Mutations were introduced into a genomic region encoding the C-termina
l portion of Gag capsid protein of pathogenic simian immunodeficiency
virus (SIVmac239). All the mutants generated were defective for virion
production and were non-infectious for monkey cells. They all efficie
ntly suppressed the replication of wild type SIVmac in monkey cells. T
hese results were in good agreement with those obtained for human immu
nodeficiency virus type 1, showing the importance of SIV/monkey model
system for studies on Gag.