B19 parvovirus can replicate in erythroid progenitor cells and in a small n
umber of human blast cell lines. To better understand and analyze the B19 v
irus replicative cycle, we performed and compared the infection of bone mar
row cells and of different blast cell lines with erythroblastoid and megaka
ryoblastoid phenotypic characteristics (UT-7, TF-I, M-07, and B1647). Follo
wing in vitro infection, B19-specific nucleic acids were characterized with
regard to the genome-replicative intermediates, the transcription pattern,
and the localization of virus-specific nucleic acids inside infected cells
. While all cell lines tested proved to be susceptible to B19 virus infecti
on, two different patterns of restriction to replication of B19 virus were
observed. In the first restriction pattern, observed in UT-7 cells, the sin
gle-stranded viral DNA was converted to double-stranded replicative interme
diates, identical to those found in bone marrow cells, and a full set of vi
ral transcripts were observed. However, replication and transcription were
restricted to a small subset of cells, and production of capsid proteins wa
s not detected. In the second restriction pattern, observed in TF-I, M-07,
and B1647 cells, the single-stranded viral DNA was not converted to double-
stranded replicative intermediates. (C) 2000 Academic Press.