Rotavirus genome segment 4 determines viral replication phenotype in cultured liver cells (HepG2).

Abstract:

:One-step growth determinations were performed with five strains of rotavirus in HepG2, a cell line derived from human liver. Three virus strains (SA11-C13, SA11-C14, and RRV) replicated in HepG2 cells and attained yields 10- to 100-fold above input titers. Two virus strains (B223 and SA11-4F) failed to replicate above input titer. Analysis of reassortants that segregated the genes of parental virus pairs able and unable to replicate revealed that the HepG2 cell growth phenotype segregated with genome segment 4. Immunofluorescence analysis of infected HepG2 cells showed that the production of detectable antigen correlated with the growth phenotype and also segregated with genome segment 4. Thus, we conclude that (i) some virus strains were capable of replication in cultured liver cells while other strains could not replicate under identical conditions and that (ii) the inability of some virus strains to replicate resulted from a segment 4-associated block in replication before protein synthesis. These results are discussed in terms of what is known of the functions of VP4.

journal_name

J Virol

journal_title

Journal of virology

authors

Ramig RF,Galle KL

doi

10.1128/JVI.64.3.1044-1049.1990

subject

Has Abstract

pub_date

1990-03-01 00:00:00

pages

1044-9

issue

3

eissn

0022-538X

issn

1098-5514

journal_volume

64

pub_type

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