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The Host-Microbiome Response to Hyperbaric Oxygen Therapy in Ulcerative Colitis Patients

BACKGROUND & AIMS: Hyperbaric oxygen therapy (HBOT) is a promising treatment for moderate-to-severe ulcerative colitis. However, our current understanding of the host and microbial response to HBOT remains unclear. This study examined the molecular mechanisms underpinning HBOT using a multi-omic...

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Autores principales: Gonzalez, Carlos G., Mills, Robert H., Kordahi, Melissa C., Carrillo-Terrazas, Marvic, Secaira-Morocho, Henry, Widjaja, Christella E., Tsai, Matthew S., Mittal, Yash, Yee, Brian A., Vargas, Fernando, Weldon, Kelly, Gauglitz, Julia M., Delaroque, Clara, Sauceda, Consuelo, Rossitto, Leigh-Ana, Ackermann, Gail, Humphrey, Gregory, Swafford, Austin D., Siegel, Corey A., Buckey, Jay C., Raffals, Laura E., Sadler, Charlotte, Lindholm, Peter, Fisch, Kathleen M., Valaseck, Mark, Suriawinata, Arief, Yeo, Gene W., Ghosh, Pradipta, Chang, John T., Chu, Hiutung, Dorrestein, Pieter, Zhu, Qiyun, Chassaing, Benoit, Knight, Rob, Gonzalez, David J., Dulai, Parambir S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9117812/
https://www.ncbi.nlm.nih.gov/pubmed/35378331
http://dx.doi.org/10.1016/j.jcmgh.2022.03.008
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author Gonzalez, Carlos G.
Mills, Robert H.
Kordahi, Melissa C.
Carrillo-Terrazas, Marvic
Secaira-Morocho, Henry
Widjaja, Christella E.
Tsai, Matthew S.
Mittal, Yash
Yee, Brian A.
Vargas, Fernando
Weldon, Kelly
Gauglitz, Julia M.
Delaroque, Clara
Sauceda, Consuelo
Rossitto, Leigh-Ana
Ackermann, Gail
Humphrey, Gregory
Swafford, Austin D.
Siegel, Corey A.
Buckey, Jay C.
Raffals, Laura E.
Sadler, Charlotte
Lindholm, Peter
Fisch, Kathleen M.
Valaseck, Mark
Suriawinata, Arief
Yeo, Gene W.
Ghosh, Pradipta
Chang, John T.
Chu, Hiutung
Dorrestein, Pieter
Zhu, Qiyun
Chassaing, Benoit
Knight, Rob
Gonzalez, David J.
Dulai, Parambir S.
author_facet Gonzalez, Carlos G.
Mills, Robert H.
Kordahi, Melissa C.
Carrillo-Terrazas, Marvic
Secaira-Morocho, Henry
Widjaja, Christella E.
Tsai, Matthew S.
Mittal, Yash
Yee, Brian A.
Vargas, Fernando
Weldon, Kelly
Gauglitz, Julia M.
Delaroque, Clara
Sauceda, Consuelo
Rossitto, Leigh-Ana
Ackermann, Gail
Humphrey, Gregory
Swafford, Austin D.
Siegel, Corey A.
Buckey, Jay C.
Raffals, Laura E.
Sadler, Charlotte
Lindholm, Peter
Fisch, Kathleen M.
Valaseck, Mark
Suriawinata, Arief
Yeo, Gene W.
Ghosh, Pradipta
Chang, John T.
Chu, Hiutung
Dorrestein, Pieter
Zhu, Qiyun
Chassaing, Benoit
Knight, Rob
Gonzalez, David J.
Dulai, Parambir S.
author_sort Gonzalez, Carlos G.
collection PubMed
description BACKGROUND & AIMS: Hyperbaric oxygen therapy (HBOT) is a promising treatment for moderate-to-severe ulcerative colitis. However, our current understanding of the host and microbial response to HBOT remains unclear. This study examined the molecular mechanisms underpinning HBOT using a multi-omic strategy. METHODS: Pre- and post-intervention mucosal biopsies, tissue, and fecal samples were collected from HBOT phase 2 clinical trials. Biopsies and fecal samples were subjected to shotgun metaproteomics, metabolomics, 16s rRNA sequencing, and metagenomics. Tissue was subjected to bulk RNA sequencing and digital spatial profiling (DSP) for single-cell RNA and protein analysis, and immunohistochemistry was performed. Fecal samples were also used for colonization experiments in IL10(-/-) germ-free UC mouse models. RESULTS: Proteomics identified negative associations between HBOT response and neutrophil azurophilic granule abundance. DSP identified an HBOT-specific reduction of neutrophil STAT3, which was confirmed by immunohistochemistry. HBOT decreased microbial diversity with a proportional increase in Firmicutes and a secondary bile acid lithocholic acid. A major source of the reduction in diversity was the loss of mucus-adherent taxa, resulting in increased MUC2 levels post-HBOT. Targeted database searching revealed strain-level associations between Akkermansia muciniphila and HBOT response status. Colonization of IL10(-/-) with stool obtained from HBOT responders resulted in lower colitis activity compared with non-responders, with no differences in STAT3 expression, suggesting complementary but independent host and microbial responses. CONCLUSIONS: HBOT reduces host neutrophil STAT3 and azurophilic granule activity in UC patients and changes in microbial composition and metabolism in ways that improve colitis activity. Intestinal microbiota, especially strain level variations in A muciniphila, may contribute to HBOT non-response.
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spelling pubmed-91178122022-05-20 The Host-Microbiome Response to Hyperbaric Oxygen Therapy in Ulcerative Colitis Patients Gonzalez, Carlos G. Mills, Robert H. Kordahi, Melissa C. Carrillo-Terrazas, Marvic Secaira-Morocho, Henry Widjaja, Christella E. Tsai, Matthew S. Mittal, Yash Yee, Brian A. Vargas, Fernando Weldon, Kelly Gauglitz, Julia M. Delaroque, Clara Sauceda, Consuelo Rossitto, Leigh-Ana Ackermann, Gail Humphrey, Gregory Swafford, Austin D. Siegel, Corey A. Buckey, Jay C. Raffals, Laura E. Sadler, Charlotte Lindholm, Peter Fisch, Kathleen M. Valaseck, Mark Suriawinata, Arief Yeo, Gene W. Ghosh, Pradipta Chang, John T. Chu, Hiutung Dorrestein, Pieter Zhu, Qiyun Chassaing, Benoit Knight, Rob Gonzalez, David J. Dulai, Parambir S. Cell Mol Gastroenterol Hepatol Original Research BACKGROUND & AIMS: Hyperbaric oxygen therapy (HBOT) is a promising treatment for moderate-to-severe ulcerative colitis. However, our current understanding of the host and microbial response to HBOT remains unclear. This study examined the molecular mechanisms underpinning HBOT using a multi-omic strategy. METHODS: Pre- and post-intervention mucosal biopsies, tissue, and fecal samples were collected from HBOT phase 2 clinical trials. Biopsies and fecal samples were subjected to shotgun metaproteomics, metabolomics, 16s rRNA sequencing, and metagenomics. Tissue was subjected to bulk RNA sequencing and digital spatial profiling (DSP) for single-cell RNA and protein analysis, and immunohistochemistry was performed. Fecal samples were also used for colonization experiments in IL10(-/-) germ-free UC mouse models. RESULTS: Proteomics identified negative associations between HBOT response and neutrophil azurophilic granule abundance. DSP identified an HBOT-specific reduction of neutrophil STAT3, which was confirmed by immunohistochemistry. HBOT decreased microbial diversity with a proportional increase in Firmicutes and a secondary bile acid lithocholic acid. A major source of the reduction in diversity was the loss of mucus-adherent taxa, resulting in increased MUC2 levels post-HBOT. Targeted database searching revealed strain-level associations between Akkermansia muciniphila and HBOT response status. Colonization of IL10(-/-) with stool obtained from HBOT responders resulted in lower colitis activity compared with non-responders, with no differences in STAT3 expression, suggesting complementary but independent host and microbial responses. CONCLUSIONS: HBOT reduces host neutrophil STAT3 and azurophilic granule activity in UC patients and changes in microbial composition and metabolism in ways that improve colitis activity. Intestinal microbiota, especially strain level variations in A muciniphila, may contribute to HBOT non-response. Elsevier 2022-04-01 /pmc/articles/PMC9117812/ /pubmed/35378331 http://dx.doi.org/10.1016/j.jcmgh.2022.03.008 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Gonzalez, Carlos G.
Mills, Robert H.
Kordahi, Melissa C.
Carrillo-Terrazas, Marvic
Secaira-Morocho, Henry
Widjaja, Christella E.
Tsai, Matthew S.
Mittal, Yash
Yee, Brian A.
Vargas, Fernando
Weldon, Kelly
Gauglitz, Julia M.
Delaroque, Clara
Sauceda, Consuelo
Rossitto, Leigh-Ana
Ackermann, Gail
Humphrey, Gregory
Swafford, Austin D.
Siegel, Corey A.
Buckey, Jay C.
Raffals, Laura E.
Sadler, Charlotte
Lindholm, Peter
Fisch, Kathleen M.
Valaseck, Mark
Suriawinata, Arief
Yeo, Gene W.
Ghosh, Pradipta
Chang, John T.
Chu, Hiutung
Dorrestein, Pieter
Zhu, Qiyun
Chassaing, Benoit
Knight, Rob
Gonzalez, David J.
Dulai, Parambir S.
The Host-Microbiome Response to Hyperbaric Oxygen Therapy in Ulcerative Colitis Patients
title The Host-Microbiome Response to Hyperbaric Oxygen Therapy in Ulcerative Colitis Patients
title_full The Host-Microbiome Response to Hyperbaric Oxygen Therapy in Ulcerative Colitis Patients
title_fullStr The Host-Microbiome Response to Hyperbaric Oxygen Therapy in Ulcerative Colitis Patients
title_full_unstemmed The Host-Microbiome Response to Hyperbaric Oxygen Therapy in Ulcerative Colitis Patients
title_short The Host-Microbiome Response to Hyperbaric Oxygen Therapy in Ulcerative Colitis Patients
title_sort host-microbiome response to hyperbaric oxygen therapy in ulcerative colitis patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9117812/
https://www.ncbi.nlm.nih.gov/pubmed/35378331
http://dx.doi.org/10.1016/j.jcmgh.2022.03.008
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