Butyrate enhances disease resistance of chickens by inducing antimicrobial host defense peptide gene expression.

Host defense peptides (HDPs) constitute a large group of natural broad-spectrum antimicrobials and an important first line of immunity in virtually all forms of life. Specific augmentation of synthesis of endogenous HDPs may represent a promising antibiotic-alternative approach to disease control. I...

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Autores principales: Lakshmi T Sunkara, Mallika Achanta, Nicole B Schreiber, Yugendar R Bommineni, Gan Dai, Weiyu Jiang, Susan Lamont, Hyun S Lillehoj, Ali Beker, Robert G Teeter, Guolong Zhang
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Publicado: Public Library of Science (PLoS) 2011
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spelling oai:doaj.org-article:cff3b215220048be9d3d3affffe0ec3d2021-11-18T07:34:56ZButyrate enhances disease resistance of chickens by inducing antimicrobial host defense peptide gene expression.1932-620310.1371/journal.pone.0027225https://doaj.org/article/cff3b215220048be9d3d3affffe0ec3d2011-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22073293/?tool=EBIhttps://doaj.org/toc/1932-6203Host defense peptides (HDPs) constitute a large group of natural broad-spectrum antimicrobials and an important first line of immunity in virtually all forms of life. Specific augmentation of synthesis of endogenous HDPs may represent a promising antibiotic-alternative approach to disease control. In this study, we tested the hypothesis that exogenous administration of butyrate, a major type of short-chain fatty acids derived from bacterial fermentation of undigested dietary fiber, is capable of inducing HDPs and enhancing disease resistance in chickens. We have found that butyrate is a potent inducer of several, but not all, chicken HDPs in HD11 macrophages as well as in primary monocytes, bone marrow cells, and jejuna and cecal explants. In addition, butyrate treatment enhanced the antibacterial activity of chicken monocytes against Salmonella enteritidis, with a minimum impact on inflammatory cytokine production, phagocytosis, and oxidative burst capacities of the cells. Furthermore, feed supplementation with 0.1% butyrate led to a significant increase in HDP gene expression in the intestinal tract of chickens. More importantly, such a feeding strategy resulted in a nearly 10-fold reduction in the bacterial titer in the cecum following experimental infections with S. enteritidis. Collectively, the results indicated that butyrate-induced synthesis of endogenous HDPs is a phylogenetically conserved mechanism of innate host defense shared by mammals and aves, and that dietary supplementation of butyrate has potential for further development as a convenient antibiotic-alternative strategy to enhance host innate immunity and disease resistance.Lakshmi T SunkaraMallika AchantaNicole B SchreiberYugendar R BommineniGan DaiWeiyu JiangSusan LamontHyun S LillehojAli BekerRobert G TeeterGuolong ZhangPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 11, p e27225 (2011)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Lakshmi T Sunkara
Mallika Achanta
Nicole B Schreiber
Yugendar R Bommineni
Gan Dai
Weiyu Jiang
Susan Lamont
Hyun S Lillehoj
Ali Beker
Robert G Teeter
Guolong Zhang
Butyrate enhances disease resistance of chickens by inducing antimicrobial host defense peptide gene expression.
description Host defense peptides (HDPs) constitute a large group of natural broad-spectrum antimicrobials and an important first line of immunity in virtually all forms of life. Specific augmentation of synthesis of endogenous HDPs may represent a promising antibiotic-alternative approach to disease control. In this study, we tested the hypothesis that exogenous administration of butyrate, a major type of short-chain fatty acids derived from bacterial fermentation of undigested dietary fiber, is capable of inducing HDPs and enhancing disease resistance in chickens. We have found that butyrate is a potent inducer of several, but not all, chicken HDPs in HD11 macrophages as well as in primary monocytes, bone marrow cells, and jejuna and cecal explants. In addition, butyrate treatment enhanced the antibacterial activity of chicken monocytes against Salmonella enteritidis, with a minimum impact on inflammatory cytokine production, phagocytosis, and oxidative burst capacities of the cells. Furthermore, feed supplementation with 0.1% butyrate led to a significant increase in HDP gene expression in the intestinal tract of chickens. More importantly, such a feeding strategy resulted in a nearly 10-fold reduction in the bacterial titer in the cecum following experimental infections with S. enteritidis. Collectively, the results indicated that butyrate-induced synthesis of endogenous HDPs is a phylogenetically conserved mechanism of innate host defense shared by mammals and aves, and that dietary supplementation of butyrate has potential for further development as a convenient antibiotic-alternative strategy to enhance host innate immunity and disease resistance.
format article
author Lakshmi T Sunkara
Mallika Achanta
Nicole B Schreiber
Yugendar R Bommineni
Gan Dai
Weiyu Jiang
Susan Lamont
Hyun S Lillehoj
Ali Beker
Robert G Teeter
Guolong Zhang
author_facet Lakshmi T Sunkara
Mallika Achanta
Nicole B Schreiber
Yugendar R Bommineni
Gan Dai
Weiyu Jiang
Susan Lamont
Hyun S Lillehoj
Ali Beker
Robert G Teeter
Guolong Zhang
author_sort Lakshmi T Sunkara
title Butyrate enhances disease resistance of chickens by inducing antimicrobial host defense peptide gene expression.
title_short Butyrate enhances disease resistance of chickens by inducing antimicrobial host defense peptide gene expression.
title_full Butyrate enhances disease resistance of chickens by inducing antimicrobial host defense peptide gene expression.
title_fullStr Butyrate enhances disease resistance of chickens by inducing antimicrobial host defense peptide gene expression.
title_full_unstemmed Butyrate enhances disease resistance of chickens by inducing antimicrobial host defense peptide gene expression.
title_sort butyrate enhances disease resistance of chickens by inducing antimicrobial host defense peptide gene expression.
publisher Public Library of Science (PLoS)
publishDate 2011
url https://doaj.org/article/cff3b215220048be9d3d3affffe0ec3d
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