The role of HMGB2 in the immune response of Nile tilapia (Oreochromis niloticus) to streptococcal infection

被引:0
作者
Dong, Yuhang [1 ]
Zhang, Zhiqiang [1 ]
Huang, Yongxiong [1 ]
Tan, Xuyan [1 ]
Li, Xing [1 ]
Huang, Meiling [1 ]
Feng, Jiaming [1 ]
Huang, Yu [1 ,2 ,3 ]
Jian, Jichang [1 ,2 ,3 ]
机构
[1] Guangdong Ocean Univ, Key Lab Control Dis Aquat Econ Anim, Guangdong Prov Key Lab Pathogen Biol & Epidemiol, Guangdong Higher Educ Inst,Coll Fishery, Zhanjiang, Peoples R China
[2] Lab Marine Biol & Biotechnol, Qingdao Natl Lab Marine Sci & Technol, Qingdao, Peoples R China
[3] Guangdong Prov Engn Res Ctr Aquat Anim Hlth Assess, Shenzhen, Peoples R China
基金
芬兰科学院; 中国国家自然科学基金;
关键词
HMGB2; Streptococcus agalactiae; Nile tilapia; Immune response; GROUP BOX 2; RNA INTERFERENCE; PROTEIN; EXPRESSION; SPERMATOGENESIS; ANTIBACTERIAL; MAINTENANCE; CLONING; DNA;
D O I
10.1016/j.fsi.2024.109845
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
High mobility group protein B2 (HMGB2) is an abundant chromatin-associated protein with pivotal roles in transcription, cell proliferation, differentiation, inflammation, and tumorigenesis. However, its immune function in Nile tilapia (Oreochromis niloticus) remains unclear. In this study, we identified a homologue of HMGB2 from Nile tilapia (On-HMGB2) and investigated its functions in the immune response against streptococcus infection. The open reading frame (ORF) of On-HMGB2 spans 642 bp, encoding 213 amino acids, and contains two conserved HMG domains. On-HMGB2 shares over 80 % homology with other fish species and 74%-76 % homology with mammals. On-HMGB2 was widely distributed in various tissues, with its highest transcript levels in the liver and the lowest in the intestine. Knockdown of On-HMGB2 promoted the inflammatory response in Nile tilapia, increased the bacterial load in the tissues, and led to elevated mortality in Nile tilapia following Streptococcus agalactiae infection. Taken together, On-HMGB2 significantly influences the immune system of Nile tilapia in response to streptococcus infection.
引用
收藏
页数:11
相关论文
共 43 条
[1]   RNA interference: Biology, mechanism, and applications [J].
Agrawal, N ;
Dasaradhi, PVN ;
Mohmmed, A ;
Malhotra, P ;
Bhatnagar, RK ;
Mukherjee, SK .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2003, 67 (04) :657-+
[2]   Mitochondrial transcription and its regulation in mammalian cells [J].
Asin-Cayuela, Jordi ;
Gustafsson, Claes M. .
TRENDS IN BIOCHEMICAL SCIENCES, 2007, 32 (03) :111-117
[3]  
BUCCI LR, 1984, J BIOL CHEM, V259, P8840
[4]   Expression of HMGB2 indicates worse survival of patients and is required for the maintenance of Warburg effect in pancreatic cancer [J].
Cai, Xin ;
Ding, Hongjian ;
Liu, Yanxia ;
Pan, Gaofeng ;
Li, Qingguo ;
Yang, Zhen ;
Liu, Weiyan .
ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 2017, 49 (02) :119-127
[5]   LECT2 improves the outcomes in ayu with Vibrio anguillarum infection via monocytes/macrophages [J].
Chen, Jiong ;
Chen, Qiang ;
Lu, Xin-Jiang ;
Li, Chang-Hong .
FISH & SHELLFISH IMMUNOLOGY, 2014, 41 (02) :586-592
[6]   Teleost innate immunity, an intricate game between immune cells and parasites of fish organs: who wins, who loses [J].
Dezfuli, Bahram Sayyaf ;
Lorenzoni, Massimo ;
Carosi, Antonella ;
Giari, Luisa ;
Bosi, Giampaolo .
FRONTIERS IN IMMUNOLOGY, 2023, 14
[7]   Antiviral RNA interference in mammals [J].
Ding, Shou-Wei ;
Han, Qingxia ;
Wang, Jinyan ;
Li, Wan-Xiang .
CURRENT OPINION IN IMMUNOLOGY, 2018, 54 :109-114
[8]   The regulatory effect of acetylation of HMGN2 and H3K27 on pyocyanin-induced autophagy in macrophages by affecting Ulk1 transcription [J].
Du, Yu ;
Guo, Hongjun ;
Guo, Lijuan ;
Miao, Junming ;
Ren, Hongyu ;
Liu, Keyun ;
Ren, Laibin ;
He, Jinchen ;
Wang, Xiaoying ;
Chen, Junli ;
Li, Jingyu ;
Wang, Yi ;
Wang, Ji ;
Huang, Ning .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2021, 25 (15) :7524-7537
[9]   Bioinformatics analysis of the prognosis and biological significance of HMGB1, HMGB2, and HMGB3 in gastric cancer [J].
Fang, Jian ;
Ge, Xuhui ;
Xu, Wenjing ;
Xie, Jingjing ;
Qin, Zhongke ;
Shi, Liqing ;
Yin, Wenjie ;
Bian, Maohong ;
Wang, Hao .
JOURNAL OF CELLULAR PHYSIOLOGY, 2020, 235 (04) :3438-3446
[10]   Targeting innate immunity protein kinase signalling in inflammation [J].
Gaestel, Matthias ;
Kotlyarov, Alexey ;
Kracht, Michael .
NATURE REVIEWS DRUG DISCOVERY, 2009, 8 (06) :480-499