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" Full genome characterization of 12 citrus tatter leaf virus isolates for the development of a detection assay. "
Tan, Shih-Hua; Osman, Fatima; Bodaghi, Sohrab; Dang, Tyler; Greer, Greg; Huang, Amy; Hammado, Sarah; Abu-Hajar, Shurooq; Campos, Roya; Vidalakis, Georgios
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AL
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| Record Number
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907884
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LA5cr080wf
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| Title & Author
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Full genome characterization of 12 citrus tatter leaf virus isolates for the development of a detection assay. [Article]\ Tan, Shih-Hua; Osman, Fatima; Bodaghi, Sohrab; Dang, Tyler; Greer, Greg; Huang, Amy; Hammado, Sarah; Abu-Hajar, Shurooq; Campos, Roya; Vidalakis, Georgios
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2019
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| Title of Periodical
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UC Riverside
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| Abstract
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Citrus tatter leaf virus (CTLV) threatens citrus production worldwide because it induces bud-union crease on the commercially important Citrange (Poncirus trifoliata × Citrus sinensis) rootstocks. However, little is known about its genomic diversity and how such diversity may influence virus detection. In this study, full-length genome sequences of 12 CTLV isolates from different geographical areas, intercepted and maintained for the past 60 years at the Citrus Clonal Protection Program (CCPP), University of California, Riverside, were characterized using next generation sequencing. Genome structure and sequence for all CTLV isolates were similar to Apple stem grooving virus (ASGV), the type species of Capillovirus genus of the Betaflexiviridae family. Phylogenetic analysis highlighted CTLV's point of origin in Asia, the virus spillover to different plant species and the bottleneck event of its introduction in the United States of America (USA). A reverse transcription quantitative polymerase chain reaction assay was designed at the most conserved genome area between the coat protein and the 3'-untranslated region (UTR), as identified by the full genome analysis. The assay was validated with different parameters (e.g. specificity, sensitivity, transferability and robustness) using multiple CTLV isolates from various citrus growing regions and it was compared with other published assays. This study proposes that in the era of powerful affordable sequencing platforms the presented approach of systematic full-genome sequence analysis of multiple virus isolates, and not only a small genome area of a small number of isolates, becomes a guideline for the design and validation of molecular virus detection assays, especially for use in high value germplasm programs.
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