Taks, N. W.; van Hulten, M.; van Splunter-Berg, J. A.; Chatterjee, S.; Paauw, M.; Pfeilmeier, S.; van den Burg, H. A.

Bacterial plant pathogens exploit natural openings, such as pores or wounds, to enter the plant interior and cause disease. Plants actively guard these openings through defense mechanisms that have been described extensively for stomates, the most common points of entry. However, bacteria from the genus Xanthomonas have specialized in that they enter their host via hydathodes--a poorly studied organ at the leaf margin involved in guttation. While hydathodes can mount an effective immune response against bacteria, a dedicated perception mechanism still needs to be discovered. To identify a hydathode-specific immune receptor, we mapped a novel resistance gene against X. campestris pv. campestris (Xcc) in Arabidopsis using an inoculation procedure that promotes natural entry via hydathodes. Using Recombinant Inbred Lines (RILs) between susceptible accession Oy-0 and resistant Col-0, a QTL for resistance was identified on the right arm of Chromosome 5 in Col-0. Combining this finding with results of a genome-wide association analysis, a single candidate gene was fine-mapped that encoded a coiled-coil nucleotide-binding leucine-rich repeat (CNL) immune receptor protein called SUPPRESSOR OF TOPP4 1 (SUT1). Whereas the ZAR1 immune receptor acts in the vasculature against Xcc, we establish that SUT1 already restricts Xcc in hydathodes but is ineffective in the vasculature. In corroboration, we confirm promoter activity of SUT1 in the epithem tissue within hydathodes. Altogether, we provide evidence for an NLR that confers hydathode-specific resistance in Arabidopsis against infection by Xcc.