Abstract
Designing an effective human immunodeficiency virus type 1 (HIV-1) vaccine will rely on understanding which variants, from among the myriad of circulating HIV-1 strains, are most commonly transmitted and determining whether such variants have an Achilles heel. Here we show that heterosexually acquired subtype A HIV-1 envelopes have signature sequences that include shorter V1-V2 loop sequences and fewer predicted N-linked glycosylation sites relative to the overall population of circulating variants. In contrast, recently transmitted subtype B variants did not, and this was true for cases where the major risk factor was homosexual contact, as well as for cases where it was heterosexual contact. This suggests that selection during HIV-1 transmission may vary depending on the infecting subtype. There was evidence from 23 subtype A-infected women for whom there was longitudinal data that those who were infected with viruses with fewer potential N-linked glycosylation sites in V1-V2 had lower viral set point levels. Thus, our study also suggests that the extent of glycosylation in the infecting virus could impact disease progression.
Publication types
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Comparative Study
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Research Support, N.I.H., Extramural
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Disease Progression
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Disease Transmission, Infectious
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Female
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Genetic Variation
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Glycosylation
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HIV Envelope Protein gp120 / genetics
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HIV Infections / diagnosis
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HIV Infections / transmission
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HIV Infections / virology*
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HIV-1 / genetics*
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Heterosexuality
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Humans
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Kenya
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Male
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Molecular Sequence Data
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Peptide Fragments / genetics
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Viral Envelope Proteins / genetics*
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Viral Load
Substances
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HIV Envelope Protein gp120
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HIV envelope protein gp120 (135-148)
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Peptide Fragments
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Viral Envelope Proteins
Associated data
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GENBANK/AF004888
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GENBANK/AF004894
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