| Literature DB >> 32340991 |
Rana Abdelnabi1, Kristina Kovacikova2, Johan Neyts1, Leen Delang3, Julia Moesslacher4, Kim Donckers1, Verena Battisti5, Pieter Leyssen1, Thierry Langer5, Gerhard Puerstinger4, Gilles Quérat6, Changqing Li7, Etienne Decroly7, Ali Tas2, Arnaud Marchand8, Patrick Chaltin8, Bruno Coutard6, Martijn van Hemert2.
Abstract
Despite the worldwide reemergence of the chikungunya virus (CHIKV) and the high morbidity associated with CHIKV infections, there is no approved vaccine or antiviral treatment available. Here, we aimed to identify the target of a novel class of CHIKV inhibitors, i.e., the CHVB series. CHVB compounds inhibit the in vitro replication of CHIKV isolates with 50% effective concentrations in the low-micromolar range. A CHVB-resistant variant (CHVBres) was selected that carried two mutations in the gene encoding nsP1 (responsible for viral RNA capping), one mutation in nsP2, and one mutation in nsP3. Reverse genetics studies demonstrated that both nsP1 mutations were necessary and sufficient to achieve ∼18-fold resistance, suggesting that CHVB targets viral mRNA capping. Interestingly, CHVBres was cross-resistant to the previously described CHIKV capping inhibitors from the MADTP series, suggesting they share a similar mechanism of action. In enzymatic assays, CHVB inhibited the methyltransferase and guanylyltransferase activities of alphavirus nsP1 proteins. To conclude, we identified a class of CHIKV inhibitors that targets the viral capping machinery. The potent anti-CHIKV activity makes this chemical scaffold a potential candidate for CHIKV drug development.Entities:
Keywords: CHIKV; MADTP; antivirals; capping; chikungunya virus; nonstructural protein 1; nsP1
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Year: 2020 PMID: 32340991 PMCID: PMC7317993 DOI: 10.1128/AAC.00649-20
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191