Sequencing of Cytomegalovirus UL97 Gene for Genotypic Antiviral Resistance Testing

Author:

Lurain Nell S.1,Weinberg Adriana2,Crumpacker Clyde S.3,Chou Sunwen4

Affiliation:

1. Rush-Presbyterian-St. Luke's Medical Center, Chicago, Illinois1;

2. University of Colorado Health Sciences Center, Denver, Colorado2;

3. Beth-Israel Deaconess Medical Center, Boston, Massachusetts3; and

4. VA Medical Center, Portland, Oregon4

Abstract

ABSTRACT The widespread use of ganciclovir (GCV) to treat cytomegalovirus (CMV) infections in immunosuppressed patients has led to the development of drug resistance. Phenotypic assays for CMV drug resistance are presently too time-consuming to be therapeutically useful. To support the development of genotypic assays for GCV resistance, the complete sequences of the UL97 phosphotransferase genes in 28 phenotypically GCV-sensitive CMV clinical isolates were determined. The gene was found to be highly conserved, with nucleotide sequence identity among strains ranging from 98.6 to 100% and amino acid sequence identity of >99%. Primers for a genotypic assay were designed to amplify codons 400 to 707, because all known UL97 mutations conferring drug resistance occur at three sites within this region. This part of the UL97 gene was amplified from over 50 clinical isolates, and two sequencing reactions for the coding strand were successfully used to identify GCV resistance mutations. This genotypic assay can be performed in 48 h using genomic DNA extracted from cell monolayers at very low levels of virus infectivity, thus rapidly providing therapeutically useful results.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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