English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/174186
Share/Impact:
Statistics
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:
Title

Contribution of a multifunctional polymerase region of foot-and-mouth disease virus to lethal mutagenesis

AuthorsHiguera, Ignacio de la ; Ferrer-Orta, Cristina ; Moreno, Elena ; Ávila, Ana Isabel de; Soria, María Eugenia; Singh, Kamalendra; Flavia Caridi,; Sobrino, Francisco; Sarafianos, Stefan G.; Perales, Celia ; Verdaguer, Núria ; Domingo, Esteban
KeywordsViral quasispecies
Nucleotide recognition
Polymerase structure
Ribavirin
Error threshold
Antiviral therapy
Issue DateOct-2018
PublisherAmerican Society for Microbiology
CitationJournal of Virology 92(20): e01119-18 (2018)
AbstractViral RNA-dependent RNA polymerases (RdRps) are major determinants of high mutation rates and generation of mutant spectra that mediate RNA virus adaptability. The RdRp of the picornavirus foot-and-mouth disease virus (FMDV), termed 3D, is a multifunctional protein that includes a nuclear localization signal (NLS) in its N-terminal region. Previous studies documented that some amino acid substitutions within the NLS altered nucleotide recognition and enhanced the incorporation of the mutagenic purine analogue ribavirin in viral RNA, but the mutants tested were not viable and their response to lethal mutagenesis could not be studied. Here we demonstrate that NLS amino acid substitution M16A of FMDV serotype C does not affect infectious virus production but accelerates ribavirin-mediated virus extinction. The mutant 3D displays polymerase activity, RNA binding, and copying processivity that are similar to those of the wild-type enzyme but shows increased ribavirin-triphosphate incorporation. Crystal structures of the mutant 3D in the apo and RNA-bound forms reveal an expansion of the template entry channel due to the replacement of the bulky Met by Ala. This is a major difference with other 3D mutants with altered nucleotide analogue recognition. Remarkably, two distinct loop β9-α11 conformations distinguish 3Ds that exhibit higher or lower ribavirin incorporation than the wild-type enzyme. This difference identifies a specific molecular determinant of ribavirin sensitivity of FMDV. Comparison of several polymerase mutants indicates that different domains of the molecule can modify nucleotide recognition and response to lethal mutagenesis. The connection of this observation with current views on quasispecies adaptability is discussed.
Publisher version (URL)https://doi.org/10.1128/JVI.01119-18
URIhttp://hdl.handle.net/10261/174186
DOI10.1128/JVI.01119-18
ISSN0022-538X
E-ISSN1098-5514
Appears in Collections:(IBMB) Artículos
Files in This Item:
File Description SizeFormat 
Multifunctuional_poly-post-print.pdf17,65 MBAdobe PDFThumbnail
View/Open
Show full item record
Review this work
 

Related articles:


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.