A. Bobkov et al., IDENTIFICATION OF AN ENV-G SUBTYPE AND HETEROGENEITY OF HIV-1 STRAINSIN THE RUSSIAN-FEDERATION AND BYELARUS, AIDS, 8(12), 1994, pp. 1649-1655
Objective: To identify HIV-1 envelope sequence subtypes in infected in
dividuals from the Russian Federation and Belarus. Patients: A cohort
of children infected after exposure to non-sterile needles during the
1988-1989 HIV-1 epidemic in southern Russia (n = 20) and HIV-1-seropos
itive individuals from Russia (n = 1) and Belarus (n = 7) infected via
sexual transmission. Methods: DNA samples derived from peripheral blo
od mononuclear cells were analysed for their HIV-1 genotypes by the he
teroduplex mobility assay (HMA). The 1.3 kilobase-pair env gene fragme
nts encoding a portion of gp120 were amplified by nested polymerase ch
ain reaction, cloned and sequenced. The env sequences derived from the
se patients were aligned and phylogenetic neighbour-joining and maximu
m parsimony-derived trees generated. Results: The env sequences derive
d from eight individuals infected in Russia and Belarus belong to subt
ype A (one), B (four), C (two), and D (one). Sequences derived from ch
ildren, infected during parenteral manipulations in southern Russia, a
nd one mother were closely related, but highly divergent, as a group,
from all prototypic strains (genetic divergence, 17.2-22.9%). However,
they clustered together with env sequences of the VI525 and LBV21-7 i
solates from Gabon, recently described to be members of a new HIV-1 en
v subtype G. Conclusion: Extensive heterogeneity of HIV-1 subtypes was
evident in the Russian Federation and Belarus. Our data also support
the existence of an HIV-1 env genetic subtype G, and such isolates are
now apparently present on both the African and European continents. T
hese variants were identified through V3 peptide enzyme-linked immunos
orbent assay screening and subsequent HMA analysis. The combination of
these techniques represents a model for screening HIV variants within
a large population.