A transitional endogenous lentivirus from the genome of a basal primate and implications for lentivirus evolution

  1. Robert J. Gifforda,1,2,
  2. Aris Katzourakisb,c,1,
  3. Michael Tristemd,
  4. Oliver G. Pybusb,
  5. Mark Wintersa and
  6. Robert W. Shafera
  1. aDivision of Infectious Diseases, Stanford University, Stanford, CA 94305;
  2. bDepartment of Zoology, University of Oxford, South Parks Road, Oxford OX1 3PS, United Kingdom;
  3. dDivision of Biology, Imperial College London, Silwood Park, Ascot, Berkshire SL5 7PY, United Kingdom; and
  4. cInstitute for Emergent Infections, The James Martin 21st Century School, Oxford University, Oxford OX1 3PS, United Kingdom
  1. Edited by John M. Coffin, Tufts University School of Medicine, Boston, MA, and approved October 22, 2008

  2. 1R.J.G. and A.K. contributed equally to this work. (received for review August 11, 2008)

Abstract

Lentiviruses chronically infect a broad range of mammalian species and have been transmitted from primates to humans, giving rise to multiple outbreaks of HIV infection over the past century. Although the circumstances surrounding these recent zoonoses are becoming clearer, the nature and timescale of interaction between lentiviruses and primates remains unknown. Here, we report the discovery of an endogenous lentivirus in the genome of the gray mouse lemur (Microcebus murinus), a strepsirrhine primate from Madagascar, demonstrating that lentiviruses are capable of invading the primate germ line. Phylogenetic analysis places gray mouse lemur prosimian immunodeficiency virus (pSIVgml) basal to all known primate lentiviruses and, consistent with this, its genomic organization is intermediate between the nonprimate lentiviruses and their more derived primate counterparts. Thus, pSIVgml represents the first unambiguous example of a viral transitional form, revealing the acquisition and loss of genomic features during lentiviral evolution. Furthermore, because terrestrial mammal populations in Madagascar and Africa are likely to have been isolated from one another for at least 14 million years, the presence of pSIVgml in the gray mouse lemur genome indicates that lentiviruses must have been infecting primates for at least this period of time, or have been transmitted between Malagasy and African primate populations by a vector species capable of traversing the Mozambique channel. The discovery of pSIVgml illustrates the utility of endogenous sequences for the study of contemporary retroviruses and indicates that primate lentiviruses may be considerably older and more broadly distributed than previously thought.

Keywords:

Footnotes

  • 2To whom correspondence may be addressed. E-mail: robjgiff{at}gmail.com or a.katzourakis{at}googlemail.com
  • Author contributions: R.J.G. and A.K. designed research; R.J.G., A.K., and M.W. performed research; R.J.G. and A.K. contributed new reagents/analytic tools; R.J.G., A.K., and M.T. analyzed data; and R.J.G., A.K., M.T., O.G.P., and R.W.S. wrote the paper.

  • The authors declare no conflict of interest.

  • This article is a PNAS Direct Submission.

  • Data deposition: The sequences reported in this paper have been deposited in the GenBank database (accession nos. FJ461356, FJ461357, and FJ461358).

  • See Commentary on page 20051.

  • This article contains supporting information online at www.pnas.org/cgi/content/full/0807873105/DCSupplemental.

  • Freely available online through the PNAS open access option.

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