Effects of dietary polyunsaturated fatty acids on in vivo splenic cytokinemRNA expression in layer chicks immunized with Salmonella typhimurium lipopolysaccharide

Citation
Jwc. Sijben et al., Effects of dietary polyunsaturated fatty acids on in vivo splenic cytokinemRNA expression in layer chicks immunized with Salmonella typhimurium lipopolysaccharide, POULTRY SCI, 80(8), 2001, pp. 1164-1170
Citations number
33
Categorie Soggetti
Animal Sciences
Journal title
POULTRY SCIENCE
ISSN journal
00325791 → ACNP
Volume
80
Issue
8
Year of publication
2001
Pages
1164 - 1170
Database
ISI
SICI code
0032-5791(200108)80:8<1164:EODPFA>2.0.ZU;2-I
Abstract
Effects of dietary polyunsaturated fatty acids (PUFA) on immune responses i n poultry have been reported. However, effects on the underlying mechanisms , such as the role of cytokines, have not been documented because the neces sary tools were lacking. Recently, primer sets for chicken interleukin (IL) -1 beta, IL-2, interferon-gamma (IFN-gamma), myelomonocytic growth factor ( MGF), and transforming growth factor (TGF)-beta (2) have become available. Therefore, in the present study we first examined the in vivo effects of an inflammatory challenge with Salmonella typhimurium lipopolysaccharide (LPS ) on cytokine profiles in growing laying-type chicks. Second, we examined w hether dietary fat sources affected the observed cytokine profiles. Two hun dred forty chicks were assigned in a 2 x 4 factorial design of treatments, with injection with LPS or saline and dietary fat source as factors. Factor s were i.v. injection with S. typhimurium LPS or saline (control) and four dietary fat sources: corn oil, linseed oil, menhaden oil, and tallow. Two h ours after injection, birds were killed, and their spleens were removed for RNA extraction. Reverse transcription polymerase chain reactions with prim er sets for chicken IL-1 beta, IL-2, IFN-gamma, MGF, TGF-beta (2), and beta -actin were performed with RNA samples pooled by pen. The expression of cy tokine mRNA was expressed relative to the level of beta -actin mRNA. Interl eukin-1 (P < 0.001), MGF (P < 0.0001), IL-2 (P < 0.001), and IFN-gamma (P < 0.001) mRNA expressions were enhanced by challenge with LPS. Immunization treatment had no effect on TGF-beta2 or beta -actin expression. Dietary tre atment did not affect mRNA expression of IL-1, MGF, IFN-gamma, TGF-beta (2) , or beta -actin. Interleukin-2 expression in LPS-injected birds that were fed the fish-oil-enriched diet was enhanced (P = 0.05). The present study i ndicates that in vivo effects of immune challenge on cytokine mRNA expressi on can be measured in poultry. The observation that mRNA level of IL-2, but not the mRNA levels of IFN-gamma or MGF, is enhanced by dietary fish oil a t 2 h suggests that dietary PUFA at this moment initially affected naive T lymphocytes.