Location: Soil Dynamics Research
Title: Development and analysis of infectious and fluorescent clones of cotton leafroll dwarf virus- ALAuthor
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CLARK, WILSON - Auburn University |
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LIVINGSTON, RACHEL - Auburn University |
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HIRSCH, KAYLEE - Auburn University |
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KOEBERNICK, JENNY - Auburn University |
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KANG, S - Auburn University |
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Price, Andrew |
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CONNER, KASSIE - Auburn University |
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JACOBSON, ALANA - Auburn University |
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MARTIN, KATE - Auburn University |
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Submitted to: PhytoFrontiers
Publication Type: Peer Reviewed Journal Publication Acceptance Date: 5/6/2025 Publication Date: N/A Citation: N/A Interpretive Summary: Cotton leafroll dwarf virus (CLRDV) is a plant pathogen that was first detected in the United States in 2017 and has caused yield loss in cotton (Gossypium hirsutum L) production. In Argentina, infectious clones of both the typical and atypical strains of CLRDV were developed to further research into the virus. In this study two infectious clones based on the original Alabama isolate were developed to help further research into this emerging pathogen. This clone produces EGFP and is visible by fluorescence microscopy in infiltrated cotton cotyledons and can be detected with commercial antibodies. This study presents the first infectious clones of CLRDV in the United States and adds to the growing knowledge of Poleroviruses. Technical Abstract: Cotton leafroll dwarf virus (CLRDV) is a plant pathogen that was first detected in the United States in 2017 and has caused yield loss in cotton (Gossypium hirsutum L) production. In Argentina, infectious clones of both the typical and atypical strains of CLRDV were developed to further research into the virus. In this study two infectious clones based on the original Alabama isolate were developed to help further research into this emerging pathogen. Both are Agrobacterium tumefaciens expression constructs which are agroinfiltrated into plants to cause infection. CLRDV-Macon1 (abbreviated CLRDV-Ma1) was created by inserting the full sequence of CLRDV into pJL89, an agrobacterium expression vector. This virus clone systemically infects both cotton and Nicotiana benthamiana and is detectable by PCR assays. CLRDV-M-GFP was created by replacing a C-terminal section of ORF3-5 from CLRDV-Ma1 with EGFP. This clone produces EGFP and is visible by fluorescence microscopy in infiltrated cotton cotyledons and can be detected with commercial antibodies. This study presents the first infectious clones of CLRDV in the United States and adds to the growing knowledge of Poleroviruses. |
