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Duplicated sequence motif in the long terminal repeat of maedi-visna virus extends cell tropism and is associated with neurovirulence
Authors:Oskarsson Thórdur  Hreggvidsdóttir Hulda S  Agnarsdóttir Gudrún  Matthíasdóttir Sigrídur  Ogmundsdóttir Margrét H  Jónsson Stefán R  Georgsson Gudmundur  Ingvarsson Sigurdur  Andrésson Olafur S  Andrésdóttir Valgerdur
Affiliation:Institute for Experimental Pathology, University of Iceland, Keldur v/Vesturlandsveg, 112 Reykjavik, Iceland.
Abstract:Maedi-visna virus (MVV) is a lentivirus of sheep causing chronic inflammatory disease of the lungs (maedi) and the nervous system (visna). We have previously shown that a duplicated sequence in the long terminal repeat (LTR) of MVV is a determinant of cell tropism. Here, we demonstrate that deletion of a CAAAT sequence from either one of the repeats resulted in poor virus growth in sheep choroid plexus cells. A duplication in the LTR encompassing the CAAAT sequence was found in four neurological field cases that were sequenced, but no duplication was present in the LTRs from seven maedi cases; one maedi isolate was mixed. These results indicate that the duplication in the LTR is associated with neurovirulence.
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