Dietary glucomannan improves the vaccinal response in pigs exposed to aflatoxin B-1 or T-2 toxin

作者:Meissonnier G M*; Raymond I; Laffitte J; Cossalter A M; Pinton P; Benoit E; Bertin G; Galtier P; Oswald I P
来源:World Mycotoxin Journal, 2009, 2(2): 161-172.
DOI:10.3920/WMJ2008.1127

摘要

The aim of the study was to investigate whether dietary supplementation with yeast-derived glucomannan protects pigs against the deleterious effects that exposure to aflatoxin B-1 (AFB(1)) or T-2 toxin has on the vaccinal immune response and drug-metabolising enzymes. Three doses of pure mycotoxin (AFB(1) trial: 482, 968 and 1,912 mu g/kg feed; T-2 toxin trial: 593, 1,155 and 2,067 mu g/kg feed) with or without dietary glucomannan supplementation (2 g/kg feed) were tested in weaned pigs for 28 days. At days 4 and 15 pigs were immunised with ovalbumin to study the humoral and cell-mediated antigen-specific immune responses. The effects of AFB(1) and T-2 toxin intake alone in pigs have already been published. In all parameters investigated no differences were apparent between animals receiving the unsupplemented control diet or the control diet containing glucomannan. In the AFB(1) trial glucomannan decreased the severity of liver lesions in animals exposed to 968 mu g/kg feed. Exposure to both AFB(1) and T-2 toxin were associated with impaired phase I liver enzyme activities, but glucomannan demonstrated a limited protective effect on these enzymes. With regard to the immune defence system, both toxins modulated the vaccinal immune response; AFB(1) impaired specific cellular response and T-2 toxin the specific humoral response. Glucomannan supplementation restored the ovalbumin-specific lymphocyte proliferation that was delayed in pigs exposed to AFB(1), regardless of dose. In the T-2 toxin trial glucomannan supplementation restored anti-ovalbumin immunoglobulin G production, which was significantly reduced in pigs exposed to both medium and high doses of the toxin. In conclusion, glucomannan dietary supplementation demonstrated no deleterious effects in control animals and protective effects against AFB(1) and T-2 toxin immunotoxicity during a vaccinal protocol.

  • 出版日期2009-5