Characterization of the Halle SSPE Measles Virus Isolate

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Abstract
The Halle 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.degree. C than at 33.degree. 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 plaque-purified to eliminate the interfering particles, producing the syn- P2 virus. This virus also plaqued more efficiently at 39.degree. C than at 33.degree. C, but caused cell fusion only at 39.degree. 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 2 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.degree. C, [35S]methionine labeling demonstrated that the hemolysin/cell fusion protein was present in syn- P2 virions. The production of interfering particles, the inability to cause cell fusion at 33.degree. C and the cold-sensitive nature of the syn- population appear to play a role in the ability of the Halle SSPE virus to establish persistent infection. [African green monkey kidney BSC-1 cells were used in this study.].