Alpha-class glutathione S-transferases involved in the detoxification of aflatoxin B1 in ducklings

被引:12
作者
Zhang, Yu [1 ,2 ]
Cao, Ke-Xin [1 ]
Niu, Qin-Jian [1 ]
Deng, Jiang [1 ]
Zhao, Ling [1 ]
Khalil, Mahmoud Mohamed [3 ]
Karrow, Niel Alexander [4 ]
Kuca, Kamil [1 ,5 ]
Sun, Lv-Hui [1 ]
机构
[1] Huazhong Agr Univ, Coll Anim Sci & Technol, Frontiers Sci Ctr Anim Breeding & Sustainable Prod, State Key Lab Agr Microbiol,Hubei Hongshan Lab, Wuhan 430070, Hubei, Peoples R China
[2] Newhope Liuhe Co Ltd, Beijing 100102, Peoples R China
[3] Massey Univ, Monogastr Res Ctr, Sch Agr & Environm, Palmerston North 4442, New Zealand
[4] Univ Guelph, Dept Anim Biosci, Guelph, ON 121, Canada
[5] Univ Hradec Kralove, Fac Sci, Dept Chem, Rokitanskeho 62, Hradec Kralove 50003, Czech Republic
关键词
AflatoxinB1; Hepatotoxicity; Glutathione S-transferase; Detoxification; Duck; B-1; BIOTRANSFORMATION; METABOLISM; MECHANISM; TOXICITY; PROTEIN; STRESS;
D O I
10.1016/j.fct.2023.113682
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The objective of this study was to identify the key glutathione S-transferase (GST) isozymes involved in the detoxification of Aflatoxin B1 (AFB1) in ducks' primary hepatocytes. The full-length cDNA encoding the 10 GST isozymes (GST, GST3, GSTM3, MGST1, MGST2, MGST3, GSTK1, GSTT1, GSTO1 and GSTZ1) were isolated/ synthesized from ducks' liver and cloned into the pcDNA3.1(+) vector. The results showed that pcDNA3.1 (+)-GSTs plasmids were successfully transferred into the ducks' primary hepatocytes and the mRNA of the 10 GST isozymes were overexpressed by 1.9-3274.7 times. Compared to the control, 75 mu g/L (IC30) or 150 mu g/L (IC50) AFB1 treatment reduced the cell viability by 30.0-50.0% and increased the LDH activity by 19.8-58.2% in the ducks' primary hepatocytes. Notably, the AFB1-induced changes in cell viability and LDH activity were mitigated by overexpression of GST and GST3. Compared to the cells treated with AFB1, exo-AFB1-8,9-epoxide (AFBO)-GSH, as the major detoxified product of AFB1, was increased in the cells overexpression of GST and GST3. Moreover, the sequences, phylogenetic and domain analysis revealed that the GST and GST3 were orthologous to Meleagris gallopavo GSTA3 and GSTA4. In conclusion, this study found that the ducks' GST and GST3 were orthologous to Meleagris gallopavo GSTA3 and GSTA4, which were involved in the detoxification of AFB1 in ducks' primary hepatocytes.
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页数:9
相关论文
共 46 条
[11]   Overexpression of ER Protein Processing and Apoptosis Regulator Genes in Human Embryonic Kidney 293 Cells Improves Gene Therapy Vectors Production [J].
Formas-Oliveira, Ana S. ;
Basilio, Joao S. ;
Rodrigues, Ana F. ;
Coroadinha, Ana S. .
BIOTECHNOLOGY JOURNAL, 2020, 15 (09)
[12]   Multi-residue analysis of 20 mycotoxins including major metabolites and emerging mycotoxins in freshwater using UHPLC-MS/MS and application to freshwater ponds in flanders, Belgium [J].
Goessens, T. ;
De Baere, S. ;
De Troyer, N. ;
Deknock, A. ;
Goethals, P. ;
Lens, L. ;
Pasmans, F. ;
Croubels, S. .
ENVIRONMENTAL RESEARCH, 2021, 196
[13]   HUMAN MU-CLASS GLUTATHIONE S-TRANSFERASES PRESENT IN LIVER, SKELETAL-MUSCLE AND TESTICULAR TISSUE [J].
HUSSEY, AJ ;
HAYES, JD .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1203 (01) :131-141
[14]   Dominant contribution of P450 3A4 to the hepatic carcinogenic activation of aflatoxin B1 [J].
Kamdem, LK ;
Meineke, I ;
Gödtel-Armbrust, U ;
Brockmöller, J ;
Wojnowski, L .
CHEMICAL RESEARCH IN TOXICOLOGY, 2006, 19 (04) :577-586
[15]   Alpha-Class Glutathione S-Transferases in Wild Turkeys (Meleagris gallopavo): Characterization and Role in Resistance to the Carcinogenic Mycotoxin Aflatoxin B1 [J].
Kim, Ji Eun ;
Bunderson, Brett R. ;
Croasdell, Amanda ;
Reed, Kent M. ;
Coulombe, Roger A., Jr. .
PLOS ONE, 2013, 8 (04)
[16]   Duck hepatitis B virus replication in primary bile duct epithelial cells [J].
Lee, JY ;
Culvenor, JG ;
Angus, P ;
Smallwood, R ;
Nicoll, A ;
Locarnini, S .
JOURNAL OF VIROLOGY, 2001, 75 (16) :7651-7661
[17]  
Lee SE, 2000, ARCH INSECT BIOCHEM, V45, P166, DOI 10.1002/1520-6327(200012)45:4<166::AID-ARCH4>3.0.CO
[18]  
2-8
[19]   Baicalin alleviates deoxynivalenol-induced intestinal inflammation and oxidative stress damage by inhibiting NF-κB and increasing mTOR signaling pathways in piglets [J].
Liao, Peng ;
Li, Yunhu ;
Li, Meijun ;
Chen, Xingfa ;
Yuan, Daixiu ;
Tang, Min ;
Xu, Kang .
FOOD AND CHEMICAL TOXICOLOGY, 2020, 140
[20]   Ferroptosis is involved in deoxynivalenol-induced intestinal damage in pigs [J].
Liu, Meng ;
Zhang, Lei ;
Mo, Yixin ;
Li, Jiahuan ;
Yang, Jiacheng ;
Wang, Juan ;
Karrow, Niel Alexander ;
Wu, Hao ;
Sun, Lvhui .
JOURNAL OF ANIMAL SCIENCE AND BIOTECHNOLOGY, 2023, 14 (01)