, McDonough Ryan T, Joardar Nikhilesh, Santiago-Borges Jesús, Tomera Christopher P, Luo Wentai, John Audrey R Odom, Kau Andrew L
Division of Allergy and Immunology, Department of Medicine and Center for Women's Infectious Disease Research, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
medRxiv. 2024 Aug 8:2024.08.02.24311413. doi: 10.1101/2024.08.02.24311413.
The gut microbiota is widely implicated in host health and disease, inspiring translational efforts to implement our growing body of knowledge in clinical settings. However, the need to characterize gut microbiota by its genomic content limits the feasibility of rapid, point-of-care diagnostics. The microbiota produces a diverse array of xenobiotic metabolites that disseminate into tissues, including volatile organic compounds (VOCs) that may be excreted in breath. We hypothesize that breath contains gut microbe-derived VOCs that inform the composition and metabolic state of the microbiota. To explore this idea, we compared the breath volatilome and fecal gut microbiomes of 27 healthy children and found that breath VOC composition is correlated with gut microbiomes. To experimentally interrogate this finding, we devised a method for capturing exhaled breath from gnotobiotic mice. Breath volatiles are then profiled by gas-chromatography mass-spectrometry (GC-MS). Using this novel methodology, we found that the murine breath profile is markedly shaped by the composition of the gut microbiota. We also find that VOCs produced by gut microbes in pure culture can be identified in the breath of mice monocolonized with the same bacteria. Altogether, our studies identify microbe-derived VOCs excreted in breath and support a mechanism by which gut bacterial metabolism directly contributes to the mammalian breath VOC profiles.
肠道微生物群与宿主健康和疾病密切相关,这激发了将我们不断增长的知识应用于临床实践的转化研究。然而,通过基因组内容来表征肠道微生物群的需求限制了快速即时诊断的可行性。微生物群产生各种各样的外源性代谢产物,这些产物会扩散到组织中,包括可能通过呼吸排出的挥发性有机化合物(VOCs)。我们假设呼出气体中含有源自肠道微生物的挥发性有机化合物,这些化合物能够反映微生物群的组成和代谢状态。为了探究这一想法,我们比较了27名健康儿童的呼出气体挥发物组和粪便肠道微生物群,发现呼出气体中的挥发性有机化合物组成与肠道微生物群相关。为了通过实验验证这一发现,我们设计了一种从无菌小鼠捕获呼出气体的方法。然后通过气相色谱 - 质谱联用(GC - MS)对呼出气体中的挥发性物质进行分析。使用这种新方法,我们发现小鼠呼出气体的成分明显受到肠道微生物群组成的影响。我们还发现,在纯培养中由肠道微生物产生的挥发性有机化合物可以在单一定植相同细菌的小鼠呼出气体中被识别出来。总之,我们的研究确定了呼出气体中源自微生物的挥发性有机化合物,并支持了一种机制,即肠道细菌代谢直接影响哺乳动物呼出气体的挥发性有机化合物谱。