Interaction of minute virus of mice with differentiated cells: strain-dependent target cell specificity is mediated by intracellular factors
- PMID: 6602221
- PMCID: PMC256568
- DOI: 10.1128/JVI.46.3.937-943.1983
Interaction of minute virus of mice with differentiated cells: strain-dependent target cell specificity is mediated by intracellular factors
Abstract
The prototype strain of minute virus of mice and the immunosuppressive strain are unable to grow lytically in each other's murine host cell type. To characterize these strain-dependent virus-host cell interactions further, we have compared the early events of both productive and restrictive infections. Each virus binds to specific receptors on the surface of both productive and restrictive cell types. Competition experiments show that both viruses recognize the same receptor on each cell type. Penetration and uncoating are presumed to be similar in both productive and restrictive infections, since incoming viral genomes are converted to parental replicative form DNA independent of the final outcome of the virus-host cell interaction. In contrast to the majority of other systems studied to date, these differences in minute virus of mice target cell specificity are not mediated at the cell surface, but by the interaction of a strain-specific viral determinant with intracellular host factors that are expressed in particular cell types as a function of differentiation. These cellular factors catalyze a step in viral replication which occurs after the initiation of viral DNA synthesis, but before the detectable expression of the viral capsid polypeptide genes.
Similar articles
-
Reciprocal productive and restrictive virus-cell interactions of immunosuppressive and prototype strains of minute virus of mice.J Virol. 1983 Jun;46(3):944-55. doi: 10.1128/JVI.46.3.944-955.1983. J Virol. 1983. PMID: 6602222 Free PMC article.
-
Growth of the parvovirus minute virus of mice MVMp3 in EL4 lymphocytes is restricted after cell entry and before viral DNA amplification: cell-specific differences in virus uncoating in vitro.J Virol. 1997 Oct;71(10):7769-80. doi: 10.1128/JVI.71.10.7769-7780.1997. J Virol. 1997. PMID: 9311862 Free PMC article.
-
Characterization of the cell type-specific determinant in the genome of minute virus of mice.J Virol. 1988 Feb;62(2):552-7. doi: 10.1128/JVI.62.2.552-557.1988. J Virol. 1988. PMID: 3257270 Free PMC article.
-
Development-dependent replication of minute virus of mice in differentiated mouse testicular cell lines.J Gen Virol. 1986 Nov;67 ( Pt 11):2549-54. doi: 10.1099/0022-1317-67-11-2549. J Gen Virol. 1986. PMID: 3783131
-
The parvoviruses.Virol Monogr. 1976;15:1-109. Virol Monogr. 1976. PMID: 181899 Review. No abstract available.
Cited by
-
DNA sequence comparison between two tissue-specific variants of the autonomous parvovirus, minute virus of mice.Nucleic Acids Res. 1985 May 24;13(10):3617-33. doi: 10.1093/nar/13.10.3617. Nucleic Acids Res. 1985. PMID: 3855242 Free PMC article.
-
Virulent variants emerging in mice infected with the apathogenic prototype strain of the parvovirus minute virus of mice exhibit a capsid with low avidity for a primary receptor.J Virol. 2005 Sep;79(17):11280-90. doi: 10.1128/JVI.79.17.11280-11290.2005. J Virol. 2005. PMID: 16103180 Free PMC article.
-
DNA sequence of the lymphotropic variant of minute virus of mice, MVM(i), and comparison with the DNA sequence of the fibrotropic prototype strain.J Virol. 1986 Feb;57(2):656-69. doi: 10.1128/JVI.57.2.656-669.1986. J Virol. 1986. PMID: 3502703 Free PMC article.
-
Autonomous parvoviruses neither stimulate nor are inhibited by the type I interferon response in human normal or cancer cells.J Virol. 2014 May;88(9):4932-42. doi: 10.1128/JVI.03508-13. Epub 2014 Feb 19. J Virol. 2014. PMID: 24554651 Free PMC article.
-
Aleutian mink disease parvovirus infection of mink peritoneal macrophages and human macrophage cell lines.J Virol. 1993 Apr;67(4):2075-82. doi: 10.1128/JVI.67.4.2075-2082.1993. J Virol. 1993. PMID: 8383229 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources