This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Currently, there is no animal model for HIV-1 infection and disease because the virus is highly specific for humans. Macaques are generally resistant to HIV-1, with the exception being pig-tailed macaques. A number of reports from WaNPRC in 1990's indicated that certain strains of HIV-1 could infect pig-tailed macaques, although viremia was transient and infection was variable. In the intervening years, there has been significant progress in the understanding of factors that restrict HIV-1 replication in primate species. Two host factors are primarily responsible for restricting HIV-1 infection in rhesus macaques: TRIM5alpha and APOBEC3G/F. These factors interact, respectively, with viral capsid and the Vif proteins. Our lab recently showed that pig-tailed macaques are unable to express functional isoforms of TRIM5 alpha. Although they express a novel form of TRIM, TRIMCyp, it does not restrict HIV-1. Therefore, it is possible that HIV-1 will only need to overcome APOBEC3G/F-mediated restriction to replicate successfully in pig-tailed macaques. To test this hypothesis, we collaborated with Dr. J. Kimata of Baylor College of Medicine, who engineered an HIV-1 clone that includes the vif gene of SIVmne, allowing it to counteract APOBEC3G/F-mediated restriction. This chimeric virus, HSIV-vif, is 96% HIV-1 and 4% SIV. It replicates in stimulated pig-tailed macaque blood cells as efficiently as SIVmne. In this pilot study, we inoculated 2 pig-tailed macaques intravenously with HSIV-vif. Both animals became infected, with plasma viremia detectable 1 wk after infection and reaching a peak between 104-105 copies/ml at wk 2. Both animals seroconverted by wk 4. Although it is too early to tell if infection will sustain, these preliminary data are encouraging and support our notion that studies of diverse macaque species are essential for the understanding of primate lentivirus pathogenesis and the development of relevant animal models for the evaluation of novel therapies and vaccines against HIV/AIDS.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
5P51RR000166-48
Application #
7958868
Study Section
Special Emphasis Panel (ZRR1-CM-8 (02))
Project Start
2009-05-01
Project End
2010-04-30
Budget Start
2009-05-01
Budget End
2010-04-30
Support Year
48
Fiscal Year
2009
Total Cost
$331,394
Indirect Cost
Name
University of Washington
Department
Type
Other Domestic Higher Education
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
Pham, Amelie; Carrasco, Marisa; Kiorpes, Lynne (2018) Endogenous attention improves perception in amblyopic macaques. J Vis 18:11
Zanos, Stavros; Rembado, Irene; Chen, Daofen et al. (2018) Phase-Locked Stimulation during Cortical Beta Oscillations Produces Bidirectional Synaptic Plasticity in Awake Monkeys. Curr Biol 28:2515-2526.e4
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Hasegawa, Yu; Curtis, Britni; Yutuc, Vernon et al. (2018) Microbial structure and function in infant and juvenile rhesus macaques are primarily affected by age, not vaccination status. Sci Rep 8:15867
Oleskiw, Timothy D; Nowack, Amy; Pasupathy, Anitha (2018) Joint coding of shape and blur in area V4. Nat Commun 9:466
Balakrishnan, Ashwini; Goodpaster, Tracy; Randolph-Habecker, Julie et al. (2017) Analysis of ROR1 Protein Expression in Human Cancer and Normal Tissues. Clin Cancer Res 23:3061-3071
Shooner, Christopher; Hallum, Luke E; Kumbhani, Romesh D et al. (2017) Asymmetric Dichoptic Masking in Visual Cortex of Amblyopic Macaque Monkeys. J Neurosci 37:8734-8741

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