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Host Restriction Factors APOBEC3G/3F and Other Interferon-Related Gene Expressions Affect Early HIV-1 Infection in Northern Pig-Tailed Macaque (Macaca leonina)
2019-01-04 | Author: | From:

Host Restriction Factors APOBEC3G/3F and Other Interferon-Related Gene Expressions Affect Early HIV-1 Infection in Northern Pig-Tailed Macaque (Macaca leonina). Front Immunol, 2018, 9: 1965

Title:  Host Restriction Factors APOBEC3G/3F and Other Interferon-Related Gene Expressions Affect Early HIV-1 Infection in Northern Pig-Tailed Macaque (Macaca leonina).    

Author:  Pang W, Song JH, Lu Y, Zhang XL, Zheng HY, Jiang J, Zheng YT

Pub Year: 2018

Publication Name: Front Immunol

Volume: 9

Issue: 4

Page Number: 1965

IF: 5.511

Abstract:

The northern pig-tailed macaques (NPMs) lack TRIM5 alpha, an antiviral restriction factor, and instead have TRIM5-CypA. In our previous study, we demonstrated that HIV-1(NL4-3) successfully infected NPMs and formed a long-term viral reservoir in vivo. However, the HIV-1-infected NPMs showed relatively high viremia in the first 6 weeks of infection, which declined thereafter suggesting that HIV-1 (NL4-3) infection in these animals was only partly permissive. To optimize HIV-1 infection in NPMs therefore, we generated HIV-1(NL4-R3A) and stHIV-1sv, and infected NPMs with these viruses. HIV-1(NL4-R3A) and stHIV-1sv can replicate persistently in NPMs during 41 weeks of acute infection stage. Compared to the HIV-1(NL4-R3A), stHIV-1sv showed a notably higher level of replication, and the NPMs infected with the latter induced a more robust neutralizing antibody but a weaker cellular immune response. In addition, IFN-I signaling was significantly up-regulated with the viral replication, and was higher in the stHIV-1sv infected macaques. Consequently, the sequences of pro-viral env showed fewer G-A hyper-mutations in stHIV-1sv, suggesting that vif gene of SIV could antagonize the antiviral effects of APOBEC3 proteins in NPMs. Taken together, NPMs infected with HIV-1(NL4-R3A) and stHIV-1sv show distinct virological and immunological features. Furthermore, interferon-related gene expression might play a role in controlling primary HIV-1(NL4-R3A) and stHIV-1sv replication in NPMs. This result suggests NPM is a potential HIV/AIDS animal model.

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