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Novel Cytomegalovirus UL54 DNA Polymerase Gene Mutations Selected In Vitro That Confer Brincidofovir Resistance.
Chou, Sunwen; Ercolani, Ronald J; Lanier, E Randall.
Afiliação
  • Chou S; Division of Infectious Diseases, Oregon Health and Science University, Portland, Oregon, USA Research Service, VA Portland Health Care System, Portland, Oregon, USA chous@ohsu.edu.
  • Ercolani RJ; Research Service, VA Portland Health Care System, Portland, Oregon, USA.
  • Lanier ER; Chimerix, Durham, North Carolina, USA.
Antimicrob Agents Chemother ; 60(6): 3845-8, 2016 06.
Article em En | MEDLINE | ID: mdl-27044553
Eight in vitro selection experiments under brincidofovir pressure elicited the known cytomegalovirus DNA polymerase amino acid substitutions N408K and V812L and the novel exonuclease domain substitutions D413Y, E303D, and E303G, which conferred ganciclovir and cidofovir resistance with 6- to 11-fold resistance to brincidofovir or 17-fold when E303G was combined with V812L. The new exonuclease domain I resistance mutations selected under brincidofovir pressure add to the single instance previously reported and show the expected patterns of cross-resistance.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / Proteínas Virais / Citomegalovirus / Citosina / DNA Polimerase Dirigida por DNA / Organofosfonatos / Mutação Limite: Humans Idioma: En Revista: Antimicrob Agents Chemother Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / Proteínas Virais / Citomegalovirus / Citosina / DNA Polimerase Dirigida por DNA / Organofosfonatos / Mutação Limite: Humans Idioma: En Revista: Antimicrob Agents Chemother Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos