HIV-1 diversity and prevalence differ between urban and rural areas in the Mbeya region of Tanzania

Miguel A. Arroyo*, Michael Hoelscher, Warren Sateren, Eleuter Samky, Leonard Maboko, Oliver Hoffmann, Gustavo Kijak, Merlin Robb, Deborah L. Birx, Francine E. McCutchan

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

42 Scopus citations

Abstract

Objective: To characterize HIV-1 strains in a potential vaccine trial cohort (CODE) in the Mbeya region of southwest Tanzania. Design: Study volunteers (n = 3096) were recruited from urban areas in Mbeya Town, using two different recruitment strategies, and in a nearby rural village. Methods: Cryopreserved plasma from 507 HIV-1 prevalent cases was the source of viral RNA for HIV-1 genotyping by the Multi-region Hybridization Assay, the MHA acd, and selected strains were confirmed by complete genome sequencing. Results: The overall HIV-1 prevalence was 16.6% [95% confidence interval (CI), 15.3-17.9] within the cohort. HIV-1 prevalence was higher among women, and in urban areas. Recruitment through advertisement targeted a high-risk urban male population for HIV-1 infection [adjusted odds ratio (adj. OR), 1.68; 95% CI, 1.13-2.51] when compared with men recruited door-to-door. The complexity of the HIV-1 epidemic was also higher in urban areas evidenced by the high-risk of HIV-1 infection with a recombinant strain (adj. OR, 2.69; 95% CI, 1.08-6.69) and HIV-1 dual infection (adj. OR, 5.16; 95% CI, 1.07-24.9), mainly driven by urban men recruited through advertisement. Conclusions: Overall the urban epidemic was more genetically complex, with higher prevalence and more recombinants and dual infections. Vaccine trials in Mbeya region can assess a complex HIV-1 population dynamic and determine vaccine efficacy in relationship to the genetic diversity of HIV-1 strains that challenge vaccines.

Original languageEnglish
Pages (from-to)1517-1524
Number of pages8
JournalAIDS
Volume19
Issue number14
DOIs
StatePublished - 23 Sep 2005

Keywords

  • Dual infection
  • HIV-1 variability/subtypes
  • Molecular epidemiology
  • Recombination
  • Tanzania

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