The hallmarks of the spumaretrovirus or human foamy virus (HFV) are su
mmarized and discussed with special focus on the potentials to use HFV
as a new retroviral vector system. The special features of HFV are th
e expression of pol by splicing and start of translation at a defined
initiation codon. The first Met of Pol is conserved in the six known f
oamy virus genomic sequences. Another remarkable characteristic of HFV
is the presence of a Gly-Arg-rich sequence instead of the Cys-Cys mot
if of the classical retroviral nuclecapsid proteins. The preferential
budding of HFV into cytoplasmic vesicles and the potential to exploit
it in the application of corresponding vector systems is discussed. In
addition, recent reports of transducing marker genes into susceptible
cells will be reviewed.