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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 : 000260

A 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 :

RBID : PMC:6813131

Abstract

Background

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.

Results

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 AvrSr50 and AVRa1 by their respective cereal NLRs Sr50 and Mla1 upon overexpression of the AVR and NLR pairs in mesophyll protoplast of both, wheat and barley.

Conclusions

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 NLR and AVR effectors or AVR effector candidate genes from diverse fungal pathogens within 24 h.


Url:
DOI: 10.1186/s13007-019-0502-0
PubMed: 31666804
PubMed Central: 6813131


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<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>
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<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>
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<italic>a1</italic>
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and
<italic>AVR</italic>
effectors or
<italic>AVR</italic>
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