Immunofluorescent demonstration of double-stranded RNA and virus antigen in RNA virus-infected cells
The indirect immunofluorescence procedure has been used for demonstration of double-stranded RNA in cells infected with reovirus, poliomyelitis, and tick-borne encephalitis (TBE) viruses. Rabbit sera against poly(A)-poly(U) and poly(I)-poly(C) react specifically with double-stranded RNA. Double-stra...
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Published in | Virology (New York, N.Y.) Vol. 62; no. 1; pp. 276 - 279 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.11.1974
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Subjects | |
Online Access | Get full text |
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Summary: | The indirect immunofluorescence procedure has been used for demonstration of double-stranded RNA in cells infected with reovirus, poliomyelitis, and tick-borne encephalitis (TBE) viruses. Rabbit sera against poly(A)-poly(U) and poly(I)-poly(C) react specifically with double-stranded RNA. Double-stranded RNA is found in the cytoplasm of the cells infected with high multiplicities of poliomyelitis and tick-borne encephalitis viruses 3 hr postinoculation. In parallel, preparations were stained with sera against viral proteins. During one cycle of reproduction the dynamics of accumulation of double-stranded RNA and virus protein was synchronous both for poliomyelitis and tick-borne encephalitis viruses. When poliovirus-infected cells degenerated, the number of cells containing TBE virus double-stranded RNA decreased markedly while the proportion of cells containing virus protein remained high. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0042-6822 1096-0341 |
DOI: | 10.1016/0042-6822(74)90322-5 |