Academic Journal
Viral Polymerase-Helicase Complexes Regulate Replication Fidelity To Overcome Intracellular Nucleotide Depletion
العنوان: | Viral Polymerase-Helicase Complexes Regulate Replication Fidelity To Overcome Intracellular Nucleotide Depletion |
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المؤلفون: | Stapleford, Kenneth A., Rozen-Gagnon, Kathryn, Das, Pratyush Kumar, Saul, Sirle, Poirier, Enzo Z., Blanc, Hervé, Vidalain, Pierre-Olivier, Merits, Andres, Vignuzzi, Marco |
المساهمون: | Dermody, T. S. |
المصدر: | Journal of Virology ; volume 89, issue 22, page 11233-11244 ; ISSN 0022-538X 1098-5514 |
بيانات النشر: | American Society for Microbiology |
سنة النشر: | 2015 |
الوصف: | To date, the majority of work on RNA virus replication fidelity has focused on the viral RNA polymerase, while the potential role of other viral replicase proteins in this process is poorly understood. Previous studies used resistance to broad-spectrum RNA mutagens, such as ribavirin, to identify polymerases with increased fidelity that avoid misincorporation of such base analogues. We identified a novel variant in the alphavirus viral helicase/protease, nonstructural protein 2 (nsP2) that operates in concert with the viral polymerase nsP4 to further alter replication complex fidelity, a functional linkage that was conserved among the alphavirus genus. Purified chikungunya virus nsP2 presented delayed helicase activity of the high-fidelity enzyme, and yet purified replication complexes manifested stronger RNA polymerization kinetics. Because mutagenic nucleoside analogs such as ribavirin also affect intracellular nucleotide pools, we addressed the link between nucleotide depletion and replication fidelity by using purine and pyrimidine biosynthesis inhibitors. High-fidelity viruses were more resistant to these conditions, and viral growth could be rescued by the addition of exogenous nucleosides, suggesting that mutagenesis by base analogues requires nucleotide pool depletion. This study describes a novel function for nsP2, highlighting the role of other components of the replication complex in regulating viral replication fidelity, and suggests that viruses can alter their replication complex fidelity to overcome intracellular nucleotide-depleting conditions. IMPORTANCE Previous studies using the RNA mutagen ribavirin to select for drug-resistant variants have highlighted the essential role of the viral RNA-dependent RNA polymerase in regulating replication fidelity. However, the role of other viral replicase components in replication fidelity has not been studied in detail. We identified here an RNA mutagen-resistant variant of the nsP2 helicase/protease that conferred increased fidelity and yet could ... |
نوع الوثيقة: | article in journal/newspaper |
اللغة: | English |
DOI: | 10.1128/jvi.01553-15 |
DOI: | 10.1128/JVI.01553-15 |
الاتاحة: | http://dx.doi.org/10.1128/jvi.01553-15 https://journals.asm.org/doi/pdf/10.1128/JVI.01553-15 |
Rights: | http://creativecommons.org/licenses/by-nc-sa/3.0/ ; https://journals.asm.org/non-commercial-tdm-license |
رقم الانضمام: | edsbas.6D5ABDB8 |
قاعدة البيانات: | BASE |
DOI: | 10.1128/jvi.01553-15 |
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