Impact of an oligosaccharide-based polymer on the metabolic profiles and microbial ecology of weanling pigs experimentally infected with a pathogenic E. coli.

Carbadox Colon microbiota Enterotoxigenic E. coli F18 Metabolomics Oligosaccharide-based polymer Weaned pigs

Journal

Journal of animal science and biotechnology
ISSN: 1674-9782
Titre abrégé: J Anim Sci Biotechnol
Pays: England
ID NLM: 101581293

Informations de publication

Date de publication:
02 Jan 2024
Historique:
received: 18 07 2023
accepted: 29 10 2023
medline: 4 1 2024
pubmed: 4 1 2024
entrez: 3 1 2024
Statut: epublish

Résumé

Our previous study has reported that supplementation of oligosaccharide-based polymer enhances gut health and disease resistance of pigs infected with enterotoxigenic E. coli (ETEC) F18 in a manner similar to carbadox. The objective of this study was to investigate the impacts of oligosaccharide-based polymer or antibiotic on the host metabolic profiles and colon microbiota of weaned pigs experimentally infected with ETEC F18. Multivariate analysis highlighted the differences in the metabolic profiles of serum and colon digesta which were predominantly found between pigs supplemented with oligosaccharide-based polymer and antibiotic. The relative abundance of metabolic markers of immune responses and nutrient metabolisms, such as amino acids and carbohydrates, were significantly differentiated between the oligosaccharide-based polymer and antibiotic groups (q < 0.2 and fold change > 2.0). In addition, pigs in antibiotic had a reduced (P < 0.05) relative abundance of Lachnospiraceae and Lactobacillaceae, whereas had greater (P < 0.05) Clostridiaceae and Streptococcaceae in the colon digesta on d 11 post-inoculation (PI) compared with d 5 PI. The impact of oligosaccharide-based polymer on the metabolic and microbial profiles of pigs is not fully understood, and further exploration is needed. However, current research suggest that various mechanisms are involved in the enhanced disease resistance and performance in ETEC-challenged pigs by supplementing this polymer.

Sections du résumé

BACKGROUND BACKGROUND
Our previous study has reported that supplementation of oligosaccharide-based polymer enhances gut health and disease resistance of pigs infected with enterotoxigenic E. coli (ETEC) F18 in a manner similar to carbadox. The objective of this study was to investigate the impacts of oligosaccharide-based polymer or antibiotic on the host metabolic profiles and colon microbiota of weaned pigs experimentally infected with ETEC F18.
RESULTS RESULTS
Multivariate analysis highlighted the differences in the metabolic profiles of serum and colon digesta which were predominantly found between pigs supplemented with oligosaccharide-based polymer and antibiotic. The relative abundance of metabolic markers of immune responses and nutrient metabolisms, such as amino acids and carbohydrates, were significantly differentiated between the oligosaccharide-based polymer and antibiotic groups (q < 0.2 and fold change > 2.0). In addition, pigs in antibiotic had a reduced (P < 0.05) relative abundance of Lachnospiraceae and Lactobacillaceae, whereas had greater (P < 0.05) Clostridiaceae and Streptococcaceae in the colon digesta on d 11 post-inoculation (PI) compared with d 5 PI.
CONCLUSIONS CONCLUSIONS
The impact of oligosaccharide-based polymer on the metabolic and microbial profiles of pigs is not fully understood, and further exploration is needed. However, current research suggest that various mechanisms are involved in the enhanced disease resistance and performance in ETEC-challenged pigs by supplementing this polymer.

Identifiants

pubmed: 38169416
doi: 10.1186/s40104-023-00956-8
pii: 10.1186/s40104-023-00956-8
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1

Subventions

Organisme : National Institute of Food and Agriculture
ID : W4002 and NC1202

Informations de copyright

© 2024. The Author(s).

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Auteurs

Kwangwook Kim (K)

Department of Animal Science, University of California, Davis, CA, 95616, USA.
Present Affiliation: Department of Animal Science, Michigan State University, East Lansing, MI, 48824, USA.

Cynthia Jinno (C)

Department of Animal Science, University of California, Davis, CA, 95616, USA.
Present Affiliation: Cedars-Sinai Medical Center, Los Angeles, CA, 90084, USA.

Xunde Li (X)

School of Veterinary Medicine, University of California, Davis, CA, 95616, USA.

David Bravo (D)

Pancosma|ADM, 1180, Rolle, Switzerland.
Present Affiliation: Nutreco Exploration, Nutreco, The Netherlands.

Eric Cox (E)

Department of Virology, Parasitology and Immunology, Ghent University, 9000, Ghent, Belgium.

Peng Ji (P)

Department of Nutrition, University of California, Davis, CA, 95616, USA.

Yanhong Liu (Y)

Department of Animal Science, University of California, Davis, CA, 95616, USA. yahliu@ucdavis.edu.

Classifications MeSH