Am. Bonneau et al., RESISTANCE OF HERPES-SIMPLEX VIRUS TYPE-1 TO PEPTIDOMIMETIC RIBONUCLEOTIDE REDUCTASE INHIBITORS - SELECTION AND CHARACTERIZATION OF MUTANT ISOLATES, Journal of virology, 70(2), 1996, pp. 787-793
Herpes simplex virus (HSV) encodes its own ribonucleotide reductase (R
R), which provides the high levels of deoxynucleoside triphosphates re
quired for viral DNA replication in infected cells. HSV RR is composed
of two distinct subunits, R1 and R2, whose association is required fo
r enzymatic activity. Peptidomimetic inhibitors that mimic the C-termi
nal amino acids of R2 inhibit HSV RR by preventing the association of
R1 and R2, These compounds are candidate antiviral therapeutic agents.
Here we describe the in vitro selection of HSV type 1 KOS variants wi
th three- to ninefold-decreased sensitivity to the RR inhibitor BILD 7
33. The resistant isolates have growth properties in vitro similar to
those of wild-type KOS but are more sensitive to acyclovir, possibly a
s a consequence of functional impairment of their RRs. A single amino
acid substitution in R1 (Ala-1091 to Ser) was associated with threefol
d resistance to BILD 733, whereas an additional substitution (Pro-1090
to Leu) was required for higher levels of resistance. These mutations
were reintroduced into HSV type 1 KOS and shown to be sufficient to c
onfer the resistance phenotype, Studies in vitro with RRs isolated fro
m cells infected with these mutant viruses demonstrated that these RRs
bind BILD 733 more weakly than the wild-type enzyme and are also func
tionally impaired, exhibiting an elevated dissociation constant (K-d)
for R1-R2 subunit association and/or reduced activity (k(cat)). This w
ork provides evidence that the C-terminal end of HSV R1 (residues 1090
and 1091) is involved in R2 binding interactions and demonstrates tha
t resistance to subunit association inhibitors may be associated with
compromised activity of the target enzyme.