Induction of porcine host defense peptide gene expression by short-chain fatty acids and their analogs

PLoS One. 2013 Aug 30;8(8):e72922. doi: 10.1371/journal.pone.0072922. eCollection 2013.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Butyrates / chemistry
  • Butyrates / pharmacology
  • Cell Line
  • Enterocytes / drug effects
  • Enterocytes / metabolism
  • Fatty Acids, Volatile / chemistry
  • Fatty Acids, Volatile / pharmacology*
  • Gene Expression Regulation / drug effects*
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Monocytes / drug effects
  • Monocytes / metabolism
  • Sus scrofa / genetics*
  • beta-Defensins / genetics*
  • beta-Defensins / metabolism

Substances

  • Butyrates
  • Fatty Acids, Volatile
  • beta-Defensins

Grants and funding

This work was supported by a United States Department of Agriculture/National Institute of Food and Agriculture grant (2008-35204-04544), Oklahoma Center for the Advancement of Science and Technology grants AR12.2-077 and HR12-051, Oklahoma State University Technology Business Development Program grant, and Oklahoma Agricultural Experiment Station project H-2811. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.