Molecular Features of the V1-V4 Coding Region of Sexually Transmitted Human Immunodeficiency Virus Type 1

Jun Yong Choi, Sergei L.Kosakovsky Pond, Christy M. Anderson, Douglas D. Richman, Davey M. Smith

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)1506-1513
Number of pages8
JournalJournal of Infectious Diseases
Volume215
Issue number10
DOIs
Publication statusPublished - 2017 May 15

Bibliographical note

Publisher Copyright:
© The Author 2016. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved.

All Science Journal Classification (ASJC) codes

  • Immunology and Allergy
  • Infectious Diseases

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