We have previously described avian leukosis virus-based packaging cell
lines that express gag, pol, and env proteins from two transcomplemen
ting genomes and produce helper-free stocks of retroviral vectors with
different host ranges. In this report, we demonstrated that (i) despi
te the deletion of the psi packaging sequence, the packaging-defective
transcomplementing retroviral transcripts were packaged into virions
at a level that could reach 2.3% of a wild-type virus packaging level
and (ii) despite deletion of the 3' LTR, these genomes were transferre
d along with the vector to target cells. As these genomes were also be
aring a selectable gene, titers of the resulting contaminant particles
could be estimated, depending on the cell line to be between 0 and 6
infectious particles/ml of supernatant. (C) 1995 Academic Press, Inc.