We previously identified a group of 10 long-term nonprogressors (LTNP) with
HIV-1 infection. In this study, we have sequenced the envelope gene (C2-V3
-C3) from the 10 LTNPs and from a control group of 9 people with rapidly pr
ogressing infection (RPI). The 19 individuals' CCR5 genotype and virus phen
otype (i.e., syncytium-inducing/non-syncytium-inducing [SI/NSI]) were obtai
ned from a previous study. A phylogenetic tree was constructed containing t
he 19 envelope sequences together with 42 local control env sequences obtai
ned from other studies. Analysis of the phylogenetic tree did not reveal an
y relation between the envelope gene (C2-V3-C3) from LTNPs versus RPIs. Whe
n data from the CCR5 genotype and the virus phenotype were assembled in the
phylogenetic tree, no significant clustering was observed. From alignment
of the protein sequences, we found a possible N-glycan in position aa294 in
env that was conserved in only 1 of 10 LTNPs; however, it was conserved in
6 of 9 RPIs. Our study could not demonstrate any association between LTNPs
and the sequenced envelope gene segment (C2-V3-C3). This lack of associati
on could be due to the relatively small sample size of the data set. Nor di
d we find any relation between the CCR5 genotype or the SI/NSI phenotype wi
th the sequenced envelope genes from the 19 participants. The possible N-gl
ycan position we have described is an interesting observation that may requ
ire further investigation.