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

被引:12
|
作者
Zheng, Xin [1 ]
Feng, Lin [1 ,2 ,3 ]
Jiang, Wei-Dan [1 ,2 ,4 ]
Wu, Pei [1 ,2 ,4 ]
Liu, Yang [1 ,2 ,5 ]
Kuang, Sheng-Yao [6 ]
Tang, Ling [5 ]
Zhou, Xiao-Qiu [1 ,2 ,3 ]
机构
[1] Sichuan Agr Univ, Anim Nutr Inst, Chengdu 611130, Sichuan, Peoples R China
[2] Sichuan Agr Univ, Fish Nutr & Safety Prod Univ Key Lab Sichuan Prov, Chengdu 611130, Sichuan, Peoples R China
[3] China Minist Educ, Key Lab Anim Dis Resistance Nutr, Chengdu, Sichuan, Peoples R China
[4] Agr Univ, Minist Educ, Key Lab Anim Dis Resistant Nutr, Chengdu 611130, Sichuan, Peoples R China
[5] Minist Agr & Rural Affairs, Key Lab Anim Dis Resistant Nutr & Feed, Chengdu, Peoples R China
[6] Sichuan Acad Anim Sci, Anim Nutr Inst, Chengdu 610066, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Pyridoxine; Challenge trial; Gill function; Signalling pathway; Requirement; Ctenopharyngodon idella; NF-KAPPA-B; DIETARY VITAMIN-C; PROTEIN TRANSCRIPT ABUNDANCE; MESSENGER-RNA EXPRESSION; PHYSICAL BARRIER; STRUCTURAL INTEGRITY; HEAD-KIDNEY; GROWTH-PERFORMANCE; SIGNALING MOLECULES; DISEASE RESISTANCE;
D O I
10.1016/j.fsi.2020.07.036
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
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.
引用
收藏
页码:209 / 223
页数:15
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