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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1988 Dec;85(24):9572–9575. doi: 10.1073/pnas.85.24.9572

LR1: a candidate RNA virus of Leishmania.

P I Tarr 1, R F Aline Jr 1, B L Smiley 1, J Scholler 1, J Keithly 1, K Stuart 1
PMCID: PMC282800  PMID: 3200841

Abstract

Although viruses are important biological agents and useful molecular tools, little is known about the viruses of parasites. We report here the discovery of a candidate for an RNA virus in a kinetoplastid parasite. This potential virus, which we term LR1, is present in the promastigote form of the human pathogen Leishmania braziliensis guyanensis CUMC1-1A but not in 11 other stocks of Leishmania that were examined nor in Trypanosoma brucei. The candidate viral RNA has a size of approximately 6000 nucleotides, is single-stranded, and is largely, if not exclusively, located in the cytoplasm. No homologous LR1 sequences are detected in genomic DNA. The candidate viral RNA is associated with a spherical particle 32 nm in diameter that has a sedimentation coefficient of approximately 130 S. There is as yet no evident effect of this potential virus on parasite physiology or the disease caused by the parasite.

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Selected References

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  1. Beverley S. M., Coderre J. A., Santi D. V., Schimke R. T. Unstable DNA amplifications in methotrexate-resistant Leishmania consist of extrachromosomal circles which relocalize during stabilization. Cell. 1984 Sep;38(2):431–439. doi: 10.1016/0092-8674(84)90498-7. [DOI] [PubMed] [Google Scholar]
  2. Croft S. L., Chance M. L., Gardener P. J. Ultrastructural and biochemical characterization of stocks of Endotrypanum. Ann Trop Med Parasitol. 1980 Dec;74(6):585–589. doi: 10.1080/00034983.1980.11687391. [DOI] [PubMed] [Google Scholar]
  3. Croft S. L., Molyneux D. H. Studies on the ultrastructure, virus-like particles and infectivity of Leishmania hertigi. Ann Trop Med Parasitol. 1979 Jun;73(3):213–226. doi: 10.1080/00034983.1979.11687251. [DOI] [PubMed] [Google Scholar]
  4. Diamond L. S., Mattern C. F. Protozoal viruses. Adv Virus Res. 1976;20:87–112. doi: 10.1016/s0065-3527(08)60502-3. [DOI] [PubMed] [Google Scholar]
  5. Feagin J. E., Jasmer D. P., Stuart K. Apocytochrome b and other mitochondrial DNA sequences are differentially expressed during the life cycle of Trypanosoma brucei. Nucleic Acids Res. 1985 Jun 25;13(12):4577–4596. doi: 10.1093/nar/13.12.4577. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Grunstein M., Hogness D. S. Colony hybridization: a method for the isolation of cloned DNAs that contain a specific gene. Proc Natl Acad Sci U S A. 1975 Oct;72(10):3961–3965. doi: 10.1073/pnas.72.10.3961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Gubler U., Hoffman B. J. A simple and very efficient method for generating cDNA libraries. Gene. 1983 Nov;25(2-3):263–269. doi: 10.1016/0378-1119(83)90230-5. [DOI] [PubMed] [Google Scholar]
  8. McEwen C. R. Tables for estimating sedimentation through linear concentration gradients of sucrose solution. Anal Biochem. 1967 Jul;20(1):114–149. doi: 10.1016/0003-2697(67)90271-0. [DOI] [PubMed] [Google Scholar]
  9. Milhausen M., Nelson R. G., Parsons M., Newport G., Stuart K., Agabian N. Molecular characterization of initial variants from the IsTat I serodeme of Trypanosoma brucei. Mol Biochem Parasitol. 1983 Nov;9(3):241–254. doi: 10.1016/0166-6851(83)90100-7. [DOI] [PubMed] [Google Scholar]
  10. Molyneux D. H. Virus-like particles in Leishmania parasites. Nature. 1974 Jun 7;249(457):588–589. doi: 10.1038/249588a0. [DOI] [PubMed] [Google Scholar]
  11. Scholler J. K., Reed S. G., Stuart K. Molecular karyotype of species and subspecies of Leishmania. Mol Biochem Parasitol. 1986 Sep;20(3):279–293. doi: 10.1016/0166-6851(86)90108-8. [DOI] [PubMed] [Google Scholar]
  12. Shapiro S. Z., Young J. R. An immunochemical method for mRNA purification. Application to messenger RNA encoding trypanosome variable surface antigen. J Biol Chem. 1981 Feb 25;256(4):1495–1498. [PubMed] [Google Scholar]
  13. Steiger R. F., Opperdoes F. R., Bontemps J. Subcellular fractionation of Trypanosoma brucei bloodstream forms with special reference to hydrolases. Eur J Biochem. 1980 Mar;105(1):163–175. doi: 10.1111/j.1432-1033.1980.tb04486.x. [DOI] [PubMed] [Google Scholar]
  14. Wang A. L., Wang C. C. A linear double-stranded RNA in Trichomonas vaginalis. J Biol Chem. 1985 Mar 25;260(6):3697–3702. [PubMed] [Google Scholar]
  15. Wang A. L., Wang C. C. Discovery of a specific double-stranded RNA virus in Giardia lamblia. Mol Biochem Parasitol. 1986 Dec;21(3):269–276. doi: 10.1016/0166-6851(86)90132-5. [DOI] [PubMed] [Google Scholar]

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