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dc.contributor.authorBraidwood, Luke Anthony
dc.date.accessioned2018-03-02T11:36:16Z
dc.date.available2018-03-02T11:36:16Z
dc.date.submitted2017-09-29
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/273678
dc.description.abstractModern agriculture is dependent on both global supply chains and crop monocultures. These features aid the evolution and spread of novel plant pathogens. Limited genetic diversity in commercial crop lines can result in widespread susceptibility to emerging pathogens. Pathogen resistance may be developed through conventional breeding approaches, or a number of transgenic strategies. This thesis focuses on the characterisation of an emerging maize disease, Maize lethal necrosis (MLN), and engineering resistant maize lines using an artificial microRNA (amiRNA) approach. MLN is a synergistic viral disease caused by the interaction of Maize chlorotic mottle virus (MCMV) with any maize-infecting member of the potyviridae. I used next-generation RNA sequencing to characterise the MLN outbreak in East Africa, discovering that local and Chinese strains of the potyvirus Sugarcane mosaic virus (SCMV) typically coinfect with MCMV. A first global MCMV phylogeny was constructed using these samples combined with new Sanger sequencing of samples in Ecuador and Hawaii. The phylogeny supported previous hypotheses of a link between the Chinese and African outbreaks, and suggested a novel link between the Hawaiian and Ecuadorian outbreaks. The SCMV sequences generated demonstrated strong evidence of extensive recombination, in line with previous reports on SCMV and potyviruses. These data also produced first reports of a number of RNA viruses in East Africa, and five novel viral-like sequences, with their presence confirmed by RT-PCR. RNA silencing is an important component of the plant immune response to viral infection. amiRNAs can be used to generate specific and effective viral resistance through Watson- Crick base pairing between the amiRNA and the (RNA) viral genome. Previous amiRNA approaches have targeted invariable genomic regions using consensus sequences. However, the high mutation rate of RNA viruses means single cells contain a variety of mutant genomes, collectively called a quasispecies. To deter the evolution of resistance breaking I devised a novel strategy to include intra-sample variation from NGS data in amiRNA design, and constructs, each containing five of these amiRNAs, were transformed into tropical maize lines. RNA silencing may be hampered by the expression of viral suppressors of silencing (VSRs). Local VSR assays demonstrated that there are no local VSRs in the MCMV genome, while systemic VSR assays showed a possible systemic VSR role for the unique P32 protein, and an interesting link between photoperiod and systemic silencing more generally.
dc.description.sponsorshipBBSRC DTP
dc.language.isoen
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectmaize chlorotic mottle virus
dc.subjectmaize
dc.subjectvirology
dc.subjectmolecular biology
dc.subjectNGS
dc.titleEngineering resistance to maize lethal necrosis
dc.typeThesis
dc.type.qualificationlevelDoctoral
dc.type.qualificationnameDoctor of Philosophy (PhD)
dc.publisher.institutionUniversity of Cambridge
dc.publisher.departmentPlant Sciences
dc.date.updated2018-03-01T17:46:05Z
dc.identifier.doi10.17863/CAM.20731
dc.contributor.orcidBraidwood, Luke Anthony [0000-0002-0233-3605]
dc.publisher.collegeTrinity
dc.type.qualificationtitlePhD in Plant Sciences
cam.supervisorBaulcombe, David Charles
cam.supervisor.orcidBaulcombe, David Charles [0000-0003-0780-6878]
rioxxterms.freetoread.startdate2018-03-01


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Attribution 4.0 International
Except where otherwise noted, this item's licence is described as Attribution 4.0 International