Interaction of the monoxenic trypanosomatid Blastocrithidia culicis with the Aedes aegypti salivary gland

Acta Tropica

Volumn 113, Issue 3, 2010, Pages 269-278

  Nascimento, Michelle Tanny C ^a   Garcia, Maria Carolina F ^a   da Silva, Karen Pereira ^a   Pinto da Silva, Lucia Helena ^b   Atella, Georgia C ^a   Motta, Maria Cristina M ^a   Saraiva, Elvira M ^a  

^a FEDERAL UNIVERSITY OF RIO DE JANEIRO   (Brazil)

^b Hospital Pedro Ernesto   (Brazil)

Author keywords

Aedes aegypti; Blastocrithidia; Monoxenic trypanosomatid; Mosquito salivary gland carbohydrates; Mosquito salivary gland lectin; Protozoa insect interaction

Indexed keywords

ALPHA METHYL MANNOSIDE; CARBOHYDRATE; FUCOSE; LECTIN; N ACETYLGLUCOSAMINE; PEANUT LECTIN; SOYBEAN AGGLUTININ; UNCLASSIFIED DRUG; WHEAT GERM AGGLUTININ;

CARBOHYDRATE; HOST-PARASITE INTERACTION; LIFE CYCLE; MOSQUITO; PROTEIN; SALIVA; TRYPANOSOMIASIS; ULTRASTRUCTURE;

AEDES AEGYPTI; ANIMAL CELL; ARTICLE; BASEMENT MEMBRANE; BINDING ASSAY; BLASTOCRITHIDIA CULICIS; CELL ADHESION; CELL COMPARTMENTALIZATION; COLONIAL SPECIES; CONTROLLED STUDY; FLAGELLUM; FLOW CYTOMETRY; FLUORESCENCE; HEMOLYMPH; IN VITRO STUDY; IN VIVO STUDY; LECTIN BINDING; MICROSCOPY; NONHUMAN; PROTOZOON; SALIVARY GLAND; SPECIES INVASION; SURVIVAL; TRANSMISSION ELECTRON MICROSCOPY; TRYPANOSOMA; ULTRASTRUCTURE;

AEDES AEGYPTI; BLASTOCRITHIDIA; BLASTOCRITHIDIA CULICIS; HEXAPODA; PROTOZOA; TRYPANOSOMATIDAE;

EID: 77649184269     PISSN: 0001706X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.actatropica.2009.11.010     Document Type: Article

References (38)

1. Barreto-de-Souza V., Medeiros T.X., Motta M.C.M., Bou-Habib D.C., Saraiva E.M. HIV-1 infection and HIV-1 Tat protein permit the survival and replication of a non-pathogenic trypanosomatid in macrophages through TGF-β1 production. Microbes Infect. 2008, 10:642-649.
2. Basseri H.R., Tew I.F., Ratcliffe N.A. Identification and distribution of carbohydrate moieties on the salivary glands of Rhodnius prolixus and their possible involvement in attachment/invasion by Trypanosoma rangeli. Exp. Parasitol. 2002, 100:226-234.
3. Barreau C., Touray M., Pimenta P.F., Miller L.H., Vernick K.D. Plasmodium gallinaceum: sporozoite invasion of Aedes aegypti salivary glands is inhibited by anti-gland antibodies and by lectins. Exp. Parasitol. 1995, 81:332-343.
4. Butcher B.A., Turco S.J., Hilty B.A., Pimenta P.F., Panunzio M., Sacks D.L. Deficiency in beta 1,3-galactosyltransferase of a Leishmania major lipophosphoglycan mutant adversely influences the Leishmania-sand fly interaction. J. Biol Chem. 1996, 271:20573-20579.
5. Corrêa-da-Silva M.S., Fampa P., Lessa L.P., Silva E.R., Santos J.R.M., Saraiva E.M., Motta M.C.M. Colonization of Aedes aegypti midgut by the endosymbiont-bearing trypanosomatid Blastocrithidia culicis. Parasitol. Res. 2006, 99:384-391.
6. D'Avila-Levy C.M., Araújo F.M., Vermelho A.B., Soares R.M., Santos A.L., Branquinha M.H. Proteolytic expression in Blastocrithidia culicis: influence of the endosymbiont and similarities with virulence factors of pathogenic trypanosomatids. Parasitology 2005, 130:413-420.
7. Ellis D.S., Evans D.A., Stamford S. The penetration of the salivary glands of Rhodnius prolixus by Trypanosoma rangeli. Z. Parasitenkd. 1980, 62:63-74.
8. Fampa P., Corrêa-da-Silva M.S., Lima D.C., Oliveira S.M., Motta M.C., Saraiva E.M. Interaction of insect trypanosomatids with mosquitoes, sand fly and the respective insect cell lines. Int. J. Parasitol. 2003, 33:1019-1026.
9. Ghosh A.K., Devenport M., Jethwaney D., Kalume D.E., Pandey A., Anderson V.E., Sultan A.A., Kumar N., Jacobs-Lorena M. Malaria parasite invasion of the mosquito salivary gland requires interaction between the Plasmodium TRAP and the Anopheles saglin proteins. PLoS Pathog. 2009, 5:e1000265.
10. Gomes S.A., Fonseca de Souza A.L., Kiffer-Moreira T., Dick C.F., Santos A.L., Meyer-Fernandes J.R. Ecto-phosphatase activity on the external surface of Rhodnius prolixus salivary glands: modulation by carbohydrates and Trypanosoma rangeli. Acta Trop. 2008, 106:137-142.
11. Gregório E.A., Ratcliffe N.A. The distribution of agglutinins and lytic activity against Trypanosoma rangeli and erythrocytes in Rhodnius prolixus and Triatoma infestans tissue extracts and haemolymph. Mem. Inst. Oswaldo Cruz 1991, 86:181-186.
12. Hagedorn H.H., Turner S., Hagedorn E.A., Pontecorvo D., Greenbaum P., Pfeiffer D., Wheelock G., Flanagan T.R. Postemergence growth of the ovarian follicles of Aedes aegypti. J. Insect Physiol. 1977, 23:203-206.
13. Hecker H., Schwarzenbach M., Rudin W. Development and interactions of Trypanosoma rangeli in and with the reduviid bug Rhodnius prolixus. Parasitol. Res. 1990, 76:311-318.
14. Hillyer J.F., Barreau C., Vernick K.D. Efficiency of salivary gland invasion by malaria sporozoites is controlled by rapid sporozoite destruction in the mosquito haemocoele. Int. J. Parasitol. 2007, 37:673-681.
15. Jansen A.M., Carreira J.C., Deane M.P. Infection of a mammal by monogenetic insect trypanosomatids (Kinetoplastida, Trypanosomatidae). Mem. Inst. Oswaldo Cruz 1988, 83:271-272.
16. Kamhawi S., Ramalho-Ortigão M., Pham V.M., Kumar S., Lawyer P.G., Turco S.J., Barillas-Mury C., Sacks D.L., Valenzuela J.G. A role for insect galectins in parasite survival. Cell 2004, 119:329-341.
17. Meirelles R.M., Henriques-Pons A., Soares M.J., Steindel M. Penetration of the salivary glands of Rhodnius domesticus Neiva & Pinto, 1923 (Hemiptera: Reduviidae) by Trypanosoma rangeli Tejera, 1920 (Protozoa: Kinetoplastida). Parasitol. Res. 2005, 97:259-269.
18. McGhee R.B. Infection of chick embryos by a Crithidia from a phytophagous hemipteron. Science 1957, 125:157-158.
19. Mohamed H.A., Ingram G.A. Salivary gland surface carbohydrate variations in three species of the Anopheles gambiae complex. Ann. Soc. Belg. Med. Trop. 1993, 73:197-207.
20. Molyneux D.H., Okolo C.J., Lines J.D., Kamhawi M. Variation in fluorescein-labelled lectin staining of salivary glands in the Anopheles gambiae complex. Med. Vet. Entomol. 1990, 4:459-462.
21. Morio F., Reynes J., Dollet M., Pratlong F., Dedet J.P., Ravel C. Isolation of a protozoan parasite genetically related to the insect trypanosomatid Herpetomonas samuelpessoai from a human immunodeficiency virus-positive patient. J. Clin. Microbiol. 2008, 46:3845-3847.
22. Müller U., Vogel P., Alber G., Schaub G.A. The innate immune system of mammals and insects. Contrib. Microbiol. 2008, 15:21-44.
23. Okolo C.J., Jenni l., Molineaux D.H., Wallbanks K.R. Surface carbohydrate differences of Glossina salivary glands and infectivity of Trypanosoma brucei gambiense to Glossina. Ann. Soc. Belg. Med. Trop. 1990, 70:39-47.
24. Pacheco R.S., Marzochi M.C.A., Pires M.Q., Brito C.M.M., Madeira M.F., Barbosa-Santos E.G.O. Parasite genotypically related to a monoxenous trypanosomatid of dog's flea causing opportunistic infection in an HIV positive patient. Mem. Inst. Oswaldo Cruz 1998, 93:531-537.
25. Parodi A.J. N-glycosylation in trypanosomatid protozoa. Glycobiology 1993, 3:193-199.
26. Perrone J.B., DeMaio J., Spielman A. Regions of mosquito salivary glands distinguished by surface lectin-binding characteristics. Insect Biochem. 1986, 16:313-318.
27. Pimenta P.F., Turco S.J., McConville M.J., Lawyer P.G., Perkins P.V., Sacks D.L. Stage-specific adhesion of Leishmania promastigotes to the sand fly midgut. Science 1992, 256:1812-1815.
28. Pimenta P.F., Touray M., Miller L. The journey of malaria sporozoites in the mosquito salivary gland. J. Eukaryot. Microbiol. 1994, 41:608-624.
29. Podlipaev S.A. Insect trypanosomatids: the need to know more. Mem. Inst. Oswaldo Cruz 2000, 95:517-522.
30. +2 signaling activity. Biochem. J. 1998, 330:505-511.
31. Santos A.L., Abreu C.M., Batista L.M., Alviano C.S., de Araújo Soares R.M. Cell-associated and extracellular proteinases in Blastocrithidia culicis: influence of growth conditions. Curr. Microbiol. 2001, 43:100-106.
32. Saraiva E.M., Pimenta P.F., Brodin T.N., Rowton E., Modi G.B., Sacks D.L. Changes in lipophosphoglycan and gene expression associated with the development of Leishmania major in Phlebotomus papatasi. Parasitolology 1995, 111:275-287.
33. Schaub G.A. The effects of trypanosomatids on insects. Adv. Parasitol. 1992, 31:255-319.
34. Schaub G.A. Pathogenicity of trypanosomatids on insects. Parasitol. Today 1994, 10:463-468.
35. Schaub G.A., Reduth D., Pudney M. The peculiarities of Blastocrithidia triatomae. Parasitol. Today 1990, 6:361-363.
36. Schaub G.A., Schnitker A. Influence of Blastocrithidia triatomae (Trypanosomatidae) on the reduviid bug Triatoma infestans: alterations in the Malpighian tubules. Parasitol. Res. 1988, 75:88-97.
37. Wallace F.G. The trypanosomatids parasites of insects and arachnids. Exp. Parasitol. 1966, 18:124-193.
38. Warren L.G. Metabolism of Schizotrypanum cruzi, Chagas. 1. Effect of culture age and substrate concentration on respiratory rate. J. Parasitol. 1960, 46:529-539.