We systematically evaluated multiple and recombinant infections in an HIV-i
nfected population selected for vaccine trials. Seventy-nine HIV-I infected
persons in a clinical cohort study in Rio de Janeiro, Brazil, were evaluat
ed for 1 year. A combination of molecular screening assays and DNA sequenci
ng showed 3 dual infections (3.8%), 6 recombinant infections (7.6%), and 70
(88.6%) infections involving single viral subtypes. In the th ree dual inf
ections, we identified HIV-1 subtypes F and B, F and D, and B and D; in con
trast, the single and recombinant infections involved only HIV-1 subtypes B
and F. The recombinants had five distinct B/F mosaic patterns: Bgag-p17/Bg
ag-p24/F-pol/B-env, Fgag-p17/Bgag-p24/F-pol/F-env, Bgag-p17/B-Fgag-p24/F-po
l/F-env, Bgag-p17/B-Fgag-p24/F-pol/B-env, and Fgag-p17/B-Fgag-p24/F-pol/F-e
nv. No association was found between dual or recombinant infections and dem
ographic or clinical variables. These findings indicate that dual and recom
binant infections are emerging as an integral part of the HIV/AIDS epidemic
in Brazil and emphasize the heterogenous character of epidemics emerging i
n countries where multiple viral subtypes coexist.