TY - JOUR
T1 - Microbes vs. chemistry in the origin of the anaerobic gut lumen
AU - Friedman, Elliot S.
AU - Bittinger, Kyle
AU - Esipova, Tatiana V.
AU - Hou, Likai
AU - Chau, Lillian
AU - Jiang, Jack
AU - Mesaros, Clementina
AU - Lund, Peder J.
AU - Liang, Xue
AU - FitzGerald, Garret A.
AU - Goulian, Mark
AU - Lee, Daeyeon
AU - Garcia, Benjamin A.
AU - Blair, Ian A.
AU - Vinogradov, Sergei A.
AU - Wu, Gary D.
N1 - Funding Information:
ACKNOWLEDGMENTS. This work was supported by the following: NIH Grant R01 GM103591 and NIH Human-Microbial Analytic and Repository Core of the Center for Molecular Studies in Digestive and Liver Disease Grant P30 DK 050306 (to G.D.W.); NIH Grants R01 EB018464 (to S.A.V.), R01 GM080279 (to M.G.), R24 NS092986 (to S.A.V.), and 2T32CA009140-41A1 (to P.J.L.); the PennCHOP Microbiome Program (G.D.W.); National Science Foundation Penn Materials Research Science and Engineering Center Grant DMR11-20901 and the NSF Optical Microscopy Program (to S.A.V.); and NSF Grants P42ES023720 and P30ES013508.
Funding Information:
This work was supported by the following: NIH Grant R01 GM103591 and NIH Human-Microbial Analytic and Repository Core of the Center for Molecular Studies in Digestive and Liver Disease Grant P30 DK 050306 (to G.D.W.); NIH Grants R01 EB018464 (to S.A.V.), R01 GM080279 (to M.G.), R24 NS092986 (to S.A.V.), and 2T32CA009140-41A1 (to P.J.L.); the PennCHOP Microbiome Program (G.D.W.); National Science Foundation Penn Materials Research Science and Engineering Center Grant DMR11-20901 and the NSF Optical Microscopy Program (to S.A.V.); and NSF Grants P42ES023720 and P30ES013508.
Publisher Copyright:
© 2018 National Academy of Sciences. All Rights Reserved.
PY - 2018/4/17
Y1 - 2018/4/17
N2 - The succession from aerobic and facultative anaerobic bacteria to obligate anaerobes in the infant gut along with the differences between the compositions of the mucosally adherent vs. luminal microbiota suggests that the gut microbes consume oxygen, which diffuses into the lumen from the intestinal tissue, maintaining the lumen in a deeply anaerobic state. Remarkably, measurements of luminal oxygen levels show nearly identical pO2 (partial pressure of oxygen) profiles in conventional and germ-free mice, pointing to the existence of oxygen consumption mechanisms other than microbial respiration. In vitro experiments confirmed that the luminal contents of germ-free mice are able to chemically consume oxygen (e.g., via lipid oxidation reactions), although at rates significantly lower than those observed in the case of conventionally housed mice. For conventional mice, we also show that the taxonomic composition of the gut microbiota adherent to the gut mucosa and in the lumen throughout the length of the gut correlates with oxygen levels. At the same time, an increase in the biomass of the gut microbiota provides an explanation for the reduction of luminal oxygen in the distal vs. proximal gut. These results demonstrate how oxygen from the mammalian host is used by the gut microbiota, while both the microbes and the oxidative chemical reactions regulate luminal oxygen levels, shaping the composition of the microbial community throughout different regions of the gut.
AB - The succession from aerobic and facultative anaerobic bacteria to obligate anaerobes in the infant gut along with the differences between the compositions of the mucosally adherent vs. luminal microbiota suggests that the gut microbes consume oxygen, which diffuses into the lumen from the intestinal tissue, maintaining the lumen in a deeply anaerobic state. Remarkably, measurements of luminal oxygen levels show nearly identical pO2 (partial pressure of oxygen) profiles in conventional and germ-free mice, pointing to the existence of oxygen consumption mechanisms other than microbial respiration. In vitro experiments confirmed that the luminal contents of germ-free mice are able to chemically consume oxygen (e.g., via lipid oxidation reactions), although at rates significantly lower than those observed in the case of conventionally housed mice. For conventional mice, we also show that the taxonomic composition of the gut microbiota adherent to the gut mucosa and in the lumen throughout the length of the gut correlates with oxygen levels. At the same time, an increase in the biomass of the gut microbiota provides an explanation for the reduction of luminal oxygen in the distal vs. proximal gut. These results demonstrate how oxygen from the mammalian host is used by the gut microbiota, while both the microbes and the oxidative chemical reactions regulate luminal oxygen levels, shaping the composition of the microbial community throughout different regions of the gut.
KW - Gut microbiota
KW - Luminal oxygen
KW - Microbial ecology
KW - Oxygen probes
KW - Phosphorescence quenching
UR - http://www.scopus.com/inward/record.url?scp=85045523003&partnerID=8YFLogxK
U2 - 10.1073/pnas.1718635115
DO - 10.1073/pnas.1718635115
M3 - Article
C2 - 29610310
AN - SCOPUS:85045523003
SN - 0027-8424
VL - 115
SP - 4170
EP - 4175
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 16
ER -