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APOBEC3 inhibits mouse mammary tumour virus replication in vivo

Abstract

Genomes of all mammals encode apobec3 genes, which are thought to have a function in intrinsic cellular immunity to several viruses including human immunodeficiency virus type 1 (HIV-1)1. APOBEC3 (A3) proteins are packaged into virions and inhibit retroviral replication in newly infected cells, at least in part by deaminating cytidines on the negative strand DNA intermediates2. However, the role of A3 in innate resistance to mouse retroviruses is not understood. Here we show that A3 functions during retroviral infection in vivo and provides partial protection to mice against infection with mouse mammary tumour virus (MMTV). Both mouse A3 and human A3G proteins interacted with the MMTV nucleocapsid in an RNA-dependent fashion and were packaged into virions. In addition, mouse A3-containing and human A3G-containing virions showed a marked decrease in titre. Last, A3-/- mice were more susceptible to MMTV infection, because virus spread was more rapid and extensive than in their wild-type littermates.

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Figure 1: mA3 and hA3G are incorporated into MMTV virions and bind NC.
Figure 2: mA3 and hA3G inhibit MMTV replication in vitro.
Figure 3: mA3 inhibits MMTV infection in vivo.
Figure 4: mA3 inhibits virus infection and spread in vivo.

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References

  1. Sheehy, A. M., Gaddis, N. C., Choi, J. D. & Malim, M. H. Isolation of a human gene that inhibits HIV-1 infection and is suppressed by the viral Vif protein. Nature 418, 646–650 (2002)

    Article  ADS  CAS  Google Scholar 

  2. Mangeat, B. et al. Broad antiretroviral defense by human APOBEC3G through lethal editing of nascent reverse transcripts. Nature 424, 99–103 (2003)

    Article  ADS  CAS  Google Scholar 

  3. Zheng, Y. H. et al. Human APOBEC3F is another host factor that blocks human immunodeficiency virus type 1 replication. J. Virol. 78, 6073–6076 (2004)

    Article  CAS  Google Scholar 

  4. Holmes, R. K., Koning, F. A., Bishop, K. N. & Malim, M. H. APOBEC3F can inhibit the accumulation of HIV-1 reverse transcription products in the absence of hypermutation: Comparisons with APOBEC3G. J. Biol. Chem. advance online publication, doi:10.1074/jbc.M607298200 (22 November 2006)

  5. Harris, R. S. et al. DNA deamination mediates innate immunity to retroviral infection. Cell 113, 803–809 (2003)

    Article  CAS  Google Scholar 

  6. Bishop, K. N. et al. Cytidine deamination of retroviral DNA by diverse APOBEC proteins. Curr. Biol. 14, 1392–1396 (2004)

    Article  CAS  Google Scholar 

  7. Doehle, B. P., Schafer, A., Wiegand, H. L., Bogerd, H. P. & Cullen, B. R. Differential sensitivity of murine leukemia virus to APOBEC3-mediated inhibition is governed by virion exclusion. J. Virol. 79, 8201–8207 (2005)

    Article  CAS  Google Scholar 

  8. Kobayashi, M. et al. APOBEC3G targets specific virus species. J. Virol. 78, 8238–8244 (2004)

    Article  CAS  Google Scholar 

  9. Esnault, C. et al. APOBEC3G cytidine deaminase inhibits retrotransposition of endogenous retroviruses. Nature 433, 430–433 (2005)

    Article  ADS  CAS  Google Scholar 

  10. Cen, S. et al. The interaction between HIV-1 Gag and APOBEC3G. J. Biol. Chem. 279, 33177–33184 (2004)

    Article  CAS  Google Scholar 

  11. Indik, S., Gunzburg, W. H., Salmons, B. & Rouault, F. Mouse mammary tumor virus infects human cells. Cancer Res. 65, 6651–6659 (2005)

    Article  CAS  Google Scholar 

  12. Zhang, Y., Rassa, J. C., deObaldia, E. M., Albritton, L. & Ross, S. R. Identification of the mouse mammary tumor virus envelope receptor-binding domain. J. Virol. 77, 10468–10478 (2003)

    Article  CAS  Google Scholar 

  13. Nandi, S. & McGrath, C. M. Mammary neoplasia in mice. Adv. Cancer Res. 17, 353–414 (1973)

    Article  Google Scholar 

  14. Mikl, M. C. et al. Mice deficient in APOBEC2 and APOBEC3. Mol. Cell. Biol. 25, 7270–7277 (2005)

    Article  CAS  Google Scholar 

  15. Su, A. I. et al. A gene atlas of the mouse and human protein-encoding transcriptomes. Proc. Natl Acad. Sci. USA 101, 6062–6067 (2004)

    Article  ADS  CAS  Google Scholar 

  16. Svarovskaia, E. S. et al. Human apolipoprotein B mRNA-editing enzyme-catalytic polypeptide-like 3G (APOBEC3G) is incorporated into HIV-1 virions through interactions with viral and nonviral RNAs. J. Biol. Chem. 279, 35822–35828 (2004)

    Article  CAS  Google Scholar 

  17. Ross, S. R. Using genetics to probe host–virus interactions: the mouse mammary tumor virus model. Microbes Infect. 2, 1215–1223 (2000)

    Article  CAS  Google Scholar 

  18. Uz-Zaman, T., Ignatowicz, L. & Sarkar, N. H. Mouse mammary tumor viruses expressed by RIII/Sa mice with a high incidence of mammary tumors interact with the Vβ-2- and Vβ-8-specific T cells during viral infection. Virology 314, 294–304 (2003)

    Article  CAS  Google Scholar 

  19. Chiu, Y. L. et al. Cellular APOBEC3G restricts HIV-1 infection in resting CD4+ T cells. Nature 435, 108–114 (2005)

    Article  ADS  CAS  Google Scholar 

  20. Newman, E. N. et al. Antiviral function of APOBEC3G can be dissociated from cytidine deaminase activity. Curr. Biol. 15, 166–170 (2005)

    Article  CAS  Google Scholar 

  21. Cullen, B. R. Role and mechanism of action of the APOBEC3 family of antiretroviral resistance factors. J. Virol. 80, 1067–1076 (2006)

    Article  CAS  Google Scholar 

  22. Doehle, B. P. et al. The betaretrovirus Mason–Pfizer Monkey Virus selectively excludes simian APOBEC3G from virion particles. J. Virol. 80, 12102–12108 (2006)

    Article  CAS  Google Scholar 

  23. Baillie, G. J., van de Lagemaat, L. N., Baust, C. & Mager, D. L. Multiple groups of endogenous betaretroviruses in mice, rats and other mammals. J. Virol. 78, 5784–5798 (2004)

    Article  CAS  Google Scholar 

  24. Morris, V. L., Medeiros, E., Ringold, G. M., Bishop, J. M. & Varmus, H. E. Comparison of mouse mammary tumor virus-specific DNA in inbred, wild and Asian mice, and in tumors and normal organs from inbred mice. J. Mol. Biol. 114, 73–91 (1977)

    Article  CAS  Google Scholar 

  25. Berkhout, B., Grigoriev, A., Bakker, M. & Lukashov, V. V. Codon and amino acid usage in retroviral genomes is consistent with virus-specific nucleotide pressure. AIDS Res. Hum. Retroviruses 18, 133–141 (2002)

    Article  CAS  Google Scholar 

  26. Golovkina, T. V., Dudley, J. P., Jaffe, A. & Ross, S. R. Mouse mammary tumor viruses with functional superantigen genes are selected during in vivo infection. Proc. Natl Acad. Sci. USA 92, 4828–4832 (1995)

    Article  ADS  CAS  Google Scholar 

  27. Rassa, J. C., Meyers, J. L., Zhang, Y., Kudaravalli, R. & Ross, S. R. Murine retroviruses activate B cells via interaction with Toll-like receptor 4. Proc. Natl Acad. Sci. USA 99, 2281–2286 (2002)

    Article  ADS  CAS  Google Scholar 

  28. Golovkina, T. V. et al. A novel membrane protein is a mouse mammary tumor virus receptor. J. Virol. 72, 3066–3071 (1998)

    CAS  PubMed  PubMed Central  Google Scholar 

  29. Dzuris, J. L., Golovkina, T. V. & Ross, S. R. Both T and B cells shed infectious MMTV. J. Virol. 71, 6044–6048 (1997)

    CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

The CGRES6 cells and pGR102ES plasmid were a gift from F. Roualt and W. Günzburg. This study was supported by grants from the National Institutes of Health to S.R.R. and M.B.P. C.O. was supported by a training grant from the National Cancer Institute of the National Institutes of Health and N.L. was funded in part by the Slovenian Research Agency.

Author Contributions C.M.O, N.L., B.M.P. and S.R.R. designed the research. C.M.O. and N.L. performed the research. C.M.O, N.L., B.M.P. and S.R.R. wrote the paper.

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Correspondence to Susan R. Ross.

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Reprints and permissions information is available at www.nature.com/reprints. The authors declare no competing financial interests.

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Okeoma, C., Lovsin, N., Peterlin, B. et al. APOBEC3 inhibits mouse mammary tumour virus replication in vivo. Nature 445, 927–930 (2007). https://doi.org/10.1038/nature05540

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