1887

Abstract

The nucleotide changes of the DNA polymerase gene and the susceptibility of acyclovir (ACV)-resistant varicella-zoster virus (VZV) mutants to anti-herpetic drugs were determined and compared to those of herpes simplex virus type 1 (HSV-1) mutants. The seven ACV-resistant VZV mutants were classified into three groups, NS, GC and VM, according to the sequences of their DNA polymerase genes. The amino acid substitutions NS and GC were identical in position to the NS and GC mutations in the HSV-1 DNA polymerase mutants, respectively, and the VM amino acid substitution was similar to the HSV-1 VM mutation. All three groups of VZV mutants were susceptible to ACV, phosphonoacetic acid, vidarabine and aphidicolin, at levels similar to those seen with the respective HSV-1 mutants, except for subtle differences that were due possibly to the non-conserved regions in their sequences. Although both the HSV-1 and the VZV DNA polymerase genes show 53% sequence similarity, both viruses essentially show a similar biochemical behaviour.

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2001-11-01
2019-09-18
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