Skip to Main content Skip to Navigation
Journal articles

Mutations on VEEV nsP1 relate RNA capping efficiency to ribavirin susceptibility

Abstract : Alphaviruses are arthropod-borne viruses of public health concern. To date no efficient vaccine nor antivirals are available for safe human use. During viral replication the nonstructural protein 1 (nsP1) catalyzes capping of genomic and subgenomic RNAs. The capping reaction is unique to the Alphavirus genus. The whole three-step process follows a particular order: (i) transfer of a methyl group from S-adenosyl methionine (SAM) onto a GTP forming m7GTP; (ii) guanylylation of the enzyme to form a m7GMP-nsP1adduct; (iii) transfer of m7GMP onto 5′-diphosphate RNA to yield capped RNA. Specificities of these reactions designate nsP1 as a promising target for antiviral drug development. In the current study we performed a mutational analysis on two nsP1 positions associated with Sindbis virus (SINV) ribavirin resistance in the Venezuelan equine encephalitis virus (VEEV) context through reverse genetics correlated to enzyme assays using purified recombinant VEEV nsP1 proteins. The results demonstrate that the targeted positions are strongly associated to the regulation of the capping reaction by increasing the affinity between GTP and nsP1. Data also show that in VEEV the S21A substitution, naturally occurring in Chikungunya virus (CHIKV), is a hallmark of ribavirin susceptibility. These findings uncover the specific mechanistic contributions of these residues to nsp1-mediated methyl-transfer and guanylylation reactions.
Document type :
Journal articles
Complete list of metadata
Contributor : Etienne Decroly Connect in order to contact the contributor
Submitted on : Monday, November 30, 2020 - 11:42:29 AM
Last modification on : Wednesday, January 19, 2022 - 4:58:35 PM




Nadia Rabah, Oney Ortega Granda, Gilles Quérat, Bruno Canard, Etienne Decroly, et al.. Mutations on VEEV nsP1 relate RNA capping efficiency to ribavirin susceptibility. Antiviral Research, Elsevier Masson, 2020, 182, pp.104883. ⟨10.1016/j.antiviral.2020.104883⟩. ⟨hal-03030827⟩



Record views