Dynamic Changes of the Fungal Microbiome in Alcohol Use Disorder
Alcohol-associated liver disease (ALD) is an important cause of morbidity and mortality worldwide. The intestinal microbiota is involved in the development and progression of ALD; however, little is known about commensal fungi therein. We studied the dynamic changes of the intestinal fungal microbio...
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Published in | Frontiers in physiology Vol. 12; p. 699253 |
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Main Authors | , , , , , , , , , , |
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Abstract | Alcohol-associated liver disease (ALD) is an important cause of morbidity and mortality worldwide. The intestinal microbiota is involved in the development and progression of ALD; however, little is known about commensal fungi therein.
We studied the dynamic changes of the intestinal fungal microbiome, or mycobiome, in 66 patients with alcohol use disorder (AUD) and after 2 weeks of alcohol abstinence using internal transcribed spacer 2 (ITS2) amplicon sequencing of fecal samples.
Patients with AUD had significantly increased abundance of the genera
,
,
,
, and
, and of the species
and
compared with control subjects. Significantly improved liver health markers caspase-cleaved and intact cytokeratin 18 (CK18-M65) levels and controlled attenuation parameter (CAP) in AUD patients after 2 weeks of alcohol abstinence were associated with significantly lower abundance of the genera
,
,
,
,
, and the species
and
. This was mirrored by significantly higher specific anti-
immunoglobulin G (IgG) and M (IgM) serum levels in AUD patients in relation to control participants, and significantly decreased anti-
IgG levels in AUD subjects after 2 weeks of abstinence. The intestinal abundance of the genus
was significantly higher in AUD subjects with progressive liver disease compared with non-progressive liver disease.
In conclusion, improved liver health in AUD patients after alcohol abstinence was associated with lower intestinal abundances of
and
, and lower serum anti-
IgG levels. Intestinal fungi might serve as a therapeutic target to improve the outcome of patients in ALD. |
---|---|
AbstractList | BackgroundAlcohol-associated liver disease (ALD) is an important cause of morbidity and mortality worldwide. The intestinal microbiota is involved in the development and progression of ALD; however, little is known about commensal fungi therein.MethodsWe studied the dynamic changes of the intestinal fungal microbiome, or mycobiome, in 66 patients with alcohol use disorder (AUD) and after 2 weeks of alcohol abstinence using internal transcribed spacer 2 (ITS2) amplicon sequencing of fecal samples.ResultsPatients with AUD had significantly increased abundance of the genera Candida, Debaryomyces, Pichia, Kluyveromyces, and Issatchenkia, and of the species Candida albicans and Candida zeylanoides compared with control subjects. Significantly improved liver health markers caspase-cleaved and intact cytokeratin 18 (CK18-M65) levels and controlled attenuation parameter (CAP) in AUD patients after 2 weeks of alcohol abstinence were associated with significantly lower abundance of the genera Candida, Malassezia, Pichia, Kluyveromyces, Issatchenkia, and the species C. albicans and C. zeylanoides. This was mirrored by significantly higher specific anti-C. albicans immunoglobulin G (IgG) and M (IgM) serum levels in AUD patients in relation to control participants, and significantly decreased anti-C. albicans IgG levels in AUD subjects after 2 weeks of abstinence. The intestinal abundance of the genus Malassezia was significantly higher in AUD subjects with progressive liver disease compared with non-progressive liver disease.ConclusionIn conclusion, improved liver health in AUD patients after alcohol abstinence was associated with lower intestinal abundances of Candida and Malassezia, and lower serum anti-C. albicans IgG levels. Intestinal fungi might serve as a therapeutic target to improve the outcome of patients in ALD. Alcohol-associated liver disease (ALD) is an important cause of morbidity and mortality worldwide. The intestinal microbiota is involved in the development and progression of ALD; however, little is known about commensal fungi therein. We studied the dynamic changes of the intestinal fungal microbiome, or mycobiome, in 66 patients with alcohol use disorder (AUD) and after 2 weeks of alcohol abstinence using internal transcribed spacer 2 (ITS2) amplicon sequencing of fecal samples. Patients with AUD had significantly increased abundance of the genera , , , , and , and of the species and compared with control subjects. Significantly improved liver health markers caspase-cleaved and intact cytokeratin 18 (CK18-M65) levels and controlled attenuation parameter (CAP) in AUD patients after 2 weeks of alcohol abstinence were associated with significantly lower abundance of the genera , , , , , and the species and . This was mirrored by significantly higher specific anti- immunoglobulin G (IgG) and M (IgM) serum levels in AUD patients in relation to control participants, and significantly decreased anti- IgG levels in AUD subjects after 2 weeks of abstinence. The intestinal abundance of the genus was significantly higher in AUD subjects with progressive liver disease compared with non-progressive liver disease. In conclusion, improved liver health in AUD patients after alcohol abstinence was associated with lower intestinal abundances of and , and lower serum anti- IgG levels. Intestinal fungi might serve as a therapeutic target to improve the outcome of patients in ALD. Alcohol-associated liver disease (ALD) is an important cause of morbidity and mortality worldwide. The intestinal microbiota is involved in the development and progression of ALD; however, little is known about commensal fungi therein.BACKGROUNDAlcohol-associated liver disease (ALD) is an important cause of morbidity and mortality worldwide. The intestinal microbiota is involved in the development and progression of ALD; however, little is known about commensal fungi therein.We studied the dynamic changes of the intestinal fungal microbiome, or mycobiome, in 66 patients with alcohol use disorder (AUD) and after 2 weeks of alcohol abstinence using internal transcribed spacer 2 (ITS2) amplicon sequencing of fecal samples.METHODSWe studied the dynamic changes of the intestinal fungal microbiome, or mycobiome, in 66 patients with alcohol use disorder (AUD) and after 2 weeks of alcohol abstinence using internal transcribed spacer 2 (ITS2) amplicon sequencing of fecal samples.Patients with AUD had significantly increased abundance of the genera Candida, Debaryomyces, Pichia, Kluyveromyces, and Issatchenkia, and of the species Candida albicans and Candida zeylanoides compared with control subjects. Significantly improved liver health markers caspase-cleaved and intact cytokeratin 18 (CK18-M65) levels and controlled attenuation parameter (CAP) in AUD patients after 2 weeks of alcohol abstinence were associated with significantly lower abundance of the genera Candida, Malassezia, Pichia, Kluyveromyces, Issatchenkia, and the species C. albicans and C. zeylanoides. This was mirrored by significantly higher specific anti-C. albicans immunoglobulin G (IgG) and M (IgM) serum levels in AUD patients in relation to control participants, and significantly decreased anti-C. albicans IgG levels in AUD subjects after 2 weeks of abstinence. The intestinal abundance of the genus Malassezia was significantly higher in AUD subjects with progressive liver disease compared with non-progressive liver disease.RESULTSPatients with AUD had significantly increased abundance of the genera Candida, Debaryomyces, Pichia, Kluyveromyces, and Issatchenkia, and of the species Candida albicans and Candida zeylanoides compared with control subjects. Significantly improved liver health markers caspase-cleaved and intact cytokeratin 18 (CK18-M65) levels and controlled attenuation parameter (CAP) in AUD patients after 2 weeks of alcohol abstinence were associated with significantly lower abundance of the genera Candida, Malassezia, Pichia, Kluyveromyces, Issatchenkia, and the species C. albicans and C. zeylanoides. This was mirrored by significantly higher specific anti-C. albicans immunoglobulin G (IgG) and M (IgM) serum levels in AUD patients in relation to control participants, and significantly decreased anti-C. albicans IgG levels in AUD subjects after 2 weeks of abstinence. The intestinal abundance of the genus Malassezia was significantly higher in AUD subjects with progressive liver disease compared with non-progressive liver disease.In conclusion, improved liver health in AUD patients after alcohol abstinence was associated with lower intestinal abundances of Candida and Malassezia, and lower serum anti-C. albicans IgG levels. Intestinal fungi might serve as a therapeutic target to improve the outcome of patients in ALD.CONCLUSIONIn conclusion, improved liver health in AUD patients after alcohol abstinence was associated with lower intestinal abundances of Candida and Malassezia, and lower serum anti-C. albicans IgG levels. Intestinal fungi might serve as a therapeutic target to improve the outcome of patients in ALD. |
Author | Hartmann, Phillipp Duan, Yi Kruglov, Andrey Schnabl, Bernd Wang, Yanhan Zeng, Suling Zhang, Xinlian Fouts, Derrick E. Lang, Sonja Bondareva, Marina Stärkel, Peter |
AuthorAffiliation | 3 Department of Medicine, VA San Diego Healthcare System , San Diego, CA , United States 8 Cliniques Universitaires Saint-Luc, Université catholique de Louvain , Brussels , Belgium 6 Belozerskiy Research Institute for Physical and Chemical Biology and Faculty of Bioengineering and Bioinformatics, M.V. Lomonosov Moscow State University , Moscow , Russia 4 Division of Biostatistics and Bioinformatics, Department of Family Medicine and Public Health, University of California , San Diego, La Jolla, CA , United States 2 Department of Medicine, University of California , San Diego, La Jolla, CA , United States 5 Chronic Inflammation Lab, German Rheumatism Research Center, a Leibniz Institute , Berlin , Germany 1 Department of Pediatrics, University of California , San Diego, La Jolla, CA , United States 7 Department of Genomic Medicine, J. Craig Venter Institute , Rockville, MD , United States |
AuthorAffiliation_xml | – name: 2 Department of Medicine, University of California , San Diego, La Jolla, CA , United States – name: 1 Department of Pediatrics, University of California , San Diego, La Jolla, CA , United States – name: 4 Division of Biostatistics and Bioinformatics, Department of Family Medicine and Public Health, University of California , San Diego, La Jolla, CA , United States – name: 3 Department of Medicine, VA San Diego Healthcare System , San Diego, CA , United States – name: 7 Department of Genomic Medicine, J. Craig Venter Institute , Rockville, MD , United States – name: 8 Cliniques Universitaires Saint-Luc, Université catholique de Louvain , Brussels , Belgium – name: 5 Chronic Inflammation Lab, German Rheumatism Research Center, a Leibniz Institute , Berlin , Germany – name: 6 Belozerskiy Research Institute for Physical and Chemical Biology and Faculty of Bioengineering and Bioinformatics, M.V. Lomonosov Moscow State University , Moscow , Russia |
Author_xml | – sequence: 1 givenname: Phillipp surname: Hartmann fullname: Hartmann, Phillipp – sequence: 2 givenname: Sonja surname: Lang fullname: Lang, Sonja – sequence: 3 givenname: Suling surname: Zeng fullname: Zeng, Suling – sequence: 4 givenname: Yi surname: Duan fullname: Duan, Yi – sequence: 5 givenname: Xinlian surname: Zhang fullname: Zhang, Xinlian – sequence: 6 givenname: Yanhan surname: Wang fullname: Wang, Yanhan – sequence: 7 givenname: Marina surname: Bondareva fullname: Bondareva, Marina – sequence: 8 givenname: Andrey surname: Kruglov fullname: Kruglov, Andrey – sequence: 9 givenname: Derrick E. surname: Fouts fullname: Fouts, Derrick E. – sequence: 10 givenname: Peter surname: Stärkel fullname: Stärkel, Peter – sequence: 11 givenname: Bernd surname: Schnabl fullname: Schnabl, Bernd |
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Cites_doi | 10.1136/gutjnl-2016-313170 10.1016/j.jhep.2019.09.029 10.1186/s12866-020-01907-3 10.1016/j.jhep.2013.03.007 10.1038/nature12820 10.1172/JCI90562 10.1038/nmeth.2604 10.1016/S0140-6736(07)61602-X 10.1002/hep.29099 10.1002/hep.30832 10.3389/fphys.2012.00402 10.1128/aem.01541-09 10.1111/2041-210X.12073 10.1007/s00535-020-01740-5 10.1093/alcalc/agw053 10.1111/acer.12704 10.1128/aem.02576-16 10.1007/s00134-017-4717-0 10.1186/s40168-017-0373-4 10.1016/j.jhep.2014.03.021 10.1186/gb-2011-12-6-r60 10.1016/j.cgh.2017.11.045 10.1128/AEM.01996-06 10.1007/s11357-019-00098-8 10.1038/s41598-020-64747-1 10.14806/ej.17.1.200 10.3389/fcimb.2020.00198 10.1136/gutjnl-2018-317791 10.1080/19490976.2020.1782157 10.1016/j.chom.2019.01.007 10.1093/nar/gky1022 10.1016/j.jim.2015.04.004 |
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Copyright | Copyright © 2021 Hartmann, Lang, Zeng, Duan, Zhang, Wang, Bondareva, Kruglov, Fouts, Stärkel and Schnabl. Copyright © 2021 Hartmann, Lang, Zeng, Duan, Zhang, Wang, Bondareva, Kruglov, Fouts, Stärkel and Schnabl. 2021 Hartmann, Lang, Zeng, Duan, Zhang, Wang, Bondareva, Kruglov, Fouts, Stärkel and Schnabl |
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Keywords | abstinence mycobiome alcohol-associated liver disease fungi microbiome |
Language | English |
License | Copyright © 2021 Hartmann, Lang, Zeng, Duan, Zhang, Wang, Bondareva, Kruglov, Fouts, Stärkel and Schnabl. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
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References | Hartmann (B12) 2015; 39 Bengtsson-Palme (B4) 2013; 4 Mueller (B21) 2017; 66 Lemoinne (B16) 2020; 69 Limon (B17) 2019; 25 Tang (B30) 2015; 421 Lozupone (B18) 2007; 73 Yang (B34) 2017; 127 Lang (B15) 2020; 71 Nilsson (B23) 2019; 47 Singh (B28) 2019; 41 Hartmann (B11) 2012; 3 Taylor (B31) 2016; 82 Bassetti (B3) 2017; 43 David (B7) 2014; 505 Kabwe (B14) 2020; 20 Segata (B27) 2011; 12 Gianni (B10) 2017; 52 von Elm (B32) 2007; 370 Maccioni (B19) 2020; 12 Nash (B22) 2017; 5 Rehm (B25) 2013; 59 Martin (B20) 2011; 17 Schloss (B26) 2009; 75 Freire (B9) 2020; 10 Edgar (B8) 2013; 10 Cholankeril (B5) 2018; 16 Wickham (B33) 2021 (B24) 2018 Jiang (B13) 2021; 56 Sparber (B29) 2020; 10 Chu (B6) 2020; 72 Bartoletti (B2) 2014; 61 Bajaj (B1) 2018; 67 |
References_xml | – volume: 67 start-page: 1146 year: 2018 ident: B1 article-title: Fungal dysbiosis in cirrhosis. publication-title: Gut doi: 10.1136/gutjnl-2016-313170 – volume: 72 start-page: 391 year: 2020 ident: B6 article-title: The Candida albicans exotoxin candidalysin promotes alcohol-associated liver disease. publication-title: J. Hepatol. doi: 10.1016/j.jhep.2019.09.029 – volume: 20 year: 2020 ident: B14 article-title: The gut mycobiota of rural and urban individuals is shaped by geography. publication-title: BMC Microbiol. doi: 10.1186/s12866-020-01907-3 – volume: 59 start-page: 160 year: 2013 ident: B25 article-title: Global burden of alcoholic liver diseases. publication-title: J. Hepatol. doi: 10.1016/j.jhep.2013.03.007 – volume: 505 start-page: 559 year: 2014 ident: B7 article-title: Diet rapidly and reproducibly alters the human gut microbiome. publication-title: Nature doi: 10.1038/nature12820 – volume: 127 start-page: 2829 year: 2017 ident: B34 article-title: Intestinal fungi contribute to development of alcoholic liver disease. publication-title: J. Clin. Invest. doi: 10.1172/JCI90562 – volume: 10 start-page: 996 year: 2013 ident: B8 article-title: UPARSE: highly accurate OTU sequences from microbial amplicon reads. publication-title: Nat. Methods doi: 10.1038/nmeth.2604 – volume: 370 start-page: 1453 year: 2007 ident: B32 article-title: The strengthening the reporting of observational studies in epidemiology (STROBE) statement: guidelines for reporting observational studies. publication-title: Lancet doi: 10.1016/S0140-6736(07)61602-X – volume: 66 start-page: 96 year: 2017 ident: B21 article-title: Caspase-cleaved keratin-18 fragments increase during alcohol withdrawal and predict liver-related death in patients with alcoholic liver disease. publication-title: Hepatology doi: 10.1002/hep.29099 – volume: 71 start-page: 522 year: 2020 ident: B15 article-title: Intestinal fungal dysbiosis and systemic immune response to fungi in patients with alcoholic hepatitis. publication-title: Hepatology doi: 10.1002/hep.30832 – volume: 3 year: 2012 ident: B11 article-title: The intestinal microbiome and the leaky gut as therapeutic targets in alcoholic liver disease. publication-title: Front. Physiol. doi: 10.3389/fphys.2012.00402 – volume: 75 start-page: 7537 year: 2009 ident: B26 article-title: Introducing mothur: open-source, platform-independent, community-supported software for describing and comparing microbial communities. publication-title: Appl. Environ. Microbiol. doi: 10.1128/aem.01541-09 – volume: 4 start-page: 914 year: 2013 ident: B4 article-title: Improved software detection and extraction of ITS1 and ITS2 from ribosomal ITS sequences of fungi and other eukaryotes for analysis of environmental sequencing data. publication-title: Methods Ecol. Evol. doi: 10.1111/2041-210X.12073 – volume: 56 start-page: 1 year: 2021 ident: B13 article-title: The gut mycobiome: a novel player in chronic liver diseases. publication-title: J. Gastroenterol. doi: 10.1007/s00535-020-01740-5 – volume: 52 start-page: 42 year: 2017 ident: B10 article-title: Prospective evaluation of liver stiffness using transient elastography in alcoholic patients following abstinence. publication-title: Alcohol Alcohol. doi: 10.1093/alcalc/agw053 – volume: 39 start-page: 763 year: 2015 ident: B12 article-title: Alcoholic liver disease: the gut microbiome and liver cross talk. publication-title: Alcohol. Clin. Exp. Res. doi: 10.1111/acer.12704 – volume: 82 start-page: 7217 year: 2016 ident: B31 article-title: Accurate estimation of fungal diversity and abundance through improved lineage-specific primers optimized for illumina amplicon sequencing. publication-title: Appl. Environ. Microbiol. doi: 10.1128/aem.02576-16 – volume: 43 start-page: 509 year: 2017 ident: B3 article-title: Clinical characteristics and predictors of mortality in cirrhotic patients with candidemia and intra-abdominal candidiasis: a multicenter study. publication-title: Intensive Care Med. doi: 10.1007/s00134-017-4717-0 – volume: 5 year: 2017 ident: B22 article-title: The gut mycobiome of the human microbiome project healthy cohort. publication-title: Microbiome doi: 10.1186/s40168-017-0373-4 – volume: 61 start-page: 51 year: 2014 ident: B2 article-title: Epidemiology and outcomes of bloodstream infection in patients with cirrhosis. publication-title: J. Hepatol. doi: 10.1016/j.jhep.2014.03.021 – volume: 12 year: 2011 ident: B27 article-title: Metagenomic biomarker discovery and explanation. publication-title: Genome Biol. doi: 10.1186/gb-2011-12-6-r60 – volume: 16 start-page: 1356 year: 2018 ident: B5 article-title: Alcoholic liver disease replaces hepatitis C virus infection as the leading indication for liver transplantation in the United States. publication-title: Clin. Gastroenterol. Hepatol. doi: 10.1016/j.cgh.2017.11.045 – volume: 73 start-page: 1576 year: 2007 ident: B18 article-title: Quantitative and qualitative beta diversity measures lead to different insights into factors that structure microbial communities. publication-title: Appl. Environ. Microbiol. doi: 10.1128/AEM.01996-06 – volume: 41 start-page: 907 year: 2019 ident: B28 article-title: Gastro-intestinal and oral microbiome signatures associated with healthy aging. publication-title: Geroscience doi: 10.1007/s11357-019-00098-8 – volume: 10 year: 2020 ident: B9 article-title: Longitudinal study of oral microbiome variation in twins. publication-title: Sci. Rep. doi: 10.1038/s41598-020-64747-1 – volume: 17 start-page: 10 year: 2011 ident: B20 article-title: Cutadapt removes adapter sequences from high-throughput sequencing reads. publication-title: EMBnet J. doi: 10.14806/ej.17.1.200 – year: 2018 ident: B24 publication-title: R: A Language and Environment for Statistical Computing. – volume: 10 year: 2020 ident: B29 article-title: Host immunity to publication-title: Front. Cell. Infect. Microbiol. doi: 10.3389/fcimb.2020.00198 – volume: 69 start-page: 92 year: 2020 ident: B16 article-title: Fungi participate in the dysbiosis of gut microbiota in patients with primary sclerosing cholangitis. publication-title: Gut doi: 10.1136/gutjnl-2018-317791 – year: 2021 ident: B33 publication-title: log_Trans: Log Transformations in Scales: Scale Functions for Visualization. – volume: 12 year: 2020 ident: B19 article-title: Intestinal permeability, microbial translocation, changes in duodenal and fecal microbiota, and their associations with alcoholic liver disease progression in humans. publication-title: Gut Microbes doi: 10.1080/19490976.2020.1782157 – volume: 25 start-page: 377 year: 2019 ident: B17 article-title: Malassezia is associated with Crohn’s disease and exacerbates colitis in mouse models. publication-title: Cell Host Microbe doi: 10.1016/j.chom.2019.01.007 – volume: 47 start-page: D259 year: 2019 ident: B23 article-title: The UNITE database for molecular identification of fungi: handling dark taxa and parallel taxonomic classifications. publication-title: Nucleic Acids Res. doi: 10.1093/nar/gky1022 – volume: 421 start-page: 112 year: 2015 ident: B30 article-title: Mycobiome: approaches to analysis of intestinal fungi. publication-title: J. Immunol. Methods. doi: 10.1016/j.jim.2015.04.004 |
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Snippet | Alcohol-associated liver disease (ALD) is an important cause of morbidity and mortality worldwide. The intestinal microbiota is involved in the development and... BackgroundAlcohol-associated liver disease (ALD) is an important cause of morbidity and mortality worldwide. The intestinal microbiota is involved in the... |
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SubjectTerms | abstinence alcohol-associated liver disease fungi microbiome mycobiome Physiology |
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Title | Dynamic Changes of the Fungal Microbiome in Alcohol Use Disorder |
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