Please use this identifier to cite or link to this item: http://hdl.handle.net/10637/15647

Structure of Foot-and-Mouth Disease Virus Mutant Polymerases with Reduced Sensitivity to Ribavirin

Title: Structure of Foot-and-Mouth Disease Virus Mutant Polymerases with Reduced Sensitivity to Ribavirin
Authors : Ferrer-Orta, Cristina
Sierra, Macarena
Agudo Torres, Rubén
De la Higuera, Ignacio
Arias, Armando
Pérez-Luque, Rosa
Escarmís, Cristina
Domingo, Esteban
Verdaguer, Nuria
Keywords: Foot-and-Mouth DiseaseRibavirinVirus
Publisher: American Society for Microbiology
Citation: Structure of foot-and-mouth disease virus mutant polymerases with reduced sensitivity to ribavirin. Ferrer-Orta C, Sierra M, Agudo R, de la Higuera I, Arias A, Pérez-Luque R, Escarmis C, Domingo E, Verdaguer E. Journal of Virology 84(12), pp. 6188 - 6199 (2010)
Abstract: Passage of poliovirus (PV) or foot-and-mouth disease virus (FMDV) in the presence of ribavirin (R) selected for viruses with decreased sensitivity to R, which included different mutations in their polymerase (3D): G64S located in the finger subdomain in the case of PV and M296I located within loop 9- 11 at the active site in the case of FMDV. To investigate why disparate substitutions were selected in two closely related 3Ds, we constructed FMDVs with a 3D that included either G62S (the equivalent replacement in FMDV of PV G64S), M296I, or both substitutions. G62S, but not M296I, inflicts upon FMDV a strong selective disadvantage which is partially compensated for by the substitution M296I. The corresponding mutant polymerases, 3D(G62S), 3D(M296I), and 3D(G62S-M296I), were analyzed functionally and structurally. G62S in 3D impairs RNA-binding, polymerization, and R monophosphate incorporation activities. The X-ray structures of the 3D(G62S)-RNA, 3D(M296I)-RNA, and 3D(G62S-M296I)-RNA complexes show that although the two positions are separated by 13.1 Å, the loops where the replacements reside are tightly connected through an extensive network of interactions that reach the polymerase active site. In particular, G62S seems to restrict the flexibility of loop 9- 11 and, as a consequence, the flexibility of the active site and its ability to bind the RNA template. Thus, a localized change in the finger subdomain of 3D may affect the catalytic domain. The results provide a structural interpretation of why different amino acid substitutions were selected to confer R resistance in closely related viruses and reveal a complex network of intra-3D interactions that can affect the recognition of both the RNA template and incoming nucleotide.
URI: http://hdl.handle.net/10637/15647
Rights : http://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
ISSN: 1098-5514
Issue Date: 14-Apr-2010
Appears in Collections:Facultad de Farmacia





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