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. 2005 Feb;49(2):606-11.
doi: 10.1128/AAC.49.2.606-611.2005.

Genotypic characterization of the DNA polymerase and sensitivity to antiviral compounds of foscarnet-resistant herpes simplex virus type 1 (HSV-1) derived from a foscarnet-sensitive HSV-1 strain

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Genotypic characterization of the DNA polymerase and sensitivity to antiviral compounds of foscarnet-resistant herpes simplex virus type 1 (HSV-1) derived from a foscarnet-sensitive HSV-1 strain

Masayuki Saijo et al. Antimicrob Agents Chemother. 2005 Feb.

Abstract

Foscarnet is widely used for the treatment of acyclovir-resistant herpesvirus infections, and foscarnet-resistant herpesvirus infections are a serious concern in immunocompromised patients. Twenty-seven single-plaque isolates of herpes simplex virus type 1 (HSV-1) resistant to foscarnet were selected from foscarnet- and acyclovir-sensitive HSV-1 strain TAS by exposure to foscarnet, and the DNA polymerase genes were analyzed. The sensitivities of these mutants to foscarnet, cidofovir, S2242, acyclovir, ganciclovir, and penciclovir were determined. A single amino acid substitution, double amino acid substitutions, and a combination of a single amino acid substitution with a deletion or insertion of amino acid residues in the viral DNA polymerase were demonstrated in 21, 4, and 2 isolates, respectively. Of the 27 isolates, an amino acid substitution of serine for asparagine at amino acid position 724 in the DNA polymerase (724 S-N) was detected in 8 isolates. An amino acid substitution in conserved region II was demonstrated in these eight isolates as well as four other isolates. The mutation in the DNA polymerase responsible for resistance to foscarnet was located between the pre-IV region and conserved region V, especially within conserved region II. All the isolates were sensitive or hypersensitive to cidofovir and ganciclovir. Seven, 5, and 15 of the 27 isolates were also sensitive to S2242, acyclovir, and penciclovir, respectively. Thus, most of the foscarnet-resistant HSV-1 isolates were sensitive or hypersensitive to cidofovir and ganciclovir.

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Figures

FIG. 1.
FIG. 1.
Schematic representation of the procedures used for the selection of PFAr HSV-1 isolates.
FIG. 2.
FIG. 2.
IC50s of PFA (A), CDV (B), S2242 (C), ACV (D), GCV (E), and PCV (F) for all 27 plaque-purified PFAr isolates that survived in the medium with PFA and those for the 5 plaque-purified wild-type HSV-1 TAS strains (gray bars, isolates 1S to 5S). The last five plaque-purified wild-type HSV-1 TAS strains are considered wild-type HSV-1. The 10average ± 2 SD and 10average ± 3 SD ranges of each compound calculated from the IC50s for plaque-purified isolates (isolates 1S to 5S) are shown. The former are the reference values for the determination of moderately sensitive and moderately resistant, while the latter are those for the determination of highly sensitive and highly resistant. The red, orange, yellow, green, and blue bars indicate highly resistant, moderately resistant, sensitive with normal range, moderately sensitive, and highly sensitive, respectively.

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References

    1. Alvarez-McLeod, A., J. Havlik, and K. E. Drew. 1999. Foscarnet treatment of genital infection due to acyclovir-resistant herpes simplex virus type 2 in a pregnant patient with AIDS: case report. Clin. Infect. Dis. 29:937-938. - PubMed
    1. Andrei, G., R. Snoeck, and E. De Clercq. 1995. Susceptibilities of several drug-resistant herpes simplex virus type 1 strains to alternative antiviral compounds. Antimicrob. Agents Chemother. 39:1632-1635. - PMC - PubMed
    1. Bestman-Smith, J., and G. Boivin. 2003. Drug resistance patterns of recombinant herpes simplex virus DNA polymerase mutants generated with a set of overlapping cosmids and plasmids. J. Virol. 77:7820-7829. - PMC - PubMed
    1. Blot, N., P. Schneider, P. Young, C. Janvresse, D. Dehesdin, P. Tron, and J. P. Vannier. 2000. Treatment of an acyclovir and foscarnet-resistant herpes simplex virus infection with cidofovir in a child after an unrelated bone marrow transplant. Bone Marrow Transplant. 26:903-905. - PubMed
    1. Bryant, P., J. Sasadeusz, J. Carapetis, K. Waters, and N. Curtis. 2001. Successful treatment of foscarnet-resistant herpes simplex stomatitis with intravenous cidofovir in a child. Pediatr. Infect. Dis. J. 20:1083-1086. - PubMed

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