SUMMARYThe Hall~ subacute sclerosing panencephalitis (SSPE) measles virus isolate and its plaque-purified progeny were investigated to determine whether any unusual properties could be associated with its ability to cause persistent infection. Three types of plaque-purified progeny were isolated. One population appeared to be similar in biological and biochemical properties to laboratory-adapted measles virus and had the ability to induce syncytia (syn+). A second population (syn-) plaqued more efficiently at 39 °C than at 33 °C, did not cause normal cell fusion at either temperature, and produced particles that interfered with the replication of other measles virus isolates in vivo and in vitro. This syn-virus was further plaquepurified to eliminate the interfering particles, producing the syn-P2 virus. This virus also plaqued more efficiently at 39 °C than at 33 °C, but caused cell fusion only at 39 °C. Both syn-viruses and the parental virus were significantly less virulent in vivo than the syn + virus and caused a more prolonged infection. Biochemical analysis showed that the syn-P2 population produced particles that banded at two different densities in potassium tartrate gradients; both densities were less than those of the standard laboratory measles virus and the syn + virus. Although the syn-P2 virus did not cause cell fusion at 33 °C, [35S]methionine labelling demonstrated that the haemolysin/cell fusion protein was present in syn-P2 virions. The production of interfering particles, the inability to cause cell fusion at 33 °C, and the cold-sensitive nature of the syn-population appear to play a role in the ability of the Hall6 SSPE virus to establish persistent infection.