Salivary gland hyaluronidase in various species of phlebotomine sand flies (Diptera: psychodidae)

Insect Biochemistry and Molecular Biology

Volumn 32, Issue 12, 2002, Pages 1691-1697

  Cerna P ^a   Mikes L ^a   Volf, P ^a  

^a CHARLES UNIVERSITY   (Czech Republic)

Author keywords

Hyaluronate glycanohydrolase EC 3.2.1.35; Hyaluronidase; Lutzomyia; Phlebotomus; Saliva; Sand fly; Spreading factor

Indexed keywords

HYALURONOGLUCOSAMINIDASE;

ANIMAL; ARTICLE; COMPARATIVE STUDY; ENZYMOLOGY; KINETICS; METABOLISM; PH; PHLEBOTOMUS; SALIVARY GLAND; SPECIES DIFFERENCE;

ANIMALS; HYALURONOGLUCOSAMINIDASE; HYDROGEN-ION CONCENTRATION; KINETICS; PHLEBOTOMUS; SALIVARY GLANDS; SPECIES SPECIFICITY;

DIPTERA; HYMENOPTERA; LUTZOMYIA LONGIPALPIS; MAMMALIA; PHLEBOTOMINAE; PHLEBOTOMUS DUBOSCQI; PHLEBOTOMUS PAPATASI; PHLEBOTOMUS PERNICIOSUS; PHLEBOTOMUS SERGENTI; PSYCHODIDAE;

EID: 0036891453     PISSN: 09651748     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0965-1748(02)00109-1     Document Type: Article

References (29)

1. Champagne, D.E., Valenzuela, J.G., 1996. Pharmacology of haematophagous arthropod saliva. In: Wikel, S.K. (Ed.), The Immunology of Host-ectoparasitic Arthropod Relationships. CAB International, Wallingford, Oxon, UK, pp. 85-106.
2. Charlab, R., Valenzuela, J.G., Rowton, E.D., Ribeiro, J.M.C., 1999. Toward an understanding of the biochemical and pharmacological complexity of the saliva of a hematophagous sand fly Lutzomyia longipalpis. Proceedings of the National Academy of Sciences of the United States of America 96, 15155-15160.
3. Deng, X.N., Czymmek, K., Martin-DeLeon, P.A., 1999. Biochemical maturation of Spam1 (PH-20) during epididymal transit of mouse sperm involves modifications of N-linked oligosaccharides. Molecular Reproduction and Development 52, 196-206.
4. Frost, G.I., Stern, R., 1997. A microtiter-based assay for hyaluronidase activity not requiring specialized reagents. Analytical Biochemistry 251, 263-269.
5. Gillespie, R.D., Mbow, M.L., Titus, R.G., 2000. The immunomodulatory factors of bloodfeeding arthropod saliva. Parasite Immunology 22, 319-331.
6. Giulian, G.G., Moss, R.L., Greaser, M., 1983. Improved methodology for analysis and quantitation of proteins on one-dimensional silver-stained slab gels. Analytical Biochemistry 129, 277-287.
7. Gmachl, M., Kreil, G., 1993. Bee venom hyaluronidase is homologous to a membrane protein of mammalian sperm. Proceedings of the National Academy of Sciences of the United States of America 90, 3569-3573.
8. Hall, L.R., Titus, R.G., 1995. Sand fly vector saliva selectively modulates macrophage functions that inhibit killing of Leishmania major and nitric oxide production. Journal of Immunology 155, 3501-3506.
9. Harrison, R.A.P., 1988. Preliminary characterization of the multiple forms of ram sperm hyaluronidase. Biochemical Journal 252, 875-882.
10. Katz, O., Waitumbi, J.N., Zer, R., Warburg, A., 2000. Adenosine, AMP and protein phosphatase activity in sandfly saliva. American Journal of Tropical Medicine and Hygiene 62, 145-150.
11. Kemeny, D.M., Dalton, N., Lawrence, A.J., Pearce, F.L., Vernon, C.A., 1984. The purification and characterization of hyaluronidase from the venom of the honey bee, Apis mellifera. European Journal of Biochemistry 139, 217-223.
12. Kreil, G., 1995. Hyaluronidases - A group of neglected enzymes. Protein Science 4, 1666-1669.
13. Lerner, E.A., Ribeiro, J.M.C., Nelson, R.J., Lerner, M.R., 1991. Isolation of maxadilan, a potent vasodilatory peptide from the salivary glands of the sand fly Lutzomyia longipalpis. Journal of Biological Chemistry 266, 11234-11236.
14. Lesley, J., Hyman, R., English, N., Catterall, J.B., Turner, G.A., 1997. CD44 in inflammation and metastasis. Glycoconjugate Journal 14, 611-622.
15. Li, M.W., Yudin, A.I., Robertson, K.R., Cherr, G.N., Overstreet, J.W., 2002. Importance of glycosylation and disulfide bonds in hyaluronidase activity of macaque sperm surface PH-20. Journal of Andrology 23, 211-219.
16. McKee, C.M., Lowenstein, C.J., Horton, M.R., Wu, J., Bao, C., Chin, B.Y., Choi, A.M.K., Noble, P.W., 1997. Hyaluronan fragments induce nitric-oxide synthase in murine macrophages through a nuclear factor kappa B-dependent mechanism. Journal of Biological Chemistry 272, 8013-8018.
17. Neitz, A.W., Howel, C.J., Potgieter, D.J., Bezuidenhout, J.D., 1978. Proteins and free amino acids in the salivary secretion and haemolymph of the tick Amblyomma hebraeum. Onderstepoort Journal of Veterinary Research 45, 235-240.
18. Ribeiro, J.M.C., Rossignol, P.A., Spielman, A., 1986. Blood-finding strategy of a capillary-feeding sandfiy, Lutzomyia longipalpis. Comparative Biochemistry and Physiology 83A, 683-686.
19. Ribeiro, J.M.C., Charlab, R., Rowton, E.D., Cupp, E.W., 2000. Simulium vittatum (Diptera:Simuliidae) and Lutzomyia longipalpis (Diptera:Psychodidae) salivary gland hyaluronidase activity. Journal of Medical Entomology 37, 743-747.
20. Ribeiro, J.M.C., Modi, G., 2001. The salivary adenosine/AMP content of Phlebotomus argentipes Annandale and Brunetti, the main vector of kala-azar. Journal of Parasitology 87, 915-917.
21. Romano, A.E., Ladijinsky, E., Aboud, M., 1983. Effect of hyaluronidase on cell response to the antiviral and interferon inducing activity of poly (RI). Poly (RC) - Brief report. Archives of Virology 78, 315-319.
22. Theodos, C.M., Ribeiro, J.M.C., Titus, R.G., 1991. Analysis of enhancing effect of sand fly saliva on Leishmania infection in mice. Infection and Immunity 59, 1592-1598.
23. Titus, R.G., 1998. Salivary gland lysate from the sand fly Lutzomyia longipalpis suppresses the immune response of mice to sheep red blood cells in vivo and concanavalin A in vitro. Experimental Parasitology 89, 133-136.
24. Titus, R.G., Ribeiro, J.M.C., 1988. Salivary gland lysates from the sand fly Lutzomyia longipalpis enhance Leishmania infectivity. Science 239, 1306-1308.
25. Valenzuela, J.G., Belkaid, Y., Rowton, E., Ribeiro, J.M.C., 2001. The salivary apyrase of the blood-sucking sand fly Phlebotomus papatasi belongs to the novel Cimex family of apyrases. Journal of Experimental Biology 204, 229-237.
26. Volf, P., Tesarová, P., Nohýnková, E., 2000. Salivary proteins and glycoproteins in phlebotomine sandflies of various species, sex and age. Medical and Veterinary Entomology 14, 251-256.
27. Volf, P., Rohousová, I., 2001. Species-specific antigens in salivary glands of phlebotomine sandflies. Parasitology 122, 37-41.
28. Warburg, A., Schlein, Y., 1986. The effect of post-bloodmeal nutrition of Phlebotomus papatasi on the transmission of Leishmania major. American Journal of Tropical Medicine and Hygiene 35, 926-930.
29. Wikel, S.K., Ramachandra, R.N., Bergman, D.K., 1996. Arthropod modulation of host immune responses. In: Wikel, S.K. (Ed.), The Immunology of Host-Ectoparasitic Arthropod Relationships. CAB International, Wallingford, Oxon, UK, pp. 107-130.