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The Bacterial Gut Microbiota of Adult Patients Infected, Colonized or Noncolonized by Clostridioides difficile

Gut microbiota composition in patients with Clostridioides difficile colonization is not well investigated. We aimed to identify bacterial signatures associated with resistance and susceptibility to C. difficile colonization (CDC) and infection (CDI). Therefore, gut microbiota composition from patie...

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Autores principales: Crobach, Monique J. T., Ducarmon, Quinten R., Terveer, Elisabeth M., Harmanus, Celine, Sanders, Ingrid M. J. G., Verduin, Kees M., Kuijper, Ed J., Zwittink, Romy D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7284656/
https://www.ncbi.nlm.nih.gov/pubmed/32384826
http://dx.doi.org/10.3390/microorganisms8050677
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author Crobach, Monique J. T.
Ducarmon, Quinten R.
Terveer, Elisabeth M.
Harmanus, Celine
Sanders, Ingrid M. J. G.
Verduin, Kees M.
Kuijper, Ed J.
Zwittink, Romy D.
author_facet Crobach, Monique J. T.
Ducarmon, Quinten R.
Terveer, Elisabeth M.
Harmanus, Celine
Sanders, Ingrid M. J. G.
Verduin, Kees M.
Kuijper, Ed J.
Zwittink, Romy D.
author_sort Crobach, Monique J. T.
collection PubMed
description Gut microbiota composition in patients with Clostridioides difficile colonization is not well investigated. We aimed to identify bacterial signatures associated with resistance and susceptibility to C. difficile colonization (CDC) and infection (CDI). Therefore, gut microbiota composition from patients with CDC (n = 41), with CDI (n = 41), and without CDC (controls, n = 43) was determined through 16S rRNA gene amplicon sequencing. Bacterial diversity was decreased in CDC and CDI patients (p < 0.01). Overall microbiota composition was significantly different between control, CDC, and CDI patients (p = 0.001). Relative abundance of Clostridioides (most likely C. difficile) increased stepwise from controls to CDC and CDI patients. In addition, differential abundance analysis revealed that CDI patients’ gut microbiota was characterized by significantly higher relative abundance of Bacteroides and Veillonella than CDC patients and controls. Control patients had significantly higher Eubacterium hallii and Fusicatenibacter abundance than colonized patients. Network analysis indicated that Fusicatenibacter was negatively associated with Clostridioides in CDI patients, while Veillonella was positively associated with Clostridioides in CDC patients. Bacterial microbiota diversity decreased in both CDC and CDI patients, but harbored a distinct microbiota. Eubacterium hallii and Fusicatenibacter may indicate resistance against C. difficile colonization and subsequent infection, while Veillonella may indicate susceptibility to colonization and infection by C. difficile.
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spelling pubmed-72846562020-06-15 The Bacterial Gut Microbiota of Adult Patients Infected, Colonized or Noncolonized by Clostridioides difficile Crobach, Monique J. T. Ducarmon, Quinten R. Terveer, Elisabeth M. Harmanus, Celine Sanders, Ingrid M. J. G. Verduin, Kees M. Kuijper, Ed J. Zwittink, Romy D. Microorganisms Article Gut microbiota composition in patients with Clostridioides difficile colonization is not well investigated. We aimed to identify bacterial signatures associated with resistance and susceptibility to C. difficile colonization (CDC) and infection (CDI). Therefore, gut microbiota composition from patients with CDC (n = 41), with CDI (n = 41), and without CDC (controls, n = 43) was determined through 16S rRNA gene amplicon sequencing. Bacterial diversity was decreased in CDC and CDI patients (p < 0.01). Overall microbiota composition was significantly different between control, CDC, and CDI patients (p = 0.001). Relative abundance of Clostridioides (most likely C. difficile) increased stepwise from controls to CDC and CDI patients. In addition, differential abundance analysis revealed that CDI patients’ gut microbiota was characterized by significantly higher relative abundance of Bacteroides and Veillonella than CDC patients and controls. Control patients had significantly higher Eubacterium hallii and Fusicatenibacter abundance than colonized patients. Network analysis indicated that Fusicatenibacter was negatively associated with Clostridioides in CDI patients, while Veillonella was positively associated with Clostridioides in CDC patients. Bacterial microbiota diversity decreased in both CDC and CDI patients, but harbored a distinct microbiota. Eubacterium hallii and Fusicatenibacter may indicate resistance against C. difficile colonization and subsequent infection, while Veillonella may indicate susceptibility to colonization and infection by C. difficile. MDPI 2020-05-06 /pmc/articles/PMC7284656/ /pubmed/32384826 http://dx.doi.org/10.3390/microorganisms8050677 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Crobach, Monique J. T.
Ducarmon, Quinten R.
Terveer, Elisabeth M.
Harmanus, Celine
Sanders, Ingrid M. J. G.
Verduin, Kees M.
Kuijper, Ed J.
Zwittink, Romy D.
The Bacterial Gut Microbiota of Adult Patients Infected, Colonized or Noncolonized by Clostridioides difficile
title The Bacterial Gut Microbiota of Adult Patients Infected, Colonized or Noncolonized by Clostridioides difficile
title_full The Bacterial Gut Microbiota of Adult Patients Infected, Colonized or Noncolonized by Clostridioides difficile
title_fullStr The Bacterial Gut Microbiota of Adult Patients Infected, Colonized or Noncolonized by Clostridioides difficile
title_full_unstemmed The Bacterial Gut Microbiota of Adult Patients Infected, Colonized or Noncolonized by Clostridioides difficile
title_short The Bacterial Gut Microbiota of Adult Patients Infected, Colonized or Noncolonized by Clostridioides difficile
title_sort bacterial gut microbiota of adult patients infected, colonized or noncolonized by clostridioides difficile
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7284656/
https://www.ncbi.nlm.nih.gov/pubmed/32384826
http://dx.doi.org/10.3390/microorganisms8050677
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