tetano
Editor, Senior Moderator
Poult Sci
. 2024 Apr 30;103(7):103800.
doi: 10.1016/j.psj.2024.103800. Online ahead of print. Guanylate-binding protein 1 inhibits inflammatory factors produced by H5N1 virus through Its GTPase activity
Yanping Jiang[SUP] 1 [/SUP], Limeng Cai[SUP] 2 [/SUP], Shuo Jia[SUP] 1 [/SUP], Weichun Xie[SUP] 2 [/SUP], Xueying Wang[SUP] 2 [/SUP], Jiaxuan Li[SUP] 1 [/SUP], Wen Cui[SUP] 1 [/SUP], Guiwei Li[SUP] 3 [/SUP], Xianzhu Xia[SUP] 4 [/SUP], Lijie Tang[SUP] 5 [/SUP]
Affiliations
The combination of inflammatory factors resulting from an influenza A virus infection is one of the main causes of death in host animals. Studies have shown that guinea pig guanosine monophosphate binding protein 1 (guanylate-binding protein 1, gGBP1) can downregulate cytokine production induced by the influenza virus. Therefore, exploring the innate immune defense mechanism of GBP1 in the process of H5N1 influenza virus infection has important implications for understanding the pathogenic mechanism, disease prevention, and the control of influenza A virus infections. We found that, in addition to inhibiting the early replication of influenza virus, gGBP1 also inhibited the production of CCL2 and CXCL10 cytokines induced by the influenza virus as well as the proliferation of mononuclear macrophages induced by these cytokines. These findings further confirmed that gGBP1 inhibited the production of cytokines through its GTPase activity and cell proliferation through its C-terminal α-helix structure. This study revealed the effect of gGBP1 on the production of cellular inflammatory factors during influenza virus infection and determined the key amino acid residues that assist in the inhibitory processes mediated by gGBP1.
Keywords: GBP1; inflammatory cytokine; influenza A virus; innate immune response; key action site.
. 2024 Apr 30;103(7):103800.
doi: 10.1016/j.psj.2024.103800. Online ahead of print. Guanylate-binding protein 1 inhibits inflammatory factors produced by H5N1 virus through Its GTPase activity
Yanping Jiang[SUP] 1 [/SUP], Limeng Cai[SUP] 2 [/SUP], Shuo Jia[SUP] 1 [/SUP], Weichun Xie[SUP] 2 [/SUP], Xueying Wang[SUP] 2 [/SUP], Jiaxuan Li[SUP] 1 [/SUP], Wen Cui[SUP] 1 [/SUP], Guiwei Li[SUP] 3 [/SUP], Xianzhu Xia[SUP] 4 [/SUP], Lijie Tang[SUP] 5 [/SUP]
Affiliations
- PMID: 38743966
- DOI: 10.1016/j.psj.2024.103800
The combination of inflammatory factors resulting from an influenza A virus infection is one of the main causes of death in host animals. Studies have shown that guinea pig guanosine monophosphate binding protein 1 (guanylate-binding protein 1, gGBP1) can downregulate cytokine production induced by the influenza virus. Therefore, exploring the innate immune defense mechanism of GBP1 in the process of H5N1 influenza virus infection has important implications for understanding the pathogenic mechanism, disease prevention, and the control of influenza A virus infections. We found that, in addition to inhibiting the early replication of influenza virus, gGBP1 also inhibited the production of CCL2 and CXCL10 cytokines induced by the influenza virus as well as the proliferation of mononuclear macrophages induced by these cytokines. These findings further confirmed that gGBP1 inhibited the production of cytokines through its GTPase activity and cell proliferation through its C-terminal α-helix structure. This study revealed the effect of gGBP1 on the production of cellular inflammatory factors during influenza virus infection and determined the key amino acid residues that assist in the inhibitory processes mediated by gGBP1.
Keywords: GBP1; inflammatory cytokine; influenza A virus; innate immune response; key action site.