Research has been carried out in order to clarify the chemical nature of cell receptors interacting with a fast growing strain of hepatitis A virus (HAV) producing a cytopathic effect on Frp/3 cells. Cell surface susceptibility to HAV attachment has been studied after treatment with enzymes acting on different chemical groupings. Results obtained showed a lowering of cell susceptibility to HAV infection following the action of phospholipase A2, phospholipase C, trypsin and beta-galactosidase. These data suggested that phospholipids, proteins and galactose participate to the cellular receptorial area for HAV.

Seganti, L., Superti, F., Orsi, N., Gabrieli, R., Divizia, M., Panà, A. (1987). Study of the chemical nature of Frp/3 cell recognition units for hepatitis A virus. MEDICAL MICROBIOLOGY AND IMMUNOLOGY, 176(1), 21-26.

Study of the chemical nature of Frp/3 cell recognition units for hepatitis A virus

GABRIELI, ROSANNA;DIVIZIA, MAURIZIO;
1987-01-01

Abstract

Research has been carried out in order to clarify the chemical nature of cell receptors interacting with a fast growing strain of hepatitis A virus (HAV) producing a cytopathic effect on Frp/3 cells. Cell surface susceptibility to HAV attachment has been studied after treatment with enzymes acting on different chemical groupings. Results obtained showed a lowering of cell susceptibility to HAV infection following the action of phospholipase A2, phospholipase C, trypsin and beta-galactosidase. These data suggested that phospholipids, proteins and galactose participate to the cellular receptorial area for HAV.
1987
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/42 - IGIENE GENERALE E APPLICATA
English
Galactose; Glycoside Hydrolases; Receptors, Virus; Humans; Hepatovirus; Proteins; Cytopathogenic Effect, Viral; Fluorescent Antibody Technique; Phospholipases; Cell Line; Phospholipids
Seganti, L., Superti, F., Orsi, N., Gabrieli, R., Divizia, M., Panà, A. (1987). Study of the chemical nature of Frp/3 cell recognition units for hepatitis A virus. MEDICAL MICROBIOLOGY AND IMMUNOLOGY, 176(1), 21-26.
Seganti, L; Superti, F; Orsi, N; Gabrieli, R; Divizia, M; Panà, A
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/66629
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