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Abstract

Genetic exchange has not been shown to be a mechanism underlying the extensive diversity of Leishmania parasites. We report here evidence that the invertebrate stages of Leishmania are capable of having a sexual cycle consistent with a meiotic process like that described for African trypanosomes. Hybrid progeny were generated that bore full genomic complements from both parents, but kinetoplast DNA maxicircles from one parent. Mating occurred only in the sand fly vector, and hybrids were transmitted to the mammalian host by sand fly bite. Genetic exchange likely contributes to phenotypic diversity in natural populations, and analysis of hybrid progeny will be useful for positional cloning of the genes controlling traits such as virulence, tissue tropism, and drug resistance.

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This research was supported in part by the Intramural Research Program of the NIH, National Institute of Allergy and Infectious Diseases (NIAID), and in part by NIAID grant support (S.M.B., D.E.D., and N.S.A. A1029646 and A1020941). We thank K. Owens for inventorying and shipping parasite strains; K. Beacht for mouse infection studies; and M. Grigg, L. Miller, and A. Sher for critical review of the manuscript. Maxicircle sequences have been submitted to GenBank and had been assigned accession numbers FJ349262 to FJ349263 (12S rRNA) and FJ349264 to FJ349265 (Divergent region).

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Published In

Science
Volume 324 | Issue 5924
10 April 2009

Submission history

Received: 8 December 2008
Accepted: 18 February 2009
Published in print: 10 April 2009

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Notes

Supporting Online Material
www.sciencemag.org/cgi/content/full/324/5924/265/DC1
Materials and Methods
Figs S1 to S5
Tables S1 to S3
References

Authors

Affiliations

Natalia S. Akopyants*
Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Nicola Kimblin*
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD 20892, USA.
Nagila Secundino
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD 20892, USA.
Rachel Patrick
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD 20892, USA.
Nathan Peters
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD 20892, USA.
Phillip Lawyer
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD 20892, USA.
Deborah E. Dobson
Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Stephen M. Beverley*
Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
David L. Sacks,* [email protected]
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD 20892, USA.

Notes

To whom correspondence should be addressed. E-mail: [email protected]

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