Oral administration of synthetic porcine beta-defensin-2 improves growth performance and cecal microbial flora and down-regulates the expression of intestinal toll-like receptor-4 and inflammatory cytokines in weaned piglets challenged with enterotoxigenic Escherichia coli

Anim Sci J. 2016 Oct;87(10):1258-1266. doi: 10.1111/asj.12540. Epub 2015 Dec 28.

Abstract

Synthetic porcine beta-defensin-2 (pBD-2) was tested as an alternative to antimicrobial growth-promoters in pig production. Thirty 21-day weaned piglets were challenged with enterotoxigenic Escherichia coli, and orally dosed with either sterile water (CON), pBD-2 (BD) or neomycin sulphate (NS) twice daily for 21 days. pBD-2 and NS led to higher growth performance, jejunum villus height and increased expression of insulin-like growth factor-I compared with the CON group (P < 0.05). Hemolytic E. coli scores from rectal swabs, and copy numbers of E. coli, Bacteroides fragilis and Streptococcus in the cecal digesta of the BD- or NS-treated piglets were lower than those in the CON group (P < 0.05). Messenger RNA levels of toll-like receptor 4, tumor necrosis factor-α, interleukin (IL)-1β, and IL-8 in the jejunum mucosa of the BD and NS groups were lower than those in the CON group (P < 0.05). Copy numbers of Lactobacilli and Bifidobacteria in the cecal digesta of the BD group were higher than those of the CON and NS groups (P < 0.05). Therefore, pBD-2 has antimicrobial activity in piglets, and it can improve growth performance, reduce inflammatory cytokine expression and affect intestinal morphological indices in the same way as probiotics. © 2015 Japanese Society of Animal Science.

Keywords: antimicrobial peptide; inflammation cytokines; piglets; porcine β-defensin-2; toll-like receptor-4.

MeSH terms

  • Administration, Oral
  • Animals
  • Cecum / microbiology*
  • Cytokines / genetics*
  • Cytokines / metabolism*
  • Down-Regulation / drug effects*
  • Enterotoxigenic Escherichia coli / immunology*
  • Gastrointestinal Microbiome*
  • Gene Expression / drug effects*
  • Inflammation Mediators / metabolism*
  • Male
  • Probiotics
  • Swine / growth & development*
  • Swine / immunology*
  • Swine / microbiology
  • Toll-Like Receptor 4 / genetics*
  • Toll-Like Receptor 4 / metabolism*
  • Weaning
  • beta-Defensins / administration & dosage*
  • beta-Defensins / pharmacology*

Substances

  • Cytokines
  • Inflammation Mediators
  • Toll-Like Receptor 4
  • beta-Defensins