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Induction of Porcine Host Defense Peptide Gene Expression by Short-Chain Fatty Acids and Their Analogs

Dietary modulation of the synthesis of endogenous host defense peptides (HDPs) represents a novel antimicrobial approach for disease control and prevention, particularly against antibiotic-resistant infections. However, HDP regulation by dietary compounds such as butyrate is species-dependent. To ex...

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Autores principales: Zeng, Xiangfang, Sunkara, Lakshmi T., Jiang, Weiyu, Bible, Megan, Carter, Scott, Ma, Xi, Qiao, Shiyan, Zhang, Guolong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3758276/
https://www.ncbi.nlm.nih.gov/pubmed/24023657
http://dx.doi.org/10.1371/journal.pone.0072922
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author Zeng, Xiangfang
Sunkara, Lakshmi T.
Jiang, Weiyu
Bible, Megan
Carter, Scott
Ma, Xi
Qiao, Shiyan
Zhang, Guolong
author_facet Zeng, Xiangfang
Sunkara, Lakshmi T.
Jiang, Weiyu
Bible, Megan
Carter, Scott
Ma, Xi
Qiao, Shiyan
Zhang, Guolong
author_sort Zeng, Xiangfang
collection PubMed
description Dietary modulation of the synthesis of endogenous host defense peptides (HDPs) represents a novel antimicrobial approach for disease control and prevention, particularly against antibiotic-resistant infections. However, HDP regulation by dietary compounds such as butyrate is species-dependent. To examine whether butyrate could induce HDP expression in pigs, we evaluated the expressions of a panel of porcine HDPs in IPEC-J2 intestinal epithelial cells, 3D4/31 macrophages, and primary monocytes in response to sodium butyrate treatment by real-time PCR. We revealed that butyrate is a potent inducer of multiple, but not all, HDP genes. Porcine β-defensin 2 (pBD2), pBD3, epididymis protein 2 splicing variant C (pEP2C), and protegrins were induced markedly in response to butyrate, whereas pBD1 expression remained largely unaltered in any cell type. Additionally, a comparison of the HDP-inducing efficacy among saturated free fatty acids of different aliphatic chain lengths revealed that fatty acids containing 3–8 carbons showed an obvious induction of HDP expression in IPEC-J2 cells, with butyrate being the most potent and long-chain fatty acids having only a marginal effect. We further investigated a panel of butyrate analogs for their efficacy in HDP induction, and found glyceryl tributyrate, benzyl butyrate, and 4-phenylbutyrate to be comparable with butyrate. Identification of butyrate and several analogs with a strong capacity to induce HDP gene expression in pigs provides attractive candidates for further evaluation of their potential as novel alternatives to antibiotics in augmenting innate immunity and disease resistance of pigs.
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spelling pubmed-37582762013-09-10 Induction of Porcine Host Defense Peptide Gene Expression by Short-Chain Fatty Acids and Their Analogs Zeng, Xiangfang Sunkara, Lakshmi T. Jiang, Weiyu Bible, Megan Carter, Scott Ma, Xi Qiao, Shiyan Zhang, Guolong PLoS One Research Article Dietary modulation of the synthesis of endogenous host defense peptides (HDPs) represents a novel antimicrobial approach for disease control and prevention, particularly against antibiotic-resistant infections. However, HDP regulation by dietary compounds such as butyrate is species-dependent. To examine whether butyrate could induce HDP expression in pigs, we evaluated the expressions of a panel of porcine HDPs in IPEC-J2 intestinal epithelial cells, 3D4/31 macrophages, and primary monocytes in response to sodium butyrate treatment by real-time PCR. We revealed that butyrate is a potent inducer of multiple, but not all, HDP genes. Porcine β-defensin 2 (pBD2), pBD3, epididymis protein 2 splicing variant C (pEP2C), and protegrins were induced markedly in response to butyrate, whereas pBD1 expression remained largely unaltered in any cell type. Additionally, a comparison of the HDP-inducing efficacy among saturated free fatty acids of different aliphatic chain lengths revealed that fatty acids containing 3–8 carbons showed an obvious induction of HDP expression in IPEC-J2 cells, with butyrate being the most potent and long-chain fatty acids having only a marginal effect. We further investigated a panel of butyrate analogs for their efficacy in HDP induction, and found glyceryl tributyrate, benzyl butyrate, and 4-phenylbutyrate to be comparable with butyrate. Identification of butyrate and several analogs with a strong capacity to induce HDP gene expression in pigs provides attractive candidates for further evaluation of their potential as novel alternatives to antibiotics in augmenting innate immunity and disease resistance of pigs. Public Library of Science 2013-08-30 /pmc/articles/PMC3758276/ /pubmed/24023657 http://dx.doi.org/10.1371/journal.pone.0072922 Text en © 2013 Zeng et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zeng, Xiangfang
Sunkara, Lakshmi T.
Jiang, Weiyu
Bible, Megan
Carter, Scott
Ma, Xi
Qiao, Shiyan
Zhang, Guolong
Induction of Porcine Host Defense Peptide Gene Expression by Short-Chain Fatty Acids and Their Analogs
title Induction of Porcine Host Defense Peptide Gene Expression by Short-Chain Fatty Acids and Their Analogs
title_full Induction of Porcine Host Defense Peptide Gene Expression by Short-Chain Fatty Acids and Their Analogs
title_fullStr Induction of Porcine Host Defense Peptide Gene Expression by Short-Chain Fatty Acids and Their Analogs
title_full_unstemmed Induction of Porcine Host Defense Peptide Gene Expression by Short-Chain Fatty Acids and Their Analogs
title_short Induction of Porcine Host Defense Peptide Gene Expression by Short-Chain Fatty Acids and Their Analogs
title_sort induction of porcine host defense peptide gene expression by short-chain fatty acids and their analogs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3758276/
https://www.ncbi.nlm.nih.gov/pubmed/24023657
http://dx.doi.org/10.1371/journal.pone.0072922
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