Spelling suggestions: "subject:"rhabdoviruses"" "subject:"rhabdovirus""
1 |
The molecular basis of the interactions of rhabdoviruses with their insect and plant hostsTsai, Chi-Wei. January 2006 (has links)
Thesis (Ph. D.)--Ohio State University, 2006. / Title from first page of PDF file. Includes bibliographical references (p. 159-170).
|
2 |
Characterization of the endotoxin response in zebrafish, and synthesis of a snakehead rhabdovirus expressing red fluorescent or green fluorescent protein /Giasson, Gregory M., January 2006 (has links) (PDF)
Thesis (M.S.) in Biochemistry--University of Maine, 2006. / Includes vita. Includes bibliographical references (leaves 65-74).
|
3 |
Characterization of the Endotoxin Response in Zebrafish, and Synthesis of a Snakehead Rhabdovirus Expressing Red Fluorescent or Green Fluorescent ProteinGiasson, Gregory M. January 2006 (has links) (PDF)
No description available.
|
4 |
Molecular characterization and genetic recombination of snakehead rhabdovirusJohnson, Marc C. 25 February 1999 (has links)
The complete genome of snakehead rhabdovirus (SHRV) was cloned and
molecularly characterized. This was initially accomplished through the sequence
determination of its glycoprotein gene and the phylogenetic analysis of this gene with
orthologous genes from other rhabdoviruses. The phylogenetic analysis revealed that
SHRV groups with viruses of the genus Novirhabdovirus. The full-length glycoprotein
was expressed in mammalian cells to investigate its potential use in the production of
pseudotyped retroviruses.
The sequence of the entire SHRV genome of 11.6 kb was determined, and all
encoded proteins, intergenic transcriptional control motifs, and the leader and trailer
regions were identified. The genome was found to encode six proteins including a
nucleoprotein, a phosphoprotein, a matrix protein, a glycoprotein, a small--presumably
non-virion--protein, and a polymerase protein. The presence of a non-virion protein,
which is the hallmark feature of all Novirhabdoviruses, supported SHRV's identity as a
member of the Novirhabdovirus genus, despite the fact that the non-virion protein
showed no homology with any known protein.
A system was developed to express a full-length, error-free positive-strand copy
of SHRV's RNA genome along with all of the SHRV proteins required for viral
replication within the cytoplasm of a virus-susceptible host cell. These factors
collectively allowed the recovery of live virus entirely from cloned cDNAs. A unique
restriction site was engineered into SHRV's cDNA genome, and the presence of this
restriction site was verified following virus recovery, proving the recovered virus was
indeed a live recombinant virus. To our knowledge this achievement marks the first time
in which reverse genetics has been performed on a nonmammalian negative-stranded
RNA virus. / Graduation date: 1999
|
5 |
Characterization of the matrix proteins of the fish rhabdovirus, infectious hematopoietic necrosis virusOrmonde, Patricia A. 14 April 1995 (has links)
Graduation date: 1995
|
6 |
Characterization of a rhabdovirus isolated from the snakehead fish (Ophicephalus striatus)Kasornchandra, Jiraporn 02 December 1991 (has links)
Graduation date: 1992
|
7 |
The genetic diversity and epizootiology of infectious hematopoietic necrosis virus /Oshima, Kevin Hiroshi, January 1991 (has links)
Thesis (Ph. D.)--University of Washington, 1991. / Vita. Includes bibliographical references (leaves [47]-56).
|
8 |
Caveolin-1a and caveolin-1b mediate the clearance of snakehead rhabdovirus infection /Stevens, Chad R., January 2009 (has links)
Thesis (M.S.) in Microbiology--University of Maine, 2009. / Includes vita. Includes bibliographical references (leaves 82-87).
|
9 |
Caveolin-1A and Caveolin-1B Mediate the Clearance of Snakehead Rhabdovirus InfectionStevens, Chad R. January 2009 (has links) (PDF)
No description available.
|
10 |
Characterization of two plant rhabdoviruses not previously reported in South AfricaLamprecht, Renate Luise 08 June 2009 (has links)
Two previously uncharacterized plant rhabdoviruses, infecting Bermuda grass (Cynodon dactylon (L.) Pers) and soybean (Glycine max) respectively, have been found in South Africa. To determine the morphology and virion size of these viruses, embedded ultra-thin sections of infected plant samples were observed under a transmission electron microscope. The virion distribution within the cell, the bulletshaped morphology and the virion sizes indicated that both these viruses might belong to the Rhabdoviridae family. Degenerate polymerase chain reaction (PCR) primers were designed by alignment of the polymerase gene sequences of several plant rhabdoviruses in order to identify conserved regions. Standard PCR and sequencing protocols were used to determine a partial polymerase gene sequence of the viruses that was then compared to the most closely related sequences available on Genbank. The analysis indicated that the Cynodon rhabdovirus was most closely related to known nucleorhabdoviruses; and the rhabdovirus-infecting soybean (Soybean blotching mosaic virus proposed name) was closely related to other known cytorhabdoviruses. These results indicate that both the viruses are new members to the Nucleo- and Cytorhabdovirus genera, respectively. / Dissertation (MSc)--University of Pretoria, 2011. / Microbiology and Plant Pathology / unrestricted
|
Page generated in 0.0437 seconds