Potentiation of vesicular stomatitis New Jersey virus infection in mice by mosquito saliva

Parasite Immunology

Volumn 22, Issue 9, 2000, Pages 461-467

  Limesand, K H ^a   Higgs, S ^a   Pearson, L D ^a   Beaty, B J ^a  

^a Department of Environmental and Radiological Health Sciences   (United States)

Author keywords

Mosquito; Salivary potentiation; Vesicular stomatitis

Indexed keywords

NEUTRALIZING ANTIBODY; VIRUS ANTIBODY;

ANIMAL EXPERIMENT; ANTIBODY RESPONSE; ARTICLE; CONTROLLED STUDY; MOSQUITO; MOUSE; NEWBORN; NONHUMAN; PRIORITY JOURNAL; SALIVA; VESICULAR STOMATITIS VIRUS; VIRUS INFECTION; VIRUS TRANSMISSION;

AEDES; ANIMALS; ANIMALS, SUCKLING; ANTIBODIES, VIRAL; INSECT VECTORS; MICE; MICE, INBRED ICR; NEUTRALIZATION TESTS; RHABDOVIRIDAE INFECTIONS; SALIVA; VESICULAR STOMATITIS-INDIANA VIRUS;

ANIMALIA; ARTHROPODA; RNA VIRUSES; VERTEBRATA; VESICULAR STOMATITIS NEW JERSEY VIRUS; VESICULAR STOMATITIS VIRUS;

EID: 0033878931     PISSN: 01419838     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-3024.2000.00326.x     Document Type: Article

References (41)

1. Bissonnette E.Y., Rossignol P.A. & Befus A.D. (1993) Extracts of mosquito salivary gland inhibit tumour necrosis factor alpha release from mast cells. Parasite Immunology 15, 27-33
2. Champagne D.E. (1994) The role of salivary vasodilators in blood-feeding and parasite transmission. Parasitology Today 10, 430-433
3. Cross M.L., Cupp E.W., Ramberg F.B. & Enriquez F.J. (1994) Modulation of murine cellular immune responses and cytokines by salivary gland extract of the black fly Simulian vittatum. Parasitology 45, 119-124
4. Cupp E.W., Mar B.J., Cupp M.S. & Ramberg F.B. (1992) Biological transmission of vesicular stomatits virus New Jersey by Simulium vittatum (Diptera: Simulidae). Journal of Medical Entomology 29, L137-L140
5. Edwards J.F., Higgs S. & Beaty B.J. (1998) Mosquito feeding-induced enhancement of Cache Valley Virus (Bunyaviridae) infection in mice. Journal of Medical Entomology 35, 261-265
6. Francy D.B., Moore C.G., Smith G.C. et al. (1988) Epizootic vesicular stomatitis in Colorado, 1982: isolation of virus from insects collected along the Northern Colorado Rocky mountain front range. Journal of Medical Entomology 25, 343-347
7. Gobet R., Cerny A., Ruedi E., Hengartner H. & Zinkernagel R.M. (1988) The role of antibodies in natural and acquired resistance of mice to vesicular stomatitis virus. Experimental Cell Biology 56, 175-180
8. Grimstad P.R., Ross Q.E. & Craig G.B. Jr (1980) Aedes triseriatus (Diptera: Culicidae) and LaCrosse virus II. Modification of mosquito feeding behavior by virus infection. Journal of Medical Entomology 17, 1-7
9. Gubler D.J. & Rosen L. (1976) A simple technique for demonstrating transmission of Dengue virus by mosquitoes without the use of vertebrate hosts. American Journal of Tropical Medicine and Hygiene 25, 146-150
10. Hajnicka V., Fuchsberger N., Slovak M. et al. (1998) Tick salivary gland extracts promote virus growth in vitro. Parasitology 116, 533-538
11. Hajnicka V., Kocakova P., Slovak M. et al. (2000) Inhibition of the antiviral action by tick salivary gland extract. Parasite Immunology 22, 201-206
12. Hanson R.P. (1952) The natural history of vesicular stomatitis. Bacteriological Reviews 16, 179-204
13. Higgs S. & Beaty B. (1996) In The Biology of Disease Vectors, Beaty B. & Marquardt W.C., eds, pp. 595-605. University Press of Colorado, Colorado
14. Higgs S., Rayner J.O., Olson K.E. et al. (1998) Engineered resistance in Aedes aegypti to a West African and a South American strain of yellow fever virus. American Journal of Tropical Medicine and Hygiene 58, 663-670
15. James A.A. (1994) Molecular and biochemical analyses of the salivary glands of vector mosquitoes. Bulletin of the Institute of Pasteur 92, 133-150
16. Jones L.D., Kaufman W.R. & Nuttall P.A. (1992) Modification of the skin feeding site by tick saliva mediates virus transmission. Experientia 48, 779-782
17. Karber G. (1931) Beitrag zar Kollktiven Behandlung Pharmakologischer Reiherersuche. Archives of Experimental Pathology and Pharmakology 162, 483
18. Lam K.S. & Marshall I.D. (1968) Dual infections of Aedes aegypti with arboviruses. II. Salivary-gland damage by Semliki Forest virus in relation to dual infections. American Journal of Tropical Medicine and Hygiene 17, 637-644
19. Liu I.K. & Zee Y.C. (1976) The pathogenesis of vesicular stomatitis virus, serotype Indiana, in Aedes aegypti mosquitoes. I. Intrathoracic injection. American Journal of Tropical Medicine and Hygiene 25, 177-185
20. Mead D.G., Ramberg F.B., Besselsen D.G. & Mare C.J. (2000) Transmission of vesicular stomatitis virus from infected to uninfected black flies co-feeding on nonviremic deer mice. Science 287, 485-487
21. Nichol S.T. (1986) Vesicular stomatits viruses. In Encyclopedia of Virology, eds Webster R.G. & Granoff A., pp. 1547-1555, Academic Press, San Diego, CA, USA
22. Osorio J.E., Godsey M.S., Defoliart G.R. & Yuill T.M. (1996) LaCrosse viremias in white tailed deer and chipmunks exposed by injection or mosquito bite. American Journal of Tropical Medicine and Hygiene 54, 338-342
23. Qireshi A.A., Asahina A., Ohnuma M. et al. (1996) Immunomodulatory properties of maxadian, the vasodilator peptide from sandfly salivary gland extracts. American Journal of Tropical Medicine and Hygiene 54, 665-671
24. Ribeiro J.M.C. (1987) Role of saliva in blood-feeding by arthropods. Annual Reviews in Entomology 32, 463-478
25. Ribeiro J.M.C. (1989) Vector saliva and its role in parasite transmission. Experimental Parasitology 69, 104-106
26. Sabin A.B. & Olitsky P.K. (1937) Influence of host factors on neuroinvasiveness of vesicular stomatitis virus. Journal of Experimental Medicine 66, 35-57
27. SAS Institute (1993) SAS/STAT User's Guide, version 6. SAS Institute Inc. Cary, NC
28. Schmidt M.R., Gravel K.A. & Woodland R.T. (1995) Progression of a vesicular stomatitis virus infection in primary lymphocytes is restricted at multiple levels during B cell activation. Journal of Immunology 155, 2533-2544
29. Skinner H.H. (1957a) The virus of vesicular stomatitis in small experimental hosts. Journal of Comparative Pathology 67, 69-86
30. Skinner H.H. (1957b) The virus of vesicular stomatits in small experimental hosts. Journal of Comparative Pathology 67, 87-105
31. Tabachnick W. (2000) Pharmacological factors in the saliva of blood-feeding insects: implications for vesicular stomatitis epidemiology. Annuals of the New York Academy of Science in press
32. Theodos C.M. & Titus R.G. (1993) Salivary gland material from the sandfly Lutzomyia longipalpis as an inhibitory effect on macrophage function in vitro. Parasite Immunology 15, 481-487
33. Thurmond M., Ardans A.A., Picanso J.P., McDowell T. & Reynolds B. (1987) Vesicular stomatitis virus (New Jersey strain) infection in two California dairy herds: an epidemiologic study. Journal of the American Veterinary Medical Association 191, 965-970
34. Titus R.G. & Ribeiro J.M.C. (1988) Salivary gland lysates form the sand fly Lutzomyia longipalpus enhance leishmania infectivity. Science 239, 1306-1308
35. Titus R.G. & Ribeiro J.M.C. (1990) The role of vector saliva in transmission of arthropod-borne disease. Parasitology Today 6, 157-160
36. Vanleeuwen J.A., Rodriguez L.L. & Waltner-Toews D. (1995) Cow, farm, and ecological risk factors of clinical vesicular stomatitis on Costa Rican dairy farms. American Journal of Tropical Medicine and Hygiene 53, 342-350
37. Wagner R.R. & Rose J.K. (1996) In Fundamental Virology, 3rd edn, eds Fields B.N., Knipe D.M. & Howley P.M., pp. 561-575, Lippincott-Raven, Philadelphia, PA, USA
38. Webb P.A. & Holbrook F.R. (1989) In The Arboviruses: Epidemiology and Ecology, vol. 5., ed. Monath T.P., pp. 1-30, CRC Press, Inc., Boca Raton, FL, USA
39. Wikel S.K. (1982) Immune responses to arthropods and their products. Annual Reviews in Entomology 27, 21-48
40. Wikel S.K., Ramachandra R.N. & Bergman D.K. (1994) Tick-induced modulation of the host immune response. International Journal for Parasitology 24, 59-66
41. Zeidner N., Higgs S., Happ C.M., Beaty B. & Miller B.R. (1999) Mosquito feeding molulates Th1 and Th2 cytokines in flavivirus susceptible mice: an effect mimicked by injection of sialokinins, but not demonstrated in flavivirus resistent mice. Parasite Immunology 21, 35-44