- Research article
- Open Access
AHL-Priming Protein 1 mediates N-3-oxo-tetradecanoyl-homoserine lactone priming in Arabidopsis
BMC Biology volume 20, Article number: 268 (2022)
N-3-oxo-tetradecanoyl-L-homoserine lactone (oxo-C14-HSL) is one of the N-acyl homoserine lactones (AHL) that mediate quorum sensing in Gram-negative bacteria. In addition to bacterial communication, AHL are involved in interactions with eukaryotes. Short-chain AHL are easily taken up by plants and transported over long distances. They promote root elongation and growth. Plants typically do not uptake hydrophobic long sidechain AHL such as oxo-C14-HSL, although they prime plants for enhanced resistance to biotic and abiotic stress. Many studies have focused on priming effects of oxo-C14-HSL for enhanced plant resistance to stress. However, specific plant factors mediating oxo-C14-HSL responses in plants remain unexplored. Here, we identify the Arabidopsis protein ALI1 as a mediator of oxo-C14-HSL-induced priming in plants.
We compared oxo-C14-HSL-induced priming between wild-type Arabidopsis Col-0 and an oxo-C14-HSL insensitive mutant ali1. The function of the candidate protein ALI1 was assessed through biochemical, genetic, and physiological approaches to investigate if the loss of the ALI1 gene resulted in subsequent loss of AHL priming. Through different assays, including MAP kinase activity assay, gene expression and transcriptome analysis, and pathogenicity assays, we revealed a loss of AHL priming in ali1. This phenomenon was reverted by the reintroduction of ALI1 into ali1. We also investigated the interaction between ALI1 protein and oxo-C14-HSL using biochemical and biophysical assays. Although biophysical assays did not reveal an interaction between oxo-C14-HSL and ALI1, a pull-down assay and an indirect method employing biosensor E. coli LuxCDABE support such interaction. We expressed fluorescently tagged ALI1 in tobacco leaves to assess the localization of ALI1 and demonstrate that ALI1 colocalizes with the plasma membrane, tonoplast, and endoplasmic reticulum.
These results suggest that the candidate protein ALI1 is indispensable for oxo-C14-HSL-dependent priming for enhanced resistance in Arabidopsis and that the ALI1 protein may interact with oxo-C14-HSL. Furthermore, ALI1 protein is localized in the cell periphery. Our findings advance the understanding of interactions between plants and bacteria and provide an avenue to explore desired outcomes such as enhanced stress resistance, which is useful for sustainable crop protection.
Being in constant vicinity with microorganisms, plants depend on efficient interaction and perception mechanisms between themselves and the surrounding microbiota. The canonical perception of microorganisms by eukaryotes is based on particular structural molecules or proteins. However, plants evolved also means to respond to bacterial quorum-sensing (QS) molecules. QS allows bacterial cells to communicate with each other; this process is based on the production and detection of diverse autoinducer molecules. These molecules enable bacteria to collectively coordinate behavioral changes to regulate cellular processes like biofilm production, genetic exchange, bioluminescence, motility, sporulation, and virulence, all of which are critical for survival, adaptation, and persistence in a changing environment [1, 2]. Gram-negative bacteria generally orchestrate their cellular behavior via the synthesis of N-acyl homoserine lactones (AHL) [3,4,5]. AHL molecules are comprised of two intrinsic moieties: a core N-acylated homoserine lactone ring and an amide linked acyl side chain ranging from 4 to 18 carbons, often with the hydrogen substituted by a hydroxyl or ketone group on the third carbon position [6,7,8]. Besides orchestrating the communication within bacterial populations, increasing evidence suggests that AHL elicit specific responses in the eukaryotic hosts . Mathesius et al. demonstrated the first evidence of specific AHL responses in Medicago truncatula using a proteomic approach . N-3-oxo-tetradecanoyl-L-homoserine lactone (oxo-C14-HSL) from Ensifer meliloti (Sinorhizobium meliloti) and oxo-C16:1-HSL from Pseudomonas aeruginosa induced auxin response and flavonoid synthesis proteins as well as secretion of small compounds that mimic QS signals that may disrupt QS mechanism in associated bacteria.
Considerable research has been conducted on the impact of different AHL on diverse plants, including physiological and transcriptional changes that influence root and shoot growth. Several studies suggested that the effects of AHL on plants are dependent on the acyl-chain length and AHL concentration. Short-chained AHL molecules, such as N-hexanoyl-L-homoserine lactone (C6-HSL), N-3-oxo-hexanoyl-L-homoserine lactone (oxo-C6-HSL), and N-3-oxo-octanoyl-L-homoserine lactone (oxo-C8-HSL), increased root length in Arabidopsis [11, 12], whereas medium-chained AHL, such as N-decanoyl-L-homoserine lactone (C10-HSL), induced lateral root and root hair formation . However, the root growth-inducing effect of C6-HSL and oxo-C6-HSL was reversed when higher concentrations (> 10 μM) of these AHL were used, as inhibitory effects on root length were observed . The impact of C6-HSL treatment on growth promotion was dependent on auxin signaling processes [12, 15]. AHL-induced augmentation in root length and plant biomass was also observed in wheat, barley, and cucumber [16,17,18]. Besides, N-3-oxo-decanoyl-L-homoserine lactone (oxo-C10-HSL) induced adventitious root formation in mung beans (Vigna radiata) through enhanced transport of basipetal auxin, ensuing in the accumulation of hydrogen peroxide and nitric oxide . Nonetheless, some studies disputed the role of auxin in AHL-mediated modulation of the plant [13, 14].
In addition to modifying plant growth, AHL can prime plants for enhanced resistance against pathogens. Priming induces a physiological state characterized by faster and more robust defense responses when elicited by stress factors. This phenomenon strengthens the plant’s resistance and tolerance to biotic and abiotic stressors. A recent study presented oxo-C8-HSL-induced priming for enhanced resistance in Arabidopsis against Pseudomonas syringae pv. tomato (Pst) . Former results from our group indicate that long-chain AHL oxo-C14-HSL primes plants for enhanced resistance against biotrophic and hemibiotrophic pathogens . Moreover, AHL priming effects were also observed in crop plants, including barley, wheat, and tomato, attributed to oxo-C14-HSL by E. meliloti . C6-HSL-primed wheat seeds induced a transgenerational effect of increased yield and resistance and promoted faster germination and embryo development . Our recent study on complex interactions between the host plant and multiple AHL molecules containing both short-chain and long-chain AHL revealed that combinations of three or more AHL-primed plants for enhanced resistance against Pst, indicating enhanced resistance as a significant result of exposure to multiple AHL in Arabidopsis . Furthermore, AHL-primed plants against abiotic stressors. Arabidopsis treated with oxo-C6-HSL showed increased tolerance to high salt concentrations, probably through both ABA-dependent and ABA-independent signaling pathways [23, 24]. Hydrophilic AHL treatment improved plant stress tolerance through tissue and compound-specific modification of the activity of several antioxidants and detoxifying enzymes . A nanocomposite fertilizer using N-butanoyl-L-homoserine lactone (C4-HSL) coupled with magnetic carbon nanofibers induced growth, tolerance to oxidative and high salinity levels, and enhanced resistance to the fungal pathogen Fusarium oxysporum in chickpeas (Cicer arientinum) .
These findings suggest that plants respond specifically to different AHL molecules, implying specific perception mechanisms. Various components were identified to play a critical role in AHL-mediated responses in plants. C4-HSL-induced transient and instantaneous Ca2+ spiking in Arabidopsis root cells . The transcription factor AtMYB44 and the Arabidopsis growth and development-related protein calmodulin (AtCaM) are required for oxo-C6-HSL-induced root elongation in Arabidopsis [28, 29]. Liu et al. suggested that the G-protein-coupled receptor GCR1 and the canonical Gα subunit GPA1 are required for oxo-C6-HSL and oxo-C8-HSL-mediated root elongation effects in Arabidopsis . Different studies have verified that short-chain AHL molecules are readily taken up by roots and transported to shoots, while long-chain AHL molecules are not systemically transported, most probably due to their lipophilic nature [12, 31, 32]. Although these studies decipher plant components integral for AHL response, no studies have been conducted to decode AHL-interacting proteins in plants.
In this study, we investigated one of such components, a membrane-associated protein required for oxo-C14-HSL-mediated enhanced resistance in plants. We propose that the Arabidopsis protein AHL-Priming Protein 1 (ALI1), previously named AtGALK2 (galactokinase 2) and currently renamed and re-annotated as AtGlcAK2 (glucuronokinase 2), is an integral component of oxo-C14-HSL-mediated AHL priming.
Principal mechanism of AHL-induced priming is missing in ali1
To identify plant factors required for efficient AHL priming, we focused on the gene encoded by the At5g14470 locus since this gene was identified in previous AHL-priming-related studies (data not shown). The At5g14470 locus encodes a putative kinase from the GHMP kinase family, recently named AtGlcAK2 or glucuronokinase 2 and formerly known as AtGALK2 or galactokinase 2. However, because of unclarities in the current annotation and its primary function prediction, we propose to rename it to AHL-Priming Protein 1 (ALI1).
In a first step, to verify if oxo-C14-HSL influences the expression of AtGlcAK2/ALI1, quantitative PCR analysis was carried out with wild-type Col-0 seedlings that were pretreated with 6 µM oxo-C14-HSL for 3 days and subsequently elicited with 100 nM flg22. The results revealed that pretreatment with oxo-C14-HSL had no impact on the expression of At5g14470 locus encoded gene, when compared to the control (acetone)-treated Col-0 plants. However, 2 h after flg22 elicitation, we could observe a twofold increase in AtGlcAK2/ALI1 expression level in the Col-0 plants, irrespective of the pretreatment. Furthermore, the enhanced expression of AtGlcAK2/ALI1 in Col-0 due to flg22 challenge appears to be transient since the expression level returned to the basal level 24 h after flg22 challenge, irrespective of the pretreatment (Additional file 2: Fig. S1). This suggests that AtGlcAK2/ALI1 might play a role in the early response to bacteria.
To further corroborate the role of AtGlcAK2/ALI1 during AHL priming, we used a mutant line with a T-DNA insertion in At5g14470 locus, along with wild-type Col-0. The segregating line N560407 was obtained from Salk Institute and propagated, and a non-segregating line (ali1) was characterized in a PCR approach (Additional file 2: Fig. S2). We performed quantitative PCR and western blot-based kinase assays to verify whether AHL priming depends on the presence of functional AtGlcAK2/ALI1 in Arabidopsis . Higher expression of TLP5 and DFR genes, usually observed upon AHL priming , was missing in the ali1 mutant (Fig. 1a). Furthermore, both Col-0 and the ali1 mutant responded to the flg22 challenge and activated MPK6 transiently. In control Col-0 plants, the phosphorylation on the MPK6 activation loop was detectable 30 min after challenge with 100 nM flg22, but the phosphorylation level declined 60 min post-challenge. No phosphorylation of the activation loop was observed 120 min after the flg22 challenge. On the contrary, oxo-C14-HSL-pretreated plants exhibited enhanced and prolonged activation of MPK6 since the pTEpY epitope was observed until 120 min after the flg22 challenge (Fig. 1b and Additional file 2: Table S1). In ali1 mutant pretreated with either acetone or oxo-C14-HSL, the pattern of MPK6 phosphorylation was identical to control Col-0 plants (Fig. 1b and Additional file 2: Table S1). These results indicate that the AtGlcAK2/ALI1 is required for the oxo-C14-HSL-mediated enhanced and prolonged activation of MPK6 in response to the flg22 challenge in AHL-primed plants.
To determine whether AHL priming reflected by enhanced upregulation of defense-related genes after a challenge [20, 34, 35] is influenced by the absence of ALI1, we assessed genes’ expression using a qPCR approach. Analysis of WRKY22 and WRKY29 expression in Col-0 and ali1 revealed that the seedlings could perceive 100 nM flg22 and elicit a response (Fig. 1d). However, the comparison between Col-0 and ali1 revealed higher transcript abundance in oxo-C14-HSL-pretreated Col-0 seedlings. This difference was missing in the ali1 mutant. Additional expression profiles of GST6 and Hsp70 revealed similar results (Additional file 2: Fig. S3). To comprehensively investigate whether the ali1 mutant responds to oxo-C14-HSL, we carried out an additional whole transcriptome analysis. Using an RNA sequencing approach, we examined differences in gene expression of plants challenged with 100 nM flg22 after priming with 6 µM oxo-C14-HSL using an RNA sequencing approach. Differentially expressed genes were set as showing a log2 fold change of 1 or more and a moderate p < 0.05 (Additional file 3, 4, 5 and 6: Datasets S1-S4). Comparison between control and oxo-C14-HSL-pretreated Col-0 seedlings challenged with 100 nM flg22 revealed upregulation of 441 (Additional file 3: Dataset S1) and downregulation of 28 genes (Additional file 4: Dataset S2). A similar comparison between control and oxo-C14-HSL-pretreated ali1 revealed upregulation of four (Additional file 5: Dataset S3) and downregulation of 66 genes (Additional file 6: Dataset S4) (Fig. 2). Gene Ontology (GO) analysis of Col-0 genes differentially expressed between oxo-C14-HSL-pretreated and control plants, 2 h after the challenge with flg22 showed enrichment of several terms. These are associated with mRNA transcription, movement of cellular components, systemic acquired resistance, cell wall organization, auxin-activated signaling pathway, and cellular response (Fig. 2b). The differentially downregulated genes showed enrichment for GO terms associated with abiotic stimulus related to decreased oxygen levels, temperature, salt, osmotic and oxidative stress in the case of Col-0 (Fig. 2b), and glucosinolate metabolism in the case of ali1. Taken together, the upregulation of defense-related genes, a typical phenomenon in AHL-primed plants, seems to depend on the presence of AtGlcAK2/ALI1.
To assess whether the absence of the AtGlcAK2/ALI1 gene impacts on the oxo-C14-HSL-priming for enhanced resistance, we performed two different Pseudomonas syringae pathovar tomato (Pst)-based pathogen assays. The first assay was performed using the AHL molecule under sterile conditions. Pst proliferated on Arabidopsis leaves from c. 104 colony-forming units (CFU) mg−1 FW leaf (2 h after inoculation) to about 107 CFU mg−1 FW leaf (96 h after the inoculation) (Fig. 3a). However, we observed a reduction in the bacterial CFU number, 96 h after Pst inoculation in Col-0 seedlings that were grown on oxo-C14-HSL-supplemented media when compared to control plants. In contrast to the wild type, no enhanced resistance was observed in the ali1 mutant (Fig. 3a). We performed a similar assay using the oxo-C14-HSL-producing bacterium Ensifer meliloti expR + . In a glasshouse experiment, plants were inoculated three times over 3 weeks with either 10 mM MgCl2 (control), the E. meliloti attM strain unable to accumulate the oxo-C14-HSL molecule (bacterial control), or the E. meliloti expR + strain. Leaves of Col-0 and ali1 were infiltrated with Pst suspension of 2 × 107 CFU ml−1 and the presence of Pst was monitored for 96 h. A significant reduction of the bacterial count was observed only in leaves of Col-0 plants, pretreated with the E. meliloti expR + strain (Fig. 3b). This indicates that the AHL priming for enhanced resistance with oxo-C14-HSL is lost in plants when the AtGlcAK2/ALI1 gene is nonfunctional.
YFP-ALI1 is associated with the plasma membrane, tonoplast, and endoplasmic reticulum
Thereupon, we examined the cellular localization of AtGlcAK2/ALI1. To this end, leaves of 4-week-old tobacco (Nicotiana benthamiana) were infiltrated with a mixture of Agrobacterium tumefaciens GV3101 carrying a plasmid with sequences of YFP-tagged AtGlcAK2/ALI1 and LBA4404 carrying a plasmid with mCherry-tagged gene sequences of proteins that localizes at diverse subcellular locations (Additional file 2: Table S3) . The results revealed that the YFP-ALI1 fusion protein colocalized with the plasma membrane, endoplasmic reticulum (ER), and partially with the tonoplast (Fig. 4) and not with other subcellular organelles including Golgi, nucleolus, plastids, and peroxisome (Additional file 2: Fig. S4) and cell wall as indicated after the plasmolysis (Additional file 2: Fig. S5). Interestingly, we observed no translocation of the YFP-ALI1 fusion protein after an oxo-C14-HSL treatment (Fig. 4).
ALI1 has a strong affinity to the bacterial quorum-sensing molecule, oxo-C14-HSL
In order to assess if bacterial quorum-sensing molecules interact with plant protein(s), we took advantage of the biotinylated derivative of the N-3-oxo-tetradecanoyl-L-homoserine lactone (oxo-C14-HSL) molecule, M4 . We sought to verify the interaction between oxo-C14-HSL and AtGlcAK2/ALI1 using the fusion 6xHis-ALI1 protein and M4. 6xHis-ALI1 protein was retained on beads bound to M4 but not on beads exposed to the biotin control, suggesting positive interaction between the ALI1 and M4 (Fig. 5a). A 6xHis-tagged Salmonella Plasmid Virulence C (SpvC) protein, a virulence protein in Salmonella enterica, was used as a negative control to verify that M4 does not bind to the 6xHis-tag. Modeling the predicted interaction between AtGlcAK2/ALI1 and oxo-C14-HSL revealed that the ligand could interact with the central groove of the protein (Fig. 5b,c and Additional file 2: Fig. S6).
To further assess the potential interaction between AtGlcAK2/ALI1 and oxo-C14-HSL, we performed a microscale thermophoresis (MST) assay. The combined dose–response curve from both experimental replicates indicated no interaction between ALI1 and oxo-C14-HSL in the analyzed ligand concentration range and under the applied experimental conditions (Additional file 2: Fig. S7a). One of the reasons for the low chances of observing a binding event could be the distant location of the dye in respect to the protein–ligand binding site. Therefore, we also examined the influence of oxo-C14-HSL on the thermal stability of AtGlcAK2/ALI1 protein by characterizing its thermal stability and unfolding profile utilizing a nano-differential scanning fluorimetry (nanoDSF) assay. For 6xHis-ALI1, two clear unfolding transitions at 50.88 °C (inflection point #1) and 66.51 °C (inflection point # 2) were observed while for 6xHis-SpvC, one clear unfolding transition at 43.99 °C (inflection point #1) was observed (Additional file 2: Fig. S7b). The presence of oxo-C14-HSL led to a shift of − 1.91 °C (∆ IP #1 column) and − 0.88 °C (∆ IP #2 column) in 6xHis-ALI1 and − 0.80 °C (∆ IP #1 column) in 6xHis-SpvC (Additional file 2: Fig. S7b). Since both proteins (6xHis-ALI1 and 6xHis-SpvC) showed comparable thermal shifts, we concluded that this was probably an artifact. However, thermal shift assays can be biased by unspecific effects such as a change in ionic strength, impurities that increase with increasing ligand concentration, or other unspecific binding events. Both proteins were shown to be destabilized by a ligand molecule implying that interaction between ALI1 and oxo-C14-HSL was not observed under the applied experimental conditions, which led us to an indirect method.
The concentration of free oxo-C14-HSL was monitored in the presence of both 6 nmol 6xHis-ALI1 or 6 nmol 6xHis-LuxR (used as a positive control) and BSA (used as a negative control). Proteins were incubated overnight with different concentrations of oxo-C14-HSL, and the presence of free molecules was monitored using the reporter E. coli strain (E. coli LuxCDABE). As revealed, mock and BSA variants induced about 80 to 100% of the possible lux activity (light production capacity) in the reporter E. coli strain in the presence of 3 nmol oxo-C14-HSL, indicating that the molecule is freely available. Moreover, 3 nmol oxo-C14-HSL seemed to be sufficient to fully induce the LuxCDABE operon. In comparison, the presence of 6 nmol 6xHis-LuxR from E. meliloti or 6 nmol of 6xHis-ALI1 from Arabidopsis in the system inhibited the induction of the LuxCDABE operon significantly. This inhibition was observable until the 9 nmol oxo-C14-HSL variant. In the presence of 6 nmol oxo-C14-HSL (equimolar amount), 50% of the possible LuxCDABE-originated luminescence was observed. We concluded, therefore, that LuxR (the native oxo-C14-HSL receptor from E. meliloti) and AtGlcAK2/ALI1 are equivalently able to sequestrate oxo-C14-HSL molecule from the solution (Fig. 5d).
AHL-induced priming is restored in complemented ali1 and ALI1-dependent phenotypes are oxo-C14-HSL specific
In order to assess if the reintroduction of the AtGlcAK2/ALI1 gene restores oxo-C14-HSL-dependent phenotypes, we performed gene expression analysis and Pst assay using homozygous ali1 lines expressing Myc-tagged ALI1 under the 35S promoter (35S::10xMyc-ALI1); line #10–2 and #10–19 together with an outcrossed line #10–3 (used as a negative control) (Additional file 2: Fig. S8). The expression patterns in both complemented #10–2 and #10–19 and the outcrossed (non-complemented) line #10–3 revealed that all seedlings responded to the flg22 challenge (Fig. 6a–c). Furthermore, expression levels of defense-related WRKY22, WRKY29, and GST6 genes 2 h after flg22 challenge in the complemented #10–19 line, and WRKY22, WRKY29 in the #10–2 line showed higher transcript abundance when pretreated with oxo-C14-HSL (Fig. 6a–c). This difference was missing in the outcrossed line #10–3. Similarly, the Pst assay validated that reintroducing AtGlcAK2/ALI1 gene into the ali1 mutant reinstates the ability of AHL priming. We observed a reduction in the proliferation of Pst in oxo-C14-HSL-treated plants compared to control plants in Col-0, 96 h after inoculation (Fig. 6d). Furthermore, we observed a similar reduction in Pst proliferation in complemented lines, #10–2 and #10–19 after an oxo-C14-HSL pretreatment, indicating enhanced resistance due to AHL priming (Fig. 6d). This reduction was missing in the non-complemented line #10–3 since no difference in the CFU count between the treatments was observed (Fig. 6d). These results suggest that reintroducing AtGlcAK2/ALI1 into the ali1 background restores the ability of AHL priming.
Finally, we aimed to investigate if ALI1-dependent phenotypes are specific to oxo-C14-HSL. Our previous reports described AHL-induced growth promotion in plants treated with a short-chained AHL molecule, C6-HSL [20, 22]. We performed, therefore, a root growth assay on 1-week-old Col-0 and ali1 seedlings on ½-strength MS agar supplemented with either 6 µM oxo-C14-HSL or 6 µM C6-HSL. The plants were grown vertically to observe the root growth for 4 weeks. We observed that C6-HSL treatment enhanced root length in Col-0 (Fig. 7a). Moreover, we observed a similar phenomenon of longer roots upon C6-HSL treatment in ali1 seedlings (Fig. 7a). There was no significant difference in the root length of both Col-0 and ali1 seedlings between control and oxo-C14-HSL treatments (Fig. 7a). Similarly, we also observed that both Col-0 and ali1 seedlings growing on plates containing 6 µM C6-HSL had higher biomass (Fig. 7b). Taken together, the influence of short-chained AHL molecules on plant growth does not seem to depend on the presence of functional AtGlcAK2/ALI1.
In this study, we presented several levels of evidence that ALI1 encoded by the At5g14470 locus is required for oxo-C14-HSL-induced priming for enhanced resistance. ALI1 is a putative protein kinase belonging to the GHMP (galactose, homoserine kinase, mevalonate kinase, phosphomevalonate kinase) super kinase family protein. This protein was formerly annotated as galactokinase 2 (AtGALK2) and was proposed to catalyze the phosphorylation of α-D-galactose (Gal). However, the only galactokinase in Arabidopsis is encoded by another locus At3g06580 . Here, we propose that the currently annotated as glucuronokinase 2 (AtGlcAK2) protein, supposedly an isoform of glucuronokinase 1 (AtGlcAK1), which catalyzes the phosphorylation of D-glucuronic acid, should be renamed to ALI1. Pieslinger et al. demonstrated that amino acid sequences of both proteins encoded by the At3g01640 locus (AtGlcAK1) and the At5g14470 locus are highly homologous, predicting the latter gene to be the second isoform of glucuronokinase, AtGlcAK2 . Another study on AtGlcAK1 by the same group suggested that the ineffective loss of function of glcak1 mutants was probably due to the activity of the other isoform, AtGlcAK2 . However, enzymatic analysis has yet to confirm the protein function of AtGlcAK2. Despite being highly homologous to the AtGlcAK1, there is no evidence that AtGlcAK2 has glucuronokinase activity of catalyzing the phosphorylation of D-glucuronic acid. According to another study, the gene encoded by At5g14470, which was erroneously designated as AtGALK2 in this study, is involved in root and flower development, the abscisic acid signaling pathway, and stress response influencing the expression of various ABA-related genes . Nonetheless, we propose a new function for this protein based on our experimental findings.
Previously, Thomanek et al. demonstrated that the biotin-tagged oxo-C14-HSL probe directly interacts with the bacterial LuxR-type receptor. Here, we used the biotin-tagged probe for a pull-down assay with Arabidopsis proteins . Additional pull-down assay with a His-tagged ALI1 revealed that ALI1 indeed might interact with oxo-C14-HSL. Other binding assays, such as the MST and nanoDSF assays, could not confirm the interaction. However, it does not rule out the possibility of interaction since we could ensure an oxo-C14-HSL-sequestering ability of AtGlcAK2/ALI1 using an indirect technique based on the detection of free oxo-C14-HSL by the bacterial biosensor E. coli LuxCDABE.
MAPKs translate extracellular signal perception into intracellular responses [42, 43]. They are also linked to priming in plants, as AHL priming for enhanced resistance resulted in robust and extended activation of MAP kinases in Arabidopsis and barley [20, 34, 35, 44]. Furthermore, several genes, including the WRKY transcription factors WRKY22 and WRKY29, GST6, and Hsp70, are upregulated during oxo-C14-HSL-priming in Arabidopsis [22, 33, 35]. Our current findings are consistent with these studies, as oxo-C14-HSL-primed wild-type Col-0 showed stronger and prolonged activation of MAP kinases and increased expression of mentioned genes. The ali1 mutant showed neither increased kinase activity nor an augmented expression of defense-related genes, both hallmarks of AHL priming. The enhanced resistance against pathogens in Arabidopsis and other crop plants, including barley and tomato, induced by the Ensifer meliloti was attributed to oxo-C14-HSL produced by E. meliloti [21, 35, 45]. Similarly, the pathogenicity assay with Pseudomonas syringae pv. tomato (Pst) indicated that the AHL priming for enhanced resistance is absent in plants lacking functional ALI1. Nonetheless, AHL priming is restored by reintroducing the ALI1 gene into the ali1 mutant, as we observed enhanced resistance against Pst in complemented plants after AHL priming but not in outcrossed lines. Therefore, we concluded that the presence of functional ALI1 is required for oxo-C14-HSL-induced priming for enhanced resistance.
A previous study from our group found that oxo-C14-HSL-priming increased the expression of genes involved in Ca2+ signaling, G-proteins, defense, cell wall, and flavonoid metabolism using transcriptomic approaches . Furthermore, in response to flg22, oxo-C14-HSL-primed Col-0 showed upregulation of genes associated with systemic acquired resistance, cell wall organization, auxin-activated signaling pathway, and movement of cellular components while downregulation of genes related to abiotic stimulus such as temperature, salt, decreased oxygen levels, and osmotic and oxidative stress. In ali1 mutants, however, none of those GO terms were regulated, while genes involved in glucosinolate metabolism were downregulated. Overall, the upregulation of defense-related genes, a typical phenomenon in AHL-primed plants, appears to depend on the presence of ALI1.
YFP-ALI1 colocalizes with the endoplasmic reticulum (ER), tonoplast, and the plasma membrane (PM). PM and ER, in particular, contain components essential for signal transduction and homeostasis regulation. ER-PM contact sites (EPCS) are functional signaling hubs formed when ER anchors and couples with PM . Since there was no translocation of ALI1 observed after an oxo-C14-HSL treatment, signal transduction is most likely mediated by the activity of ALI1 or its interacting proteins rather than translocation. Although the actual downstream events are unknown, several components have already been proposed for other AHL molecules. A previous study found that in Arabidopsis, oxo-C6-HSL and oxo-C8-HSL induce root elongation by activating the G-protein-coupled receptors GCR1 and GPA1 . Furthermore, the transcription factor AtMYB44 and the Arabidopsis growth and development-related protein calmodulin (AtCaM) are involved in oxo-C6-HSL-induced root elongation in Arabidopsis [28, 29]. Those specific components are, however, most likely involved in response to a particular, in this case, short-chained AHL molecule(s) and are not required for ALI1-mediated responses to oxo-C14-HSL.
We presented here evidence from several levels that AtGlcAK2/ALI1 is required for the oxo-C14-HSL-induced primed state in Arabidopsis. Different physiological assays used in this study with ali1 mutant show that the plant responses to flg22 elicitor are similar to naïve plants despite oxo-C14-HSL treatment. A plant’s ability to be primed with oxo-C14-HSL is entirely lost in the absence of a functional ALI1 gene as only AHL-primed wild-type Arabidopsis exhibited enhanced resistance against Pst, while the mutant did not. However, this phenomenon was reverted once the candidate gene was reintroduced into the mutant, as was shown by the expression of priming marker genes and pathogenic assays with Pst. The current study shows that the candidate protein ALI1 might interact with oxo-C14-HSL. Although biophysical assays did not demonstrate the interaction between oxo-C14-HSL and ALI1, pull-down assay and indirect technique using biosensor E. coli LuxCDABE successfully substantiated that the candidate protein ALI1 might interact with oxo-C14-HSL. Transcriptomic analysis showed that flg22 elicitation of AHL-primed wild-type Col-0 plants resulted in enhanced expression of genes involved in systemic acquired resistance, cell wall organization, and auxin-activated signaling pathway while downregulated genes were related to the abiotic stimulus. However, AHL pretreatment did not have any impact on the ali1 mutant. Furthermore, assessing the localization of the candidate protein in plants showed that the ALI1 proteins are localized in the ER, PM, and tonoplast. This study will enable identifying AHL priming mechanisms and different plant factors that mediate AHL priming after AHL perception, which could be exploited through plant breeding and novel genetic technologies to improve AHL priming effects in plants. From a larger perspective, this research will help us uncover another layer of coevolutionary inter-kingdom communication between plants and bacteria, which involves quorum sensing molecules that confer plant benefits by priming plants for enhanced resistance.
Plant materials and growth conditions
Seeds from wild-type Arabidopsis thaliana Col-0 and the ali1 (N560407; At5g14470) mutant obtained from the Salk Institute, as well as complemented (pGWB21; 35S::10xMyc-ALI1) and outcrossed lines, were used in the study. Seed sterilization and Arabidopsis growth were carried out as was described in Shrestha et al. . For the MAP kinase assay, gene expression analysis, and RNA sequencing approaches, 2-week-old seedlings were transferred to six-well plates with 3 ml ½-strength MS medium prior to pretreatment with N-acyl homoserine lactone (AHL). Root growth assay and sterile Pseudomonas syringae pathogenicity assay were performed as described in Shrestha et al. , except for AHL molecules used. For non-sterile P. syringae pathogenicity assay and ali1 mutant complementation, 2-week-old seedlings were transferred to pots with standard bedding soil (Fruhstorfer Erde: Perlite (1:1)) and grown under short-day conditions at 8 h:16 h (light: dark) photoperiod at 22 °C for another 3 weeks in the glasshouse. Six-week-old plants were grown under long-day conditions (light:dark 16 h:8 h and 22 °C photoperiod, light intensity of 150 µmol m−2 s−1 and 60% humidity) to induce flowering.
Characterization of ali1 mutant
For genotyping of the T-DNA insertion ali1 mutants, PCR-based screening was performed for knockout mutation. Genomic DNA was extracted from wild type Col-0, mutant ali1 and T-DNA insertion mutant that were growing on soil for 3 weeks using Qiagen DNeasy Plant Mini Kit following the manufacturer’s protocol. The first PCR was performed with left border primer LBb1-3 and gene-specific forward primer (Additional file 2: Table S1). The band was observed only in ali1 mutant and not in the other T-DNA insertion mutant and wild-type Col-0 indicating that T-DNA was indeed inserted in ALI1 locus (Additional file 2: Fig. S2). Similarly, the second PCR that was performed with ALI1 gene-specific primers (Additional file 2: Table S1) resulted in the band in wild-type Col-0 and T-DNA insertion mutant but not in ali1 mutant validating that there is a modification in the gene (Additional file 2: Fig. S2). Furthermore, third PCR was carried out with ALI1 cDNA-specific primers (Additional file 2: Table S1) to verify whether the transcription of ALI1 gene was impeded or not. The band was seen in cDNA of Col-0 pretreated with both oxo-C14-HSL and acetone control but not for ali1.
Pretreatment with AHL
Pretreatment with AHL was conducted as in Shrestha et al. , except for the AHL molecules used. N-hexanoyl-L-homoserine lactone (C6-HSL) and N-3-oxo-tetradecanoyl-L-homoserine lactone (oxo-C14-HSL) (Sigma-Aldrich) at concentrations as indicated were used in this study.
MAP kinase activity assay
Arabidopsis seedlings Col-0 and ali1 (N560407) mutant were pretreated with 6 µM oxo-C14-HSL or acetone for 3 days and collected 0, 30, 60, or 120 min after eliciting with 100 nM flg22 peptide. Protein extraction from Arabidopsis seedlings and western blotting were performed as in Shrestha et al. .
Gene expression analysis
Wild-type Col-0 and ali1 (N560407) Arabidopsis seedlings pretreated with oxo-C14-HSL were harvested at 0, 2, 4, 6, 24, and 48 h post 100 nM flg22 treatment. Extraction of RNA and synthesis of cDNA was carried out as described in Shrestha et al. . Quantitative RT-PCR (qPCR) was performed using primers listed in Additional file 2: Table S2 [20, 47]. All expression levels were normalized to the expression of Ubiquitin ligase (At5g25760).
cDNA library construction, sequence processing, and transcriptome analysis
We performed transcriptome analysis of Col-0 and ali1 seedlings that were pretreated for 3 days with 6 µM oxo-C14-HSL or acetone control and subsequently elicited with 100 nM flg22 in order to determine the differences in their defense responses. All treatments were performed in triplicates. RNA was isolated from Arabidopsis seedlings using RNeasy Plant Mini Kit (Qiagen) according to the manufacturer’s recommendations. One microgram of total RNA was taken for DNAse digestion using the PerfeCTa DNAse I (Quanta Biosciences), and subsequently, cDNA synthesis was carried out using the qScript cDNA Synthesis kit (Quanta Biosciences) according to the manufacturer’s recommendations. Library construction and sequencing were performed on BGISEQ-500 (BGI Tech Solutions, Hong Kong). Raw sequencing reads were cleaned by removing adaptor sequences, reads containing poly N-sequences and low-quality reads. The cleaned sequence reads (100 bp single end) were analyzed using RNAStar (Version 2.4.0d-2) , cufflinks (Version 22.214.171.124), cuffmerge (Version 126.96.36.199), and cuffdiff (Version 188.8.131.52) . The FPKM (fragments per kilobase million) and the significant differences between transcriptional profiles of Arabidopsis seedlings Col-0 and ali1 between the treatments were calculated based on q-value < 0.05 and fold change > 2 (Additional file 3, 4, 5 and 6: Dataset S1-S4). Significantly enriched genes related to specific GOs (Gene Ontology) were identified using web-based tool PANTHER (http://geneontology.org) using the PANTHER Overrepresentation Test (Released 2020–02-14), Arabidopsis thaliana (TAIR), GO biological process complete, and Fisher’s exact test with false discovery rate (FDR). The raw data were uploaded to GEO NCBI Sequence Read Archive with the number GSE156726. The Euler diagram was created using the R package “eulerr” .
Inoculation with Ensifer meliloti strains
Ensifer meliloti Rm2011 expR + (M. McIntosh) and E. meliloti Rm2011 (pBBR2-attM) carrying the lactonase gene attM from Agrobacterium tumefaciens  were grown in Tryptone Yeast extract (TY) medium until the OD600 reached 0.6–0.8. Bacterial cultures were centrifuged at 2500 g for 10 min and resuspended in 10 mM MgCl2. The rhizosphere of Arabidopsis was inoculated three times over 3 weeks with 10 ml of OD600 = 0.1 using: E. meliloti expR + , E. meliloti attM culture solution or 10 mM MgCl2 as control. The production of AHL on the root surface as well as establishment of the bacteria was previously demonstrated by .
Challenge with Pseudomonas syringae
Pseudomonas syringae pv. tomato DC3000 (Pst) pathogen assay on sterile Arabidopsis was performed as in Shrestha et al. . The bacterial culture was adjusted to OD600 = 0.1. For Pst challenge on non-sterile condition, 3 days after the last inoculation with E. meliloti or MgCl2, four leaves from each treated plant were infiltrated with Pst inoculation solution adjusted to OD600 = 0.02. The leaves were infiltrated with Pst using a needleless syringe and four-leaf discs were collected from two leaves at 12, 48, and 96 h post infiltration. The leaf discs were homogenized in 10 mM MgCl2 and subsequently diluted. Duplicates of the dilution were plated on King’s B agar plates containing selective antibiotics to assess the colony-forming units (CFU) number.
Assessment of localization of ALI1
To assess the subcellular localization of ALI1, ALI1 ORF was subcloned into pGWB441 vector containing yellow fluorescent protein (YFP) gene and the Cauliflower Mosaic Virus (CaMV) 35S promoter and transformed into NEB 5-alpha Competent E. coli (New England Biolabs). Cloned vector extracted from transformed E. coli DH5α was used to transform competent Agrobacterium tumefaciens GV3101. YFP-tagged ALI1 in A. tumefaciens GV3101 along with several A. tumefaciens LBA4404 containing mCherry-tagged gene sequence of proteins (Additional file 2: Table S3) that localizes at different subcellular organelles were grown overnight in 5 ml LB liquid medium with selective antibiotics at 28 °C. The bacterial cultures were centrifuged at 2500 g for 10 min, resuspended with infiltration buffer at final OD600 of 0.05, and infiltrated into leaves of 4-week-old tobacco (N. benthamiana) plants. Equal OD600 0.05 of A. tumefaciens GV3101 containing YFP-tagged ALI1 and A. tumefaciens LBA4404 containing mCherry-tagged gene sequence of a protein that localizes at a subcellular organelle were mixed in infiltration buffer and infiltrated on the abaxial side of the leaves with 1-ml needleless syringe. The infiltrated leaves were visualized for protein localization on confocal laser scanning microscopy (CLSM) 2 to 3 days after infiltration. YFP was observed using 514 nm Ex and 520–550 nm Em range, and mCherry using 560 Ex and 570–600 Em settings.
Localization of ALI1 upon oxo-C14-HSL treatment
In order to assess a possible relocalization of ALI1 upon oxo-C14-HSL treatment, the leaves that were pre-infiltrated for 24 h with A. tumefaciens mix solution were infiltrated again with 6 µM oxo-C14-HSL. Similarly, acetone on infiltration buffer was used as a control. The infiltrated leaves were visualized for ALI1 localization 1 and 2 days after the infiltration with oxo-C14-HSL.
ALI1 expression and purification
Gateway destination vector pDEST17 subcloned with ALI1 ORF was transformed into E. coli BL21 competent cells (New England Biolabs). Colonies were screened and selected with gene-specific and vector-specific primers (Additional file 2: Table S1). Positive colonies were grown in 50 ml of LB containing 100 mg ml−1 ampicillin at 37 °C until OD600 reached 0.6. The expression of the protein was induced by adding 1 mM isopropyl β-D-1-thiogalactopyranoside (IPTG) overnight at room temperature (RT). All further steps were carried out at 4 °C or on ice. Bacterial cells were collected and centrifuged at 7379 g for 15 min and lysed through sonication with ice-cold lysis buffer (50 mM Tris–HCl, 300 mM NaCl, 0.1% Triton-X, DNase, lysozyme supplemented with protease inhibitor (Roche) and thereafter centrifuged at 14,462 g for 10 min. The resulting supernatant was added to a solution containing nickel resin beads (HisPur™ Ni–NTA Resin, Thermo Fisher Scientific) and binding buffer (50 mM sodium phosphate buffer at pH 8, 500 mM NaCl, 10 mM imidazole, 2.5% glycerol) for 30 min with continuous rotation. Lysate-bead mix was subsequently transferred to column and washed 5 times with washing buffer (50 mM sodium phosphate buffer at pH 8, 500 mM NaCl, 20 mM imidazole, 2.5% glycerol) and eluted with elution buffer (50 mM sodium phosphate buffer at pH 8, 500 mM NaCl, 250 mM imidazole, 2.5% glycerol). The concentration of 6xHis-tagged proteins was quantified using Bradford assay (Roti-Quant, Roth). E. coli BL21 transformed with pDEST17-SpvC was used as a 6xHis-tagged protein control.
Pull-down and binding assays
The interaction of ALI1 protein with oxo-C14-HSL was verified by pull-down assay. 6xHis-tagged ALI1 and 6xHis-tagged control protein were incubated with streptavidin beads (Sepharose® Bead Conjugate, Cell Signaling Technology) that were already loaded with M4 (oxo-C14-HSL tagged with biotin) or biotin control and incubated overnight before washing with washing buffer. The final bead-bound protein fractions were eluted with Laemmli buffer (62.5 mM Tris–HCl (pH 6.8), 2% SDS, 10% glycerol, 0.01% bromophenol blue) containing 2% β-mercaptoethanol and subjected to western blotting.
Thirty microliters of streptavidin beads were blocked using blocking buffer (0.05% (w/v) BSA in 100 mM phosphate buffer at pH 7.4) for half an hour at RT and further loaded with 60 mM biotin or 60 mM biotin-labeled oxo-C14-HSL (M4) for 30 min and centrifuged at 67 g for 1 min. After removal of supernatant, 100 µg 6xHis-tagged proteins were added and incubated overnight at constant stirring at 4 °C. After the beads were washed five times with blocking buffer, bound proteins were eluted by adding 40 µl of Laemmli buffer and heated at 95 °C for 5 min. Twenty microliters of eluted protein samples was separated on SDS gel (12%) and transferred to PVDF membrane (Immun-Blot® PVDF, Bio-Rad) through semi-wet blotting protocol. The membranes were blocked with 5% fat-free milk and subsequently probed with primary antibodies 6xHis Tag Monoclonal Antibody (Invitrogen) followed by incubation with horseradish peroxidase-labeled secondary antibody. Blots were developed using ServaLight chemiluminescent substrate (SERVA).
To verify the binding capacity of ALI1 to oxo-C14-HSL, we used an additional indirect technique based on the detection of free oxo-C14-HSL by the bacterial biosensor E. coil LuxCDABE. We used BSA as a negative control and the E. meliloti-originated LuxR receptor as purified His and GST versions, as positive control, and the ALI1, purified as GST-ALI1 and 6xHis-ALI1 fusion proteins. Six nanomoles of each protein was used. The oxo-C14-HSL was added in a range from 0 to 18 nmol and incubated with proteins overnight. Unbound oxo-C14-HSL was detected after overnight incubation using the bacterial biosensor E. coli LuxCDABE, as described in Schenk et al. .
Microscale thermophoresis (MST) binding assay
Preceding to MST bioassay, both proteins (6xHis-ALI1 and 6xHis-SpvC used as His-tagged protein control) were labeled with Red-Tris-NTA fluorescent dye and diluted into the labeling buffer (50 mM phosphate buffer at pH 8.0, 150 mM NaCl, 0.005% Tween-20, and 0.16% acetone) to reach the labeling concentration of 0.2 µM. After labeling, dye removal was not required as all dye molecules were bound by a protein due to labeling stoichiometry and, therefore, no free dye was present in the labeling batch. The final concentration of total protein and fluorescence was 200 and 100 nM respectively. Premium-coated capillaries were chosen for further experiments as no adhesion of both labeled proteins was observed. The intrinsic MST noise of both labeled proteins was acceptably low (< 5.0 units) under the applied experimental parameters and the used assay buffer. MST binding assay was performed on Monolith NT.115 Pico (red-nano) at 25 °C, with 90% LED power and 40% laser power. Five microliters of the fluorescent target proteins was used at constant 50 nM where 5 µl of the ligand oxo-C14-HSL was titrated from 100 µM down in 16 (1:1 dilution) steps. To ensure reproducibility, measurements were taken repeatedly on two independent experiments. The data were analyzed by ligand concentration (mol l−1) against normalized fluorescence of labeled proteins. Curve fitting were performed by using the KD fit derived from the law of mass action according to the binding model, and the affinity is calculated and stated as EC50 or KD values. The amplitude of the binding curve was assessed and signal to noise ratio which is amplitude divided by noise. Noise is standard deviation of difference between experimental data and fitted data.
Nano-differential scanning fluorimetry (nanoDSF) assay
Prior to nanoDSF assay, both protein samples (6xHis-ALI1 and 6xHis-SpvC used as His-tagged protein control) and ligand oxo-C14-HSL were diluted in assay buffer (50 mM phosphate buffer at pH 8.0, 150 mM NaCl, 0.005% Tween-20 and 0.167% acetone) to have a final concentration of 5 and 100 µM respectively. The experiments were performed on a Prometheus NT.48 device equipped with additional back reflection options for detection of target protein aggregation via light scattering method. The temperature of the assay ranged from 20 to 95 °C with heating speed of 1 °C min−1. The analysis method of ratio 350/330 nm for protein unfolding (Tm) was used, and data were analyzed using the PR.StabilityAnalysissoftware from Nanotemper Technologies. The thermal denaturation of the target proteins were monitored via its intrinsic tryptophan fluorescence. Thermal shift was calculated by assessing difference of melting temperatures (Tm) between ligand-bound and apo-state of a protein.
In silico screening for docking of oxo-C14-HSL against ALI1 (At5g14470)
The sequence of the ALI1 (AtGlcAK2) protein was obtained from TAIR, and the best predicted model of ALI1 was generated using i-TASSER server (https://zhanglab.ccmb.med.umich.edu/I-TASSER/) . Similarly, 3D conformer of the ligand oxo-C14-HSL was retrieved from PubChem Structure . The 3D structure of both protein and ligand was visualized using UCSF Chimera  where the model was prepared for docking in order to attain a clean protein model for further analysis. Docking simulations of ALI1 protein and oxo-C14-HSL ligand was performed in SwissDock (http://www.swissdock.ch/docking) , a web server that provides prediction of molecular interaction between the ligand and the target protein. The “docking type” was set to accurate type and “Definition of the region of interest” was set to default and so was “flexibility” which allows flexibility for side chains within 0 Å of any atom of the ligand in its reference binding mode. The binding modes were scored using their FullFitness and clustered, of which they were ranked on the basis of the average FullFitness of their elements . The prediction file from SwissDock was further inspected in UCSF Chimera, and the chimera model with the lowest energy was selected for the identification of amino acid residues that were at a distance of less than 5 Å from each atom of the ligand.
ALI1 ORF sequence (At5g14470) was amplified from cDNA of Col-0 Arabidopsis using ALI1-specific primers (Additional file 2: Table S1). Subsequently, ALI1 ORF sequence was supplemented with attB sites using sequence-specific primers containing attB sites (Additional file 2: Table S1). Thereafter, the PCR product was purified using PEG precipitation protocol . BP clonase recombination reaction was performed to subclone ALI1 into the pDONR207 vector using Gateway® BP Clonase™ II Enzyme Mix following the manufacturer’s protocol. NEB 5-alpha Competent E. coli (New England Biolabs) cells were transformed with the product of recombination reaction using the heat shock method. Colony PCR was performed using DNR3 and DNR5 primers and amplicons were digested with BamHI and ran on a gel for further analysis. Positive constructs were sent for sequencing. LR clonase recombination reaction was performed to insert ALI1 ORF into different destination vectors (pGWB21 or pGWB441) using Gateway™ LR Clonase™ II Enzyme Mix following the manufacturer’s protocol. Different destination vectors were used for the study. For protein expression and purification, pDEST17 was used whereas pGWB441 was used for cellular localization studies.
Complementation of ali1 mutant
For complementation of the ali1 mutant (N560407), pGWB21 (35S, N-ter 10xMyc) destination vector was used. Competent E. coli DH5α was transformed with the product of LR recombination reaction using heat shock method. Colony PCR was performed using vector and gene-specific primers (Additional file 2: Table S1) and obtained constructs were verified via sequencing. A. tumefaciens strain GV3101 was transformed with the desired vector constructs by electroporation, and selection of the positive colonies was performed through colony PCR using vector and gene-specific primers (Additional file 2: Table S1). The positive cells were used to transform the ali1 mutant using the floral-dip method. Seeds of the ali1 mutant were first surface sterilized and grown on ½-strength MS media plates for 2 weeks and later transferred on standard bedding soil (Fruhstorfer erde: Perlite (1:1)). The 2-week-old seedlings were grown on controlled condition (day/night 8/16 h and 22 °C photoperiod, light intensity of 150 µmol/ m−2 s−1 and 60% humidity) in a growth chamber for 2 months before transferring them to the greenhouse condition (day/night 16/8 h and 22 °C photoperiod, light intensity of 150 µmol m−2 s−1 and 60% humidity) until flowering. A. tumefaciens GV3101 strains containing ALI1 ORF in pGWB21 was grown overnight in LB medium containing selective antibiotics. Two hundred fifty microliters of pre-culture was inoculated on 250 ml LB medium containing selective antibiotics and was grown overnight at 28 °C until the O.D600 reached 1. The culture was collected and centrifuged at 2500 g for 10 min at RT. The pellets were resuspended in 250 ml of 5% sucrose solution, and Silwet L-77 was added at a concentration of 0.02%. Floral-dip method  was employed to stably transform the ali1 mutant. Inflorescences were dipped into the Agrobacterium suspension for 30 s. The plants were then covered with a hood for 48 h and left to grow in the greenhouse under long-day conditions. Watering of the plants was stopped after the first pods began to dry. Seeds were harvested after complete drying of the inflorescences, and seeds were selected on selective ½-strength MS medium plates. The seedlings growing on selective plates were transferred on soil pots and later genotyped in order to identify the positive heterozygous complemented lines (T0). The positive complemented lines were self-pollinated and the generated seeds (F1) were checked for homozygosity using gene-specific and tag-specific primers (Additional file 2: Table S1).
Western blot on complemented ali1 lines
Arabidopsis seedlings Col-0, complemented ali1 (N560407) mutants #10–2 and #10–19, and outcross line #10–3 were first grown on ½-strength MS plates for 2 weeks and then transferred on soil pots. The plants were grown for additional 4 weeks and one leaf was collected and homogenized. Proteins were extracted from homogenized plant samples using Laemmli buffer (62.5 mM Tris–HCl (pH 6.8), 2% SDS, 10% glycerol, 0.01% bromophenol blue) further supplemented with Triton-X (10%) and additional SDS (4%). The homogenized plant samples were vortexed vigorously, subsequently cooked at 95 °C for 10 min and briefly centrifuged. Fifteen microliters of total protein was run on SDS gel (12%) and transferred to PVDF membrane through semi-wet blotting protocol. The membranes were blocked with 5% w/v fat-free milk and thereafter probed with primary antibody Myc-tag antibody (Chromotek GmbH), followed by incubation with horseradish peroxidase-labeled secondary antibody Anti-rat IgG (Cell Signaling Technology). Blots were developed using chemiluminescent substrate (ServaLight Vega Luminol solution, SERVA).
All experiments were performed with at least three independent biological replicates. The GENMOD procedure from SAS 9.4 (SAS Institute Inc., Cary, NC, USA) was used for the analysis of variance. For multiple comparisons in root growth assay, the p-value was adjusted by the method of Tukey’s honestly significant difference (HSD) post hoc test. The class variable was treatment (C6-HSL, oxo-C14-HSL and acetone control). Quantitative PCR assays were performed in four biologically independent experiments and Pst assays were performed in three biologically independent experiments. p values < 0.05 in Student’s t test were considered as indicative for a significant difference. Western blot analysis was performed in three independent experiments, representative blot is shown.
Availability of data and materials
All data generated or analyzed during this study are included in this published article, its supplementary information files (Additional files 1, 2, 3, 4, 5 and 6) and publicly available repositories. The raw sequences of transcriptome analysis were uploaded to Gene Expression Omnibus (GEO) NCBI Sequence Read Archive with the accession number GSE156726 inhttps://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE156726.
N-Acyl homoserine lactones
Bovine serum albumin
Confocal laser scanning microscopy
Nano-differential scanning fluorimetry
Pseudomonas syringae Pv. tomato
Quantitative polymerase chain reaction
Salmonella Plasmid virulence C
Yellow fluorescent protein
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The authors thank Wolfgang Maison, Annette Niehl, Hendrik Reuper, Khalid Amari Baba, Davide Faggionato, Svenja Lindenau, and Miriam Breuer for their help in providing us with materials to perform some of the experiments. We would also like to thank Dr. Thomas Schubert and 2bind GmbH for their generous support in performing MST binding and nanoDSF assays.
Open Access funding enabled and organized by Projekt DEAL. The work of AbS was supported by Deutsche Forschungsgemeinschaft research (DFG), grant nr. SCHI 1132–11 granted to AS. The work of CSR was supported by Consejo Nacional de Ciencia y Tecnología (CONACYT).
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Additional file 1.
Supporting individual data values displayed in Figure 1a, 1d, 3a-b, 5d, 6 a-d, 7a-b, and Additional file 2: Figure S1 and S3.
Additional file 2: Supplementary materials. Figure S1.
The expression of ALI1 is not influenced by oxo-C14-HSL. Figure S2. The ali1 mutant has a T-DNA insertion in At5g14470 position and is homozygous. Figure S3. Enhanced activation of defense-related genes due to AHL-priming is missing in ali1. Figure S4. ALI1 does not colocalize with Golgi, plastids, and peroxisomes. Figure S5. Localization of ALI1 upon plasmolysis. Figure S6. Representative images of predicted docking between ALI1 protein and oxo-C14-HSL ligand. Figure S7. Interaction between ALI1 and oxo-C14-HSL was missing in biophysical assays but indicated to be present in indirect binding assay. Figure S8. The complemented lines of ali1 mutant express ALI1. Table S1. Densitometric analysis of Western blot results. Table S2. Primers used in the study. Table S3. Fluorescence-tagged strains used in the localization study.
Additional file 3: Dataset S1.
List of genes differentially expressed (upregulated) in Col-0 after 3-day pretreatment with oxo-C14-HSL and additional challenge with 100 nM flg22 for 2 h.
Additional file 4: Dataset S2.
List of genes differentially expressed (downregulated) in Col-0 after 3-day pretreatment with oxo-C14-HSL and additional challenge with 100 nM flg22 for 2 h.
Additional file 5: Dataset S3.
List of genes differentially expressed (upregulated) in ali1 after 3-day pretreatment with oxo-C14-HSL and additional challenge with 100 nM flg22 for 2 h.
Additional file 6: Dataset S4.
List of genes differentially expressed (downregulated) in ali1 after 3-day pretreatment with oxo-C14-HSL and additional challenge with 100 nM flg22 for 2 h.
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Shrestha, A., Hernández-Reyes, C., Grimm, M. et al. AHL-Priming Protein 1 mediates N-3-oxo-tetradecanoyl-homoserine lactone priming in Arabidopsis. BMC Biol 20, 268 (2022). https://doi.org/10.1186/s12915-022-01464-3
- AHL priming
- Enhanced resistance
- N-acyl homoserine lactone
- Plant immunity
- Plant–microbe interaction
- Quorum sensing