A cell death assay in barley and wheat protoplasts for identification and validation of matching pathogen AVR effector and plant NLR immune receptors
Identifieur interne : 000259 ( Main/Exploration ); précédent : 000258; suivant : 000260A cell death assay in barley and wheat protoplasts for identification and validation of matching pathogen AVR effector and plant NLR immune receptors
Auteurs : Isabel M. L. Saur [Allemagne] ; Saskia Bauer [Allemagne] ; Xunli Lu [Allemagne, République populaire de Chine] ; Paul Schulze-Lefert [Allemagne]Source :
- Plant Methods [ 1746-4811 ] ; 2019.
Abstract
Plant disease resistance to host-adapted pathogens is often mediated by host nucleotide-binding and leucine-rich repeat (NLR) receptors that detect matching pathogen avirulence effectors (AVR) inside plant cells. AVR-triggered NLR activation is typically associated with a rapid host cell death at sites of attempted infection and this response constitutes a widely used surrogate for NLR activation. However, it is challenging to assess this cell death in cereal hosts.
Here we quantify cell death upon NLR-mediated recognition of fungal pathogen AVRs in mesophyll leaf protoplasts of barley and wheat. We provide measurements for the recognition of the fungal AVRs
Our data demonstrate that the here described approach can be effectively used to detect and quantify death of wheat and barley cells induced by overexpression of
Url:
DOI: 10.1186/s13007-019-0502-0
PubMed: 31666804
PubMed Central: 6813131
Affiliations:
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<series><title level="j">Plant Methods</title>
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<front><div type="abstract" xml:lang="en"><sec><title>Background</title>
<p id="Par1">Plant disease resistance to host-adapted pathogens is often mediated by host nucleotide-binding and leucine-rich repeat (NLR) receptors that detect matching pathogen avirulence effectors (AVR) inside plant cells. AVR-triggered NLR activation is typically associated with a rapid host cell death at sites of attempted infection and this response constitutes a widely used surrogate for NLR activation. However, it is challenging to assess this cell death in cereal hosts.</p>
</sec>
<sec><title>Results</title>
<p id="Par2">Here we quantify cell death upon NLR-mediated recognition of fungal pathogen AVRs in mesophyll leaf protoplasts of barley and wheat. We provide measurements for the recognition of the fungal AVRs <italic>AvrSr50</italic>
and <italic>AVR</italic>
<sub><italic>a1</italic>
</sub>
by their respective cereal NLRs <italic>Sr50</italic>
and <italic>Mla1</italic>
upon overexpression of the <italic>AVR</italic>
and <italic>NLR</italic>
pairs in mesophyll protoplast of both, wheat and barley.</p>
</sec>
<sec><title>Conclusions</title>
<p id="Par3">Our data demonstrate that the here described approach can be effectively used to detect and quantify death of wheat and barley cells induced by overexpression of <italic>NLR</italic>
and <italic>AVR</italic>
effectors or <italic>AVR</italic>
effector candidate genes from diverse fungal pathogens within 24 h.</p>
</sec>
</div>
</front>
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<li>République populaire de Chine</li>
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