Zearalenone induces immuno-compromised status via TOR/NF/κB pathway and aggravates the spread of Aeromonas hydrophila to grass carp gut (Ctenopharyngodon idella)

被引:18
作者
Zhang, Hong-Yun [1 ]
Wang, Ya-Li [1 ]
Zhou, Xiao-Qiu [1 ,2 ,3 ]
Jiang, Wei-Dan [1 ,2 ,4 ]
Wu, Pei [1 ,2 ,4 ]
Liu, Yang [1 ,2 ,4 ,5 ]
Zhang, Lu [6 ]
Mi, Hai-Feng [6 ]
Jiang, Jun [1 ]
Kuang, Sheng-Yao [7 ]
Tang, Ling [7 ]
Feng, Lin [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, Peoples R China
[3] Key Lab Anim Dis Resistance Nutr, Chengdu 611130, Peoples R China
[4] Minist Educ, Key Lab Anim Dis Resistant Nutr, Chengdu 611130, Peoples R China
[5] Minist Agr & Rural Affairs, Key Lab Anim Dis Resistant Nutr & Feed, Chengdu 611130, Peoples R China
[6] Tongwei Res Inst, Chengdu 600438, Peoples R China
[7] Sichuan Acad Anim Sci, G Anim Nutr Inst, Chengdu 610066, Peoples R China
基金
中国国家自然科学基金;
关键词
Zearalenone; Immune; Pathogen infection; Mucus layer; Grass carp; NF-KAPPA-B; INTESTINAL INFLAMMATION; NATURAL OCCURRENCE; OXIDATIVE STRESS; INNATE; ACTIVATION; TOXICITY; MUCINS; WHEAT; EXPRESSION;
D O I
10.1016/j.ecoenv.2021.112786
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The occurrence of immuno-compromised status in animals with zearalenone (ZEA) exposure may be a critical contributor to associated mucosal (gastrointestinal tract) diseases. However, it is difficult to assess the associated risks with limited reference data. This study comprehensively discussed the effects of ZEA on intestinal immune components, cytokines and molecular mechanism of juvenile grass carp infected with Aeromonas hydrophila. Specifically, the fish were fed six graded levels of dietary ZEA (0-2507 mu g kg(-1) diet) for 70 d. The results pointed out that the average residual amount of ZEA in the intestines increased with dose level after ZEA feeding. We further performed an infection assay using A. hydrophila. After 14 d, ZEA groups increased enteritis morbidity rate compared with controls. The acid phosphatase (ACP), lysozyme (LZ) activities and immunoglobulin M (IgM) content were significantly decreased in three intestinal segments. Furthermore, ZEA could reduce the transcription of beta-defensin-1, Hepcidin, liver expressed antimicrobial peptide 2A/2B (LEAP-2A/2B) and Mucin-2. We next confirmed the loss of these immune components accompanied by the invasion of the intestinal barrier by bacteria, as indicated by activation of the nuclear factor kappa B (NF-kappa B) and the expression of downstream cytokines. Notably, the phosphorylated target of rapamycin (TOR) plays an important role in regulating these genes, thus indicating a possible target caused by ZEA. In summary, the extensive inhibition of immune components by ZEA promotes the spread of pathogens, which may increase the possibility of intestinal mucosa exposure and the risk of transforming disease.
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页数:12
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