Dietary sophorolipid accelerates growth by modulation of gut microbiota population and intestinal environments in broiler chickens.

Broilers Gut microbiota Gut morphology Local inflammation Mucus barrier Sophorolipids

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:
12 Jul 2021
Historique:
received: 12 01 2021
accepted: 13 05 2021
entrez: 12 7 2021
pubmed: 13 7 2021
medline: 13 7 2021
Statut: epublish

Résumé

Gut is a crucial organ for the host's defense system due to its filtering action of the intestinal membrane from hazardous foreign substances. One strategy to strengthen the gut epithelial barrier function is to upregulate beneficial microflora populations and their metabolites. Sophorolipid (SPL), which is a glycolipid bio-surfactant, could increase beneficial microflora and decrease pathogenic bacteria in the gastrointestinal tract. Therefore, herein, we conducted an experiment with broiler chickens to investigate the fortifying effects of SPL on the host's gut defense system by modulating the microbiota population. A total of 540 1-day-old chicks (Ross 308) were used, and they were immediately allotted into three treatment groups (6 replications with 30 chicks/pen) according to their initial body weight. The dietary treatments consisted of CON (basal diet), BAM (10 mg/kg bambermycin), and SPL (10 mg/kg SPL). During the experiment, birds freely accessed feed and water, and body weight and feed intake were measured at the end of each phase. On d 35, birds (one bird/pen) were sacrificed to collect jejunum and cecum samples. Dietary SPL and BAM supplementation significantly accelerated birds' growth and also significantly improved feed efficiency compared to CON. Intestinal microbial community was significantly separated by dietary SPL supplementation from that of CON, and dietary SPL supplementation significantly increased Lactobacillus spp. and Akkermansia muciniphila. Moreover, birds fed with dietary SPL also showed the highest concentration of cecal butyrate among all treatment groups. Gut morphological analysis showed that dietary SPL significantly increased villus height, ratio of villus height to crypt depth, goblet cell numbers, and the gene expression levels of claudin-1 and mucin 2. Additionally, dietary SPL significantly decreased the mRNA expression level of pro-inflammatory cytokine, interleukin-6, and increased that of anti-inflammatory cytokine, interleukin-10, compared to other treatments. Dietary SPL increases the beneficial bacterial population and butyrate concentration, which leads to a strengthened gut barrier function. In addition, the intestinal inflammation was also downregulated by dietary SPL supplementation.

Sections du résumé

BACKGROUND BACKGROUND
Gut is a crucial organ for the host's defense system due to its filtering action of the intestinal membrane from hazardous foreign substances. One strategy to strengthen the gut epithelial barrier function is to upregulate beneficial microflora populations and their metabolites. Sophorolipid (SPL), which is a glycolipid bio-surfactant, could increase beneficial microflora and decrease pathogenic bacteria in the gastrointestinal tract. Therefore, herein, we conducted an experiment with broiler chickens to investigate the fortifying effects of SPL on the host's gut defense system by modulating the microbiota population.
METHODS METHODS
A total of 540 1-day-old chicks (Ross 308) were used, and they were immediately allotted into three treatment groups (6 replications with 30 chicks/pen) according to their initial body weight. The dietary treatments consisted of CON (basal diet), BAM (10 mg/kg bambermycin), and SPL (10 mg/kg SPL). During the experiment, birds freely accessed feed and water, and body weight and feed intake were measured at the end of each phase. On d 35, birds (one bird/pen) were sacrificed to collect jejunum and cecum samples.
RESULTS RESULTS
Dietary SPL and BAM supplementation significantly accelerated birds' growth and also significantly improved feed efficiency compared to CON. Intestinal microbial community was significantly separated by dietary SPL supplementation from that of CON, and dietary SPL supplementation significantly increased Lactobacillus spp. and Akkermansia muciniphila. Moreover, birds fed with dietary SPL also showed the highest concentration of cecal butyrate among all treatment groups. Gut morphological analysis showed that dietary SPL significantly increased villus height, ratio of villus height to crypt depth, goblet cell numbers, and the gene expression levels of claudin-1 and mucin 2. Additionally, dietary SPL significantly decreased the mRNA expression level of pro-inflammatory cytokine, interleukin-6, and increased that of anti-inflammatory cytokine, interleukin-10, compared to other treatments.
CONCLUSIONS CONCLUSIONS
Dietary SPL increases the beneficial bacterial population and butyrate concentration, which leads to a strengthened gut barrier function. In addition, the intestinal inflammation was also downregulated by dietary SPL supplementation.

Identifiants

pubmed: 34247658
doi: 10.1186/s40104-021-00606-x
pii: 10.1186/s40104-021-00606-x
pmc: PMC8274033
doi:

Types de publication

Journal Article

Langues

eng

Pagination

81

Subventions

Organisme : Pathway intermediates
ID : Q1813691

Informations de copyright

© 2021. The Author(s).

Références

Poult Sci. 2019 Sep 1;98(9):3902-3913
pubmed: 31329958
Oxid Med Cell Longev. 2020 Jul 23;2020:6538930
pubmed: 32774682
Poult Sci. 2008 Sep;87(9):1823-33
pubmed: 18753451
PLoS One. 2019 Dec 10;14(12):e0216853
pubmed: 31821320
Poult Sci. 2010 Jul;89(7):1549-55
pubmed: 20548086
Vet Immunol Immunopathol. 2016 Nov 1;180:21-28
pubmed: 27692091
Front Immunol. 2019 Mar 11;10:277
pubmed: 30915065
Vet Med Sci. 2021 Mar 25;:
pubmed: 33764629
Nat Microbiol. 2018 Aug;3(8):898-908
pubmed: 30038308
Vet Med Int. 2010;2010:262604
pubmed: 20671938
Avian Dis. 2017 Mar;61(1):115-122
pubmed: 28301240
Int J Syst Evol Microbiol. 2017 May;67(5):1613-1617
pubmed: 28005526
Front Microbiol. 2012 Nov 19;3:392
pubmed: 23181058
Food Chem Toxicol. 2019 Mar;125:85-94
pubmed: 30597221
Poult Sci. 2019 Dec 1;98(12):6693-6701
pubmed: 31801309
Clin Nutr. 2010 Dec;29(6):832-9
pubmed: 20605664
PLoS One. 2015 May 15;10(5):e0126507
pubmed: 25978355
Folia Microbiol (Praha). 2016 Jan;61(1):85-9
pubmed: 26126789
J Biol Chem. 2003 Jul 11;278(28):25481-9
pubmed: 12711604
Psychoneuroendocrinology. 2013 Sep;38(9):1738-47
pubmed: 23566632
Neuroscience. 2015 Dec 3;310:561-77
pubmed: 26408987
Sci Rep. 2019 Jun 20;9(1):8872
pubmed: 31222159
Gastroenterol Rep (Oxf). 2019 Feb;7(1):3-12
pubmed: 30792861
Nat Rev Immunol. 2008 Jun;8(6):411-20
pubmed: 18469830
Jpn J Infect Dis. 2013;66(4):334-6
pubmed: 23883848
Sci Rep. 2019 Oct 30;9(1):15683
pubmed: 31666581
PLoS One. 2011;6(11):e27949
pubmed: 22114729
Int J Food Sci Nutr. 2020 Dec;71(8):965-978
pubmed: 32306796
Anaerobe. 2012 Aug;18(4):386-91
pubmed: 22579985
J Anim Physiol Anim Nutr (Berl). 2018 Feb;102(1):268-275
pubmed: 28295656
Gastroenterol Hepatol Bed Bench. 2019 Spring;12(2):163-168
pubmed: 31191842
Int J Syst Evol Microbiol. 2004 Sep;54(Pt 5):1469-1476
pubmed: 15388697
J Antimicrob Chemother. 1994 Oct;34(4):507-14
pubmed: 7868403
J Surg Res. 2007 Oct;142(2):314-9
pubmed: 17719064

Auteurs

Min-Jin Kwak (MJ)

Department of Biotechnology, Korea University, 145 Anam-ro, Seoul, 02841, Republic of Korea.

Min-Young Park (MY)

Department of Biotechnology, Korea University, 145 Anam-ro, Seoul, 02841, Republic of Korea.

Yong-Soon Choi (YS)

Department of Biotechnology, Korea University, 145 Anam-ro, Seoul, 02841, Republic of Korea.

Junghwan Cho (J)

Department of Biotechnology, Korea University, 145 Anam-ro, Seoul, 02841, Republic of Korea.

Duleepa Pathiraja (D)

Department of Biotechnology, Korea University, 145 Anam-ro, Seoul, 02841, Republic of Korea.

Jonggun Kim (J)

Department of Biotechnology, Korea University, 145 Anam-ro, Seoul, 02841, Republic of Korea.

Hanbae Lee (H)

Pathway Intermediates, Seoul, 02841, Republic of Korea.

In-Geol Choi (IG)

Department of Biotechnology, Korea University, 145 Anam-ro, Seoul, 02841, Republic of Korea.

Kwang-Youn Whang (KY)

Department of Biotechnology, Korea University, 145 Anam-ro, Seoul, 02841, Republic of Korea. kwhang@korea.ac.kr.

Classifications MeSH