
Novel Class of Chikungunya Virus Small Molecule Inhibitors That Targets the Viral Capping Machinery
Author(s) -
Rana Abdelnabi,
Kristina Kovacikova,
Julia Moesslacher,
Kim Donckers,
Verena Battisti,
Pieter Leyssen,
Thomas Langer,
Gerhard Puerstinger,
Gilles Quérat,
Changqing Li,
Étienne Decroly,
Ali Taş,
Arnaud Marchand,
Patrick Chaltin,
Bruno Coutard,
Martijn J. van Hemert,
Johan Neyts,
Leen Delang
Publication year - 2020
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.00649-20
Subject(s) - chikungunya , virology , virus , alphavirus , biology , viral replication , mutation , gene , genetics
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 (CHVB res ) 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, CHVB res 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.