Journal
POULTRY SCIENCE
Volume 98, Issue 2, Pages 722-733Publisher
OXFORD UNIV PRESS
DOI: 10.3382/ps/pey460
Keywords
incubation temperature; Pekin ducks; LPS challenge; HSP70; immune response
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During the course of multi-stage incubation, small locational differences in incubation temperature within a machine are not uncommon and so the goal of this study was to study the immune response of ducklings exposed to thermal manipulation during incubation. Commercial Pekin duck eggs (n = 200) were distributed among four treatment: SS-Control (37.5 degrees C from embryonic day [ED] 1 to 25); SS-LPS (37.5 degrees C from ED1 to 25 + LPS at DO [hatch]); HH-LPS (38 degrees C from ED1 to 25+ LPS at DO); SH-LPS (37.5 degrees C from ED1 to 10 and 38 degrees C from ED 11 to 25 + LPS at DO). At DO, ducklings received a lipopolysaccharide (LPS) injection. At D1 and D5, the HH-LPS treatment significantly reduced body weight (P <= 0.05). At D1 and D3 post-LPS injection, the SH-LPS and HH-LPS treatments significantly reduced splenic and bursal heat shock protein 70 (HSP70), mRNA abundance, and macrophage nitric oxide production compared with the SS-LPS treatment (P <= 0.05). At D1, the HH-LPS and SH-LPS treatments had increased splenic IL-10 mRNA and lower MHC I mRNA compared with the SS-LPS treatment (P <= 0.05). At D1, the HH-LPS treatment increased splenic IL-6 mRNA and bursal IFN gamma mRNA transcription while the SH-LPS treatment reduced splenic IL-6 mRNA compared with the SS-LPS treatment (P <= 0.05). The HH-LPS treatment reduced thymocyte proliferation efficiency, while at D1, D3, and D5, the SH-LPS treatment increased thymocyte proliferation efficiency compared with the SS-LPS treatment (P < 0.05). Ducklings in the HH-LPS treatment had a higher splenic CD8(+)/CD4(+) ratio compared to the SS-LPS treatment at D3 post-LPS injection (P <= 0.05). In summary, the HH-LPS treatment compromised immunocompetence via decreased NO production and thymocyte proliferation efficiency, while the SH-LPS treatment increased body weight and thymocyte proliferation and reduced IL-6 mRNA abundance. This suggests that an embryonic temperature stress during the latter half of incubation may prime the immune system which may be beneficial during secondary post-hatch inflammatory challenges.
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