Sooty mangabeys are naturally infected with simian immunodeficiency virus (SIVsmm) subtypes that have identical genomic structure and similar nucleotide sequence as HIV-2. Sooty mangabeys suffer no adverse consequences of SIV infection while rhesus macaques develop simian immunodeficiency virus induced disease after experimental infection with viruses derived from sooty mangabeys. This project previously found that naturally infected sooty mangabeys have high plasma viral load and variable anti-SIV CTL responses suggesting that greater host containment of viral replication does not explain the lack of SIV-disease in mangabeys. During the last year, 3 rhesus macaques and 3 sooty mangabeys were experimentally infected with a common stock of SIVmac239/ON to identify characteristics of primary viremia that correlate with the virologic, immunologic, and clinical outcome of pathogenic and nonpathogenic SIV infection. All three mangabeys demonstrated attenuated viremia associate d with persistent strong anti-SIV CTL responses, while the three rhesus macaques had high levels of viremia, and CTL responses that diminished during clinical progression. The onset of anti-SIV CTL responses correlated temporally with the suppression of peak viremia in both primate host species. Attenuated viremia in these experimentally infected mangabeys, in contrast with naturally infected mangabeys which have high viremia, may be attributable to macaque adaptations of the virus stock used or some characteristic of natural infection that is not reproduced by intravenous challenge. Nevertheless, these experiments demonstrate that sooty mangabeys can acquire strong anti-SIV CTL responses in the setting of attenuated infection, arguing against congenital immune tolerance in mangabeys. Identification of the factors that determine the extent of immune tolerance early in the course of SIV infection in mangabeys may provide clues to how early therapeutic intervention could alter the n atural history of pathogenic viral infections.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
5P51RR000165-37
Application #
6247331
Study Section
Project Start
1997-05-01
Project End
1998-04-30
Budget Start
1996-10-01
Budget End
1997-09-30
Support Year
37
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Emory University
Department
Type
DUNS #
042250712
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Kamara, Dennis M; Gangishetti, Umesh; Gearing, Marla et al. (2018) Cerebral Amyloid Angiopathy: Similarity in African-Americans and Caucasians with Alzheimer's Disease. J Alzheimers Dis 62:1815-1826
Ploquin, Mickaƫl J; Casrouge, Armanda; Madec, Yoann et al. (2018) Systemic DPP4 activity is reduced during primary HIV-1 infection and is associated with intestinal RORC+ CD4+ cell levels: a surrogate marker candidate of HIV-induced intestinal damage. J Int AIDS Soc 21:e25144
Fonseca, Jairo A; McCaffery, Jessica N; Caceres, Juan et al. (2018) Inclusion of the murine IgG? signal peptide increases the cellular immunogenicity of a simian adenoviral vectored Plasmodium vivax multistage vaccine. Vaccine 36:2799-2808
Tedesco, Dana; Thapa, Manoj; Chin, Chui Yoke et al. (2018) Alterations in Intestinal Microbiota Lead to Production of Interleukin 17 by Intrahepatic ?? T-Cell Receptor-Positive Cells and Pathogenesis of Cholestatic Liver Disease. Gastroenterology 154:2178-2193
Robinson, Amy A; Abraham, Carmela R; Rosene, Douglas L (2018) Candidate molecular pathways of white matter vulnerability in the brain of normal aging rhesus monkeys. Geroscience 40:31-47
Walker, Lary C (2018) Sabotage by the brain's supporting cells helps fuel neurodegeneration. Nature 557:499-500
Mascaro, Jennifer S; Rentscher, Kelly E; Hackett, Patrick D et al. (2018) Preliminary evidence that androgen signaling is correlated with men's everyday language. Am J Hum Biol 30:e23136
Forger, Nancy G; Ruszkowski, Elara; Jacobs, Andrew et al. (2018) Effects of sex and prenatal androgen manipulations on Onuf's nucleus of rhesus macaques. Horm Behav 100:39-46
Claw, Katrina G; George, Renee D; MacCoss, Michael J et al. (2018) Quantitative evolutionary proteomics of seminal fluid from primates with different mating systems. BMC Genomics 19:488
Adekambi, Toidi; Ibegbu, Chris C; Cagle, Stephanie et al. (2018) High Frequencies of Caspase-3 Expressing Mycobacterium tuberculosis-Specific CD4+ T Cells Are Associated With Active Tuberculosis. Front Immunol 9:1481

Showing the most recent 10 out of 912 publications