Literature DB >> 1534119

Monoclonal antibodies identify the NS5 yellow fever virus non-structural protein in the nuclei of infected cells.

A Buckley1, S Gaidamovich, A Turchinskaya, E A Gould.   

Abstract

Eight monoclonal antibodies (MAbs) derived using yellow fever (YF) virus (French viscerotropic virus strain) labelled the nuclei (wild-type strains) and/or the nucleoli (vaccine strains) of cells infected with different strains of YF virus. The specificity of these antibodies for YF virus-infected cells was confirmed using MAbs that bind only the YF virus envelope glycoprotein. The characteristics of fluorescent labelling in the nuclei and nucleoli of both normal cells and of nuclei separate from cell cytoplasm confirmed that the antigen was inside the nucleus rather than on the outer surface of the nuclear membrane. Virus-specific antigen was also observed in the cytoplasm of infected cells. One additional virus envelope-specific antibody, derived at the same time, identified cytoplasmic antigen exclusively. The eight antibodies that identified nuclear antigen showed no activity in neutralization, haemagglutination inhibition or mouse protection tests. Analysis of their molecular specificities by radioimmunoprecipitation of virus-infected cell lysates showed that they identified the non-structural NS5 antigen of YF virus. These results support the possibility of nuclear involvement in the replicative stages of YF virus infection.

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Year:  1992        PMID: 1534119     DOI: 10.1099/0022-1317-73-5-1125

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  25 in total

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5.  Ultrastructure of Kunjin virus-infected cells: colocalization of NS1 and NS3 with double-stranded RNA, and of NS2B with NS3, in virus-induced membrane structures.

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6.  Nuclear localization of flavivirus RNA synthesis in infected cells.

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Review 8.  Genome cyclization as strategy for flavivirus RNA replication.

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9.  Detection of genomic and intermediate replicative strands of hepatitis C virus in liver tissue by in situ hybridization.

Authors:  K T Nouri Aria; R Sallie; D Sangar; G J Alexander; H Smith; J Byrne; B Portmann; A L Eddleston; R Williams
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10.  NS5 Sumoylation Directs Nuclear Responses That Permit Zika Virus To Persistently Infect Human Brain Microvascular Endothelial Cells.

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