The surface protein Pvs25 of Plasmodium vivax ookinetes interacts with calreticulin on the midgut apical surface of the malaria vector Anopheles albimanus

Molecular and Biochemical Parasitology

Volumn 153, Issue 2, 2007, Pages 167-177

  Rodríguez, María del Carmen ^a   Martínez Barnetche, Jesús ^a   Alvarado Delgado, Alejandro ^a   Batista, César ^b   Argotte Ramos, Rocío S ^a   Hernández Martínez, Salvador ^a   González Cerón, Lilia ^a   Torres, Jorge A ^a   Margos, Gabriele ^c   Rodríguez, Mario Henry ^a  

^a INSTITUTO NACIONAL DE SALUD PÚBLICA   (Mexico)

^b INSTITUTO DE BIOTECNOLOGÍA   (Mexico)

^c University of Bath   (United Kingdom)

Author keywords

Calreticulin; Malaria transmission; Midgut; Mosquito vector; Ookinete; Pvs25

Indexed keywords

CALRETICULIN; PROTEIN PVS25; PROTEIN PVS28; PROTOZOON ANTIBODY; RECOMBINANT PROTEIN; UNCLASSIFIED DRUG; VIRUS VECTOR;

ANIMAL EXPERIMENT; ANOPHELES; ANTIBODY PRODUCTION; ARTICLE; FEMALE; HUMAN; IMMUNOFLUORESCENCE; IMMUNOPRECIPITATION; IN VIVO STUDY; MALARIA; MASS SPECTROMETRY; MIDGUT; NONHUMAN; PLASMODIUM VIVAX; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN INTERACTION;

AMINO ACID SEQUENCE; ANIMALS; ANOPHELES; ANTIGENS, PROTOZOAN; ANTIGENS, SURFACE; BASE SEQUENCE; CALRETICULIN; CLONING, MOLECULAR; DIGESTIVE SYSTEM; HUMANS; INSECT VECTORS; MALARIA VACCINES; MOLECULAR SEQUENCE DATA; PLASMODIUM VIVAX; RECOMBINANT PROTEINS; SEQUENCE ANALYSIS, DNA;

ANOPHELES ALBIMANUS; PLASMODIUM VIVAX;

EID: 34247558205     PISSN: 01666851     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molbiopara.2007.03.002     Document Type: Article

References (45)

1. Shahabuddin M., Toyoshima T., Aikawa M., and Kaslow D.C. Transmission-blocking activity of a chitinase inhibitor and activation of malarial parasite chitinase by mosquito protease. Proc Natl Acad Sci USA 90 (1993) 4266-4270
2. Zieler H., Narocki J.P., and Shahabuddin M. Plasmodium gallinaceum ookinetes adhere specifically to the midgut epithelium of Aedes aegypti by interaction with a carbohydrate ligand. J Exp Biol 202 (1999) 449-485
3. Zieler H., and Dvorak J.A. Invasion in vitro of mosquito midgut cells by the malaria parasite proceeds by a conserved mechanism and results in death of the invaded midgut cells. Proc Natl Acad Sci USA 97 (2000) 11516-11521
4. Sinden R.E. Molecular interactions between Plasmodium and its insect vectors. Cell Microbiol 4 (2002) 713-724
5. Shahabuddin M., and Costero A. Spatial distribution of factors that determine sporogonic development of malaria parasites in mosquitoes. Insect Biochem Mol Biol 1 (2001) 231-240
6. Tomas A.M., Margos G., Dimopoulos G., et al. P25 and P28 proteins of the malaria ookinete surface have multiple and partially redundant functions. EMBO J 20 (2001) 3975-3983
7. Kotsyfakis M., Ehret-Sabatier L., Siden-Kiamos I., Mendoza J., Sinden R.E., and Louis C. Plasmodium berghei ookinetes bind to Anopheles gambiae and Drosophila melanogaster annexins. Mol Microbiol 57 (2005) 171-179
8. Vlachou D., Lycett G., Siden-Kiamos I., Blass C., Sinden R.E., and Louis C. Anopheles gambiae laminin interacts with the P25 surface protein of Plasmodium berghei ookinetes. Mol Biochem Parasitol 112 (2001) 229-237
9. Rodríguez M.H., and Loyola E.G. Malaria in Mexico. Proceedings and papers of the 58th annual conference of the California Mosquito and Vector Control Association (AMCA) (1990) 49-52
10. Villarreal C., Arredondo-Jimenez J.I., Rodríguez M.H., and Ulloa A. Colonization of Anopheles pseudopunctipennis from Mexico. J Am Mosq Control Assoc 14 (1998) 369-372
11. González-Cerón L., Rodríguez M.H., Nettel J.C., Villarreal C., Kain K.C., and Hernández J.E. Differential susceptibilities of An. albimanus and An. pseudpounctipennis to infections with coindigenous Plasmodium vivax variants VK210 and VK247 in Southern Mexico. Infect Immun 67 (1999) 410-412
12. Tsuboi T., Kaslow D.C., Gozar M.M., Tachibana M., Cao Y.M., and Torii M. Sequence polymorphism in two novel Plasmodium vivax transmission-blocking vaccine candidates. Mol Med 4 (1998) 772-782
13. Luckow V.A., Lee S.C., Barry G.F., and Olins P.O. Efficient generation of infectious recombinant baculoviruses by site-specific transposon-mediated insertion of foreign genes into a baculovirus genome propagated in Escherichia coli. J Virol 67 (1993) 4566-4579
14. O'reilly D.R., Miller L.K., and Luckow V.A. Baculovirus expression vectors. A laboratory manual (1994), Oxford University Press
15. Pelham H.R. The retention signal for soluble proteins of the endoplasmic reticulum. Trends Biochem Sci 15 (1990) 483-486
16. Rodríguez M.C., Gerold P., Dessens J., et al. Characterization and expression of Pbs25, a sexual and sporogonic stage specific protein of Plasmodium berghei. Mol Biochem Parasitol 110 (2000) 147-159
17. Laemmli U.K. Cleavage of structural proteins during assembly of the head of bacteriophage T4. Nature 227 (1970) 680-685
18. Towbin H., Staehelin T., and Gordon J. Electrophoretic transfer of proteins from polyacrilamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci USA 76 (1979) 4350-4354
19. O'Farrell P.H. High resolution two-dimensional electrophoresis of proteins. J Biol Chem 250 (1975) 4007-4021
20. Celis J.E., Ratz G., and Bodil B. Cell biology: a laboratory handbook vol. 3 (1994), Academic Press p. 272-5
21. Nakamura Y., Gojobori T., and Ikemura T. Codon usage tabulated from the international DNA sequence databases: status for the year. Nucleic Acids Res 28 (2000) 292. http://www.kazusa.or.jp/codon/ URL http://www.kazusa.or.jp/codon/
22. Tabb D.L., Eng J.K., and Yates III J.R. Protein identification by SEQUEST. In: James P. (Ed). Proteome research: mass spectrometry vol. 1 (2001), Springer, New York 125-142
23. Margos G., Kurtenbach K., Posnett E., et al. Expression of the Plasmodium berghei ookinete protein Pbs21 in a baculovirus-insect cell system produces an efficient transmission blocking immunogen. Parasite Immunol 17 (1995) 167-176
24. Coppolino M.G., and Dedhar S. Calreticulin. Int J Biochem Cell Biol 30 (1998) 553-558
25. Danilczyk U.G., Cohen-Doyle M.F., and Williams D.B. Fuctional relationship between calreticulin, calnexin and the endoplasmic reticulum luminal domain of calnexin. J Biol Chem 275 (2000) 13089-13097
26. Quevillon E., Silventoinen V., Pillai S., et al. InterProScan: protein domains identifier. Nucleic Acids Res 33 (2005) W116-W120. http://www.ebi.ac.uk/InterProScan/ URL http://www.ebi.ac.uk/InterProScan/.
27. Duffy P.E., and Kaslow D.C. A novel malaria protein, Pfs28, and Pfs25 are genetically linked and synergistic as falciparum malaria transmission-blocking vaccines. Infect Immun 65 (1997) 1109-1113
28. Siden-Kiamos I., Vlachou D., Margos G., et al. Distinct roles for pbs21 and pbs25 in the in vitro ookinete to oocyst transformation of Plasmodium berghei. J Cell Sci 113 (2000) 3419-3426
29. Saxena A.K., Singh K., Su H.P., et al. The essential mosquito-stage P25 and P28 proteins from Plasmodium form tile-like triangular prisms. Nat Struct Mol Biol 13 (2006) 90-91
30. Adini A., and Warburg A. Interaction of Plasmodium gallinaceum ookinetes and oocysts with extracellular matrix proteins. Parasitology 119 (1999) 331-336
31. Arrighi R.B., and Hurd H. The role of Plasmodium berghei ookinete proteins in binding to basal lamina components and transformation into oocysts. Int J Parasitol 32 (2002) 91-98
32. Sinden R.E. A proteomic analysis of malaria biology: integration of old literature and new technologies. Int J Parasitol (2004) 1441-1450
33. Alavi Y., Arai M., Mendoza J., et al. The dynamics of interactions between Plasmodium and the mosquito: a study of the infectivity of Plasmodium berghei and Plasmodium gallinaceum, and their transmission by Anopheles stephensi, Anopheles gambiae and Aedes aegypti. Int J Parasitol 34 (2004) 245-247
34. 2+ binding domains. J Biochem Chem 266 (1991) 21458-21465
35. Ghiran I., Klickstein L.B., and Weller A.N. Calreticulin is at the surface of circulating neutrophils and uses CD59 as an adaptor molecule. J Biol Chem 278 (2003) 21024-21031
36. Fadel M.P., Dziak E., Lo C., et al. Calreticulin affects focal contact-dependent but not close contact-dependent cell-substratum adhesion. J Biol Chem 274 (1999) 15085-15094
37. Gray A.J., Par P.W., Broekelmann T.J., et al. The mitogenic effects of the B beta chain of fibrinogen are mediated through cell surface calreticulin. J Biol Chem 270 (1995) 26602-26606
38. White T.K., Zhu Q., and Tanzer M.L. Cell surface calreticulin is a putative mannoside lectin which triggers mouse melanoma cell spreading. J Biol Chem 270 (1995) 15926-15929
39. Ferreira V., Valck C., Sánchez G., et al. The classical activation pathway of the human complement system is specifically inhibited by calreticulin from Trypanosoma cruzi. J Immunol 172 (2004) 3042-3050
40. Muller-Taubenberger A., Lupas A.N., Li H., Ecke M., Simmeth E., and Gerisch G. Calreticulin and calnexin in the endoplasmic reticulum are important for phagocytosis. EMBO J 20 (2001) 6772-6782
41. Vandivier R.W., Orden C.A., Fadok V.A., et al. Role of surfactant proteins A, D, and C1q in the clearance of apoptotic cells in vivo and in vitro: calreticulin and CD91 as a common collectin receptor complex. J Immunol 169 (2002) 3978-3986
42. Choi J.Y., Whitten M.M., Cho M.Y., et al. Calreticulin enriched as an early-stage encapsulation protein in wax moth Galleria mellonella larvae. Dev Comp Immunol 26 (2002) 335-343
43. Valenzuela J.G., Pham V.M., Garfield M.K., Francischetti I.M., and Ribeiro J.M. Toward a description of the sialome of the adult female mosquito Aedes aegypti. Insect Biochem Mol Biol 32 (2002) 1101-1122
44. Jaworski D.C., Higgins J.A., Radulovic S., Vaughan J.A., and Azad A.F. Presence of calreticulin in vector fleas (Siphonaptera). J Med Entomol 33 (1996) 482-489
45. Han Y.S., Thompson J., Kafatos F.C., and Barillas-Mury C. Molecular interactions between Anopheles stephensi midgut cells and Plasmodium berghei: the time bomb theory of ookinete invasion of mosquitoes. EMBO J 19 (2000) 6030-6040