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Foscarnet resistance mutations mapping to atypical domains of the cytomegalovirus DNA polymerase gene
- Source :
- Antiviral Research. 138:57-60
- Publication Year :
- 2017
- Publisher :
- Elsevier BV, 2017.
-
Abstract
- Human cytomegalovirus UL54 DNA polymerase gene mutations that confer foscarnet resistance in clinical practice typically cluster in the amino terminal 2, palm and finger domains. Exposure to foscarnet in cell culture selected for mutations elsewhere in UL54, including amino acid substitutions S290R in the amino terminal 1 domain and E951D in the palm 2 domain. These are newly confirmed to confer foscarnet resistance and slightly decreased ganciclovir susceptibility. Other emergent substitutions N495K, T552N and T838A are known to confer foscarnet resistance, while additional ones Q783R and V798A only slightly affected susceptibility. An expanded set of domains is involved in foscarnet resistance and its genotypic diagnosis.
- Subjects :
- 0301 basic medicine
Foscarnet
Human cytomegalovirus
Ganciclovir
Genotype
DNA polymerase
030106 microbiology
Cytomegalovirus
DNA-Directed DNA Polymerase
Gene mutation
Antiviral Agents
Article
Viral Proteins
03 medical and health sciences
Virology
Drug Resistance, Viral
medicine
Humans
Polymerase Gene
Pharmacology
chemistry.chemical_classification
Genetics
biology
virus diseases
biochemical phenomena, metabolism, and nutrition
medicine.disease
Amino acid
Phenotype
Amino Acid Substitution
chemistry
Cytomegalovirus Infections
DNA, Viral
Mutation
biology.protein
medicine.drug
Subjects
Details
- ISSN :
- 01663542
- Volume :
- 138
- Database :
- OpenAIRE
- Journal :
- Antiviral Research
- Accession number :
- edsair.doi.dedup.....4db514c5e1c6cb37501c398741342322