Hostname: page-component-cd9895bd7-dzt6s Total loading time: 0 Render date: 2024-12-23T03:32:47.916Z Has data issue: false hasContentIssue false

Haemoglobin inhibits the development of infective promastigotes and chitinase secretion in Leishmania major cultures

Published online by Cambridge University Press:  06 April 2009

Y. Schlein
Affiliation:
Department of Parasitology, The Hebrew University – Hadassah Medical School, P.O.B. 1172, Jerusalem 91120, Israel
R. L. Jacobson
Affiliation:
Department of Parasitology, The Hebrew University – Hadassah Medical School, P.O.B. 1172, Jerusalem 91120, Israel

Summary

Haemoglobin or blood in the growth medium of Leishmania major inhibited the formation of infective promastigotes and the secretion of chitinases. Inoculation of mice with stationary-phase parasites from control medium caused infections in 20/29 mice, compared to 3/20 mice injected with parasites grown with 10% rabbit blood, or 1/30 mice that received parasites grown with rabbit haemoglobin. The concentration of peanut lectin (PNA) required to agglutinate promastigotes was used as an index of their infectivity, ranging from a high concentration for infective populations to a low concentration for relatively non-infective populations. Agglutination of 50% of the parasites from control medium or from medium containing rabbit haemoglobin required 4·1 μg PNA/ml and 0·1 μg PNA/ml, respectively. Chitinase activities/107 parasites decreased from 4·8 units chitinase and 12·5 units N-acetylglucosaminidase (NAGase) in the control to 2·0 units chitinase and 8·5 units NAGase in cultures containing rabbit haemoglobin. Rabbit, human, bovine and pigeon haemoglobins had various inhibitory effects on the activity of chitinases and not on the virulence, as expressed by PNA agglutination. The relevance of the results to the cycle of Leishmania is discussed.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1994

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Adler, S. & Theodor, O. (1927). The transmission of Leishmania tropica from artificially infected sandflies to man. Annals of Tropical Medicine and Parasitology 21, 89110.CrossRefGoogle Scholar
Bates, P. A. & Tetley, L. (1993). Leishmania mexicana: induction of metacyclogenesis by cultivation of promastigotes at acidic pH. Experimental Parasitology 76, 412–23.CrossRefGoogle ScholarPubMed
Bradford, M. M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein using the principle of protein dye-binding. Analytical Biochemistry 72, 248–54.CrossRefGoogle ScholarPubMed
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
Davies, C. R., Cooper, A. M., Peacock, C., Lane, R. P. & Blacewell, J. M. (1990). Expression of LPG and GP63 by different developmental stages of Leishmania major in the sandfly Phlebotomus papatasi. Parasitology 101, 337–43.CrossRefGoogle ScholarPubMed
Doran, T. I. & Herman, R. (1981). Characterization of populations of promastigotes of Leishmania donovani. Journal of Protozoology 28, 345–50.CrossRefGoogle ScholarPubMed
Feng, L. C. (1950–1). The role of the peritrophic membrane in Leishmania and Trypanosoma infections of sandflies. Peking Natural History Bulletin 19, 327–34.Google Scholar
Giannini, M. S. (1974). Effects of promastigote growth phase, frequency of subculture, and host age on promastigote-initiated infections with Leishmania donovani in the golden hamster. Journal of Protozoology 21, 521–7.CrossRefGoogle ScholarPubMed
Howard, M. K., Sayers, G. & Miles, M. A. (1987). Leishmania donovani metacyclic promastigotes: transformation in vitro, lectin agglutination, complement resistance, and infectivity. Experimental Parasitology 64, 147–56.CrossRefGoogle ScholarPubMed
Jacobson, R. L. & Schnur, L. F. (1990). Changing surface carboyhydrate configurations during the growth of Leishmania major. Journal of Parasitology 76, 218–24.CrossRefGoogle Scholar
Killick-Kendrick, R. (1986). The transmission of leishmaniasis by the bite of the sandfly. Journal of the Royal Army Medical Corps 132, 134–40.CrossRefGoogle Scholar
Killick-Kendrick, R. (1990). The life cycle of Leishmania in the sandfly with special reference to the form infective to the vertebrate host. Annales de Parasitologie Humaine et Comparée 65, Suppl. 1, 3742.CrossRefGoogle Scholar
Lang, T., Warburg, A., Sacks, D. L., Croft, S. L. & Lane, R. P. (1991). Transmission of scanning EM-immunogold labelling of Leishmania major lipophosphoglycan in the sandfly, Phlebotomus papatasi. European Journal of Cell Biology 55, 362–72.Google ScholarPubMed
McConville, M. J., Turco, S. J., Ferguson, M. A. J. & Sacks, D. L. (1992). Developmental modification of lipophosphoglycan during the differentiation of Leishmania major promastigotes to an infectious stage. EMBO Journal 11, 3593–600.CrossRefGoogle Scholar
Polacheck, I. & Rosenberger, R. F. (1978). Distribution of autolysins in hyphae of Aspergillus undulans: evidence for lipid mediated attachment to hyphal walls. Journal of Bacteriology 135, 741–7.CrossRefGoogle Scholar
Sacks, D. L., Hieny, S. & Sher, A. (1985). Identification of cell surface carbohydrate and antigenic changes between noninfective and infective developmental stages of Leishmania major promastigotes. Journal of Immunology 135, 564–9.CrossRefGoogle ScholarPubMed
Sacks, D. L. & Perkins, P. V. (1984). Identification of an infective stage of Leishmania promastigotes. Science 223, 1417–19.CrossRefGoogle ScholarPubMed
Sacks, D. L. & Perkins, P. V. (1985). Development of infective stage Leishmania promastigotes within phlebotomine sandflies. American Journal of Tropical Medicine and Hygiene 34, 456–9.CrossRefGoogle Scholar
Schlein, Y. & Jacobson, R. L. (1992). Chitinases in trypanosomatidae and in Trypanosoma brucei brucei: reply. Parasitology Today 8, 367.CrossRefGoogle ScholarPubMed
Schlein, Y., Jacobson, R. L. & Messer, G. (1992). Leishmania infections damage the feeding mechanism of the sandfly vector and implement parasite transmission by bite. Proceedings of the National Academy of Sciences, USA 89, 9944–8.CrossRefGoogle ScholarPubMed
Schlein, Y., Jacobson, R. L. & Shlomai, J. (1991). Chitinase secreted by Leishmania functions in the sandfly vector. Proceedings of the Royal Society of London, B 245, 121–6.Google ScholarPubMed
Segovia, M., Artero, J. M., Mellado, E. & Chance, M. L. (1992). Effects of long-term in vitro cultivation on the virulence of cloned lines of Leishmania major promastigotes. Annals of Tropical Medicine and Parasitology 86, 347–54.CrossRefGoogle ScholarPubMed
Turco, S. J. (1988). The lypophosphoglycan of Leishmania. Parasitology Today 4, 255–7.CrossRefGoogle ScholarPubMed
Walters, L. L. (1993). Leishmania differentiation in natural and unnatural sandfly hosts. Journal of Eukaryotic Microbiology 40, 196206.CrossRefGoogle ScholarPubMed
Walters, L. L., Modi, G. B., Tesh, R. B. & Burrage, T. (1987). Host–parasite relationship of Leishmania mexicana mexicana and Lutzomyia abonnenci (Diptera: Psychodidae). American Journal of Tropical Medicine and Hygiene 36, 294314.CrossRefGoogle ScholarPubMed