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HIV-1 Tropism and Survival in Vertically Infected Ugandan Infants
Journal article   Open access   Peer reviewed

HIV-1 Tropism and Survival in Vertically Infected Ugandan Infants

Jessica D CHURCH, Wei Huang, Neil PARKIN, Susan H ESHLEMAN, Anthony MWATHA, Jonathan TOMA, Eric STAWISKI, Deborah DONNELL, Laura A GUAY, Francis MMIRO, …
The Journal of infectious diseases, Vol.197(10), pp.1382-1388
2008
DOI: 10.1086/587492
PMID: 18444795
url
https://doi.org/10.1086/587492View
Published (Version of record) Open Access

Abstract

Background. Human immunodeficiency virus type 1 (HIV-1) may utilize the CXCR4 coreceptor (X4 virus), the CCR5 coreceptor (R5 virus), or both (dual/mixed [DM] virus). We analyzed HIV-1 coreceptor tropism in Ugandan infants enrolled in the HIVNET (HIV Network for Prevention Trials) 012 trial. Methods. Plasma or serum was analyzed using a commercial coreceptor tropism assay. HIV env subtype was determined by phylogenetic methods. Results. Tropism results were obtained for 57 samples from infants collected 6–14 weeks after birth. Fifty-two infants had only R5 virus, and 5 had either X4 or DM virus. The mothers of those 5 infants also had X4 or DM virus. In infants, subtype D infection was associated with high-level infectivity in CCR5-bearing cells and also with the detection of X4 or DM strains. High-level infectivity in CCR5-bearing cells was associated with decreased infant survival, but infection with X4 or DM virus was not. HIV clones from infants with DM viral populations showed different patterns of coreceptor use. V3 loop sequence- based algorithms predicted the tropism of some, but not all, env clones. Conclusions. Complex patterns of HIV tropism were found in HIV-infected newborn infants. Subtype D infection was associated with X4 virus and with high-level replication in CCR5-bearing cells. High-level replication of R5 virus was associated with decreased infant survival.
Infectious Diseases Microbiology Virology Fundamental and applied biological sciences. Psychology Miscellaneous Biological and medical sciences Medical sciences

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