No abstract

Plants sense potential microbial invaders by using patternrecognition receptors to recognize pathogen-associated molecular patterns (PAMPs) 1 . In Arabidopsis thaliana, the leucine-rich repeat receptor kinases flagellin-sensitive 2 (FLS2) (ref.2) and elongation factor Tu receptor (EFR) (ref.3) act as pattern-recognition receptors for the bacterial PAMPs flagellin 4 and elongation factor Tu (EF-Tu) (ref. 5) and contribute to resistance against bacterial pathogens. Little is known about the molecular mechanisms that link receptor activation to intracellular signal transduction. Here we show that BAK1 (BRI1-associated receptor kinase 1), a leucinerich repeat receptor-like kinase that has been reported to regulate the brassinosteroid receptor BRI1 (refs 6,7), is involved in signalling by FLS2 and EFR. Plants carrying bak1 mutations show normal flagellin binding but abnormal early and late flagellintriggered responses, indicating that BAK1 acts as a positive regulator in signalling. The bak1-mutant plants also show a reduction in early, but not late, EF-Tu-triggered responses. The decrease in responses to PAMPs is not due to reduced sensitivity to brassinosteroids. We provide evidence that FLS2 and BAK1 form a complex in vivo, in a specific ligand-dependent manner, within the first minutes of stimulation with flagellin. Thus, BAK1 is not only associated with developmental regulation through the plant hormone receptor BRI1 (refs 6,7), but also has a functional role in PRR-dependent signalling, which initiates innate immunity.PAMPs have key roles as activators of the innate immune response in animals 8 and, analogously, as 'general elicitors' of defence responses in plants [1][2][3][4][5][9][10][11] . We have previously characterized FLS2 and EFR as the pattern-recognition receptors (PRRs) for flagellin (represented by a 22-amino-acid peptide, flg22) and for EF-Tu (represented by the peptides elf18 and elf26, which correspond to its amino terminus), respectively 2-5,10 . Flagellin and EF-Tu rapidly induce a common set of Arabidopsis genes for leucine-rich repeat receptor-like kinases (LRR-RLKs), including FLS2 and EFR themselves 3,11 . This led to the assumption that some of these PAMPinduced LRR-RLKs might encode additional components of PAMP perception or signalling. Using a reverse genetic approach, we tested a collection of insertional mutants in these LRR-RLKs (previously used for identification of the EFR gene 3 ) for responsiveness to flg22 and found that two mutants with insertions in the LRR-RLK gene At4g33430 have reduced sensitivity to flg22 in seedling growth assays (Fig. 1a,b). In more than 10 repetitions of seedling growth assays with these mutants, we always observed a clear reduction (but never a complete loss) of sensitivity to flg22 and flg22-related peptides. By contrast, the mutants seemed to be as sensitive as the wild type to treatment with elf18 in more than five seedling growth assays (Fig. 1b and data not shown).

Plants and animals recognize microbial invaders by detecting pathogen-associated molecular patterns (PAMPs) such as flagellin. However, the importance of flagellin perception for disease resistance has, until now, not been demonstrated. Here we show that treatment of plants with flg22, a peptide representing the elicitor-active epitope of flagellin, induces the expression of numerous defence-related genes and triggers resistance to pathogenic bacteria in wild-type plants, but not in plants carrying mutations in the flagellin receptor gene FLS2. This induced resistance seems to be independent of salicylic acid, jasmonic acid and ethylene signalling. Wild-type and fls2 mutants both display enhanced resistance when treated with crude bacterial extracts, even devoid of elicitor-active flagellin, indicating the existence of functional perception systems for PAMPs other than flagellin. Although fls2 mutant plants are as susceptible as the wild type when bacteria are infiltrated into leaves, they are more susceptible to the pathogen Pseudomonas syringae pv. tomato DC3000 when it is sprayed on the leaf surface. Thus, flagellin perception restricts bacterial invasion, probably at an early step, and contributes to the plant's disease resistance.

A key aspect of the eukaryotic innate immune system is the recognition of pathogen-associated molecular patterns (PAMPs), universally conserved patterns in whole classes of microbes, mediated by germline encoded, nonrearranging receptors, the so-called pattern recognition receptors (PRRs) (Gordon 2002). In vertebrates, the most important PRRs are the Toll-like receptors (TLRs), of which 11 have been identified to date. PAMP recognition through TLRs induces a conserved host defense response including production of inflammatory cytokines and antimicrobials. Furthermore, TLR signaling influences phagocytosis and triggers adaptive immunity (Pasare and Medzhitov 2004;Underhill and Ganter 2004). Mammalian TLR5 influences host susceptibility to infection through recognition of the bacterial flagellin protein, the main subunit building the flagellar structure (Smith et al. 2003).In plants, the paradigm for a PRR is the well-characterized FLS2 receptor kinase Asai et al. 2002;Zipfel et al. 2004). Arabidopsis FLS2 mediates flagellin recognition on the basis of the highly conserved flg22 peptide Chinchilla et al. 2006). Interestingly, the epitope recognized by mammalian TLR5 is different (Smith et al. 2003;Chinchilla et al. 2006). Perception of flg22 by FLS2 leads almost immediately to the generation of reactive oxygen species (ROS), protein phosphorylation, mitogenactivated protein (MAP) kinase signaling, and transcriptional gene induction (Felix et al. 1999;Asai et al. 2002;Zipfel et al. 2004). Recent work has shown that flagellin perception is essential for efficient host defense, since fls2 mutant plants exhibit an enhanced disease susceptibility to bacterial infections . Besides basal immunity, plants contain a specific defense system based on the detection of pathogen-derived race-specific avirulence factors (Avr) through corresponding products of resistance (R) genes. Recently, RIN4, a key regulator of R-gene-mediated defense, has been shown to also modulate flg22 signaling (Kim et al. 2005). Thus, both basal and specific immune signaling pathways in plants appear to be linked.Obviously, TLR signaling needs to be kept in check by negative regulation. Several negative regulators of TLR signaling have been recently described, which function on different levels, for example, through extracellular PAMP scavengers, cytosolic adapter proteins, or transmembrane protein regulators, or by down-regulation of TLR expression (Liew et al. 2005). Although FLS2-triggered immune responses in plants are well characterized, it is not yet clear how FLS2 signaling is attenuated. FLS2 belongs to the large receptor-like kinase (RLK) family with ∼610 members in Arabidopsis (Shiu and Bleecker 2001). One possibility for down-regulating RLK signaling in plants is the kinase-associated protein phosphatase (KAPP), which has been identified to interact with several RLKs including FLS2 Becraft 2002). In addition, since RLKs are structurally related to receptor tyrosine kinases (RTK) in animals (Shiu and Bleecker 2001), mechanisms established for...

Innate immunity is based on the recognition of pathogen-associated molecular patterns (PAMPs). Here, we show that elongation factor Tu (EF-Tu), the most abundant bacterial protein, acts as a PAMP in Arabidopsis thaliana and other Brassicaceae. EF-Tu is highly conserved in all bacteria and is known to be N-acetylated in Escherichia coli. Arabidopsis plants specifically recognize the N terminus of the protein, and an N-acetylated peptide comprising the first 18 amino acids, termed elf18, is fully active as inducer of defense responses. The shorter peptide, elf12, comprising the acetyl group and the first 12 N-terminal amino acids, is inactive as elicitor but acts as a specific antagonist for EF-Tu–related elicitors. In leaves of Arabidopsis plants, elf18 induces an oxidative burst and biosynthesis of ethylene, and it triggers resistance to subsequent infection with pathogenic bacteria

In Arabidopsis, WRKY factors comprise a large gene family of plant-specific transcriptional regulators controlling several types of plant stress responses. To understand the regulatory role of WRKY proteins during such processes, we identified targets of the senescence-and defense-associated WRKY6 factor. WRKY6 was found to suppress its own promoter activity as well as that of a closely related WRKY family member, indicating negative autoregulation. On the other hand, WRKY6 positively influenced the senescence-and pathogen defense-associated PR1 promoter activity, most likely involving NPR1 function. One novel identified target gene, SIRK, encodes a receptor-like protein kinase, whose developmental expression is strongly induced specifically during leaf senescence. The transcriptional activation of SIRK is dependent on WRKY6 function. Senescing leaves of wrky6 knockout mutants showed a drastic reduction, and green leaves of WRKY6 overexpression lines showed clearly elevated SIRK transcript levels. Furthermore, the SIRK gene promoter was specifically activated by WRKY6 in vivo, functioning very likely through direct W-box interactions.

Animals and plants carry recognition systems to sense bacterial flagellin. Flagellin perception in Arabidopsis involves FLS2, a Leu-rich-repeat receptor kinase. We surveyed the early transcriptional response of Arabidopsis cell cultures and seedlings within 60 min of treatment with flg22, a peptide corresponding to the most conserved domain of flagellin. Using Affymetrix microarrays, approximately 3.0% of 8,200 genes displayed transcript level changes in flg22 elicited suspension cultures and seedlings. FLARE (Flagellin Rapidly Elicited) genes mostly encode signaling components, such as transcription factors, protein kinases/phosphatases, and proteins that regulate protein turnover. Approximately 80% of flg22-induced genes were also upregulated in Arabidopsis seedlings treated with cycloheximide. This suggests that many FLARE genes are negatively regulated by rapidly turned-over repressor proteins. Twenty-one tobacco Avr9/Cf-9 rapidly elicited (ACRE) cDNA full-length sequences were used to search for their Arabidopsis orthologs (AtACRE). We identified either single or multiple putative orthologs for 17 ACRE genes. For 13 of these ACRE genes, at least one Arabidopsis ortholog was induced in flg22-elicited Arabidopsis suspension cells and seedlings. This result revealed a substantial overlap between the Arabidopsis flg22 response and the tobacco Avr9 race-specific defense response. We also compared FLARE gene sets and genes induced in basal or gene-for-gene interactions upon different Pseudomonas syringae treatments, and infer that Pseudomonas syringae pv tomato represses the flagellin-initiated defense response.

The plant immune system is activated by microbial patterns that are detected as nonself molecules. Such patterns are recognized by immune receptors that are cytoplasmic or localized at the plasma membrane. Cell surface receptors are represented by receptor-like kinases (RLKs) that frequently contain extracellular leucine-rich repeats and an intracellular kinase domain for activation of downstream signaling, as well as receptor-like proteins (RLPs) that lack this signaling domain. It is therefore hypothesized that RLKs are required for RLPs to activate downstream signaling. The RLPs Cf-4 and Ve1 of tomato ( Solanum lycopersicum ) mediate resistance to the fungal pathogens Cladosporium fulvum and Verticillium dahliae , respectively. Despite their importance, the mechanism by which these immune receptors mediate downstream signaling upon recognition of their matching ligand, Avr4 and Ave1, remained enigmatic. Here we show that the tomato ortholog of the Arabidopsis thaliana RLK Suppressor Of BIR1-1/Evershed (SOBIR1/EVR) and its close homolog S. lycopersicum ( Sl )SOBIR1-like interact in planta with both Cf-4 and Ve1 and are required for the Cf-4– and Ve1-mediated hypersensitive response and immunity. Tomato SOBIR1/EVR interacts with most of the tested RLPs, but not with the RLKs FLS2, SERK1, SERK3a, BAK1, and CLV1. SOBIR1/EVR is required for stability of the Cf-4 and Ve1 receptors, supporting our observation that these RLPs are present in a complex with SOBIR1/EVR in planta . We show that SOBIR1/EVR is essential for RLP-mediated immunity and propose that the protein functions as a regulatory RLK of this type of cell-surface receptors.