The matrix gene expression of subacute sclerosing panencephalitis (SSPE) virus (Osaka-1 strain): A comparison of two sibling viruses isolated from different lobes of an SSPE brain
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作者:
Ayata, M
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机构:Osaka City Univ, Sch Med, Dept Virol, Abeno Ku, Osaka 5458585, Japan
Ayata, M
Hayashi, K
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机构:Osaka City Univ, Sch Med, Dept Virol, Abeno Ku, Osaka 5458585, Japan
Hayashi, K
Seto, T
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机构:Osaka City Univ, Sch Med, Dept Virol, Abeno Ku, Osaka 5458585, Japan
Seto, T
Murata, R
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机构:Osaka City Univ, Sch Med, Dept Virol, Abeno Ku, Osaka 5458585, Japan
Murata, R
Ogura, H
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机构:Osaka City Univ, Sch Med, Dept Virol, Abeno Ku, Osaka 5458585, Japan
Ogura, H
机构:
[1] Osaka City Univ, Sch Med, Dept Virol, Abeno Ku, Osaka 5458585, Japan
[2] Osaka City Univ, Sch Med, Dept Pediat, Osaka 5458585, Japan
[3] Osaka City Gen Hosp, Dept Pediat, Osaka 5340021, Japan
The Fr/V and Oc/V sibling viruses of the Osaka-1 strain of the subacute sclerosing panencephalitis (SSPE) virus were defective in cell-free virus production. By radioimmunoprecipitation assay, the matrix (M) protein was not detected in cells persistently infected with the Osaka-1 strain. This undetectable expression was consistent with the selective reduction of antibody response to the M protein in the patient from whom the Osaka-1 strain was isolated. The sequence of the M gene, however, predicted that the protein could be synthesized because the translational start and stop codons for the protein were not altered, Northern blot hybridization demonstrated the selective defect of the monocistronic mRNAs for the M protein and the phosphoprotein (P) together with the dominant presence of the P-M bicistronic mRNA, This absence of the hi mRNA was further confirmed by primer extension analysis. Therefore, the undetectable expression of the M protein in the infected cells was proved to be caused by a transcriptional defect, The two sibling viruses, isolated from remote portions of an SSPE brain, were indistinguishable in their viral characters, including the M gene sequences, which indicates the possibility of clonal expansion of the strain in the brain.