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75 Integrating Membrane Transport with Male Gametophyte ... - TAIR

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295 A Search for Transcriptional Regulators of Disease Resistance<br />

Natalie Spivey, Dong Wang, Xinnian Dong<br />

Duke University<br />

In response to pathogen attack, the plant activates several different signaling pathways and initiates changes in gene<br />

expression. While some of the transcriptional changes are well characterized and used as markers for the defense response,<br />

questions remain about the regulation of the transcriptional activation and repression events induced by infection. Using<br />

microarray technology, we sought to characterize the changes in gene expression that resulted from infection <strong>with</strong> the<br />

bacterial pathogen Pseudomonas syringae. At five different time points, we infected half of an Arabidopsis leaf <strong>with</strong> either<br />

virulent P. syringae or avirulent P. syringae/avrRpt2. The uninfected half of the leaf was then collected and prepared for<br />

microarray analysis using the Affymetrix GeneChip Arabidopsis ATH1 Genome Array. Using this approach, we were<br />

able to compare each gene’s expression pattern over time. We are currently using these data to search for transcription<br />

factors that regulate the expression changes that result from pathogen infection. We are also looking for potential cisacting<br />

regulatory elements in the promoter regions of genes whose expression pattern is highly correlated.<br />

296 Arabidopsis Virulence of Xanthomonas campestris pv. campestris Mutants Defective in<br />

Secretion Systems<br />

Wenxian Sun, Muthu Venkateshwaran, Andrew Bent<br />

Department of Plant Pathology, University of Wisconsin-Madison, Madison, WI, USA<br />

The bacterial plant pathogen Xanthomonas campestris pv. campestris causes disease in crucifer plants including<br />

Arabidopsis thaliana. We recently showed that Xcc strains that make a flagellin detectable by the Arabidopsis FLS2<br />

RLK nevertheless caused similar disease on FLS2+ and fls2-/fls2- plants (Sun et al., 2006. Plant Cell 18:491). In<br />

Pseudomonas syringae pv. tomato DC3000, both type III secretion and twin-arginine translocation systems were shown<br />

to contribute to virulence and fitness. Xanthomonas campestris pv. vesicatoria virulence was attenuated when the bacteria<br />

were defective in pilus secretion. Here, we explored the contribution of the type III secretion system (TTSS) and twinarginine<br />

translocation (TAT) system to Xcc virulence and fitness using TTSS- and TAT-defective mutants. HrcC and<br />

hrpE genes encode central key components of the type III secretion apparatus. HrcC and hrpE gene deletions caused<br />

different phenotypes in different Xcc strains. Xcc B186 strain virulence on Arabidopsis was greatly attenuated when<br />

TTSS was knocked out while Xcc B305 ΔhrcC strains had similar virulence ability to the isogenic wildtype B305 strain<br />

based on bacterial numbers in infected plants after vacuum infiltration or hydathode inoculation. Xcc mutants defective<br />

in TAT system exhibited similar pleiotropic phenotypes to a Pst DC3000 tatC knockout strain, such as hypersensitivity<br />

to copper. However, unlike Pst DC3000, the twin-arginine translocation system played a trivial role in Xcc virulence, as<br />

tested using two different inoculation approaches. Based on these data, it is speculated that other secretion systems are<br />

likely to exist in Xcc bacteria that contribute significantly to virulence. Mutants defective in other secretion systems are<br />

being made to test our hypotheses. Interestingly, TTSS mutants will also be used to test the function of TTSS virulence<br />

effectors in the suppression of PAMP-induced plant basal defenses.

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