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Updated: Mar 8, 2026

Analysis of Simian Immunodeficiency Virus-specific CD8+ T-cells in Rhesus Macaques by Peptide-MHC-I Tetramer Staining
Published on: December 23, 2016
SIV Infection Facilitates Mycobacterium tuberculosis Infection of Rhesus Macaques
Ming Guo1, Qiao-Yang Xian1, Yan Rao1
1School of Basic Medical Sciences, Center for Animal Experiment/Animal Biosafety Level III Laboratory, Wuhan University Wuhan, Hubei, China.
Abstract:
Tuberculosis (TB) is a common opportunistic infection and the leading cause of death for human immunodeficiency virus (HIV)-infected patients. Thus, it is necessary to understand the pathogenetic interactions between M.tb and HIV infection. In this study, we examined M.tb and/or simian immunodeficiency virus (SIV) infection of Chinese rhesus macaques. While there was little evidence that M.tb enhanced SIV infection of macaques, SIV could facilitate M.tb infection as demonstrated by X-rays, pathological and microbiological findings. Chest X-rays showed that co-infected animals had disseminated lesions in both left and right lungs, while M.tb mono-infected animals displayed the lesions only in right lungs. Necropsy of co-infected animals revealed a disseminated M.tb infection not only in the lungs but also in the extrapulmonary organs including spleen, pancreas, liver, kidney, and heart. The bacterial counts in the lungs, the bronchial lymph nodes, and the extrapulmonary organs of co-infected animals were significantly higher than those of M.tb mono-infected animals. The mechanistic studies demonstrated that two of three co-infected animals had lower levels of M.tb specific IFN-γ and IL-22 in PBMCs than M.tb mono-infected animals. These findings suggest that Chinese rhesus macaque is a suitable and alternative non-human primate model for SIV/M.tb coinfection studies. The impairment of the specific anti-TB immunity is likely to be a contributor of SIV-mediated enhancement M.tb infection.
Insights
Simian immunodeficiency virus (SIV) coinfection in rhesus macaques facilitates Mycobacterium tuberculosis (M.tb) infection, leading to disseminated disease and impaired immune responses. Chinese rhesus macaques serve as a valuable model for SIV/M.tb coinfection studies.
Area of Science:
- Immunology
- Infectious Diseases
- Primate Models
Background:
- Tuberculosis (TB) is a leading cause of death in HIV-infected individuals.
- Understanding the interaction between Mycobacterium tuberculosis (M.tb) and HIV is crucial.
- Simian immunodeficiency virus (SIV) is an animal model for HIV.
Purpose of the Study:
- To investigate the pathogenetic interactions between M.tb and SIV in Chinese rhesus macaques.
- To evaluate the Chinese rhesus macaque as a non-human primate model for SIV/M.tb coinfection.
Main Methods:
- Infection of Chinese rhesus macaques with M.tb and/or SIV.
- Assessment using chest X-rays, necropsy, microbiological analysis, and peripheral blood mononuclear cell (PBMC) assays.
- Measurement of M.tb-specific IFN-γ and IL-22 levels.
Main Results:
- SIV coinfection facilitated M.tb infection, unlike M.tb mono-infection.
- Co-infected animals showed disseminated lesions in lungs and extrapulmonary organs.
- Significantly higher bacterial loads were observed in co-infected animals.
- Impaired M.tb-specific IFN-γ and IL-22 responses were noted in co-infected macaques.
Conclusions:
- SIV coinfection enhances M.tb infection in Chinese rhesus macaques.
- Impaired anti-TB immunity likely contributes to SIV-mediated M.tb enhancement.
- Chinese rhesus macaques are a suitable model for SIV/M.tb coinfection research.
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