Skip to content
University of Maryland LibrariesDigital Repository at the University of Maryland
    • Login
    View Item 
    •   DRUM
    • Theses and Dissertations from UMD
    • UMD Theses and Dissertations
    • View Item
    •   DRUM
    • Theses and Dissertations from UMD
    • UMD Theses and Dissertations
    • View Item
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Role of Noncoding Regions in Newcastle Disease Virus Replication and pathogenesis

    Thumbnail
    View/Open
    umi-umd-5866.pdf (1.375Mb)
    No. of downloads: 2170

    Date
    2008-11-17
    Author
    Yan, Yongqi
    Advisor
    Samal, Siba K
    Metadata
    Show full item record
    Abstract
    The roles of the intergenic sequences (IGS) and untranslated regions (UTR) in Newcastle disease virus (NDV) transcription and pathogenesis are not clear. By our established reverse genetics system, we investigated the role of these noncoding regions in NDV life cycle. The infectious recombinant viruses containing increased/decreased length of F-HN and HN-L IGS were recovered and the transcription and pathogenicity of mutants were characterized. Our studies indicated that increased F-HN or HN-L IGS length reduced the downstream gene transcription. Morever, all IGS mutants were attenuated in chickens and the level of attenuation was increased as the length of IGS increased. The mutant viruses with modified 5' and 3' UTR of HN mRNA were also recovered. The transcription, translation and pathogenecity of these recombinant viruses were characterized. Our studies indicated that the UTRs are not essential for NDV replication in vitro. Complete deletions of 5' HN UTR down regulated its transcription, translation levels and incorporation of HN protein into virus particle, therefore, attenuated the pathogenicity of NDV in chickens. Moreover, studies on the HN UTRs replaced with corresponding NP UTRs virus suggested that UTRs can be exchanged between NDV mRNAs without affecting the replication of virus in vitro and in vivo. In summary, my research identifies for the first time the role of noncoding regions in NDV replication and pathogenesis and provides novel methods for the development of attenuated live vaccines for NDV.
    URI
    http://hdl.handle.net/1903/8838
    Collections
    • Department of Veterinary Medicine Theses and Dissertations
    • UMD Theses and Dissertations

    DRUM is brought to you by the University of Maryland Libraries
    University of Maryland, College Park, MD 20742-7011 (301)314-1328.
    Please send us your comments.
    Web Accessibility
     

     

    Browse

    All of DRUMCommunities & CollectionsBy Issue DateAuthorsTitlesSubjectsThis CollectionBy Issue DateAuthorsTitlesSubjects

    My Account

    LoginRegister
    Pages
    About DRUMAbout Download Statistics

    DRUM is brought to you by the University of Maryland Libraries
    University of Maryland, College Park, MD 20742-7011 (301)314-1328.
    Please send us your comments.
    Web Accessibility