Please use this identifier to cite or link to this item: https://doi.org/10.1126/scitranslmed.3008517
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dc.titleAn orally available, small-molecule polymerase inhibitor shows efficacy against a lethal morbillivirus infection in a large animal model
dc.contributor.authorKrumm, S.A.
dc.contributor.authorYan, D.
dc.contributor.authorHovingh, E.S.
dc.contributor.authorEvers, T.J.
dc.contributor.authorEnkirch, T.
dc.contributor.authorReddy, G.P.
dc.contributor.authorSun, A.
dc.contributor.authorSaindane, M.T.
dc.contributor.authorArrendale, R.F.
dc.contributor.authorPainter, G.
dc.contributor.authorLiotta, D.C.
dc.contributor.authorNatchus, M.G.
dc.contributor.authorVon Messling, V.
dc.contributor.authorPlemper, R.K.
dc.date.accessioned2016-06-01T10:28:33Z
dc.date.available2016-06-01T10:28:33Z
dc.date.issued2014-04-16
dc.identifier.citationKrumm, S.A., Yan, D., Hovingh, E.S., Evers, T.J., Enkirch, T., Reddy, G.P., Sun, A., Saindane, M.T., Arrendale, R.F., Painter, G., Liotta, D.C., Natchus, M.G., Von Messling, V., Plemper, R.K. (2014-04-16). An orally available, small-molecule polymerase inhibitor shows efficacy against a lethal morbillivirus infection in a large animal model. Science Translational Medicine 6 (232) : -. ScholarBank@NUS Repository. https://doi.org/10.1126/scitranslmed.3008517
dc.identifier.issn19466242
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/124761
dc.description.abstractMeasles virus is a highly infectious morbillivirus responsible for major morbidity and mortality in unvaccinated humans. The related, zoonotic canine distemper virus (CDV) induces morbillivirus disease in ferrets with 100% lethality. We report an orally available, shelf-stable pan-morbillivirus inhibitor that targets the viral RNA polymerase. Prophylactic oral treatment of ferrets infected intranasally with a lethal CDV dose reduced viremia and prolonged survival. Ferrets infected with the same dose of virus that received post-infection treatment at the onset of viremia showed low-grade viral loads, remained asymptomatic, and recovered from infection, whereas control animals succumbed to the disease. Animals that recovered also mounted a robust immune response and were protected against rechallenge with a lethal CDV dose.Drug-resistant viral recombinants were generated and found to be attenuated and transmission-impaired compared to the genetic parent virus. These findings may pioneer a path toward an effectivemorbillivirus therapy that could aid measles eradication by synergizing with vaccination to close gaps in herd immunity due to vaccine refusal.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1126/scitranslmed.3008517
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentDUKE-NUS GRADUATE MEDICAL SCHOOL S'PORE
dc.description.doi10.1126/scitranslmed.3008517
dc.description.sourcetitleScience Translational Medicine
dc.description.volume6
dc.description.issue232
dc.description.page-
dc.identifier.isiut000334586100003
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