Analysis of Variance ; Evolution, Molecular ; Glycosylation ; HIV Envelope Protein gp120/chemistry ; HIV Envelope Protein gp120/genetics* ; HIV Envelope Protein gp120/metabolism ; HIV Infections/transmission* ; HIV Infections/virology* ; HIV-1/genetics* ; HIV-1/metabolism ; HIV-1/pathogenicity ; Humans ; Peptide Fragments/genetics*
Keywords
HIV ; env ; transmitted virus ; viral evolution
Abstract
BACKGROUND: Investigations into which human immunodeficiency virus type 1 (HIV-1) sequence features may be selected for transmission during sexual exposure have been hampered by the small number of characterized transmission pairs in individual studies.
METHODS: To boost statistical power to detect differences in glycosylation, length, and electrical charge in the HIV-1 V1-V4 coding region, we reanalyzed all available 2485 env sequences derived from 114 subjects representing 58 transmission pairs from previous studies using mixed-effects linear regression and an approach to approximate the unobserved transmitted virus.
RESULTS : The recipient partner had a shorter V1-V4 region and fewer potential N-linked glycosylation sites (PNGS) than sequences from the source partner. We also detected a trend toward more PNGS and lower isoelectric points in transmitted sequences with source partner and the evolutionary tendency to shorten V1-V4 sequences, reduce the number of PNGS, and lower isoelectric points in the recipient following transmission.
CONCLUSIONS: By using all available well-characterized env sequences from transmission pairs via sexual exposure, we were able to identify several important virologic factors that may be important in the development of biomedical preventive interventions