tetano
Editor, Senior Moderator
J Med Virol
. 2023 Jul;95(7):e28968.
doi: 10.1002/jmv.28968. Discovery of ligustrazine and chalcone derivatives as novel viral nucleoprotein nuclear export inhibitors against influenza viruses
Ping Li[SUP] 1 2 [/SUP], Han Ju[SUP] 1 [/SUP], Ying Zhang[SUP] 1 [/SUP], Jazmin Galvan Achi[SUP] 3 [/SUP], Dongwei Kang[SUP] 1 [/SUP], Jinmi Zou[SUP] 1 [/SUP], Ruikun Du[SUP] 2 [/SUP], Qinghua Cui[SUP] 2 [/SUP], Xinyong Liu[SUP] 1 [/SUP], Lijun Rong[SUP] 3 [/SUP], Peng Zhan[SUP] 1 [/SUP]
Affiliations
Influenza viruses pose a significant threat to human health worldwide due to seasonal epidemics and occasional global pandemics. These viruses can cause severe upper respiratory tract infections that contribute to high morbidity and mortality rates. The emergence of drug-resistant influenza viruses has created the need for the development of novel broad-spectrum antivirals. Here, we present a novel anti-influenza agent with new targets and mechanisms of action to address this problem. Our findings led to the discovery of a novel influenza virus inhibitor, a ligustrazine derivative known as A9. We have found that it exhibits broad-spectrum antiviral properties against influenza A and B viruses (IAV and IBV, respectively), including oseltamivir-resistant strain. Through multiple bioassays such as time-of-addition assay, indirect immunofluorescence assay, and nuclear-cytoplasmic fractionation assay, we demonstrated that A9 inhibits the nuclear export of the viral ribonucleoprotein (vRNP). Furthermore, escape mutant analyses and affinity studies determined by surface plasmon resonance indicated that A9 specifically targets the nucleoprotein. In addition, four chalcone derivatives developed from A9 (B14, B29, B31, and B32), were found to effectively inhibit the replication of influenza virus through the same mechanism of action. In this manuscript we highlight A9 and its four derivatives as potential leads for the treatment of IAV and IBV infections, and their unique and novel mechanism of action probable benefit the field of anti-influenza drug discovery.
Keywords: anti-influenza viruses; chalcone derivatives; ligustrazine derivatives; nuclear export inhibitor; nucleoprotein; phenotypic screening.
. 2023 Jul;95(7):e28968.
doi: 10.1002/jmv.28968. Discovery of ligustrazine and chalcone derivatives as novel viral nucleoprotein nuclear export inhibitors against influenza viruses
Ping Li[SUP] 1 2 [/SUP], Han Ju[SUP] 1 [/SUP], Ying Zhang[SUP] 1 [/SUP], Jazmin Galvan Achi[SUP] 3 [/SUP], Dongwei Kang[SUP] 1 [/SUP], Jinmi Zou[SUP] 1 [/SUP], Ruikun Du[SUP] 2 [/SUP], Qinghua Cui[SUP] 2 [/SUP], Xinyong Liu[SUP] 1 [/SUP], Lijun Rong[SUP] 3 [/SUP], Peng Zhan[SUP] 1 [/SUP]
Affiliations
- PMID: 37489704
- DOI: 10.1002/jmv.28968
Influenza viruses pose a significant threat to human health worldwide due to seasonal epidemics and occasional global pandemics. These viruses can cause severe upper respiratory tract infections that contribute to high morbidity and mortality rates. The emergence of drug-resistant influenza viruses has created the need for the development of novel broad-spectrum antivirals. Here, we present a novel anti-influenza agent with new targets and mechanisms of action to address this problem. Our findings led to the discovery of a novel influenza virus inhibitor, a ligustrazine derivative known as A9. We have found that it exhibits broad-spectrum antiviral properties against influenza A and B viruses (IAV and IBV, respectively), including oseltamivir-resistant strain. Through multiple bioassays such as time-of-addition assay, indirect immunofluorescence assay, and nuclear-cytoplasmic fractionation assay, we demonstrated that A9 inhibits the nuclear export of the viral ribonucleoprotein (vRNP). Furthermore, escape mutant analyses and affinity studies determined by surface plasmon resonance indicated that A9 specifically targets the nucleoprotein. In addition, four chalcone derivatives developed from A9 (B14, B29, B31, and B32), were found to effectively inhibit the replication of influenza virus through the same mechanism of action. In this manuscript we highlight A9 and its four derivatives as potential leads for the treatment of IAV and IBV infections, and their unique and novel mechanism of action probable benefit the field of anti-influenza drug discovery.
Keywords: anti-influenza viruses; chalcone derivatives; ligustrazine derivatives; nuclear export inhibitor; nucleoprotein; phenotypic screening.