Abstract

Arthropod-borne viruses are diverse pathogens and are often associated with human disease. These viruses span multiple genera, including flaviviruses, alphaviruses, and bunyaviruses. In a high-throughput drug screen, we found that tenovin-1 was antiviral against the flaviviruses Zika virus and dengue virus. Tenovin-1 is a sirtuin inhibitor, and here we found that inhibition of sirtuins, but not inhibition of the related histone deacetylases, is potently antiviral against diverse arboviruses. Sirtuin inhibitors block infection of arboviruses in multiple human cell types. We found that sirtuin inhibitors arrest infection downstream of entry but that they do so at an early step, preventing the accumulation of viral RNA and protein. However, sirtuin inhibitors had no impact on the replication of flaviviral replicons, suggesting a defect in the establishment of replication. Consistent with this, we found that sirtuin inhibitors impacted double-stranded RNA (dsRNA) accumulation during flaviviral infection. Since these viruses infect vector insects, we also tested whether sirtuin inhibitors impacted infection of adult flies and found that these inhibitors blocked infection; therefore, they target highly conserved facets of replication. Taken together, these results suggest that sirtuin inhibitors represent a new class of potent host-targeting antivirals.IMPORTANCE Arthropod-borne viruses are diverse pathogens and are associated with human disease. Through high-throughput drug screening, we found that sirtuin inhibitors are potently antiviral against diverse arboviruses, including flaviviruses such as West Nile virus, bunyaviruses such as Rift Valley fever virus, and alphaviruses such as chikungunya virus. Sirtuin inhibitors block infection of these viruses in multiple human cell types. Moreover, we found that sirtuin inhibitors arrest infection downstream of entry but that they do so at an early step, preventing the accumulation of viral RNA and protein. Since these viruses infect vector insects, we also tested whether sirtuin inhibitors impacted infection of adult flies and found that these inhibitors blocked infection; therefore, they target highly conserved facets of replication. Taken together, these results suggest that sirtuin inhibitors represent a new class of potent host-targeting antivirals.

Highlights

  • Arthropod-borne viruses are diverse pathogens and are often associated with human disease

  • Flaviviruses are the most widespread group and are enveloped positivesense RNA viruses that include dengue virus (DENV), which infects hundreds of millions of people yearly; Zika virus (ZIKV), which recently emerged in the Americas; yellow fever virus (YFV), which causes high mortality in the Americas and Africa; and West Nile virus (WNV), which became endemic in the New World in the last 2 decades [2]

  • Bunyaviruses, the third major group of arboviruses, are enveloped trisegmented negativesense viruses that include many important human pathogens such as Rift Valley fever virus (RVFV), which has a devastating impact on livestock in Africa, and La Crosse virus (LACV), which is responsible for high rates of encephalitis in children in the United States [4]

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Summary

Introduction

Arthropod-borne viruses are diverse pathogens and are often associated with human disease. We found that sirtuin inhibitors arrest infection downstream of entry but that they do so at an early step, preventing the accumulation of viral RNA and protein Since these viruses infect vector insects, we tested whether sirtuin inhibitors impacted infection of adult flies and found that these inhibitors blocked infection; they target highly conserved facets of replication. Flaviviruses are the most widespread group and are enveloped positivesense RNA viruses that include dengue virus (DENV), which infects hundreds of millions of people yearly; Zika virus (ZIKV), which recently emerged in the Americas; yellow fever virus (YFV), which causes high mortality in the Americas and Africa; and West Nile virus (WNV), which became endemic in the New World in the last 2 decades [2]. Whether sirtuin inhibitors impact arbovirus infection has not yet been explored

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