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
Hauptverfasser: 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
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container_title PLoS neglected tropical diseases
container_volume 17
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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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 diseases</topic><topic>Cross-Sectional Studies</topic><topic>Defence mechanisms</topic><topic>Denervation</topic><topic>Deoxyribonucleic acid</topic><topic>Development and progression</topic><topic>Diet</topic><topic>Digestive system</topic><topic>Digestive tract</topic><topic>Discriminant analysis</topic><topic>DNA</topic><topic>DNA structure</topic><topic>Dysbiosis</topic><topic>Esophagus</topic><topic>Feces</topic><topic>Gastric motility</topic><topic>Gastrointestinal Microbiome - genetics</topic><topic>Gastrointestinal tract</topic><topic>Gene sequencing</topic><topic>Genomes</topic><topic>Health aspects</topic><topic>Health services</topic><topic>Humans</topic><topic>Immune response</topic><topic>Immunity</topic><topic>Infections</topic><topic>Intestinal flora</topic><topic>Intestinal microflora</topic><topic>Medicine and Health Sciences</topic><topic>Microbial activity</topic><topic>Microbiomes</topic><topic>Microbiota</topic><topic>Microbiota (Symbiotic organisms)</topic><topic>Microorganisms</topic><topic>Middle Aged</topic><topic>Motility</topic><topic>Outliers (statistics)</topic><topic>Parasites</topic><topic>Patients</topic><topic>Persistent Infection</topic><topic>Prospective Studies</topic><topic>Protozoa</topic><topic>Quality control</topic><topic>Recipes</topic><topic>Risk factors</topic><topic>Software</topic><topic>Taxonomy</topic><topic>Tropical diseases</topic><topic>Vector-borne diseases</topic><topic>Veganism</topic><topic>Whole genome sequencing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; 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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. 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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
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title Chagas disease is related to structural changes of the gut microbiota in adults with chronic infection (TRIPOBIOME Study)
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