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Ricin-resistant mutants of Leishmania major which express modified lipophosphoglycan remain infective for mice

Published online by Cambridge University Press:  06 April 2009

R. Cappai
Affiliation:
The Walter and Eliza Hall Institute of Medical Research, Post Office, The Royal Melbourne Hospital, Victoria 3050, Australia
L. Morris
Affiliation:
The Walter and Eliza Hall Institute of Medical Research, Post Office, The Royal Melbourne Hospital, Victoria 3050, Australia
T. Aebischer
Affiliation:
The Walter and Eliza Hall Institute of Medical Research, Post Office, The Royal Melbourne Hospital, Victoria 3050, Australia
A. Bacic
Affiliation:
Plant Cell Biology Centre, School of Botany, University of Melbourne, Parkville 3052, Australia
J. M. Curtis
Affiliation:
The Walter and Eliza Hall Institute of Medical Research, Post Office, The Royal Melbourne Hospital, Victoria 3050, Australia
M. Kelleher
Affiliation:
The Walter and Eliza Hall Institute of Medical Research, Post Office, The Royal Melbourne Hospital, Victoria 3050, Australia
K. S. McLeod
Affiliation:
The Walter and Eliza Hall Institute of Medical Research, Post Office, The Royal Melbourne Hospital, Victoria 3050, Australia
S. F. Moody
Affiliation:
The Walter and Eliza Hall Institute of Medical Research, Post Office, The Royal Melbourne Hospital, Victoria 3050, Australia
A. H. Osborn
Affiliation:
The Walter and Eliza Hall Institute of Medical Research, Post Office, The Royal Melbourne Hospital, Victoria 3050, Australia
E. Handman
Affiliation:
The Walter and Eliza Hall Institute of Medical Research, Post Office, The Royal Melbourne Hospital, Victoria 3050, Australia

Summary

Glycosylation variants of the virulent Leishmania major clone VI21 were generated by mutagenesis with N-methyl-N-nitroso-N-nitroguanidine and selected using the galactose-specific lectin Ricinus communis II (RCA II). Three mutants, 4B9, 1D1 and 1C12, which failed to bind RCA II, were found to have an altered expression of lipophosphoglycan (LPG), a molecule implicated in the attachment to host macrophages and survival within the phagolysosome. There were differences in the antigenicity, molecular weight and localization of LPG from mutant parasites as compared to V121. Expression of gp63, a surface molecule also implicated in attachment to macrophages, was unaltered. All 3 mutants caused disease when injected into genetically susceptible BALB/c mice but lesions developed at a much slower rate than those caused by the virulent V121 clone. This slow rate of lesion development did not correlate with promastigotes' ability to invade macrophages in vitro. Karyotype analysis showed that there was a reduction in the size of chromosome band number 2 in all 3 mutants. The differences in LPG and chromosome band 2 were retained by mutant clones following passage through mice, suggesting that these phenotypes are stable. Although the mutant parasites were infective and caused lesions, the changed structure of the LPG appeared to influence the virulence of the parasites.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1994

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References

REFERENCES

Bastien, P., Blaineau, C. & Pages, M. (1992). Leishmania: sex, lies and karyotype. Parasitology TodayS, 174–7.Google Scholar
Blaineau, C., Bastien, P. & Pages, M. (1992). Multiple forms of chromosome I, II and V in a restricted population of Leishmania infantum contrasting with monomorphism in individual strains suggest haploidy or automixy. Molecular and Biochemical Parasitology 50, 197204.Google Scholar
Button, L. L. & McMaster, W. R. (1988). Molecular cloning of the major surface antigen of Leishmania. Journal of Experimental Medicine 167, 724–9.Google Scholar
Chang, K.-p. & Chaudhuri, G. (1990). Molecular determinants of Leishmania virulence. Annual Review of Microbiology 44, 499529.Google Scholar
Chang, K.-p., Fong, D. & Bray, R. S. (1985). Biology of Leishmania and Leishmaniasis. In Leishmaniasis (ed. Chang, K. P. & Bray, R. S.) pp. 130. Amsterdam: Elsevier.Google Scholar
Da Silva, R. & Sacks, D. L. (1987). Metacyclogenesis is a major determinant of Leishmania promastigote virulence and attenuation. Infection and Immunity 55, 2802–6.CrossRefGoogle Scholar
Deibarra, A., Howard, J. C. & Snary, D. (1982). Monoclonal antibodies to Leishmania tropica major: specificities and antigen localization. Parasitology 85, 523–31.CrossRefGoogle Scholar
Elhay, M., Kelleher, M., Bacic, A., McConville, M. J., Tolson, D. L., Pearson, T. W. & Handman, E. (1990). Lipophosphoglycan expression and virulence in ricin-resistant variants of Leishmania major. Molecular and Biochemical Parasitology 40, 255–67.CrossRefGoogle ScholarPubMed
Elhay, M. J., McConville, M. J. & Handman, E. (1988). Immunochemical characterization of a glyco-inositol-phospholipid membrane antigen of Leishmania major. Journal of Immunology 141, 1326–31.Google Scholar
Greenblatt, C. L., Slutzky, G. M., Deibarra, A. A. & Snary, D. (1983). Monoclonal antibodies for serotyping of Leishmania strains. Journal of Clinical Microbiology 18, 191–3.Google Scholar
Grumont, R., Washtien, W. L., Caput, D. & Santi, D. V. (1986). Bifunctional thymidylate synthase-dihydrofolate reductase from Leishmania tropica: sequence homology with the corresponding monofunctional proteins. Proceedings of the National Academy of Sciences, USA 83, 5387–91.Google Scholar
Handman, E. & Goding, J. W. (1985). The Leishmania receptor for macrophages is a lipid containing glycoconjugate. EMBO Journal 4, 329–36.CrossRefGoogle ScholarPubMed
Handman, E., Schnur, L. F., Spithill, T. W. & Mitchell, G. F. (1986). Passive transfer of Leishmania lipophosphoglycan confers parasite survival in macrophages. Journal of Immunology 137, 3608–14.CrossRefGoogle Scholar
Handman, E., Barnett, L. D., Osborn, A. H., Goding, J. W. & Murray, P. J. (1994). Identification, characterization and genomic cloning of a O-linked N-acetylglucosamine-containing cytoplasmic Leishmania glycoprotein. Molecular and Biochemical Parasitology (in the Press).Google Scholar
Heisch, R. B., Grainger, W. E. & Harvey, E. C. (1959). The isolation of a Leishmania from gerbils in Kenya. American Journal of Tropical Medicine and Hygiene 62, 158–9.Google Scholar
Iovannisci, D. M. & Beverley, S. M. (1989). Structural alterations of chromosome 2 in Leishmania major as evidence for diploidy, including spontaneous amplification of the mini-exon array. Molecular and Biochemical Parasitology 34, 177–88.Google Scholar
Kelleher, M., Bacic, A. & Handman, E. (1992). Identification of a macrophage-binding determinant on lipophosphoglycan from Leishmania major promastigotes. Proceedings of the National Academy of Sciences, USA 89, 610.CrossRefGoogle ScholarPubMed
Laemmli, U. K. (1970). Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature, London 227, 680–5.CrossRefGoogle ScholarPubMed
Lighthall, G. K. & Giannini, S. H. (1992). The chromosomes of Leishmania. Parasitology Today 8, 192–9.Google Scholar
McConville, M.J. (1991). Glycosylated-phosphatidylinositols as virulence factors in Leishmania. Cell Biology International Reports 15, 779–98.Google Scholar
McNeely, T. B. & Turco, S. J. (1990). Requirement of lipophosphoglycan for intracellular survival of Leishmania donovani within human monocytes. Journal of Immunology 144, 2745–50.CrossRefGoogle ScholarPubMed
Moll, H. & Mitchell, G. F. (1988). Analysis of variables associated with promotion of resistance and its abrogation in T cell-reconstituted nude mice infected with Leishmania major. Journal of Parasitology 74, 993–8.CrossRefGoogle Scholar
Murray, P. J., Handman, E., Glaser, T. A. & Spithill, T. W. (1990). Leishmania major: expression and gene structure of the glycoprotein 63 molecule in virulent and avirulent clones and strains. Experimental Parasitology 71, 294304.Google Scholar
Murray, P. J. & Spithill, T. W. (1991). Variants of a Leishmania surface antigen derived from a multigenic family. Journal of Biological Chemistry 266, 24477–84.Google Scholar
Rovai, L., Tripp, C., Stuart, K. & Simpson, . (1992). Recurrent polymorphisms in small chromosomes of Leishmania tarentolae after nutrient stress or subcloning. Molecular and Biochemical Parasitology 50, 115–26.Google Scholar
Russell, D. G. (1990). Leishmania and the macrophage. Immunology Today 11, 74–5.Google Scholar
Russell, D. G. & talamas, R. P. (1989). Leishmania and the macrophage: a marriage of inconvenience. Immunology Today 10, 328–33.CrossRefGoogle ScholarPubMed
Samaras, N. & Spithill, T. W. (1989). The developmentally regulated PI00/11E gene of Leishmania major shows homology to a superfamily of reductase genes. Journal of Biological Chemistry 264, 4251–4.CrossRefGoogle Scholar
Sambrook, J., Fritsch, E. H. & Maniatis, T. (1989). Molecular Cloning: A Laboratory Manual 2nd Edn.Cold Spring Harbour, N.Y: Cold Spring Harbour Laboratory.Google Scholar
Spithill, T. W. & Samaras, N. (1985). The molecular karyotype of Leishmania major and mapping of α and β tubulin gene families to multiple unlinked chromosomal loci. Nucleic Acids Research 13, 4155–69.Google Scholar
Spithill, T. W. & Samaras, N. (1987). Genomic organization, chromosomal location and transcription of dispersed and repeated tubulin genes in Leishmania major. Molecular and Biochemical Parasitology 24, 2337.Google Scholar
Stanley, R. E. & Heard, P. M. (1977). Factors regulating macrophage production and growth. Journal of Biological Chemistry 252, 4305–12.CrossRefGoogle Scholar
Towbin, H., Staehelin, T. & Gordon, J. (1979). Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proceedings of the National Academy of Sciences, USA 76, 4350–4.CrossRefGoogle ScholarPubMed
Turco, S. J. (1990). The leishmanial lipophosphoglycan: a multifunctional molecule. Experimental Parasitology 70, 241–5.CrossRefGoogle ScholarPubMed
Turco, S. & Descoteaux, A. (1992). The lipophosphoglycan of Leishmania parasites. Annual Review of Microbiology 46, 6594.CrossRefGoogle ScholarPubMed