4.7 Article

The regulatory effects of pyridoxine deficiency on the grass carp (Ctenopharyngodon idella) gill barriers immunity, apoptosis, antioxidant, and tight junction challenged with Flavobacterium columnar

Journal

FISH & SHELLFISH IMMUNOLOGY
Volume 105, Issue -, Pages 209-223

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fsi.2020.07.036

Keywords

Pyridoxine; Challenge trial; Gill function; Signalling pathway; Requirement; Ctenopharyngodon idella

Funding

  1. National Key R&D Program of China [2019YFD0900200, 2018YFD0900400]
  2. National Natural Science Foundation of China for Outstanding Youth Science Foundation [31922086]
  3. National Natural Science Foundation of China [31972810]
  4. Young Top-Notch Talent Support Program of National TenThousand Talents Program
  5. Earmarked Fund for China Agriculture Research System [CARS-45]
  6. Outstanding Talents and Innovative Team of Agricultural Scientific Research (Ministry of Agriculture)
  7. Key Research and Development Plan in Sichuan Province [2018NZ0007]
  8. Sichuan Science and Technology Program [2019YFN0036]

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The effects of dietary pyridoxine (PN) on the gill immunity, apoptosis, antioxidant and tight junction of grass cap (Ctenopharyngodon idella) were investigated in this study. Fish were fed semi-purified diets containing graded levels of PN for 10 weeks, and then challenged with Flavobacterium columnare by bath immersion exposure for 3 days. The results indicated that compared with the optimal PN level, PN deficiency resulted in a decline in the antimicrobial compound production of gill. In addition, PN deficiency up-regulated the pro-inflammatory cytokines and down-regulated the anti-inflammatory cytokines gene expression, which might be associated with the enhanced nuclear factor kappa B p65 and the inhibited target of rapamycin signalling pathways, respectively, suggesting that PN deficiency could impair gill immune barrier function. Furthermore, PN deficiency (1) induced cell apoptosis, which may be partly associated with the (apoptotic protease activating factor-1, Bcl-2 associated X protein)/caspase-9 and c-Rel/tumor necrosis factor alpha (rather than FasL)/caspase-8 mediated apoptosis pathway. (2) Inhibited Kelch-like ECH-associating protein 1a/NF-E2-related factor 2 mRNA expression, decreased the mRNA expression and activities of antioxidant enzymes, increased the levels of reactive oxygen species, protein carbonyl and malondialdehyde. (3) Increased the mRNA expression level of myosin light chain kinase, which may be result in the down-regulation of tight junction complexes such as zonula occludens 1, occludin and claudins (expect claudin-12 and claudin-15). These results suggest that PN deficiency could impair gill physical barrier function. In summary, dietary PN deficiency could cause the impairment of gill barrier function associated with immunity, apoptosis, antioxidant and tight junction, which may result in the increased the susceptibility of fish to pathogenic bacteria. Moreover, based on the gill rot morbidity, LZ activity and MDA content, the dietary PN requirements for grass cap were estimated to be 4.85, 4.78 and 4.77 mg kg(-1) diet, respectively.

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