Study of the Chemical Nature of Frp/3 Cell Recognition Units for Hepatitis A Virus
Overview
Affiliations
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.
Direct-acting Antivirals and Host-targeting Agents against the Hepatitis A Virus.
Kanda T, Nakamoto S, Wu S, Nakamura M, Jiang X, Haga Y J Clin Transl Hepatol. 2015; 3(3):205-10.
PMID: 26623267 PMC: 4663202. DOI: 10.14218/JCTH.2015.00016.
Capsid functions of inactivated human picornaviruses and feline calicivirus.
Nuanualsuwan S, Cliver D Appl Environ Microbiol. 2003; 69(1):350-7.
PMID: 12514015 PMC: 152381. DOI: 10.1128/AEM.69.1.350-357.2003.
Kaplan G, Totsuka A, Thompson P, Akatsuka T, Moritsugu Y, Feinstone S EMBO J. 1996; 15(16):4282-96.
PMID: 8861957 PMC: 452154.
The effect of lipophilic amines on the growth of hepatitis A virus in Frp/3 cells.
Superti F, Seganti L, Orsi N, Divizia M, Gabrieli R, Pana A Arch Virol. 1987; 96(3-4):289-96.
PMID: 2821967 DOI: 10.1007/BF01320970.
Effect of cellular function inhibitors on the infection of Frp/3 cells by hepatitis A virus.
Superti F, Seganti L, Orsi N, Divizia M, Gabrieli R, Pana A Med Microbiol Immunol. 1989; 178(1):29-36.
PMID: 2535886 DOI: 10.1007/BF00202289.