R. Cheingsongpopov et al., SEROTYPING HIV TYPE-1 BY ANTIBODY-BINDING TO THE V3 LOOP - RELATIONSHIP TO VIRAL GENOTYPE, AIDS research and human retroviruses, 10(11), 1994, pp. 1379-1386
We have investigated whether peptides representing the HIV-1 principal
neutralization domain (V3) can be used as antigens in antibody-bindin
g assays to predict the genotypes of the subjects' virus. Serum sample
s collected from HIV-1-infected subjects from the four WHO-sponsored v
accine evaluation sites (Uganda, Rwanda, Thailand, and Brazil) were ch
aracterized by antibody binding to a panel of synthetic V3 peptides th
at were derived from the consensus sequences of the V3 region of the H
IV-1 subgroups according to the env phylogenetic analysis (A-E). An in
direct V3 peptide-binding assay was used for primary screening, and a
V3 peptide antigen-limiting ELISA was then used as a secondary assay t
o discriminate cross-reactivity if the screening assay was equivocal.
In general, V3 peptide serology could predict HIV-1 genotypes. In sera
for which the genotype of the virus was known, peptide assays could p
redict the correct genotype in approximately 90% of cases for genotype
s A, B, C, and E; Ugandan sera of genotype D were more broadly reactiv
e. There was considerable serological cross-reactivity between some HI
V-1 genotypes, in particular between A and C, and, to a lesser extent,
B and D subtypes. Owing to polymorphism at the crown of the V3 loop,
an additional B peptide (B') was required to type Brazilian B genotype
sera. These simple assays may help facilitate the determination and d
istribution of HIV-1 genotypes circulating in populations.