tetano
Editor, Senior Moderator
J Virol. 2019 Jun 5. pii: JVI.00878-19. doi: 10.1128/JVI.00878-19. [Epub ahead of print]
[h=1]Novel small molecule targeting the hemagglutinin stalk of influenza viruses.[/h] Kim JI[SUP]1[/SUP], Lee S[SUP]1[/SUP], Lee GY[SUP]2[/SUP], Park S[SUP]1[/SUP], Bae JY[SUP]1[/SUP], Heo J[SUP]2[/SUP], Kim HY[SUP]2[/SUP], Woo SH[SUP]2[/SUP], Lee HU[SUP]2[/SUP], Ahn CA[SUP]2[/SUP], Bang HJ[SUP]2[/SUP], Ju HS[SUP]2[/SUP], Ok K[SUP]3[/SUP], Byun Y[SUP]3[/SUP], Cho DJ[SUP]2[/SUP], Shin JS[SUP]2[/SUP], Kim DY[SUP]2[/SUP], Park MS[SUP]1[/SUP], Park MS[SUP]4[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Combating influenza is one of the perennial global public health issues to be managed. Antiviral drugs are useful for the treatment of influenza in the absence of an appropriate vaccine. However, the appearance of resistant strains necessitates a constant search for new drugs. In this study, we investigated novel anti-influenza drug candidates using in vitro and in vivo assays. We identified anti-influenza hit compounds using a high-throughput screening method with a green fluorescent protein-tagged recombinant influenza virus. Through subsequent analyses of their cytotoxicity and pharmacokinetic properties, one candidate (IY7640) was selected for further evaluation. In a replication kinetics analysis, IY7640 showed greater inhibitory effects during the early phase of viral infection than the viral neuraminidase-inhibitor oseltamivir. In addition, we observed that hemagglutinin (HA)-mediated membrane fusion was inhibited by the IY7640 treatment, indicating that the HA stalk region, which is highly conserved across various (sub)types of influenza viruses, may be the molecular target of IY7640. In an escape mutant analysis in cells, amino acid mutations were identified at the HA stalk region of the 2009 pandemic H1N1 (pH1N1) virus. Even though the in vivo efficacy of IY7640 did not reach to complete protection in a lethal challenge study in mice, these results suggest that IY7640 has potential to be developed as a new type of anti-influenza drug.IMPORTANCEAnti-influenza drugs with broad-spectrum efficacy against antigenically diverse influenza viruses can be highly useful when no vaccines are available. To develop new anti-influenza drugs, we screened a number of small molecules and identified a strong candidate, IY7640. When added at the time of or after influenza virus infection, IY7640 was observed to successfully inhibit or reduce viral replication in cells. We subsequently discovered that IY7640 targets the stalk region of the influenza HA protein, which exhibits a relatively high degree of amino acid sequence conservation across various (sub)types of influenza viruses. Furthermore, IY7640 was observed to block HA-mediated membrane fusion of H1N1, H3N2, and influenza B viruses in cells. Although it appears less effective against strains other than H1N1 subtype viruses in a challenge study in mice, we suggest that the small molecule IY7640 has potential to be optimized as a new anti-influenza drug.
Copyright ? 2019 American Society for Microbiology.
PMID: 31167918 DOI: 10.1128/JVI.00878-19
[h=1]Novel small molecule targeting the hemagglutinin stalk of influenza viruses.[/h] Kim JI[SUP]1[/SUP], Lee S[SUP]1[/SUP], Lee GY[SUP]2[/SUP], Park S[SUP]1[/SUP], Bae JY[SUP]1[/SUP], Heo J[SUP]2[/SUP], Kim HY[SUP]2[/SUP], Woo SH[SUP]2[/SUP], Lee HU[SUP]2[/SUP], Ahn CA[SUP]2[/SUP], Bang HJ[SUP]2[/SUP], Ju HS[SUP]2[/SUP], Ok K[SUP]3[/SUP], Byun Y[SUP]3[/SUP], Cho DJ[SUP]2[/SUP], Shin JS[SUP]2[/SUP], Kim DY[SUP]2[/SUP], Park MS[SUP]1[/SUP], Park MS[SUP]4[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Combating influenza is one of the perennial global public health issues to be managed. Antiviral drugs are useful for the treatment of influenza in the absence of an appropriate vaccine. However, the appearance of resistant strains necessitates a constant search for new drugs. In this study, we investigated novel anti-influenza drug candidates using in vitro and in vivo assays. We identified anti-influenza hit compounds using a high-throughput screening method with a green fluorescent protein-tagged recombinant influenza virus. Through subsequent analyses of their cytotoxicity and pharmacokinetic properties, one candidate (IY7640) was selected for further evaluation. In a replication kinetics analysis, IY7640 showed greater inhibitory effects during the early phase of viral infection than the viral neuraminidase-inhibitor oseltamivir. In addition, we observed that hemagglutinin (HA)-mediated membrane fusion was inhibited by the IY7640 treatment, indicating that the HA stalk region, which is highly conserved across various (sub)types of influenza viruses, may be the molecular target of IY7640. In an escape mutant analysis in cells, amino acid mutations were identified at the HA stalk region of the 2009 pandemic H1N1 (pH1N1) virus. Even though the in vivo efficacy of IY7640 did not reach to complete protection in a lethal challenge study in mice, these results suggest that IY7640 has potential to be developed as a new type of anti-influenza drug.IMPORTANCEAnti-influenza drugs with broad-spectrum efficacy against antigenically diverse influenza viruses can be highly useful when no vaccines are available. To develop new anti-influenza drugs, we screened a number of small molecules and identified a strong candidate, IY7640. When added at the time of or after influenza virus infection, IY7640 was observed to successfully inhibit or reduce viral replication in cells. We subsequently discovered that IY7640 targets the stalk region of the influenza HA protein, which exhibits a relatively high degree of amino acid sequence conservation across various (sub)types of influenza viruses. Furthermore, IY7640 was observed to block HA-mediated membrane fusion of H1N1, H3N2, and influenza B viruses in cells. Although it appears less effective against strains other than H1N1 subtype viruses in a challenge study in mice, we suggest that the small molecule IY7640 has potential to be optimized as a new anti-influenza drug.
Copyright ? 2019 American Society for Microbiology.
PMID: 31167918 DOI: 10.1128/JVI.00878-19