New Tools to Understand Mechanisms of Nutrient Transfer from Plants to Biotrophic Pathogens

The interaction between Arabidopsis and its natural downy mildew pathogen, Hyaloperonospora arabidopsidis (Hpa), provides a model for understanding how oomycetes colonize plants. Hpa is a model organism for many highly destructive oomycete pathogens and transcriptomics of this interaction have been...

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Main Author: Dinkeloo, Kasia
Other Authors: Plant Pathology, Physiology and Weed Science
Format: Others
Published: Virginia Tech 2020
Subjects:
RNA
GFP
Online Access:http://hdl.handle.net/10919/97521
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spelling ndltd-VTETD-oai-vtechworks.lib.vt.edu-10919-975212020-09-29T05:31:23Z New Tools to Understand Mechanisms of Nutrient Transfer from Plants to Biotrophic Pathogens Dinkeloo, Kasia Plant Pathology, Physiology and Weed Science Pilot, Guillaume Haak, David C. Zhao, Bingyu McDowell, John M. Plant-Pathogen Interactions Translatome Transcriptomics RNA Methods TRAP GFP The interaction between Arabidopsis and its natural downy mildew pathogen, Hyaloperonospora arabidopsidis (Hpa), provides a model for understanding how oomycetes colonize plants. Hpa is a model organism for many highly destructive oomycete pathogens and transcriptomics of this interaction have been well-documented. However, the material in these studies has been derived from infected leaves that contain a mix of pathogen-proximal and pathogen-distal plant cells. The most direct interactions between Arabidopsis and Hyaloperonospora arabidopsidis occur in haustoriated cells- where the pathogen can secrete effectors and acquire nutrients needed for successful colonization and reproduction. These cells are difficult to isolate due to their limited number and ephemeral nature. I have developed a method to isolate the translatome (i.e., mRNAs associated with ribosomes) of pathogen-proximal cells. This method utilizes translating ribosome immuno-purification technology (TRAP), regulated by both pathogen-responsive and tissue-specific promoters, to isolate mRNAs that are being translated in pathogen-proximal cells. Compared to "bulk" transcriptomics of material isolated from homogenized leaves, this method will enrich for transcripts that are differentially expressed, and translated, in pathogen-proximal cells. From this method, RNA was isolated in amount and quality sufficient for sequencing. This sequencing data will enable the discovery of plant genes that may be manipulated by the pathogen to suppress defense responses and extract nutrients. Ph. D. 2020-04-05T06:00:57Z 2020-04-05T06:00:57Z 2018-10-12 Dissertation vt_gsexam:16935 http://hdl.handle.net/10919/97521 In Copyright http://rightsstatements.org/vocab/InC/1.0/ ETD application/pdf Virginia Tech
collection NDLTD
format Others
sources NDLTD
topic Plant-Pathogen Interactions
Translatome
Transcriptomics
RNA
Methods
TRAP
GFP
spellingShingle Plant-Pathogen Interactions
Translatome
Transcriptomics
RNA
Methods
TRAP
GFP
Dinkeloo, Kasia
New Tools to Understand Mechanisms of Nutrient Transfer from Plants to Biotrophic Pathogens
description The interaction between Arabidopsis and its natural downy mildew pathogen, Hyaloperonospora arabidopsidis (Hpa), provides a model for understanding how oomycetes colonize plants. Hpa is a model organism for many highly destructive oomycete pathogens and transcriptomics of this interaction have been well-documented. However, the material in these studies has been derived from infected leaves that contain a mix of pathogen-proximal and pathogen-distal plant cells. The most direct interactions between Arabidopsis and Hyaloperonospora arabidopsidis occur in haustoriated cells- where the pathogen can secrete effectors and acquire nutrients needed for successful colonization and reproduction. These cells are difficult to isolate due to their limited number and ephemeral nature. I have developed a method to isolate the translatome (i.e., mRNAs associated with ribosomes) of pathogen-proximal cells. This method utilizes translating ribosome immuno-purification technology (TRAP), regulated by both pathogen-responsive and tissue-specific promoters, to isolate mRNAs that are being translated in pathogen-proximal cells. Compared to "bulk" transcriptomics of material isolated from homogenized leaves, this method will enrich for transcripts that are differentially expressed, and translated, in pathogen-proximal cells. From this method, RNA was isolated in amount and quality sufficient for sequencing. This sequencing data will enable the discovery of plant genes that may be manipulated by the pathogen to suppress defense responses and extract nutrients. === Ph. D.
author2 Plant Pathology, Physiology and Weed Science
author_facet Plant Pathology, Physiology and Weed Science
Dinkeloo, Kasia
author Dinkeloo, Kasia
author_sort Dinkeloo, Kasia
title New Tools to Understand Mechanisms of Nutrient Transfer from Plants to Biotrophic Pathogens
title_short New Tools to Understand Mechanisms of Nutrient Transfer from Plants to Biotrophic Pathogens
title_full New Tools to Understand Mechanisms of Nutrient Transfer from Plants to Biotrophic Pathogens
title_fullStr New Tools to Understand Mechanisms of Nutrient Transfer from Plants to Biotrophic Pathogens
title_full_unstemmed New Tools to Understand Mechanisms of Nutrient Transfer from Plants to Biotrophic Pathogens
title_sort new tools to understand mechanisms of nutrient transfer from plants to biotrophic pathogens
publisher Virginia Tech
publishDate 2020
url http://hdl.handle.net/10919/97521
work_keys_str_mv AT dinkelookasia newtoolstounderstandmechanismsofnutrienttransferfromplantstobiotrophicpathogens
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