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High-throughput sequence analysis of variants of human cytomegalovirus strains Towne and AD169.
Bradley, Amanda J; Lurain, Nell S; Ghazal, Peter; Trivedi, Urmi; Cunningham, Charles; Baluchova, Katarina; Gatherer, Derek; Wilkinson, Gavin W G; Dargan, Derrick J; Davison, Andrew J.
Afiliación
  • Bradley AJ; MRC Virology Unit, Institute of Virology, Church Street, Glasgow G11 5JR, UK.
  • Lurain NS; Department of Immunology and Microbiology, Rush University Medical Center, 1653 West Congress Parkway, Chicago, IL 60612, USA.
  • Ghazal P; Division of Pathway Medicine, University of Edinburgh Medical School, Chancellor's Building, 49 Little France Crescent, Edinburgh EH16 4SB, UK.
  • Trivedi U; The Gene Pool, Ashworth Laboratories, Institute of Evolutionary Biology, King's Buildings, Edinburgh EH9 3JT, UK.
  • Cunningham C; MRC Virology Unit, Institute of Virology, Church Street, Glasgow G11 5JR, UK.
  • Baluchova K; MRC Virology Unit, Institute of Virology, Church Street, Glasgow G11 5JR, UK.
  • Gatherer D; MRC Virology Unit, Institute of Virology, Church Street, Glasgow G11 5JR, UK.
  • Wilkinson GWG; Department of Medical Microbiology, Tenovus Building, School of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XX, UK.
  • Dargan DJ; MRC Virology Unit, Institute of Virology, Church Street, Glasgow G11 5JR, UK.
  • Davison AJ; MRC Virology Unit, Institute of Virology, Church Street, Glasgow G11 5JR, UK.
J Gen Virol ; 90(Pt 10): 2375-2380, 2009 Oct.
Article en En | MEDLINE | ID: mdl-19553388
ABSTRACT
The genomes of commonly used variants of human cytomegalovirus (HCMV) strains Towne and AD169 each contain a substantial mutation in which a region (U(L)/b') at the right end of the long unique region has been replaced by an inverted duplication of a region from the left end of the genome. Using high-throughput technology, we have sequenced HCMV strain Towne (ATCC VR-977) and confirmed the presence of two variants, one exhibiting the replacement in U(L)/b' and the other intact in this region. Both variants are mutated in genes RL13, UL1, UL40, UL130, US1 and US9. We have also sequenced a novel AD169 variant (varUC) that is intact in U(L)/b' except for a small deletion that affects genes UL144, UL142, UL141 and UL140. Like other AD169 variants, varUC is mutated in genes RL5A, RL13, UL36 and UL131A. A subpopulation of varUC contains an additional deletion affecting genes IRS1, US1 and US2.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Citomegalovirus Límite: Humans Idioma: En Revista: J Gen Virol Año: 2009 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Citomegalovirus Límite: Humans Idioma: En Revista: J Gen Virol Año: 2009 Tipo del documento: Article País de afiliación: Reino Unido