Research Note: Snapshot of the transcriptome via RNA sequencing in the ileum of broiler chickens fed subtherapeutic concentrations of avilamycin.


Journal

Poultry science
ISSN: 1525-3171
Titre abrégé: Poult Sci
Pays: England
ID NLM: 0401150

Informations de publication

Date de publication:
Feb 2021
Historique:
received: 13 07 2020
revised: 05 11 2020
accepted: 09 11 2020
entrez: 1 2 2021
pubmed: 2 2 2021
medline: 8 5 2021
Statut: ppublish

Résumé

Antibiotics have played a critical role in sustaining and improving livestock production in the past decades, but the emergence of antimicrobial resistance has led several countries to ban or limit their use. Since then, in-feed alternatives have gained a lot of attention but the development of efficacious alternatives implies a better understanding of the mode of action of antibiotic growth promoters (AGP) when administered at subtherapeutic concentrations. In the present study, 120 broiler chickens per group (8 pens/group) were fed for 35 d with either basal feed (control group) or feed supplemented with avilamycin (AGP group; 10 g/1,000 kg of feed). At the end of the trial, the ileum from the small intestine of 5 birds per group was sampled, and RNA were isolated for profiling their transcriptome via RNA sequencing (RNA-Seq). As expected, the growth of chickens in the AGP group was significantly higher than in the control group. Overall, 66 differentially expressed genes (false discovery rate ≤ 0.05 and fold change ≥ 2 or ≤ -2) were found in the ileum of chickens fed avilamycin in comparison with the control group. The functional analysis showed reduced activity of genes related to signaling by interleukins, with IL-22, SOCS3, and certain antimicrobial peptides found multiple times in these pathways in the AGP group at day 35. In addition, higher activity was predicted in a module of genes related to lipid metabolism and transport in the avilamycin group. The use of RNA-Seq allowed a snapshot of the whole transcriptome at day 35 and aimed at delivering additional data on the host-centric hypothesis regarding the mode of action of AGP (i.e. immunomodulation, reduction of the immunological stress).

Identifiants

pubmed: 33518154
pii: S0032-5791(20)30858-0
doi: 10.1016/j.psj.2020.11.012
pmc: PMC7858091
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Oligosaccharides 0
avilamycin 720WDX56D3

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

998-1003

Informations de copyright

Copyright © 2020. Published by Elsevier Inc.

Références

Poult Sci. 2007 Nov;86(11):2466-71
pubmed: 17954599
Mucosal Immunol. 2008 Sep;1(5):335-8
pubmed: 19079197
Appl Microbiol Biotechnol. 2017 Jun;101(11):4547-4559
pubmed: 28243710
Poult Sci. 2007 Apr;86(4):605-9
pubmed: 17369528
Cytokine. 2012 Dec;60(3):815-27
pubmed: 22980486
Gut Pathog. 2011 Sep 25;3(1):14
pubmed: 21943280
Int J Antimicrob Agents. 2017 Jan;49(1):12-24
pubmed: 27717740
Poult Sci. 2018 Mar 1;97(3):970-979
pubmed: 29253227
J Nutr. 2004 Jun;134(6):1487-92
pubmed: 15173416

Auteurs

Silvia Fibi-Smetana (S)

BIOMIN Research Center, BIOMIN Holding GmbH, 3430 Tulln, Austria.

Candida Vaz (C)

Bioinformatics Institute, Agency for Science Technology and Research (A∗STAR), Singapore 138671.

Jeremy Le Coz (J)

BIOMIN Research Center, BIOMIN Holding GmbH, 3430 Tulln, Austria.

Suzana Ilic (S)

BIOMIN Research Center, BIOMIN Holding GmbH, 3430 Tulln, Austria.

Roger Berrios (R)

BIOMIN Holding GmbH, Erber Campus 1, 3131 Getzersdorf, Austria.

Gerd Schatzmayr (G)

BIOMIN Research Center, BIOMIN Holding GmbH, 3430 Tulln, Austria.

Vivek Tanavde (V)

Bioinformatics Institute, Agency for Science Technology and Research (A∗STAR), Singapore 138671.

Bertrand Grenier (B)

BIOMIN Research Center, BIOMIN Holding GmbH, 3430 Tulln, Austria. Electronic address: bertrand.grenier@biomin.net.

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Classifications MeSH