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Molecular responses of maize to its foliar pathogen, Cercospora zeina

Thesis (PhD)--University of Pretoria, 2015.

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Other Authors: Berger, David Kenneth
Format: Thesis
Language:English
Published: University of Pretoria 2021
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author2 Berger, David Kenneth
author_browse Berger, David Kenneth
author_facet Berger, David Kenneth
collection Thesis
dc_rights_str_mv © 2020 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.
description Thesis (PhD)--University of Pretoria, 2015.
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institution University of Pretoria (South Africa)
language English
last_indexed 2026-06-10T12:39:16.707Z
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publisher University of Pretoria
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source_str UPSpace — University of Pretoria Institutional Repository
spelling oai:repository.up.ac.za:2263/79263 Molecular responses of maize to its foliar pathogen, Cercospora zeina Berger, David Kenneth jeann.korsman@fabi.up.ac.za Crampton, Bridget Genevieve Korsman, Jeanne Nicola UCTD Cercospora zeae-maydis Cercospora zeina Precision phenotyping Quantitative polymerase chain reaction (qPCR) Grey leaf spot Real-time PCR Natural and agricultural sciences theses SDG-02 Natural and agricultural sciences theses SDG-09 Natural and agricultural sciences theses SDG-15 Thesis (PhD)--University of Pretoria, 2015. The defence response of maize (Zea mays) to its foliar pathogen, Cercospora zeina, is not well characterized at the molecular and genetic level. C. zeina causes grey leaf spot (GLS), and high infection levels result in reduced crop yield. A molecular genetic study of the interaction between maize and C. zeina required a method to quantify the fungus within infected leaves. A quantitative PCR assay was developed for this purpose. It was based on amplification of a fungal cytochrome P450 reductase (cpr1) gene fragment, which was normalized using an amplified maize glutathione S-transferase III (gst) gene fragment. The assay was specific to C. zeina and a related species, Cercospora zeae-maydis, not yet found in Africa. In addition, a melt curve analysis enabled discrimination between these species. There was no amplification from a range of other maize foliar pathogens. The fungal quantification assay was successfully tested on glasshouse grown maize inoculated with C. zeina, and infected field grown maize. This assay can be implemented to quantify C. zeina at early stages of infection due to its sensitivity, and in the field due to its specificity. The fungal quantification assay was used to map GLS resistance QTL from a field trial of a sub-tropical maize RIL population in KwaZulu-Natal. We hypothesized that QTL involved in limiting C. zeina growth maize in leaves could be detected using in planta fungal quantity and lesion area data from digital image analysis, and that they would correspond with GLS resistance QTL previously mapped in the same population. Three QTL were mapped for in planta fungal quantity and one for lesion area. The strongest effect QTL was located on chromosome six. It was detected using both the fungal quantification assay and the lesion area data, and overlapped with a GLS resistance QTL from the same population in the same environment. Thus QTL can be successfully mapped from in planta fungal quantification and lesion area data and these QTL correspond to GLS resistance QTL. The molecular response of maize to C. zeina was studied using expression profiling of a pooled bulk of resistant RILs versus a pooled bulk of susceptible RILs from the same population used for GLS QTL mapping. We aimed to find genes with differential expression between the resistant and susceptible bulks during GLS field infection. Additionally, we hypothesized that genes contributing to the QTL effect could be identified within QTL. Candidate genes for the resistance response included an RPP13-like gene and an mlo gene. The genome positions of the differentially expressed genes were compared to the genome positions of the QTL. Candidate genes coinciding with QTL included a malectin containing RLK, an EDR1-like gene, a GTPase gene, a cytochrome b561 gene, and a chorismate synthase gene. Comparison of gene ontologies from all the genes differentially expressed between the resistant and susceptible bulks indicated that cell death was a likely strategy for resistance. The resistant response is probably an early response, with a later and continuing response to biotic stress in the susceptible maize plants. bs2026 Plant Science PhD Unrestricted SDG-02: Zero hunger SDG-09: Industry, innovation and infrastructure SDG-15: Life on land 2021-04-06T07:22:34Z 2021-04-06T07:22:34Z 2015/07/09 2015 Thesis Korsman, JN 2015, Molecular responses of maize to its foliar pathogen, Cercospora zeina, PhD Thesis, University of Pretoria, Pretoria, viewed yymmdd <http://hdl.handle.net/2263/79263> S2015 http://hdl.handle.net/2263/79263 en © 2020 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. application/pdf University of Pretoria
spellingShingle UCTD
Cercospora zeae-maydis
Cercospora zeina
Precision phenotyping
Quantitative polymerase chain reaction (qPCR)
Grey leaf spot
Real-time PCR
Natural and agricultural sciences theses SDG-02
Natural and agricultural sciences theses SDG-09
Natural and agricultural sciences theses SDG-15
Molecular responses of maize to its foliar pathogen, Cercospora zeina
title Molecular responses of maize to its foliar pathogen, Cercospora zeina
title_full Molecular responses of maize to its foliar pathogen, Cercospora zeina
title_fullStr Molecular responses of maize to its foliar pathogen, Cercospora zeina
title_full_unstemmed Molecular responses of maize to its foliar pathogen, Cercospora zeina
title_short Molecular responses of maize to its foliar pathogen, Cercospora zeina
title_sort molecular responses of maize to its foliar pathogen cercospora zeina
topic UCTD
Cercospora zeae-maydis
Cercospora zeina
Precision phenotyping
Quantitative polymerase chain reaction (qPCR)
Grey leaf spot
Real-time PCR
Natural and agricultural sciences theses SDG-02
Natural and agricultural sciences theses SDG-09
Natural and agricultural sciences theses SDG-15
url http://hdl.handle.net/2263/79263