Chagas disease is related to structural changes of the gut microbiota in adults with chronic infection (TRIPOBIOME Study)
The implications of the gut microbial communities in the immune response against parasites and gut motility could explain the differences in clinical manifestations and treatment responses found in patients with chronic Chagas disease. In this pilot prospective cross-sectional study, we included 80...
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Veröffentlicht in: | PLoS neglected tropical diseases 2023-07, Vol.17 (7), p.e0011490-e0011490 |
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creator | Pérez-Molina, José A Crespillo-Andújar, Clara Trigo, Elena Chamorro, Sandra Arsuaga, Marta Olavarrieta, Leticia Navia, Beatriz Martín, Oihane Monge-Maillo, Begoña Norman, Francesca F Lanza, Val F Serrano-Villar, Sergio |
description | The implications of the gut microbial communities in the immune response against parasites and gut motility could explain the differences in clinical manifestations and treatment responses found in patients with chronic Chagas disease.
In this pilot prospective cross-sectional study, we included 80 participants: 29 with indeterminate CD (ICD), 16 with cardiac CD (CCD), 15 with digestive CD (DCD), and 20 controls without CD. Stool was collected at the baseline visit and faecal microbial community structure DNA was analyzed by whole genome sequencing. We also performed a comprehensive dietary analysis. Ninety per cent (72/80) of subjects were of Bolivian origin with a median age of 47 years (IQR 39-54) and 48.3% (29/60) had received benznidazole treatment. There were no substantial differences in dietary habits between patients with CD and controls. We identified that the presence or absence of CD explained 5% of the observed microbiota variability. Subjects with CD exhibited consistent enrichment of Parabacteroides spp, while for Enterococcus hirae, Lactobacillus buchneri and Megamonas spp, the effect was less clear once excluded the outliers values. Sex, type of visceral involvement and previous treatment with benznidazole did not appear to have a confounding effect on gut microbiota structure. We also found that patients with DCD showed consistent Prevotella spp enrichment.
We found a detectable effect of Chagas disease on overall microbiota structure with several potential disease biomarkers, which warrants further research in this field. The analysis of bacterial diversity could prove to be a viable target to improve the prognosis of this prevalent and neglected disease. |
doi_str_mv | 10.1371/journal.pntd.0011490 |
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In this pilot prospective cross-sectional study, we included 80 participants: 29 with indeterminate CD (ICD), 16 with cardiac CD (CCD), 15 with digestive CD (DCD), and 20 controls without CD. Stool was collected at the baseline visit and faecal microbial community structure DNA was analyzed by whole genome sequencing. We also performed a comprehensive dietary analysis. Ninety per cent (72/80) of subjects were of Bolivian origin with a median age of 47 years (IQR 39-54) and 48.3% (29/60) had received benznidazole treatment. There were no substantial differences in dietary habits between patients with CD and controls. We identified that the presence or absence of CD explained 5% of the observed microbiota variability. Subjects with CD exhibited consistent enrichment of Parabacteroides spp, while for Enterococcus hirae, Lactobacillus buchneri and Megamonas spp, the effect was less clear once excluded the outliers values. Sex, type of visceral involvement and previous treatment with benznidazole did not appear to have a confounding effect on gut microbiota structure. We also found that patients with DCD showed consistent Prevotella spp enrichment.
We found a detectable effect of Chagas disease on overall microbiota structure with several potential disease biomarkers, which warrants further research in this field. The analysis of bacterial diversity could prove to be a viable target to improve the prognosis of this prevalent and neglected disease.</description><identifier>ISSN: 1935-2735</identifier><identifier>ISSN: 1935-2727</identifier><identifier>EISSN: 1935-2735</identifier><identifier>DOI: 10.1371/journal.pntd.0011490</identifier><identifier>PMID: 37478160</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adult ; Adults ; Benznidazole ; Biology and Life Sciences ; Biomarkers ; Chagas disease ; Chagas Disease - drug therapy ; Chronic infection ; Community structure ; Complications and side effects ; Congenital diseases ; Cross-Sectional Studies ; Defence mechanisms ; Denervation ; Deoxyribonucleic acid ; Development and progression ; Diet ; Digestive system ; Digestive tract ; Discriminant analysis ; DNA ; DNA structure ; Dysbiosis ; Esophagus ; Feces ; Gastric motility ; Gastrointestinal Microbiome - genetics ; Gastrointestinal tract ; Gene sequencing ; Genomes ; Health aspects ; Health services ; Humans ; Immune response ; Immunity ; Infections ; Intestinal flora ; Intestinal microflora ; Medicine and Health Sciences ; Microbial activity ; Microbiomes ; Microbiota ; Microbiota (Symbiotic organisms) ; Microorganisms ; Middle Aged ; Motility ; Outliers (statistics) ; Parasites ; Patients ; Persistent Infection ; Prospective Studies ; Protozoa ; Quality control ; Recipes ; Risk factors ; Software ; Taxonomy ; Tropical diseases ; Vector-borne diseases ; Veganism ; Whole genome sequencing</subject><ispartof>PLoS neglected tropical diseases, 2023-07, Vol.17 (7), p.e0011490-e0011490</ispartof><rights>Copyright: © 2023 Pérez-Molina et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</rights><rights>COPYRIGHT 2023 Public Library of Science</rights><rights>2023 Pérez-Molina et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 Pérez-Molina et al 2023 Pérez-Molina et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c559t-2abc1a23c3b50f8190b18bc9939cf1fe868f95b88f363fbffd92169de72652c13</citedby><cites>FETCH-LOGICAL-c559t-2abc1a23c3b50f8190b18bc9939cf1fe868f95b88f363fbffd92169de72652c13</cites><orcidid>0000-0001-8735-4124</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10395948/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10395948/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,2929,23871,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37478160$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Rogers, Matthew Brian</contributor><creatorcontrib>Pérez-Molina, José A</creatorcontrib><creatorcontrib>Crespillo-Andújar, Clara</creatorcontrib><creatorcontrib>Trigo, Elena</creatorcontrib><creatorcontrib>Chamorro, Sandra</creatorcontrib><creatorcontrib>Arsuaga, Marta</creatorcontrib><creatorcontrib>Olavarrieta, Leticia</creatorcontrib><creatorcontrib>Navia, Beatriz</creatorcontrib><creatorcontrib>Martín, Oihane</creatorcontrib><creatorcontrib>Monge-Maillo, Begoña</creatorcontrib><creatorcontrib>Norman, Francesca F</creatorcontrib><creatorcontrib>Lanza, Val F</creatorcontrib><creatorcontrib>Serrano-Villar, Sergio</creatorcontrib><title>Chagas disease is related to structural changes of the gut microbiota in adults with chronic infection (TRIPOBIOME Study)</title><title>PLoS neglected tropical diseases</title><addtitle>PLoS Negl Trop Dis</addtitle><description>The implications of the gut microbial communities in the immune response against parasites and gut motility could explain the differences in clinical manifestations and treatment responses found in patients with chronic Chagas disease.
In this pilot prospective cross-sectional study, we included 80 participants: 29 with indeterminate CD (ICD), 16 with cardiac CD (CCD), 15 with digestive CD (DCD), and 20 controls without CD. Stool was collected at the baseline visit and faecal microbial community structure DNA was analyzed by whole genome sequencing. We also performed a comprehensive dietary analysis. Ninety per cent (72/80) of subjects were of Bolivian origin with a median age of 47 years (IQR 39-54) and 48.3% (29/60) had received benznidazole treatment. There were no substantial differences in dietary habits between patients with CD and controls. We identified that the presence or absence of CD explained 5% of the observed microbiota variability. Subjects with CD exhibited consistent enrichment of Parabacteroides spp, while for Enterococcus hirae, Lactobacillus buchneri and Megamonas spp, the effect was less clear once excluded the outliers values. Sex, type of visceral involvement and previous treatment with benznidazole did not appear to have a confounding effect on gut microbiota structure. We also found that patients with DCD showed consistent Prevotella spp enrichment.
We found a detectable effect of Chagas disease on overall microbiota structure with several potential disease biomarkers, which warrants further research in this field. The analysis of bacterial diversity could prove to be a viable target to improve the prognosis of this prevalent and neglected disease.</description><subject>Adult</subject><subject>Adults</subject><subject>Benznidazole</subject><subject>Biology and Life Sciences</subject><subject>Biomarkers</subject><subject>Chagas disease</subject><subject>Chagas Disease - drug therapy</subject><subject>Chronic infection</subject><subject>Community structure</subject><subject>Complications and side effects</subject><subject>Congenital diseases</subject><subject>Cross-Sectional Studies</subject><subject>Defence mechanisms</subject><subject>Denervation</subject><subject>Deoxyribonucleic acid</subject><subject>Development and progression</subject><subject>Diet</subject><subject>Digestive system</subject><subject>Digestive tract</subject><subject>Discriminant analysis</subject><subject>DNA</subject><subject>DNA structure</subject><subject>Dysbiosis</subject><subject>Esophagus</subject><subject>Feces</subject><subject>Gastric motility</subject><subject>Gastrointestinal Microbiome - genetics</subject><subject>Gastrointestinal tract</subject><subject>Gene sequencing</subject><subject>Genomes</subject><subject>Health aspects</subject><subject>Health services</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immunity</subject><subject>Infections</subject><subject>Intestinal flora</subject><subject>Intestinal microflora</subject><subject>Medicine and Health Sciences</subject><subject>Microbial activity</subject><subject>Microbiomes</subject><subject>Microbiota</subject><subject>Microbiota (Symbiotic organisms)</subject><subject>Microorganisms</subject><subject>Middle Aged</subject><subject>Motility</subject><subject>Outliers (statistics)</subject><subject>Parasites</subject><subject>Patients</subject><subject>Persistent Infection</subject><subject>Prospective Studies</subject><subject>Protozoa</subject><subject>Quality control</subject><subject>Recipes</subject><subject>Risk factors</subject><subject>Software</subject><subject>Taxonomy</subject><subject>Tropical diseases</subject><subject>Vector-borne diseases</subject><subject>Veganism</subject><subject>Whole genome 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disease is related to structural changes of the gut microbiota in adults with chronic infection (TRIPOBIOME Study)</title><author>Pérez-Molina, José A ; Crespillo-Andújar, Clara ; Trigo, Elena ; Chamorro, Sandra ; Arsuaga, Marta ; Olavarrieta, Leticia ; Navia, Beatriz ; Martín, Oihane ; Monge-Maillo, Begoña ; Norman, Francesca F ; Lanza, Val F ; Serrano-Villar, Sergio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c559t-2abc1a23c3b50f8190b18bc9939cf1fe868f95b88f363fbffd92169de72652c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adult</topic><topic>Adults</topic><topic>Benznidazole</topic><topic>Biology and Life Sciences</topic><topic>Biomarkers</topic><topic>Chagas disease</topic><topic>Chagas Disease - drug therapy</topic><topic>Chronic infection</topic><topic>Community structure</topic><topic>Complications and side effects</topic><topic>Congenital 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Dis</addtitle><date>2023-07-01</date><risdate>2023</risdate><volume>17</volume><issue>7</issue><spage>e0011490</spage><epage>e0011490</epage><pages>e0011490-e0011490</pages><issn>1935-2735</issn><issn>1935-2727</issn><eissn>1935-2735</eissn><abstract>The implications of the gut microbial communities in the immune response against parasites and gut motility could explain the differences in clinical manifestations and treatment responses found in patients with chronic Chagas disease.
In this pilot prospective cross-sectional study, we included 80 participants: 29 with indeterminate CD (ICD), 16 with cardiac CD (CCD), 15 with digestive CD (DCD), and 20 controls without CD. Stool was collected at the baseline visit and faecal microbial community structure DNA was analyzed by whole genome sequencing. We also performed a comprehensive dietary analysis. Ninety per cent (72/80) of subjects were of Bolivian origin with a median age of 47 years (IQR 39-54) and 48.3% (29/60) had received benznidazole treatment. There were no substantial differences in dietary habits between patients with CD and controls. We identified that the presence or absence of CD explained 5% of the observed microbiota variability. Subjects with CD exhibited consistent enrichment of Parabacteroides spp, while for Enterococcus hirae, Lactobacillus buchneri and Megamonas spp, the effect was less clear once excluded the outliers values. Sex, type of visceral involvement and previous treatment with benznidazole did not appear to have a confounding effect on gut microbiota structure. We also found that patients with DCD showed consistent Prevotella spp enrichment.
We found a detectable effect of Chagas disease on overall microbiota structure with several potential disease biomarkers, which warrants further research in this field. The analysis of bacterial diversity could prove to be a viable target to improve the prognosis of this prevalent and neglected disease.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>37478160</pmid><doi>10.1371/journal.pntd.0011490</doi><orcidid>https://orcid.org/0000-0001-8735-4124</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central Open Access; Public Library of Science (PLoS) Journals Open Access; PubMed Central |
subjects | Adult Adults Benznidazole Biology and Life Sciences Biomarkers Chagas disease Chagas Disease - drug therapy Chronic infection Community structure Complications and side effects Congenital diseases Cross-Sectional Studies Defence mechanisms Denervation Deoxyribonucleic acid Development and progression Diet Digestive system Digestive tract Discriminant analysis DNA DNA structure Dysbiosis Esophagus Feces Gastric motility Gastrointestinal Microbiome - genetics Gastrointestinal tract Gene sequencing Genomes Health aspects Health services Humans Immune response Immunity Infections Intestinal flora Intestinal microflora Medicine and Health Sciences Microbial activity Microbiomes Microbiota Microbiota (Symbiotic organisms) Microorganisms Middle Aged Motility Outliers (statistics) Parasites Patients Persistent Infection Prospective Studies Protozoa Quality control Recipes Risk factors Software Taxonomy Tropical diseases Vector-borne diseases Veganism Whole genome sequencing |
title | Chagas disease is related to structural changes of the gut microbiota in adults with chronic infection (TRIPOBIOME Study) |
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