Entry of African swine fever virus into Vero cells and uncoating

Veterinary Microbiology

Volumn 60, Issue 2-4, 1998, Pages 131-140

  Valdeira, M Luisa ^a,b,c   Bernardes, Catarina ^a,b   Cruz, B ^b   Geraldes, A ^c  

^a RESEARCH INSTITUTE FOR MEDICINES IMED ULISBOA   (Portugal)

^b Laboratorio Nacional de Investigacao Veterinaria   (Portugal)

^c INSTITUTO GULBENKIAN DE CIÊNCIA   (Portugal)

Author keywords

African swine fever virus; Lysosomotropic weak bases; Protease inhibitors; Viral uncoating

Indexed keywords

2,4 DINITROPHENOL; CYTOCHALASIN B; DEMECOLCINE; MONENSIN; SODIUM AZIDE;

AFRICAN SWINE FEVER VIRUS; ANIMAL CELL; ARTICLE; NONHUMAN; OXIDATIVE PHOSPHORYLATION; VERO CELL; VIRUS CELL INTERACTION; VIRUS INFECTIVITY; VIRUS REPLICATION;

2,4-DINITROPHENOL; ADSORPTION; AFRICAN SWINE FEVER VIRUS; AMMONIUM CHLORIDE; ANIMALS; CERCOPITHECUS AETHIOPS; CHLOROQUINE; CYTOCHALASIN B; CYTOSKELETON; DEMECOLCINE; ENDOCYTOSIS; ENDOSOMES; LYSOSOMES; MEMBRANE FUSION; MONENSIN; SODIUM AZIDE; VERO CELLS;

EID: 0032574111     PISSN: 03781135     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1135(98)00152-7     Document Type: Article

References (30)

1. Alcamí A., Carrascosa A.L., Viñuela E. Saturable binding sites mediate the entry of African swine fever virus into Vero cells. Virology. 168:1989;393-398.
2. Alcamí A., Carrascosa A.L., Viñuela E. The entry of African swine fever virus into Vero cells. Virology. 171:1989;68-75.
3. Amerongen H.M., Wilson G.A.R., Fields B.N., Neutra M.R. Proteolytic processing of reovirus is required for adherence to intestinal M cells. J. Virol. 68:1994;8428-8432.
4. Andersen K.B. Leupeptin inhibits retrovirus infection in mouse fibroblasts. J. Virol. 48:1983;765-769.
5. Appleyard G., Tisdale M. Inhibition of the growth of human coronavirus 229Enn by leupeptin. J. Gen. Virol. 66:1985;363-366.
6. Bass D.M., Bodkin D., Dambrauskas R., Trier J.S., Fields B.N., Wolf J.L. Intraluminal proteolytic activation plays an important role in replication of type reovirus in the intestines of neonatal mice. J. Virol. 64:1990;1830-1833.
7. Carrascosa A.C., Del Val M., Santaren J.F., Viñuela E. Purification and properties of African swine fever virus. J. Virol. 54:1985;337-344.
8. Eagle H. Buffer combination for mammalian cell cultures. Science. 174:1971;500-503.
9. Geraldes A., Valdeira M.L. Effect of chloroquine on African swine fever virus infection. J. Gen. Virol. 66:1985;1145-1148.
10. Goldstein J.L., Brown M.S., Anderson R.G.W., Russell D.W., Schneider W.J. Receptor mediated endocytosis: Concepts emerging from the LDL receptor system. Annu. Rev. Cell Biol. 1:1985;1-39.
11. Hayashi T., Hotta H., Itoh M., Homma M. Protection of mice by a protease inhibitor, aprotinin, against lethal Sendai virus pneumonia. J. Gen. Virol. 72:1991;979-982.
12. Hoekstra D., Kok J.W. Entry mechanisms of enveloped viruses. Implications for fusion of intracellular membranes. Biosci. Rep. 9:1989;273-305.
13. Hoekstra, D., Pedroso de Lima, M.C., 1992. Molecular mechanisms of enveloped viruses entry into host cells: Protein dynamics and membrane fusion. In: Aloia R.C., Curtain, C.C. (Eds.), Advances in Membrane Fluidity. Membrane Interactions of HIV: Implications for Pathogenesis and Therapy in AIDS. Wiley-Liss, New York, pp. 71-97.
14. Ichihashi Y., Oie M. Proteolytic activation of vaccinia virus for the penetration phase of infection. Virology. 116:1982;297-305.
15. Kaljot K.T., Shaw R.D., Rubin D.H., Greenberg H.B. Infectious rotavirus enters cells by direct cell membrane penetration, not by endocytosis. J. Virol. 62:1988;1136-1144.
16. Karnovsky M.J. A formaldehyde-glutaraldehyde fixative of high osmolarity for use in electron microscopy. J. Cell Biol. 27:1965;137A.
17. Manso Ribeiro J., Rosa Azevedo J.A. Reapparition de la peste porcine africaine au Portugal. Bull. Off. Int. Epizoot. 55:1961;889-899.
18. Marsh M., Helenius A. Virus entry into animal cells. Virus Res. 36:1989;107-150.
19. Marsh M., Wellsteed J., Kern H., Harms E., Helenius A. Monensin inhibits Semliki Forest virus penetration into culture cells. Proc. Natl. Acad. Sci. U.S.A. 79:1982;5297-5301.
20. Matlin K.S., Reggio H., Helenius A., Simons K. Pathway of vesicular stomatitis virus entry leading to infection. J. Mol. Biol. 156:1982;609-631.
21. Ohkuma S., Poole B. Fluorescence probe measurement of the intralysosomal pH in living cells and the perturbation of pH by various agents. Proc. Natl. Acad. Sci. U.S.A. 79:1978;5297-5301.
22. Oie M., Ichihashi Y. Modification of vaccinia virus penetration proteins analysed by monoclonal antibodies. Virology. 157:1987;449-459.
23. Sommerfelt M.A., Marsh M. Binding and entry of animal viruses. Adv. Drug Deliv. Rev. 4:1989;1-26.
24. Sturzenbecker L.J., Nibert M., Furlong D., Fields B.N. Intracellular digestion of reovirus particles requires a low pH and is an essential step in the viral infectious cycle. J. Virol. 61:1987;2351-2361.
25. Tashiro M., Homme M. Evidence of proteolytic activation of Sendai virus in mouse lung. Arch. Virol. 77:1983;127-137.
26. Valdeira M.L., Geraldes A. Morphological study on the entry of African swine fever virus into cells. Biol. Cell. 55:1985;35-40.
27. Valdeira M.L., Duque-Magalhães M.C., Geraldes A. Evidence for an phosphatase acid in purified African swine fever virus. Arch. Virol. 113:1990;125-131.
28. Viñuela, E., 1987. Molecular biology of African swine fever virus. In: Becker, Y. (Ed.), African Swine Fever, Martinus Nijhoff, Boston, pp. 31-49.
29. White J., Kartenbeck J., Helenius A. Fusion of Semliki forest virus with the plasma membrane can be induced by low pH. J. Cell Biol. 87:1980;264-272.
30. Zhirnov O.P., Ovcharenko A.V., Bukrinskaya A.G. Suppression of influenza virus replication in infected mice by protease inhibitors. J. Gen. Virol. 65:1984;191-196.