Cargando…

Successional Dynamics in the Gut Microbiome Determine the Success of Clostridium difficile Infection in Adult Pig Models

Clostridium difficile infections (CDI) are a major cause of antibiotic-associated diarrhea. It is hypothesized that CDI develops due to the antibiotic-induced disruption of the intestinal microbial community structure, which allows C. difficile to flourish. Here, we pre-treated weaned pigs with the...

Descripción completa

Detalles Bibliográficos
Autores principales: Jurburg, Stephanie D., Cornelissen, Jan J. B. W. J., de Boer, Paulo, Smits, Mari A., Rebel, Johanna M. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6691177/
https://www.ncbi.nlm.nih.gov/pubmed/31448240
http://dx.doi.org/10.3389/fcimb.2019.00271
_version_ 1783443311702310912
author Jurburg, Stephanie D.
Cornelissen, Jan J. B. W. J.
de Boer, Paulo
Smits, Mari A.
Rebel, Johanna M. J.
author_facet Jurburg, Stephanie D.
Cornelissen, Jan J. B. W. J.
de Boer, Paulo
Smits, Mari A.
Rebel, Johanna M. J.
author_sort Jurburg, Stephanie D.
collection PubMed
description Clostridium difficile infections (CDI) are a major cause of antibiotic-associated diarrhea. It is hypothesized that CDI develops due to the antibiotic-induced disruption of the intestinal microbial community structure, which allows C. difficile to flourish. Here, we pre-treated weaned pigs with the antibiotics Clindamycin or Ciprofloxacin for 1 day, and subsequently inoculated them with a human and pig enteropathogenic C. difficile strain 078 spores. Body temperature, clinical signs of disease, and the fecal microbiome were monitored daily for 15 days. Clindamycin had a stronger effect on the pigs than Ciprofloxacin, resulting in drastic shifts in the fecal microbiome, decreases in microbial diversity and significant increases in body temperature, even in the absence of C. difficile. Fecal shedding of C. difficile was detectable for 3 and 9 days in Ciprofloxacin and Clindamycin treated pigs inoculated with C. difficile, respectively, and in both cases decreased cell proliferation rates were detected in colon tissue. The timing of C. difficile shedding coincided with the decrease in a large cluster of Firmicutes following Clindamycin treatment, a pattern which was also independent of C. difficile inoculation. The observed community patterns suggest that successional dynamics following antibiotic treatment facilitate C. difficile establishment. The similarities between the microbiome responses observed in our study and those previously reported in CDI-infected humans further support the utility of adult pigs as models for the study of CDI.
format Online
Article
Text
id pubmed-6691177
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-66911772019-08-23 Successional Dynamics in the Gut Microbiome Determine the Success of Clostridium difficile Infection in Adult Pig Models Jurburg, Stephanie D. Cornelissen, Jan J. B. W. J. de Boer, Paulo Smits, Mari A. Rebel, Johanna M. J. Front Cell Infect Microbiol Cellular and Infection Microbiology Clostridium difficile infections (CDI) are a major cause of antibiotic-associated diarrhea. It is hypothesized that CDI develops due to the antibiotic-induced disruption of the intestinal microbial community structure, which allows C. difficile to flourish. Here, we pre-treated weaned pigs with the antibiotics Clindamycin or Ciprofloxacin for 1 day, and subsequently inoculated them with a human and pig enteropathogenic C. difficile strain 078 spores. Body temperature, clinical signs of disease, and the fecal microbiome were monitored daily for 15 days. Clindamycin had a stronger effect on the pigs than Ciprofloxacin, resulting in drastic shifts in the fecal microbiome, decreases in microbial diversity and significant increases in body temperature, even in the absence of C. difficile. Fecal shedding of C. difficile was detectable for 3 and 9 days in Ciprofloxacin and Clindamycin treated pigs inoculated with C. difficile, respectively, and in both cases decreased cell proliferation rates were detected in colon tissue. The timing of C. difficile shedding coincided with the decrease in a large cluster of Firmicutes following Clindamycin treatment, a pattern which was also independent of C. difficile inoculation. The observed community patterns suggest that successional dynamics following antibiotic treatment facilitate C. difficile establishment. The similarities between the microbiome responses observed in our study and those previously reported in CDI-infected humans further support the utility of adult pigs as models for the study of CDI. Frontiers Media S.A. 2019-08-06 /pmc/articles/PMC6691177/ /pubmed/31448240 http://dx.doi.org/10.3389/fcimb.2019.00271 Text en Copyright © 2019 Jurburg, Cornelissen, de Boer, Smits and Rebel. http://creativecommons.org/licenses/by/4.0/ 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.
spellingShingle Cellular and Infection Microbiology
Jurburg, Stephanie D.
Cornelissen, Jan J. B. W. J.
de Boer, Paulo
Smits, Mari A.
Rebel, Johanna M. J.
Successional Dynamics in the Gut Microbiome Determine the Success of Clostridium difficile Infection in Adult Pig Models
title Successional Dynamics in the Gut Microbiome Determine the Success of Clostridium difficile Infection in Adult Pig Models
title_full Successional Dynamics in the Gut Microbiome Determine the Success of Clostridium difficile Infection in Adult Pig Models
title_fullStr Successional Dynamics in the Gut Microbiome Determine the Success of Clostridium difficile Infection in Adult Pig Models
title_full_unstemmed Successional Dynamics in the Gut Microbiome Determine the Success of Clostridium difficile Infection in Adult Pig Models
title_short Successional Dynamics in the Gut Microbiome Determine the Success of Clostridium difficile Infection in Adult Pig Models
title_sort successional dynamics in the gut microbiome determine the success of clostridium difficile infection in adult pig models
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6691177/
https://www.ncbi.nlm.nih.gov/pubmed/31448240
http://dx.doi.org/10.3389/fcimb.2019.00271
work_keys_str_mv AT jurburgstephanied successionaldynamicsinthegutmicrobiomedeterminethesuccessofclostridiumdifficileinfectioninadultpigmodels
AT cornelissenjanjbwj successionaldynamicsinthegutmicrobiomedeterminethesuccessofclostridiumdifficileinfectioninadultpigmodels
AT deboerpaulo successionaldynamicsinthegutmicrobiomedeterminethesuccessofclostridiumdifficileinfectioninadultpigmodels
AT smitsmaria successionaldynamicsinthegutmicrobiomedeterminethesuccessofclostridiumdifficileinfectioninadultpigmodels
AT rebeljohannamj successionaldynamicsinthegutmicrobiomedeterminethesuccessofclostridiumdifficileinfectioninadultpigmodels