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Bacteriome and Mycobiome Interactions Underscore Microbial Dysbiosis in Familial Crohn’s Disease
by
Vermeire, S.
, Sendid, B.
, Ghannoum, M. A.
, Poulain, D.
, Hoarau, G.
, Fujioka, H.
, Clemente, J.
, Colombel, J. F.
, Mukherjee, P. K.
, Retuerto, M. A.
, Chandra, J.
, Neut, C.
, Hager, C.
, Gower-Rousseau, C.
in
Abundance
/ Adult
/ Antibodies
/ Bacteria
/ Biofilms
/ Biofilms - growth & development
/ Biomarkers
/ Candida tropicalis
/ Candida tropicalis - isolation & purification
/ Crohn Disease - genetics
/ Crohn Disease - microbiology
/ Crohn's disease
/ Demographics
/ Dysbacteriosis
/ Dysbiosis - microbiology
/ E coli
/ Escherichia coli
/ Escherichia coli - isolation & purification
/ Feces - microbiology
/ Female
/ Fimbriae, Bacterial
/ France
/ Gastrointestinal Microbiome
/ Genetic factors
/ Healthy Volunteers
/ Humans
/ Hyphae
/ Hyphae - isolation & purification
/ Male
/ Microbial Interactions
/ Microbiota
/ Middle Aged
/ Mycobiome
/ Patients
/ Pili
/ Saccharomyces cerevisiae
/ Saccharomyces cerevisiae - immunology
/ Serratia marcescens
/ Serratia marcescens - isolation & purification
/ Small intestine
/ Species
/ Yeast
2016
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Bacteriome and Mycobiome Interactions Underscore Microbial Dysbiosis in Familial Crohn’s Disease
by
Vermeire, S.
, Sendid, B.
, Ghannoum, M. A.
, Poulain, D.
, Hoarau, G.
, Fujioka, H.
, Clemente, J.
, Colombel, J. F.
, Mukherjee, P. K.
, Retuerto, M. A.
, Chandra, J.
, Neut, C.
, Hager, C.
, Gower-Rousseau, C.
in
Abundance
/ Adult
/ Antibodies
/ Bacteria
/ Biofilms
/ Biofilms - growth & development
/ Biomarkers
/ Candida tropicalis
/ Candida tropicalis - isolation & purification
/ Crohn Disease - genetics
/ Crohn Disease - microbiology
/ Crohn's disease
/ Demographics
/ Dysbacteriosis
/ Dysbiosis - microbiology
/ E coli
/ Escherichia coli
/ Escherichia coli - isolation & purification
/ Feces - microbiology
/ Female
/ Fimbriae, Bacterial
/ France
/ Gastrointestinal Microbiome
/ Genetic factors
/ Healthy Volunteers
/ Humans
/ Hyphae
/ Hyphae - isolation & purification
/ Male
/ Microbial Interactions
/ Microbiota
/ Middle Aged
/ Mycobiome
/ Patients
/ Pili
/ Saccharomyces cerevisiae
/ Saccharomyces cerevisiae - immunology
/ Serratia marcescens
/ Serratia marcescens - isolation & purification
/ Small intestine
/ Species
/ Yeast
2016
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Bacteriome and Mycobiome Interactions Underscore Microbial Dysbiosis in Familial Crohn’s Disease
by
Vermeire, S.
, Sendid, B.
, Ghannoum, M. A.
, Poulain, D.
, Hoarau, G.
, Fujioka, H.
, Clemente, J.
, Colombel, J. F.
, Mukherjee, P. K.
, Retuerto, M. A.
, Chandra, J.
, Neut, C.
, Hager, C.
, Gower-Rousseau, C.
in
Abundance
/ Adult
/ Antibodies
/ Bacteria
/ Biofilms
/ Biofilms - growth & development
/ Biomarkers
/ Candida tropicalis
/ Candida tropicalis - isolation & purification
/ Crohn Disease - genetics
/ Crohn Disease - microbiology
/ Crohn's disease
/ Demographics
/ Dysbacteriosis
/ Dysbiosis - microbiology
/ E coli
/ Escherichia coli
/ Escherichia coli - isolation & purification
/ Feces - microbiology
/ Female
/ Fimbriae, Bacterial
/ France
/ Gastrointestinal Microbiome
/ Genetic factors
/ Healthy Volunteers
/ Humans
/ Hyphae
/ Hyphae - isolation & purification
/ Male
/ Microbial Interactions
/ Microbiota
/ Middle Aged
/ Mycobiome
/ Patients
/ Pili
/ Saccharomyces cerevisiae
/ Saccharomyces cerevisiae - immunology
/ Serratia marcescens
/ Serratia marcescens - isolation & purification
/ Small intestine
/ Species
/ Yeast
2016
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Bacteriome and Mycobiome Interactions Underscore Microbial Dysbiosis in Familial Crohn’s Disease
Journal Article
Bacteriome and Mycobiome Interactions Underscore Microbial Dysbiosis in Familial Crohn’s Disease
2016
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Overview
Crohn’s disease (CD) results from a complex interplay between host genetic factors and endogenous microbial communities. In the current study, we used Ion Torrent sequencing to characterize the gut bacterial microbiota (bacteriome) and fungal community (mycobiome) in patients with CD and their nondiseased first-degree relatives (NCDR) in 9 familial clusters living in northern France-Belgium and in healthy individuals from 4 families living in the same area (non-CD unrelated [NCDU]). Principal component, diversity, and abundance analyses were conducted, and CD-associated inter- and intrakingdom microbial correlations were determined. Significant microbial interactions were identified and validated using single- and mixed-species biofilms. CD and NCDR groups clustered together in the mycobiome but not in the bacteriome. Microbiotas of familial (CD and NCDR) samples were distinct from those of nonfamilial (NCDU) samples. The abundance of Serratia marcescens and Escherichia coli was elevated in CD patients, while that of beneficial bacteria was decreased. The abundance of the fungus Candida tropicalis was significantly higher in CD than in NCDR ( P = 0.003) samples and positively correlated with levels of anti- Saccharomyces cerevisiae antibodies (ASCA). The abundance of C. tropicalis was positively correlated with S. marcescens and E. coli , suggesting that these organisms interact in the gut. The mass and thickness of triple-species ( C. tropicalis plus S. marcescens plus E. coli ) biofilm were significantly greater than those of single- and double-species biofilms. C. tropicalis biofilms comprised blastospores, while double- and triple-species biofilms were enriched in hyphae. S. marcescens used fimbriae to coaggregate or attach with C. tropicalis / E. coli , while E. coli was closely apposed with C. tropicalis . Specific interkingdom microbial interactions may be key determinants in CD. IMPORTANCE Here, we characterized the gut bacterial microbiota (bacteriome) and fungal community (mycobiome) in multiplex families with CD and healthy relatives and defined the microbial interactions leading to dysbiosis in CD. We identified fungal ( Candida tropicalis ) and bacterial ( Serratia marcescens and Escherichia coli ) species that are associated with CD dysbiosis. Additionally, we found that the level of anti- Saccharomyces cerevisiae antibodies (ASCA; a known CD biomarker) was associated with the abundance of C. tropicalis . We also identified positive interkingdom correlations between C. tropicalis , E. coli , and S. marcescens in CD patients and validated these correlations using in vitro biofilms. These results provide insight into the roles of bacteria and fungi in CD and may lead to the development of novel treatment approaches and diagnostic assays. Here, we characterized the gut bacterial microbiota (bacteriome) and fungal community (mycobiome) in multiplex families with CD and healthy relatives and defined the microbial interactions leading to dysbiosis in CD. We identified fungal ( Candida tropicalis ) and bacterial ( Serratia marcescens and Escherichia coli ) species that are associated with CD dysbiosis. Additionally, we found that the level of anti- Saccharomyces cerevisiae antibodies (ASCA; a known CD biomarker) was associated with the abundance of C. tropicalis . We also identified positive interkingdom correlations between C. tropicalis , E. coli , and S. marcescens in CD patients and validated these correlations using in vitro biofilms. These results provide insight into the roles of bacteria and fungi in CD and may lead to the development of novel treatment approaches and diagnostic assays.
Publisher
American Society for Microbiology
Subject
/ Adult
/ Bacteria
/ Biofilms
/ Biofilms - growth & development
/ Candida tropicalis - isolation & purification
/ Crohn Disease - microbiology
/ E coli
/ Escherichia coli - isolation & purification
/ Female
/ France
/ Humans
/ Hyphae
/ Hyphae - isolation & purification
/ Male
/ Patients
/ Pili
/ Saccharomyces cerevisiae - immunology
/ Serratia marcescens - isolation & purification
/ Species
/ Yeast
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