Broilers divergently selected for digestibility differ for their digestive microbial ecosystems.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 17 12 2019
accepted: 14 04 2020
entrez: 19 5 2020
pubmed: 19 5 2020
medline: 1 8 2020
Statut: epublish

Résumé

Improving the digestive efficiency of broiler chickens (Gallus gallus) could reduce organic waste, increase the use of alternative feed not used for human consumption and reduce the impact of feed in production costs. By selecting chicken lines divergently for their digestive efficiency, we showed previously that digestive efficiency is under genetic control and that the two resulting divergent lines, D+ (high digestive efficiency or "digestibility +") and D- (low digestive efficiency or "digestibility -"), also differ for the abundance of specific bacteria in their caeca. Here we perform a more extensive census of the bacteria present in the digestive microbiota of 60 chickens selected for their low apparent metabolizable energy corrected for nitrogen balance (AMEn-) or high (AMEn+) digestive efficiency in a [D+ x D-] F8 progeny of 200 individuals. We sequenced the 16S rRNA genes of the ileal, jejunal and caecal microbiotas, and compared the compositions and predicted functions of microbiotas from the different intestinal segments for 20 AMEn+ and 19 AMEn- birds. The intestinal segment of origin was the main factor structuring the samples. The caecal microbiota was the most impacted by the differences in digestive efficiency, with 41 bacterial species with abundances differing between highly and poorly efficient birds. Furthermore, we predicted that the caecal microbiota of efficient birds might be enriched in genes contributing to the degradation of short chain fatty acids (SCFA) from non-starch polysaccharides. These results confirm the impact of the genetic selection led on digestibility on the caecal microbiota taxonomic composition. They open the way toward the identification of specific, causal genes of the host controlling variations in the abundances of bacterial taxons.

Identifiants

pubmed: 32421690
doi: 10.1371/journal.pone.0232418
pii: PONE-D-19-34898
pmc: PMC7233591
doi:

Substances chimiques

RNA, Ribosomal, 16S 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0232418

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Références

PLoS One. 2015 Aug 12;10(8):e0135488
pubmed: 26267269
Appl Microbiol Biotechnol. 2014 May;98(10):4301-10
pubmed: 24643736
Poult Sci. 2004 Jun;83(6):860-7
pubmed: 15206610
Genet Sel Evol. 2015 Sep 25;47:74
pubmed: 26407557
Sci Rep. 2017 Mar 28;7:45308
pubmed: 28349946
Front Microbiol. 2016 Feb 19;7:187
pubmed: 26925052
Br Poult Sci. 2002 Jul;43(3):404-15
pubmed: 12195800
Poult Sci. 2018 Sep 1;97(9):3009-3014
pubmed: 29800328
Poult Sci. 2014 May;93(5):1245-50
pubmed: 24795318
Br Poult Sci. 1990 Sep;31(3):567-76
pubmed: 2245351
Front Microbiol. 2016 Sep 21;7:1416
pubmed: 27708624
Nat Methods. 2013 Jan;10(1):57-9
pubmed: 23202435
Int J Syst Evol Microbiol. 2008 Dec;58(Pt 12):2799-802
pubmed: 19060061
J Anim Sci. 2013 Feb;91(2):613-22
pubmed: 23243164
Genetics. 1995 Nov;141(3):1199-207
pubmed: 8582624
PLoS One. 2017 Nov 15;12(11):e0187766
pubmed: 29141016
BMC Genomics. 2015 May 28;16:418
pubmed: 26017153
PeerJ. 2014 Aug 21;2:e545
pubmed: 25177538
Front Microbiol. 2016 Dec 19;7:2033
pubmed: 28066358
Animal. 2010 Nov;4(11):1861-72
pubmed: 22445147
PLoS One. 2015 Nov 06;10(11):e0142334
pubmed: 26544955
Genet Sel Evol. 2016 Nov 28;48(1):93
pubmed: 27894254
Avian Pathol. 2014;43(1):78-81
pubmed: 24320598
PLoS One. 2014 Mar 07;9(3):e89862
pubmed: 24608294
Vet Microbiol. 2013 May 31;164(1-2):85-92
pubmed: 23434185
Genet Sel Evol. 2014 Apr 03;46:25
pubmed: 24708200
Appl Environ Microbiol. 1997 Jul;63(7):2802-13
pubmed: 9212428
Nat Methods. 2013 Dec;10(12):1200-2
pubmed: 24076764
FEMS Microbiol Lett. 2014 Nov;360(2):100-12
pubmed: 25263745
PLoS One. 2014 Mar 21;9(3):e91941
pubmed: 24657972
PLoS One. 2015 Nov 20;10(11):e0143442
pubmed: 26588075
Poult Sci. 2010 Sep;89(9):1955-61
pubmed: 20709981
Science. 2016 Apr 29;352(6285):532-5
pubmed: 27126034
Nat Biotechnol. 2013 Sep;31(9):814-21
pubmed: 23975157
BMC Genomics. 2018 Dec 13;19(1):928
pubmed: 30545300
Sci Rep. 2016 Nov 23;6:37376
pubmed: 27876778
Nat Methods. 2010 May;7(5):335-6
pubmed: 20383131
Sci Rep. 2013;3:1163
pubmed: 23362462
Appl Environ Microbiol. 2011 Sep;77(17):5868-78
pubmed: 21742925

Auteurs

Marion Borey (M)

Université Paris-Saclay, INRAE, AgroParisTech, GABI, Jouy-en-Josas, France.

Jordi Estellé (J)

Université Paris-Saclay, INRAE, AgroParisTech, GABI, Jouy-en-Josas, France.

Aziza Caidi (A)

Université Paris-Saclay, INRAE, AgroParisTech, GABI, Jouy-en-Josas, France.

Nicolas Bruneau (N)

Université Paris-Saclay, INRAE, AgroParisTech, GABI, Jouy-en-Josas, France.

Jean-Luc Coville (JL)

Université Paris-Saclay, INRAE, AgroParisTech, GABI, Jouy-en-Josas, France.

Christelle Hennequet-Antier (C)

BOA, INRAE, Université de Tours, Nouzilly, France.

Sandrine Mignon-Grasteau (S)

BOA, INRAE, Université de Tours, Nouzilly, France.

Fanny Calenge (F)

Université Paris-Saclay, INRAE, AgroParisTech, GABI, Jouy-en-Josas, France.

Articles similaires

Genome, Chloroplast Phylogeny Genetic Markers Base Composition High-Throughput Nucleotide Sequencing

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH