Doctor of Philosophy / Department of Plant Pathology / Dorith Rotenberg / Frankliniella occidentalis, the western flower thrips, transmits the plant-pathogenic virus, Tomato spotted wilt virus (TSWV), through a circulative-propagative transmission strategy. The virus infects and replicates in the insect, traversing membrane barriers as it moves from the midgut to the salivary glands for subsequent inoculation of a plant host. Based on well-characterized virus-vector systems, many molecular interactions occur as the virus completes an infection cycle in the vector, and knowledge of transcriptome-wide response of thrips to TSWV has been limited. My research goals were to gain insight into i) the molecular responses that occur in thrips vectors of orthotospoviruses, ii) the role of antiviral defense in viruliferous thrips, and iii) plant transgenic-based strategies for studying thrips gene function and crop-pest control. To this end, my specific research objectives were to: 1) generate, assemble, and annotate a RNA-Seq-derived transcriptome for F. occidentalis using the thrips genome, and to quantify global gene expression in response to TSWV activity in larval, pre-pupal, and adult developmental stages, 2) conduct a time-course experiment to determine the effect(s) of challenging TSWV-exposed and non-exposed thrips with dsRNAs of F. occidentalis Dcr-2 or AGO2 by hemocoel injection, and 3) construct transgenic plants expressing a thrips-gene specific dsRNA hairpin to target a vital gene. My research has catalogued insect response to TSWV activity in thrips during development and provides candidate sequences for functional analysis of genes involved in insect development and defense. Successful silencing of the antiviral RNAi pathway in thrips revealed increased mortality and decreased offspring production in both virus-exposed and non-exposed insects. Arabidopsis plants were developed to express dsRNA of vacuolar ATP synthase (V-ATPase) and preliminary feeding bioassays to explore the effect of these transgenics on thrips fitness indicate a need for further description of thrips dsRNA uptake. In total, my research contributes new basic knowledge underpinning the complex and dynamic relationship between thrips vectors and the plant viruses they transmit.

京都大学 / 0048 / 新制・論文博士 / 博士(農学) / 乙第13073号 / 論農博第2843号 / 新制||農||1046(附属図書館) / 学位論文||H29||N5029(農学部図書室) / 33224 / 京都大学大学院農学研究科農学専攻 / (主査)教授 北島 宣, 教授 土井 元章, 教授 田尾 龍太郎 / 学位規則第4条第2項該当 / Doctor of Agricultural Science / Kyoto University / DFAM

Typescript (photocopy). / Digitized by Kansas Correctional Industries

Ácaros Brevipalpus yothersi Baker (1949) são vetores do citrus leprosis virus C (CiLV-C), o mais comum causador da leprose dos citros. Esta é considerada, atualmente, a doença viral de maior importância na cultura dos citros no Brasil e ocorre também em países da América do Sul e Central, além do México, na América do Norte. A doença prejudica a vida útil da planta, devido à queda de folhas e frutos, e seca de ramos, podendo levá-la à morte quando o ataque é demasiadamente severo. O controle e manejo da leprose são basicamente atribuídos ao uso de acaricidas, demandando dos produtores um acréscimo significativo no orçamento por defensivos agrícolas e potencial risco ao ambiente. Nos últimos anos, análises de expressão gênica (transcriptoma), envolvendo ácaros praga da agricultura, resultaram em informações importantes como o envolvimento de genes específicos no processo de resistência a acaricidas e desenvolvimento biológico. No entanto, ainda pouco se sabe sobre a interação do ácaro B. yothersi com o CiLV-C, tornando o estudo de transcriptoma muito significativo para a obtenção de informações aprofundadas sobre o atípico padrão vírus-vetor do patossistema leprose. Assim, através do sequenciamento de RNA (RNAseq), foi investigado o perfil de expressão diferencial entre ácaros B. yothersi virulíferos e avirulíferos. O RNAseq foi realizado em sistema Illumina HiSeq 2500, e os dados analisados com base em linguagem R e ferramentas do software Bioconductor. Os reads sequenciados foram mapeados no genoma de B. yothersi e foi feita análise de expressão utilizando DESeq2. Foram observados 5.690 genes diferencialmente expressos (GDE), sendo 2.736 transcritos induzidos em ácaros virulíferos. Os GDE foram analisados em banco de dados do NCBI, buscando por proteínas similares em artrópodes. Dentre os transcritos induzidos em B. yothersi, potencialmente em resposta ao CiLV-C, foram encontrados genes relacionados ao processo de detoxificação de xenobióticos, metabolismo primário e imunidade, com possível envolvimento na interação vírus-vetor. A expressão de 23 genes foi verificada por RT-PCR quantitativo em tempo real (RT-qPCR). As análises indicaram que os genes envolvidos em detoxificação são induzidos durante a interação entre o ácaro da leprose e o CiLV-C. / The false spider mite Brevipalpus yothersi Baker (1949) is recognized as vector of citrus leprosis virus C (CiLV-C), the most common causal agent of citrus leprosis disease. Currently, it is considered the viral disease of major importance in citrus in Brazil and occurs in countries of South and Central America, as well as in Mexico, North America. It reduces the lifespam of the plants due to leaf and fruit drop, dried branches, and can lead to death when the attack is severe. The management of leprosis is based primarily on the chemical control of the mite vector, increasing significantly the cost of production and harming the environment. On the last years, gene expression (transcriptome) analyzes involving phytophagous mites resulted in important data, such as the involvement of specific genes in the process of resistance to acaricides and biological development. However, there is little information about B. yothersi-CiLV-C interaction, making the transcriptome a very interesting tool to obtaining data regarding the atypical virus-vector relationship of the leprosis pathosystem. RNA sequencing (RNAseq) was used to investigate the differential expression profiles between viruliferous and aviruliferous B. yothersi mites. The RNAseq was performed using the Illumina HiSeq 2500 system, the data were analyzed using the R language and Bioconductor software packages. The sequenced reads were mapped on the genome of B. yothersi and expression analysis was performed in DESeq2. We identified 5.690 differentially expressed genes (DEGs), of which 2.736 transcripts were induced in viruliferous mites. The DEGs were analyzed in NCBI database, searching for similar proteins in arthropods. Among the transcripts induced in response to CiLV-C, there are genes related to the detoxification of xenobiotics, primary metabolism, immunity and possible involvement in the virus-vector interaction. Expression of 23 genes was verified by quantitative real-time RT-PCR (RT-qPCR). The analyzes indicate that detoxification genes are induced during the interaction between the false spider mite and CiLV-C.

"February, 2002" / Includes bibliographical references (leaves 156-182) / xiv, 182, [26] leaves : ill. (some col.) ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Thesis (Ph.D.)--University of Adelaide, Dept. of Molecular Biosciences, 2002

The coat protein of satellite panicum mosaic virus (SPMV) was used to stabilize viral vector gene inserts in planta. A Potato virus X (PVX) vector carrying the SPMV capsid protein (CP) gene was successfully stabilized through three serial passages in Nicotiana benthamiana from the upper non-inoculated leaves following rub inoculation. The presence of SPMV CP expression from the PVX vector was confirmed by necrotic lesions that occur only when SPMV CP is present and by western blot and reversetranscription PCR analyses. In addition, PVX-SPCP was co-inoculated onto N. benthamiana with a Tomato bushy stunt virus vector carrying a green fluorescent protein gene, which normally does not yield GFP expression in upper tissue due to loss of the insert. However, upon co-inoculation with PVX-SPCP, upper non-inoculated leaves exhibited GFP accumulation based on green fluorescence by UV illumination at 488 nm and western blot analysis. GFP expression was more abundant in upper non-inoculated N. benthamiana leaves as well as systemic tissues when the co-inoculation experiments were performed at 20°C compared to 25°C. These results suggest that SPMV CP is a viable molecular tool for stabilizing viral vector gene inserts in planta.

Dissertation (Ph.D.)--Auburn University, 2009. / Abstract. Includes bibliographic references.

Ribonuclease T1 oligonucleotide fingerprint (ONF) analysis was used to study genomic stability of La Crosse virus (Bunyaviridae) during vertical and horizontal transmission in the laboratory. No RNA genomic changes were detected in vertebrate cell culture-propagated virus isolated (following oral ingestion and replication) from the natural mosquito host, Aedes triseriatus. Genomic changes were not detected during transovarial passage of virus through two generations of mosquitoes or in virus isolated from suckling mice infected by transovarially infected mosquitoes. These results demonstrate that the La Crosse virus genome can remain relatively stable during transovarial transmission (TOT) in the insect host and during transfer between insect and vertebrate hosts. ONF analysis was used to demonstrate TOT of reassortant California serogroup bunyaviruses in Aedes treiseriatus. Mosquitoes were simultaneously inoculated with temperature sensitive mutants of La Crosse and Snowshoe hare viruses able to replicate at 33°C but not at 40°C. Putative reassortants, selected by replication at 40°C, were isolated from progeny mosquitoes and mice infected by these mosquitoes. ONF analysis confirmed that they were reassortants. Approximately 75% of the M segment and 25% of the L segment nucleotide sequences of Inkoo virus (Bunyaviridae) were determined by Sanger dideoxynucleotide sequencing of cDNA clones. Comparison of the M segment nucleotide and deduced amino acid sequences with those of four other bunyaviruses, representing two serogroups, revealed greater conservation of nucleotide than of amino acid sequence between serogroups. Areas of the sequences representing nonstructural protein(s) were less conserved than glycoprotein regions. The L segment nucleotide sequence begins with the known 3' end of the viral L segment and contains an open reading frame encoding the amino terminal 505 amino acids of the viral L protein. The amino acid sequence contains the glycine-aspartate-aspartate motif which is conserved in many RNA-dependent RNA polymerases. Comparison of the L segment sequences with those in the GEN Bank Data Base revealed no significant similarities with any other sequence.

Thesis (M.S.)--University of Nevada, Reno, 2006. / "December, 2006." Includes bibliographical references (leaves 29-33). Online version available on the World Wide Web. Library also has microfilm. Ann Arbor, Mich. : ProQuest Information and Learning Company, [2006]. 1 microfilm reel ; 35 mm.

Thesis (M.S.)--University of Wisconsin--Madison, 1982. / Typescript. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 53-56).