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Detail publikace
Eyer, L., Kondo, H., Zouharova, D., Hirano, M., Valdés, J.J., Muto, M., Kastl, T., Kobayashi, S., Haviernik, J., Igarashi, M., Kariwa, H., Vaculovicova, M., Cerny, J., Kizek, R., Kröger, A., Lienenklaus, S., Dejmek, M., Nencka, R., Palus, M., Salat, J., De Clercq, E., Yoshii, K., Ruzek, D.
Originální název
Escape of tick-borne flavivirus from 2'-C-methylated nucleoside antivirals is mediated by a single conservative mutation in NS5 that has a dramatic effect on viral fitness
Typ
článek v časopise ve Web of Science, Jimp
Jazyk
angličtina
Originální abstrakt
Tick-borne encephalitis virus (TBEV) causes a severe and potentially fatal neuroinfection in humans. Despite its high medical relevance, no specific antiviral therapy is currently available. Here we demonstrate that treatment with a nucleoside analog, 7-deaza-2=-C-methyladenosine (7-deaza-2=-CMA), substantially improved disease outcomes, increased survival, and reduced signs of neuroinfection and viral titers in the brains of mice infected with a lethal dose of TBEV. To investigate the mechanism of action of 7-deaza-2=-CMA, two drug-resistant TBEV clones were generated and characterized. The two clones shared a signature amino acid substitution, S603T, in the viral NS5 RNA-dependent RNA polymerase (RdRp) domain. This mutation conferred resistance to various 2=-C-methylated nucleoside derivatives, but no cross-resistance was seen with other nucleoside analogs, such as 4=-C-azidocytidine and 2=-deoxy-2=-beta-hydroxy-4=-azidocytidine (RO-9187). All-atom molecular dynamics simulations revealed that the S603T RdRp mutant repels a water molecule that coordinates the position of a metal ion cofactor as 2=-C-methylated nucleoside analogs approach the active site. To investigate its phenotype, the S603T mutation was introduced into a recombinant TBEV strain (Oshima-IC) generated from an infectious cDNA clone and into a TBEV replicon that expresses a reporter luciferase gene (Oshima- REP-luc2A). The mutants were replication impaired, showing reduced growth and a small plaque size in mammalian cell culture and reduced levels of neuroinvasiveness and neurovirulence in rodent models. These results indicate that TBEV resistance to 2=-C-methylated nucleoside inhibitors is conferred by a single conservative mutation that causes a subtle atomic effect within the active site of the viral NS5 RdRp and is associated with strong attenuation of the virus.
Klíčová slova
antiviral agents; antiviral therapy; escape mutant; tick-borne encephalitis virus; tick-borne pathogens
Autoři
Vydáno
1. 11. 2017
ISSN
0022-538X
Periodikum
JOURNAL OF VIROLOGY
Ročník
91
Číslo
21
Stát
Spojené státy americké
Strany od
1
Strany do
20
Strany počet
BibTex
@article{BUT141910, author="Markéta {Vaculovičová} and Daniel {Růžek} and Luděk {Eyer} and James Jason {Valdés} and Jiří {Černý} and Martin {Palus} and Jiří {Salát} and Darina {Zouharová} and Tomáš {Kastl} and Jan {Haviernik} and René {Kizek}", title="Escape of tick-borne flavivirus from 2'-C-methylated nucleoside antivirals is mediated by a single conservative mutation in NS5 that has a dramatic effect on viral fitness", journal="JOURNAL OF VIROLOGY", year="2017", volume="91", number="21", pages="1--20", doi="10.1128/JVI.01028-17", issn="0022-538X" }