Cargando…

Fumonisin-Exposure Impairs Age-Related Ecological Succession of Bacterial Species in Weaned Pig Gut Microbiota

Pigs are highly affected by dietary mycotoxin contamination and particularly by fumonisin. The effects of fumonisin on pig intestinal health are well documented, but little is known regarding its impact on gut microbiota. We investigate the effects of the fumonisin (FB1, 12 mg/kg feed) on the fecal...

Descripción completa

Detalles Bibliográficos
Autores principales: Mateos, Ivan, Combes, Sylvie, Pascal, Géraldine, Cauquil, Laurent, Barilly, Céline, Cossalter, Anne-Marie, Laffitte, Joëlle, Botti, Sara, Pinton, Philippe, Oswald, Isabelle P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6024561/
https://www.ncbi.nlm.nih.gov/pubmed/29874877
http://dx.doi.org/10.3390/toxins10060230
_version_ 1783336082165727232
author Mateos, Ivan
Combes, Sylvie
Pascal, Géraldine
Cauquil, Laurent
Barilly, Céline
Cossalter, Anne-Marie
Laffitte, Joëlle
Botti, Sara
Pinton, Philippe
Oswald, Isabelle P.
author_facet Mateos, Ivan
Combes, Sylvie
Pascal, Géraldine
Cauquil, Laurent
Barilly, Céline
Cossalter, Anne-Marie
Laffitte, Joëlle
Botti, Sara
Pinton, Philippe
Oswald, Isabelle P.
author_sort Mateos, Ivan
collection PubMed
description Pigs are highly affected by dietary mycotoxin contamination and particularly by fumonisin. The effects of fumonisin on pig intestinal health are well documented, but little is known regarding its impact on gut microbiota. We investigate the effects of the fumonisin (FB1, 12 mg/kg feed) on the fecal microbiota of piglets (n = 6) after 0, 8, 15, 22, and 29 days of exposure. A control group of six piglets received a diet free of FB1. Bacterial community diversity, structure and taxonomic composition were carried out by V3–V4 16S rRNA gene sequencing. Exposure to FB1 decreases the diversity index, and shifts and constrains the structure and the composition of the bacterial community. This takes place as early as after 15 days of exposure and is at a maximum after 22 days of exposure. Compared to control, FB1 alters the ecological succession of fecal microbiota species toward higher levels of Lactobacillus and lower levels of the Lachnospiraceae and Veillonellaceae families, and particularly OTUs (Operational Taxonomic Units) of the genera Mitsuokella, Faecalibacterium and Roseburia. In conclusion, FB1 shifts and constrains age-related evolution of microbiota. The direct or indirect contribution of FB1 microbiota alteration in the global host response to FB1 toxicity remains to be investigated.
format Online
Article
Text
id pubmed-6024561
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-60245612018-07-09 Fumonisin-Exposure Impairs Age-Related Ecological Succession of Bacterial Species in Weaned Pig Gut Microbiota Mateos, Ivan Combes, Sylvie Pascal, Géraldine Cauquil, Laurent Barilly, Céline Cossalter, Anne-Marie Laffitte, Joëlle Botti, Sara Pinton, Philippe Oswald, Isabelle P. Toxins (Basel) Article Pigs are highly affected by dietary mycotoxin contamination and particularly by fumonisin. The effects of fumonisin on pig intestinal health are well documented, but little is known regarding its impact on gut microbiota. We investigate the effects of the fumonisin (FB1, 12 mg/kg feed) on the fecal microbiota of piglets (n = 6) after 0, 8, 15, 22, and 29 days of exposure. A control group of six piglets received a diet free of FB1. Bacterial community diversity, structure and taxonomic composition were carried out by V3–V4 16S rRNA gene sequencing. Exposure to FB1 decreases the diversity index, and shifts and constrains the structure and the composition of the bacterial community. This takes place as early as after 15 days of exposure and is at a maximum after 22 days of exposure. Compared to control, FB1 alters the ecological succession of fecal microbiota species toward higher levels of Lactobacillus and lower levels of the Lachnospiraceae and Veillonellaceae families, and particularly OTUs (Operational Taxonomic Units) of the genera Mitsuokella, Faecalibacterium and Roseburia. In conclusion, FB1 shifts and constrains age-related evolution of microbiota. The direct or indirect contribution of FB1 microbiota alteration in the global host response to FB1 toxicity remains to be investigated. MDPI 2018-06-05 /pmc/articles/PMC6024561/ /pubmed/29874877 http://dx.doi.org/10.3390/toxins10060230 Text en © 2018 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
Mateos, Ivan
Combes, Sylvie
Pascal, Géraldine
Cauquil, Laurent
Barilly, Céline
Cossalter, Anne-Marie
Laffitte, Joëlle
Botti, Sara
Pinton, Philippe
Oswald, Isabelle P.
Fumonisin-Exposure Impairs Age-Related Ecological Succession of Bacterial Species in Weaned Pig Gut Microbiota
title Fumonisin-Exposure Impairs Age-Related Ecological Succession of Bacterial Species in Weaned Pig Gut Microbiota
title_full Fumonisin-Exposure Impairs Age-Related Ecological Succession of Bacterial Species in Weaned Pig Gut Microbiota
title_fullStr Fumonisin-Exposure Impairs Age-Related Ecological Succession of Bacterial Species in Weaned Pig Gut Microbiota
title_full_unstemmed Fumonisin-Exposure Impairs Age-Related Ecological Succession of Bacterial Species in Weaned Pig Gut Microbiota
title_short Fumonisin-Exposure Impairs Age-Related Ecological Succession of Bacterial Species in Weaned Pig Gut Microbiota
title_sort fumonisin-exposure impairs age-related ecological succession of bacterial species in weaned pig gut microbiota
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6024561/
https://www.ncbi.nlm.nih.gov/pubmed/29874877
http://dx.doi.org/10.3390/toxins10060230
work_keys_str_mv AT mateosivan fumonisinexposureimpairsagerelatedecologicalsuccessionofbacterialspeciesinweanedpiggutmicrobiota
AT combessylvie fumonisinexposureimpairsagerelatedecologicalsuccessionofbacterialspeciesinweanedpiggutmicrobiota
AT pascalgeraldine fumonisinexposureimpairsagerelatedecologicalsuccessionofbacterialspeciesinweanedpiggutmicrobiota
AT cauquillaurent fumonisinexposureimpairsagerelatedecologicalsuccessionofbacterialspeciesinweanedpiggutmicrobiota
AT barillyceline fumonisinexposureimpairsagerelatedecologicalsuccessionofbacterialspeciesinweanedpiggutmicrobiota
AT cossalterannemarie fumonisinexposureimpairsagerelatedecologicalsuccessionofbacterialspeciesinweanedpiggutmicrobiota
AT laffittejoelle fumonisinexposureimpairsagerelatedecologicalsuccessionofbacterialspeciesinweanedpiggutmicrobiota
AT bottisara fumonisinexposureimpairsagerelatedecologicalsuccessionofbacterialspeciesinweanedpiggutmicrobiota
AT pintonphilippe fumonisinexposureimpairsagerelatedecologicalsuccessionofbacterialspeciesinweanedpiggutmicrobiota
AT oswaldisabellep fumonisinexposureimpairsagerelatedecologicalsuccessionofbacterialspeciesinweanedpiggutmicrobiota