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Unbiased, next-generation sequencing for the characterization of Citrus tristeza virus populations

A high-throughput sequencing pipeline to characterize Citrus tristeza virus isolates was developed. Three alternative viral templates (total RNA, double-stranded RNA and virus particles) were first tested on a single, previously characterized GFMS12 sub-isolate for their enrichment qualities, and combined with random RT-PCR amplification were subjected to Illumina paired-end sequencing. Double-stranded RNA was found to be most useful and was selected for further characterization of additional isolates (glasshouse-kept and field-derived). A novel South African genotype, named CT-ZA3 was assembled de novo and shown to be the dominant component in all GFMS12 sub-isolates tested. Genotype distributions within field-derived isolates collected from commercial orange (Citrus sinensis) orchards revealed a mixed infection status, dominated by a resistance breaking (RB)-like component (Tai-SP) coupled with a minor, VT-like (mild) (Kpg3) component. Based on read mapping patterns from field isolates, it is further suggested that two previously unknown recombinants may be present: a SP/Kpg3 and HA16-5/Kpg3 combination. This study underlined the effectiveness of next-generation sequencing for genotype discovery as well as whole-genome characterization of CTV isolates to a level of detail previously unreachable with classical methods such as SSCP and Sanger sequencing of multiple clones. / Dissertation (MSc)--University of Pretoria, 2013. / gm2014 / Microbiology and Plant Pathology / unrestricted

Identiferoai:union.ndltd.org:netd.ac.za/oai:union.ndltd.org:up/oai:repository.up.ac.za:2263/33177
Date January 2013
CreatorsZablocki, Olivier
ContributorsPietersen, Gerhard, ozablocki@hotmail.com
Source SetsSouth African National ETD Portal
LanguageEnglish
Detected LanguageEnglish
TypeDissertation
Rights© 2013 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.

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