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

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 identi...

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Veröffentlicht in:Fish & shellfish immunology 2024-10, Vol.153, p.109845, Article 109845
Hauptverfasser: Dong, Yuhang, Zhang, Zhiqiang, Huang, Yongxiong, Tan, Xuyan, Li, Xing, Huang, Meiling, Feng, Jiaming, Huang, Yu, Jian, Jichang
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Sprache:eng
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Zusammenfassung: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. •High mobility group protein B2 (On-HMGB2) was cloned from Oreochromis niloticus.•On-HMGB2 was knocked down by RNA interference.•HMGB2 protected O. niloticus against S. agalactiae infection in vivo.•HMGB2 is associated with an antimicrobial response with anti-inflammatory and anti-apoptotic effects.
ISSN:1050-4648
1095-9947
1095-9947
DOI:10.1016/j.fsi.2024.109845