
Replicative
capacity results complicated by minority wild-type virus

The unique
co-transfection step inherent to single-cycle HIV resistance assays, can
result in even relatively small amounts of wild-type virus (WT) within
a viral population significantly affecting the apparent replication capacity
(RC) and phenotype of mutant strains, conclude researchers from Abbott
Laboratories in Illinois, USA.
The replication
capacity and susceptibility of plasma isolates from patients who are off
therapy or not adherent to treatment, in which wild-type virus may expand
to significant levels, should be interpreted with caution, they say in
an abstract presented to the Mexico resistance meeting.
In a typical
single-cycle HIV phenotypic assay - the most common test for RC and phenotypic
resistance - the ‘pool’ of DNA generated from patient plasma
is transfected into target cells in order to capture and preserve the
protease and reverse transcriptase sequence heterogeneity of the plasma
virus. However, co-transfection of different viral variants into the same
cell might provide the opportunity for genetic recombination or complementation,
or both.
Hongmei Mo
and colleagues found that four mutant constructs with different genotypes
derived from dual protease inhibitor-experienced subjects receiving lopinavir/ritonavir
(LPV/r) therapy displayed <5% RC when transfected alone. Co-transfection
of as little as 9% of the WT clone increased the RC of the mutant clones
to up to 14%. Co-transfection of a higher proportion of the WT clone further
enhanced the RC of the mutants to 31–81%.
The LPV susceptibility
of four mutant clones with sufficient RC for phenotypic evaluation when
transfected alone ranged from 44- to 302-fold, compared to the WT clone.
Incremental cotransfection of 9–50% of the WT clone decreased the
LPV IC50 of the mutant clones by up to 96%, compared to WT.
Ref: Mo H, Lu L,
Kempf D et al. The impact of minor populations of wild-type HIV on the
replication capacity and phenotype of mutant variants in a single-cycle
HIV resistance assay. Abstract 85.
|