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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Disclosures
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Quantification of pathogen growth is a powerful tool to characterize various Arabidopsis thaliana (hereafter: Arabidopsis) immune responses. The method described here presents an optimized syringe infiltration assay to quantify the Pseudomonas syringae pv. maculicola ES4326 growth in adult Arabidopsis leaves.

Abstract

In the absence of specialized mobile immune cells, plants utilize their localized programmed cell death and Systemic Acquired Resistance to defend themselves against pathogen attack. The contribution of a specific Arabidopsis gene to the overall plant immune response can be specifically and quantitatively assessed by assaying the pathogen growth within the infected tissue. For over three decades, the hemibiotrophic bacterium Pseudomonas syringae pv. maculicola ES4326 (Psm ES4326) has been widely applied as the model pathogen to investigate the molecular mechanisms underlying the Arabidopsis immune response. To deliver pathogens into the leaf tissue, multiple inoculation methods have been established, e.g., syringe infiltration, dip inoculation, spray, vacuum infiltration, and flood inoculation. The following protocol describes an optimized syringe infiltration method to deliver virulent Psm ES4326 into leaves of adult soil-grown Arabidopsis plants and accurately screen for enhanced disease susceptibility (EDS) towards this pathogen. In addition, this protocol can be supplemented with multiple pre-treatments to further dissect specific immune defects within different layers of plant defense, including Salicylic Acid (SA)-Triggered Immunity (STI) and MAMP-Triggered Immunity (MTI).

Introduction

Due to their sessile nature, plants are constantly threatened by a plethora of pathogens exhibiting various lifestyles and nutritional strategies1. To a first approximation, biotrophic pathogens maintain their host alive to retrieve nutrients, while necrotrophic pathogens actively secret toxins and enzymes to kill host tissue and feed on the dead cells1. Another group of pathogens, termed hemibiotrophs, begins their infection course with the biotrophic stage and shifts to the necrotrophic stage upon reaching a certain threshold of pathogen accumulation2. In order to effectively defend themselves against these microorganisms, plants hav....

Protocol

The following text describes a stepwise protocol to perform optimized Psm ES4326 syringe infiltration assay in Arabidopsis. Major procedures of this assay are represented in a simplified flowchart (Figure 1).

1. Plant Growth Conditions

  1. Sow seeds
    1. Prepare 2 pots (4 in diameter, 3.75 in tall) loosely filled with soil and water pots by soaking them from the bottom O/N before draining the excess water.
    2. Sow 50-100 Arabidopsis see.......

Representative Results

The protocol we describe here represents an optimized P. syringae syringe infiltration assay to quantitatively evaluate the immune response in Arabidopsis plants. As illustrated in Figure 1, the syringe infiltration of Psm ES4326 is followed by pathogen extraction and quantification via serial dilutions and colonies enumeration.

As described in Step 3 within the protocol text, Enhanced Disease Susceptibility (EDS) against Psm ES4326 can be a.......

Discussion

With decreasing available farmland and increasing population, researchers around the world are challenged with pressing needs for crop improvement. The yield can be greatly influenced by various biotic and abiotic stresses. Among them, pathogen infection is one of the leading causes of crop yield reduction, responsible for approximately 12% losses in the U.S. alone45. To resolve this issue, massive research has been conducted in the model Arabidopsis - P. syringae pathosystem to comprehensively charac.......

Disclosures

The authors have nothing to disclose.

Acknowledgements

We thank Dr. Shahid Mukhtar for critiquing the manuscript and Dr. Xinnian Dong for the sample data analysis file. This work is supported by a NSF-CAREER award (IOS-1350244) to KPM and the UAB Biology Department.

....

Materials

NameCompanyCatalog NumberComments
MetroMix 360 GrosouthSNGMM360
Large potsGrosouthTEKUVCC10TC
12x6 InsertsGrosouthLM1206
11x21 Flats with no holesGrosouthLM1020
11x21 Flats with holesGrosouthLM1020H
Vinyl propagation domesGrosouthCW-221
Proteose PeptoneFisher ScientificDF0122-17-4
Potassium Phosphate Dibasic Trihydrate MP Biomedicals151946
Agar Fisher ScientificA360-500
Streptomycin sulfateBio Basic IncSB0494
100x15mm Petri dishesFisher ScientificFB0875713
150x15mm Petri dishesFisher ScientificR80150
Rectangular plateFisher Scientific12-565-450 
MgCl2 HexahydrateBio Basic IncMB0328
GlycerolBio Basic IncGB0232
MgSOBio Basic IncMN1988
1 mL syringeFisher ScientificNC9992493 
KimwipeFisher Scientific06-666-A
Grinding tubes Denville ScientificB1257
Caps for grinding tubesDenville ScientificB1254
Stainless steel grinding ballFisher Scientific2150
96-well plate Fisher Scientific12-556-008
Sodium SalicylateSigma Aldrichs3007-1kg
flg22 (QRLSTGSRINSAKDDAAGLQIA)GenescriptMade to order
elf18 (Ac-SKEKFERTKPHVNVGTIG)GenescriptMade to order
Hole puncherStaples146308
Biophotometer plusEppendorf952000006
PowerGen High-Throughput HomogenizerFisher Scientific02-215-503
Accu spin micro centrifugeFisher Scientific13-100-675
Multichannel pipette (10-100 µl)Eppendorf3122 000.043
Multichannel pipette (30-300µl)Eppendorf3122 000.060
Pipette (20µl)Eppendorf3120 000.038
Pipette tipsFisher Scientific3552-HR
Sharpie permanent markerStaples507130
1.5 mL tubeEppendorf22363204
ForcepsFisher Scientific08-890

References

  1. Glazebrook, J. Contrasting mechanisms of defense against biotrophic and necrotrophic pathogens. Annu. Rev. Phytopathol. 43, 205-227 (2005).
  2. Hammond-Kosack, K. E., Jones, J. D. Plant disease resistance genes.

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Bacterial Leaf InfiltrationArabidopsis ThalianaPseudomonas SyringaePathogen Growth AssaySystemic Acquired ResistanceProgrammed Cell DeathSyringe InfiltrationEnhanced Disease SusceptibilitySalicylic Acid triggered ImmunityMAMP triggered Immunity

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