tetano
Editor, Senior Moderator
J Virol. 2020 Jan 2. pii: JVI.01888-19. doi: 10.1128/JVI.01888-19. [Epub ahead of print] [h=1]Repurposing papaverine as an antiviral agent against influenza viruses and paramyxoviruses.[/h]
Aggarwal M[SUP]1,[/SUP][SUP]1[/SUP], Leser GP[SUP]1,[/SUP][SUP]1[/SUP], Lamb RA[SUP]2,[/SUP][SUP]1[/SUP].
[h=3]Author information[/h] 1 Department of Molecular Biosciences and Howard Hughes Medical Institute, Northwestern University, Evanston, Illinois, 60208-3500 USA. 2 Department of Molecular Biosciences and Howard Hughes Medical Institute, Northwestern University, Evanston, Illinois, 60208-3500 USA ralamb@northwestern.edu.
[h=3]Abstract[/h] Influenza viruses are highly infectious and are the leading cause of human respiratory diseases and may trigger severe epidemics and occasional pandemics. Although antiviral drugs against influenza virus have been developed, there is an urgent need to design new strategies to develop influenza virus inhibitors due to the increasing resistance of viruses towards currently available drugs. In this study, we examined the antiviral activity of natural compounds against influenza virus strains: A/WSN/33 (H1N1), A/Udorn/72 (H3N2) and B/Lee/40. Papaverine (a non-narcotic alkaloid that has been used for the treatment of heart disease, impotency and psychosis) was found to be an effective inhibitor of multiple strains of influenza virus. Kinetic studies demonstrated that papaverine inhibited influenza virus infection at a late stage in the virus life cycle. An alteration in influenza virus morphology and viral ribonucleoproteins (vRNPs) localization was observed as an effect of papaverine treatment. Papaverine is a well-known phosphodiesterase inhibitor and also modifies MAPK (mitogen-activated protein kinase) pathway by downregulating the phosphorylation of MEK and ERK (Extracellular signal-related kinase). Thus, the modulation of host cell signaling pathways by papaverine may be associated with the nuclear retention of vRNPs and the reduction of influenza virus titers. Interestingly, papaverine also inhibited paramyxoviruses PIV5, HPIV3 and RSV infection. We propose that papaverine can be a potential candidate to be used as an antiviral agent against a broad range of influenza viruses and paramyxoviruses.Importance Influenza viruses are important human pathogens which are the causative agents of epidemics and pandemics. Despite the availability of an annual vaccine, a large number of cases occur every year globally. Here, we report that papaverine, a vasodilator, shows inhibitory action against various strains of influenza virus as well as the paramyxoviruses PIV5, HPIV3 and RSV. A significant effect of papaverine on the influenza virus morphology was observed. Papaverine treatment of influenza virus infected cells resulted in the inhibition of virus at a later time in the virus life cycle through the suppression of nuclear export of vRNP and also interfered with the host cellular cAMP and MEK/ERK cascade pathways. This study explores the use of papaverine as an effective inhibitor of both influenza viruses as well as paramyxoviruses.
Copyright ? 2020 American Society for Microbiology.
PMID: 31896588 DOI: 10.1128/JVI.01888-19
Aggarwal M[SUP]1,[/SUP][SUP]1[/SUP], Leser GP[SUP]1,[/SUP][SUP]1[/SUP], Lamb RA[SUP]2,[/SUP][SUP]1[/SUP].
[h=3]Author information[/h] 1 Department of Molecular Biosciences and Howard Hughes Medical Institute, Northwestern University, Evanston, Illinois, 60208-3500 USA. 2 Department of Molecular Biosciences and Howard Hughes Medical Institute, Northwestern University, Evanston, Illinois, 60208-3500 USA ralamb@northwestern.edu.
[h=3]Abstract[/h] Influenza viruses are highly infectious and are the leading cause of human respiratory diseases and may trigger severe epidemics and occasional pandemics. Although antiviral drugs against influenza virus have been developed, there is an urgent need to design new strategies to develop influenza virus inhibitors due to the increasing resistance of viruses towards currently available drugs. In this study, we examined the antiviral activity of natural compounds against influenza virus strains: A/WSN/33 (H1N1), A/Udorn/72 (H3N2) and B/Lee/40. Papaverine (a non-narcotic alkaloid that has been used for the treatment of heart disease, impotency and psychosis) was found to be an effective inhibitor of multiple strains of influenza virus. Kinetic studies demonstrated that papaverine inhibited influenza virus infection at a late stage in the virus life cycle. An alteration in influenza virus morphology and viral ribonucleoproteins (vRNPs) localization was observed as an effect of papaverine treatment. Papaverine is a well-known phosphodiesterase inhibitor and also modifies MAPK (mitogen-activated protein kinase) pathway by downregulating the phosphorylation of MEK and ERK (Extracellular signal-related kinase). Thus, the modulation of host cell signaling pathways by papaverine may be associated with the nuclear retention of vRNPs and the reduction of influenza virus titers. Interestingly, papaverine also inhibited paramyxoviruses PIV5, HPIV3 and RSV infection. We propose that papaverine can be a potential candidate to be used as an antiviral agent against a broad range of influenza viruses and paramyxoviruses.Importance Influenza viruses are important human pathogens which are the causative agents of epidemics and pandemics. Despite the availability of an annual vaccine, a large number of cases occur every year globally. Here, we report that papaverine, a vasodilator, shows inhibitory action against various strains of influenza virus as well as the paramyxoviruses PIV5, HPIV3 and RSV. A significant effect of papaverine on the influenza virus morphology was observed. Papaverine treatment of influenza virus infected cells resulted in the inhibition of virus at a later time in the virus life cycle through the suppression of nuclear export of vRNP and also interfered with the host cellular cAMP and MEK/ERK cascade pathways. This study explores the use of papaverine as an effective inhibitor of both influenza viruses as well as paramyxoviruses.
Copyright ? 2020 American Society for Microbiology.
PMID: 31896588 DOI: 10.1128/JVI.01888-19