Rhizobacteria-mediated induced systemic resistance (ISR) in Arabidopsis is not associated with a direct effect on expression of known defense-related genes but stimulates the expression of the jasmonate-inducible gene Atvsp upon challenge
Publication date
1999
Authors
Wees, A.C.M. van
Luijendijk, M.
Smoorenburg, I.
Loon, L.C. van
Pieterse, C.M.J.
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Article
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Abstract
Selected strains of nonpathogenic rhizobacteria from the genus Pseudomonas are capable of eliciting broadspectrum
induced systemic resistance (ISR) in plants that is phenotypically similar to pathogen-induced systemic
acquired resistance (SAR). In Arabidopsis, the ISR pathway functions independently of salicylic acid (SA) but
requires responsiveness to jasmonate and ethylene. Here, we demonstrate that known defense-related genes, i.e.
the SA-responsive genes PR-1, PR-2, and PR-5, the ethylene-inducible gene Hel, the ethylene- and jasmonateresponsive
genes ChiB and Pdf1.2, and the jasmonate-inducible genes Atvsp, Lox1, Lox2, Pal1, and Pin2, are
neither induced locally in the roots nor systemically in the leaves upon induction of ISR by Pseudomonas fluorescens
WCS417r. In contrast, plants infected with the virulent leaf pathogen Pseudomonas syringae pv. tomato
(Pst) or expressing SAR induced by preinfecting lower leaves with the avirulent pathogen Pst(avrRpt2) exhibit
elevated expression levels of most of the defense-related genes studied. Upon challenge inoculation with Pst, PR
gene transcripts accumulated to a higher level in SAR-expressing plants than in control-treated and ISR-expressing
plants, indicating that SAR involves potentiation of SA-responsive PR gene expression. In contrast, pathogen
challenge of ISR-expressing plants led to an enhanced level of Atvsp transcript accumulation. The other jasmonateresponsive
defense-related genes studied were not potentiated during ISR, indicating that ISR is associated with
the potentiation of specific jasmonate-responsive genes.