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The construction of an infectious clone of grapevine virus A (GV A)

Thesis (MSc (Genetics))--University of Stellenbosch, 2005.

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Main Author: Du Preez, Jacques
Other Authors: Burger, J. T.
Format: Thesis
Language:English
Published: Stellenbosch : University of Stellenbosch 2008
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access_status_str Open Access
author Du Preez, Jacques
author2 Burger, J. T.
author_browse Burger, J. T.
Du Preez, Jacques
author_facet Burger, J. T.
Du Preez, Jacques
author_sort Du Preez, Jacques
collection Thesis
dc_rights_str_mv University of Stellenbosch
description Thesis (MSc (Genetics))--University of Stellenbosch, 2005.
format Thesis
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institution Stellenbosch University (South Africa)
language English
last_indexed 2026-06-10T12:41:41.074Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from SUNScholar — Stellenbosch University Repository
publishDate 2008
publishDateRange 2008
publishDateSort 2008
publisher Stellenbosch : University of Stellenbosch
publisherStr Stellenbosch : University of Stellenbosch
record_format dspace
source_str SUNScholar — Stellenbosch University Repository
spelling oai:scholar.sun.ac.za:10019.1/2650 The construction of an infectious clone of grapevine virus A (GV A) Du Preez, Jacques Burger, J. T. University of Stellenbosch. Faculty of Agrisciences. Dept. of Genetics. Dissertations -- Genetics Theses -- Genetics Grapes -- Diseases and pests -- Control Virus diseases of plants -- Genetic aspects RNA viruses -- Reproduction Thesis (MSc (Genetics))--University of Stellenbosch, 2005. An infectious clone of a viral RNA genome is one that can be used, either as an in vitro transcript or as cDNA, to produce an infection in a susceptible plant. Infectious clones serve as a tool to study viral RNA genomes at a molecular level to gain deeper insight into genome organization, viral gene function, presence of regulatory sequences and gene expression. In the Western Cape (and elsewhere) a new crippling grapevine disease, known as Shiraz disease, is emerging of which the aetiology and pathogenic agents involved are not yet fully understood. Grapevine virus A (GVA), genus Vitivirus, family Flexiviridae, is thought to be the associated with this disease. The aim of this study was to construct a full-length infectious cDNA clone of GVA, which will aid in the molecular study of the viral genome. This clone could ultimately be used to investigate GVA’s involvement in Shiraz disease, which could lead to the unravelling of the aetiology and control of the disease. A full-length clone of GVA, named GVA-IC2/T7-2972-3, was constructed in several steps using restriction digestion/ligation and primer overlap extension PCR. Grapevine virus A cDNA fragments were obtained from GVAinfected Nicotiana benthamiana and Vitis vinifera plants using three different techniques, of which the Rapid direct-one-tube RT-PCR was most successful. A 5’ T7 promoter and a 3’ poly-A tail were incorporated and the full-length clone was cloned into pBluescript II SK (+). Full-length sequencing of the clone, revealed two significant frameshift mutations. The first mutation was a single base pair insertion (one G) in a slippery site of 6 G’s at position 1380 – 1385 in open reading frame one (ORF 1) of the viral genome. This mutation was corrected by PCR-based site-directed mutagenesis, which resulted in pSK-GVA-mutagen-3 and pSK-GVA-mutagen-4. The second mutation was a single base pair deletion (one G) at position 6959 in ORF4, which coded for the coat protein (CP). Several techniques were attempted to correct this mutation, but none were successful. Even though the second mutation could not be corrected, in vitro transcriptions were performed on three clones followed by subsequent infections of N. benthamiana plants. The three clones included pSK-GVA-mutagen-3, pSKGVA- mutagen-4 (both hosting the mutation at position 6959) and GVA-IC2/T7-2972-3 (hosting both mutations). At 21 days post-inoculation no significant visual symptoms were observed in plants infected with in vitro RNA or in plants infected with wild type GVA. Rapid direct-one-tube RT-PCR results revealed the presence of viral RNA in infected leaves and apical leaves of infected plants, and provided preliminary evidence that the mutated clones were still capable of systemic infection and viral movement. These results are still inconclusive, and several post-infection studies will have to be performed to confirm these findings. Koch's postulates will also have to be proved in order to confirm the infectious nature of the clones. The effect of the two mutations in the constructed clones will be investigated further and post-infection analysis performed to deduce whether the viral progeny are devoid of the mutations. Three full-length GVA cDNA clones (hosting mutations) seemingly capable of systemic infection in N. benthamiana plants were constructed in this study and have laid the foundation for molecular and mutational analysis of the GVA genome. This could lead to the study of pathogen-host interactions in order to unravel the aetiology of Shiraz disease in the future. Masters 2008-07-08T09:45:22Z 2010-06-01T08:54:28Z 2008-07-08T09:45:22Z 2010-06-01T08:54:28Z 2005-04 Thesis http://hdl.handle.net/10019.1/2650 en University of Stellenbosch application/pdf Stellenbosch : University of Stellenbosch
spellingShingle Dissertations -- Genetics
Theses -- Genetics
Grapes -- Diseases and pests -- Control
Virus diseases of plants -- Genetic aspects
RNA viruses -- Reproduction
Du Preez, Jacques
The construction of an infectious clone of grapevine virus A (GV A)
title The construction of an infectious clone of grapevine virus A (GV A)
title_full The construction of an infectious clone of grapevine virus A (GV A)
title_fullStr The construction of an infectious clone of grapevine virus A (GV A)
title_full_unstemmed The construction of an infectious clone of grapevine virus A (GV A)
title_short The construction of an infectious clone of grapevine virus A (GV A)
title_sort construction of an infectious clone of grapevine virus a gv a
topic Dissertations -- Genetics
Theses -- Genetics
Grapes -- Diseases and pests -- Control
Virus diseases of plants -- Genetic aspects
RNA viruses -- Reproduction
url http://hdl.handle.net/10019.1/2650
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