Abstract

Hepatitis A virus (HAV) is a member of the picornavirus family. It was first provisionally classified as enterovirus 72, but subsequent determinations of its nucleotide and amino acid sequences showed them to be sufficiently distinct to assign the virus to a new genus. Heparnavirus (Hep-A-RNA-virus) has been suggested as the genus name. HAV shares the key properties of the picornavirus family: an icosahedral particle 28 nm in diameter with cubic symmetry, composed of 30% RNA and 70% protein. The genome is single-stranded 7.48 kb RNA, linear and positive-sense. Like other picornaviruses, HAV possesses four major polypeptides cleaved from a large precursor polyprotein. The surface proteins VPI and VP3 are major antibody-binding sites. The internal protein VP4 is much smaller than the VP4s of other picornaviruses. As other picornaviruses. HAV has no envelope and replicates in the cytoplasm. HAV is stable to treatment with ether and acid, and is much more heat-resistant than other picornaviruses. It withstands 60°C for 1 h. MgCl 2 stabilizes the virus to withstand temperatures up to 80°C. The relative resistance of HAV to disinfection indicates a need for extra precautions in dealing with hepatitis patients and their products. Only one serotype is known. There is no antigenic cross-reactivity with other hepatitis viruses. HAV initially was identified in stool and liver preparations by employing immune electron microscopy as the detection system. Chimpanzees and marmoset monkeys are susceptible to HAV. HAV has been cultivated serially in primary explant cultures of adult marmoset livers and in cell lines of primate origin. The infection is usually non-cytopathic and is identified by immunologic assay for virus or its antigen, or by a hybridization assay for viral RNA.

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