Protocol: an improved method to quantify activation of systemic acquired resistance (SAR)
Abstract Background Plant responses triggered upon detection of an invading pathogen include the generation of a number of mobile signals that travel to distant tissues and determine an increased resistance in distal, uninfected tissues, a defense response known as systemic acquired resistance (SAR)...
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2019-02-01
|
Series: | Plant Methods |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s13007-019-0400-5 |
id |
doaj-53532a2f1dcf40779a3f241ec0d5b051 |
---|---|
record_format |
Article |
spelling |
doaj-53532a2f1dcf40779a3f241ec0d5b0512020-11-25T03:15:05ZengBMCPlant Methods1746-48112019-02-011511810.1186/s13007-019-0400-5Protocol: an improved method to quantify activation of systemic acquired resistance (SAR)José S. Rufián0Javier Rueda-Blanco1Carmen R. Beuzón2Javier Ruiz-Albert3Dpto. Biología Celular, Genética y Fisiología, Instituto de Hortofruticultura Subtropical y Mediterránea, Universidad de Málaga-Consejo Superior de Investigaciones Científicas (IHSM-UMA-CSIC)Dpto. Biología Celular, Genética y Fisiología, Instituto de Hortofruticultura Subtropical y Mediterránea, Universidad de Málaga-Consejo Superior de Investigaciones Científicas (IHSM-UMA-CSIC)Dpto. Biología Celular, Genética y Fisiología, Instituto de Hortofruticultura Subtropical y Mediterránea, Universidad de Málaga-Consejo Superior de Investigaciones Científicas (IHSM-UMA-CSIC)Dpto. Biología Celular, Genética y Fisiología, Instituto de Hortofruticultura Subtropical y Mediterránea, Universidad de Málaga-Consejo Superior de Investigaciones Científicas (IHSM-UMA-CSIC)Abstract Background Plant responses triggered upon detection of an invading pathogen include the generation of a number of mobile signals that travel to distant tissues and determine an increased resistance in distal, uninfected tissues, a defense response known as systemic acquired resistance (SAR). The more direct means of measuring activation of SAR by a primary local infection is the quantification of pathogen multiplication in distal, systemic sites of secondary infection. However, while such assay provides a biologically relevant quantification of SAR, it is hampered by experimental variation, requiring many repetitions for reliable results. Results We propose a modification of the SAR assay based on the Arabidopsis–Pseudomonas syringae pathosystem exploiting the knowledge of source-sink relationships (orthostichies), known to centralize SAR-competency to upper leaves in the orthostichy of a lower primary infected leaf. Although many sources of variation such as genotypes of plant and pathogen, inoculation procedure, or environmental conditions are already taken into account to improve the performance of SAR assays, a strict leaf selection based on source-sink relationships is not usually implemented. We show how enacting this latter factor considerably improves data reliability, reducing the number of experimental repetitions for results. Conclusions Direct selection of leaves for both primary and secondary inoculation exclusively within the orthostichy of the primary infected leaf is a key element on reducing the number of experimental repetitions required for statistically relevant SAR activation results.http://link.springer.com/article/10.1186/s13007-019-0400-5Systemic acquired resistance (SAR)Plant immunityPseudomonas syringae |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
José S. Rufián Javier Rueda-Blanco Carmen R. Beuzón Javier Ruiz-Albert |
spellingShingle |
José S. Rufián Javier Rueda-Blanco Carmen R. Beuzón Javier Ruiz-Albert Protocol: an improved method to quantify activation of systemic acquired resistance (SAR) Plant Methods Systemic acquired resistance (SAR) Plant immunity Pseudomonas syringae |
author_facet |
José S. Rufián Javier Rueda-Blanco Carmen R. Beuzón Javier Ruiz-Albert |
author_sort |
José S. Rufián |
title |
Protocol: an improved method to quantify activation of systemic acquired resistance (SAR) |
title_short |
Protocol: an improved method to quantify activation of systemic acquired resistance (SAR) |
title_full |
Protocol: an improved method to quantify activation of systemic acquired resistance (SAR) |
title_fullStr |
Protocol: an improved method to quantify activation of systemic acquired resistance (SAR) |
title_full_unstemmed |
Protocol: an improved method to quantify activation of systemic acquired resistance (SAR) |
title_sort |
protocol: an improved method to quantify activation of systemic acquired resistance (sar) |
publisher |
BMC |
series |
Plant Methods |
issn |
1746-4811 |
publishDate |
2019-02-01 |
description |
Abstract Background Plant responses triggered upon detection of an invading pathogen include the generation of a number of mobile signals that travel to distant tissues and determine an increased resistance in distal, uninfected tissues, a defense response known as systemic acquired resistance (SAR). The more direct means of measuring activation of SAR by a primary local infection is the quantification of pathogen multiplication in distal, systemic sites of secondary infection. However, while such assay provides a biologically relevant quantification of SAR, it is hampered by experimental variation, requiring many repetitions for reliable results. Results We propose a modification of the SAR assay based on the Arabidopsis–Pseudomonas syringae pathosystem exploiting the knowledge of source-sink relationships (orthostichies), known to centralize SAR-competency to upper leaves in the orthostichy of a lower primary infected leaf. Although many sources of variation such as genotypes of plant and pathogen, inoculation procedure, or environmental conditions are already taken into account to improve the performance of SAR assays, a strict leaf selection based on source-sink relationships is not usually implemented. We show how enacting this latter factor considerably improves data reliability, reducing the number of experimental repetitions for results. Conclusions Direct selection of leaves for both primary and secondary inoculation exclusively within the orthostichy of the primary infected leaf is a key element on reducing the number of experimental repetitions required for statistically relevant SAR activation results. |
topic |
Systemic acquired resistance (SAR) Plant immunity Pseudomonas syringae |
url |
http://link.springer.com/article/10.1186/s13007-019-0400-5 |
work_keys_str_mv |
AT josesrufian protocolanimprovedmethodtoquantifyactivationofsystemicacquiredresistancesar AT javierruedablanco protocolanimprovedmethodtoquantifyactivationofsystemicacquiredresistancesar AT carmenrbeuzon protocolanimprovedmethodtoquantifyactivationofsystemicacquiredresistancesar AT javierruizalbert protocolanimprovedmethodtoquantifyactivationofsystemicacquiredresistancesar |
_version_ |
1724640593945034752 |