Ali Jawad Alyasiri and Mohammed Qasim Waheeb
Department of Biology, College of Science, Al Muthanna University, Iraq
*Corresponding author: Ali.abdulaali.sci@mu.edu.iq
Received: May 10, 2022/ Revised: June 10, 2022 / Accepted: June 15, 2022
Abstract
Protozoa parasites of the genus Leishmania have a great ability to avoid damage in the hostile environments they encounter throughout their life cycle within the host’s body. Parasites have developed many virulence factors to ensure their persistence and replication within the host, and the first role of these factors is to attenuate the host’s defenses against them through innate and adaptive immunity, as evidence indicates that the determinants of parasite virulence are responsible for evading the host’s defenses, allowing these organisms to survive on Alive in the host’s hostile immune environment. Understanding the molecular details of how these pathogens persist with impunity under extreme conditions is beginning to begin. The fact that Leishmania parasites have adapted not only to survive but are likely to reproduce is due to the protection afforded by specialized molecules on the parasite’s cell surface. Although recent years have seen clear and significant progress in the research on Leishmania in different directions, many issues have yet to be clarified. The surface of all parasites, especially protozoa, usually undergoes pronounced changes during their life cycle. It is of particular interest in the case of protozoan parasites of the genus Leishmania whose surface is exposed to different and hostile environments within vertebrate and invertebrate organisms. Because of the importance that the cell surface of pathogenic parasites plays in their interaction with the host for survival, some efforts have been devoted to their characterization. This review aims to give an overview of the main virulence factors that contribute to parasite survival and survival. We have attempted to provide a brief picture of the factors that influence the interaction of the parasite in its host, further highlighting GP63 as a critical virulence factor affecting macrophage physiology as well as the functioning of the immune system.
Keywords Leishmania, parasite, virulence factors, GP63
Alyasiri, A. J. and Waheeb, M. Q. (2022). Global overview of Leishmania virulence factors, and the role of GP63 in promastigotes. Science Archives, Vol. 3 (2), 124–132. http://dx.doi.org/10.47587/SA.2022.3208
References
Abdellahi, L., Iraji, F., Mahmoudabadi, A., & Hejazi, S. H. (2022). Vaccination in Leishmaniasis: A Review Article. Iranian Biomedical Journal, 26(1), 1.
Al-Mayali, H. M. H., & Alyasiri, A. J. A. (2020). Molecular Detection of Virulence Factor Glycoprotein (Gp63) of Leishmania spp. in Phlebotomus Sand Flies. Int J Med Parasitol Epidemiol Sci Volume, 1(4), 92.
Barrett, A. J. (1994). [1] Classification of peptidases. In Methods in enzymology (Vol. 244, pp. 1-15). Academic Press.
Borges, A. R., Link, F., Engstler, M., & Jones, N. G. (2021). The glycosylphosphatidylinositol anchor: a linchpin for cell surface versatility of trypanosomatids. Frontiers in Cell and Developmental Biology, 2681.
Bouvier, J., Schneider, P., & Etges, R. (1995). [37] Leishmanolysin: Surface metalloproteinase of Leishmania. In Methods in enzymology (Vol. 248, pp. 614-633). Academic Press.
Chang, K. P., & McGwire, B. S. (2002). Molecular determinants and regulation of Leishmania virulence. Kinetoplastid biology and disease, 1(1), 1-7.
Chang, K. P., Reed, S. G., McGwire, B. S., & Soong, L. (2003). Leishmania model for microbial virulence: the relevance of parasite multiplication and pathoantigenicity. Acta tropica, 85(3), 375-390.
Chaudhuri, G. A. U. T. A. M., Chaudhuri, M. I. N. U., Pan, A., & Chang, K. P. (1989). Surface acid proteinase (gp63) of Leishmania mexicana: a metalloenzyme capable of protecting liposome-encapsulated proteins from phagolysosomal degradation by macrophages. Journal of Biological Chemistry, 264(13), 7483-7489.
Contreras, I., Gómez, M. A., Nguyen, O., Shio, M. T., McMaster, R. W., & Olivier, M. (2010). Leishmania-induced inactivation of the macrophage transcription factor AP-1 is mediated by the parasite metalloprotease GP63. PLoS pathogens, 6(10), e1001148.
Coombs, G. H. (1982). Proteinases of Leishmania mexicana and other flagellate protozoa. Parasitology, 84(1), 149-155.
de Assis, R. R., Ibraim, I. C., Nogueira, P. M., Soares, R. P., & Turco, S. J. (2012). Glycoconjugates in New World species of Leishmania: polymorphisms in lipophosphoglycan and glycoinositolphospholipids and interaction with hosts. Biochimica et Biophysica Acta (BBA)-General Subjects, 1820(9), 1354-1365.
de Souza, V. L., Souza, J. A., Silva, T. M. C., Veras, P. S. T., & de-Freitas, L. A. R. (2000). Different Leishmania species determine distinct profiles of immune and histopathological responses in CBA mice. Microbes and infection, 2(15), 1807-1815.
Descoteaux, A., & Turco, S. J. (1999). Glycoconjugates in Leishmania infectivity. Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease, 1455(2-3), 341-352.
Flaih, M. H. (2022). Geographical Distribution of Cutaneous Leishmaniasis and Pathogenesis. Leishmaniasis: General Aspects of a Stigmatized Disease, 99.
Gomez, M. A., Contreras, I., Hallé, M., Tremblay, M. L., McMaster, R. W., & Olivier, M. (2009). Leishmania GP63 alters host signaling through cleavage-activated protein tyrosine phosphatases. Science signaling, 2(90), ra58-ra58.
Hepburn, N. C. (2003). Cutaneous leishmaniasis: an overview. Journal of postgraduate medicine, 49(1), 50.
Ilgoutz, S. C., & McConville, M. J. (2001). Function and assembly of the Leishmania surface coat. International journal for parasitology, 31(9), 899-908.
McKerrow, J. H., Sun, E., Rosenthal, P. J., & Bouvier, J. (1993). The proteases and pathogenicity of parasitic protozoa. Annual review of microbiology, 47, 821-854.
Joshi, P. B., Kelly, B. L., Kamhawi, S., Sacks, D. L., & McMaster, W. R. (2002). Targeted gene deletion in Leishmania major identifies leishmanolysin (GP63) as a virulence factor. Molecular and biochemical parasitology, 120(1), 33-40.
Llg, T., Handman, E., & Stierhof, Y. D. (1999). Proteophosphoglycans from Leishmania promastigotes and amastigotes. Biochemical Society Transactions, 27(4), 518-525.
Markle, W. H., & Makhoul, K. (2004). Cutaneous leishmaniasis recognition and treatment. American family physician, 69(6), 1455-1460.
McConville, M. J., Mullin, K. A., Ilgoutz, S. C., & Teasdale, R. D. (2002). Secretory pathway of trypanosomatid parasites. Microbiology and Molecular Biology Reviews, 66(1), 122-154.
Medina-Acosta, E., Karess, R. E., Schwartz, H., & Russell, D. G. (1989). The promastigote surface protease (gp63) of Leishmania is expressed but differentially processed and localized in the amastigote stage. Molecular and biochemical parasitology, 37(2), 263-273.
Moody, S. F. (1993). Molecular variation in Leishmania. Acta Tropica, 53(3-4), 185-204.
Morales, G., Carrillo, G., Requena, J. M., Guzman, F., Gomez, L. C., Patarroyo, M. E., & Alonso, C. (1997). Mapping of the antigenic determinants of the Leishmania infantum gp63 protein recognized by antibodies elicited during canine visceral leishmaniasis. Parasitology, 114(6), 507-516.
Mottram, J. C., Coombs, G. H., & Alexander, J. (2004). Cysteine peptidases as virulence factors of Leishmania. Current opinion in microbiology, 7(4), 375-381.
Olivier, M., Atayde, V. D., Isnard, A., Hassani, K., & Shio, M. T. (2012). Leishmania virulence factors: focus on the metalloprotease GP63. Microbes and infection, 14(15), 1377-1389.
Pearson, R. D., & de Queiroz Sousa, A. (1996). Clinical spectrum of leishmaniasis. Clinical infectious diseases, 1-11.
Pradhan, S., Schwartz, R. A., Patil, A., Grabbe, S., & Goldust, M. (2022). Treatment options for leishmaniasis. Clinical and experimental dermatology, 47(3), 516-521.
Rafati, S., Fasel, N., & Masina, S. (2003). Leishmania cysteine proteinases: from gene to subunit vaccine. Current Genomics, 4(3), 253-261.
Rogers, M. E. (2012). The role of Leishmania proteophosphoglycans in sand fly transmission and infection of the mammalian host. Frontiers in microbiology, 3, 223.
Schlagenhauf, E., Etges, R., & Metcalf, P. (1998). The crystal structure of the Leishmania major surface proteinase leishmanolysin (gp63). Structure, 6(8), 1035-1046.
Stierhof, Y. D., Bates, P. A., Jacobson, R. L., Rogers, M. E., Schlein, Y., Handman, E., & Ilg, T. (1999). Filamentous proteophosphoglycan secreted by Leishmania promastigotes forms gel-like three-dimensional networks that obstruct the digestive tract of infected sandfly vectors. European journal of cell biology, 78(10), 675-689.
Turco, S. J., & Descoteaux, A. (1992). The lipophosphoglycan of Leishmania parasites. Annual review of microbiology, 46(1), 65-92.
Yao, C., Donelson, J. E., & Wilson, M. E. (2003). The major surface protease (MSP or GP63) of Leishmania sp. Biosynthesis, regulation of expression, and function. Molecular and biochemical parasitology, 132(1), 1-16.
License Article Metadata
This work is licensed under a Creative Commons Attribution 4.0 International License.