Original Research ARTICLE
Quantitative Disease Resistance under Elevated Temperature: Genetic Basis of New Resistance Mechanisms to Ralstonia solanacearum
- LIPM, Centre National de la Recherche Scientifique, Institut National de la Recherche Agronomique, INPT, Université de Toulouse, Castanet-Tolosan, France
In the context of climate warming, plants will be facing an increased risk of epidemics as well as the emergence of new highly aggressive pathogen species. Although a permanent increase of temperature strongly affects plant immunity, the underlying molecular mechanisms involved are still poorly characterized. In this study, we aimed to uncover the genetic bases of resistance mechanisms that are efficient at elevated temperature to the Ralstonia solanacearum species complex (RSSC), one of the most harmful phytobacteria causing bacterial wilt. To start the identification of quantitative trait loci (QTLs) associated with natural variation of response to R. solanacearum, we adopted a genome wide association (GWA) mapping approach using 176 worldwide natural accessions of Arabidopsis thaliana inoculated with the R. solanacearum GMI1000 strain. Following two different procedures of root-inoculation (root apparatus cut vs. uncut), plants were grown either at 27 or 30°C, with the latter temperature mimicking a permanent increase in temperature. At 27°C, the RPS4/RRS1-R locus was the main QTL of resistance detected regardless of the method of inoculation used. This highlights the power of GWA mapping to identify functionally important loci for resistance to the GMI1000 strain. At 30°C, although most of the accessions developed wilting symptoms, we identified several QTLs that were specific to the inoculation method used. We focused on a QTL region associated with response to the GMI1000 strain in the early stages of infection and, by adopting a reverse genetic approach, we functionally validated the involvement of a strictosidine synthase-like 4 (SSL4) protein that shares structural similarities with animal proteins known to play a role in animal immunity.
Global changes are predicted to increase the frequency of extreme climate events and to accentuate abiotic stresses such as temperature increase, drought, and water logging (Orlowsky and Seneviratne, 2012; IPCC, 2014), thereby impacting crop development (e.g., rate of photosynthetic carbon assimilation, rate of leaf initiation, leaf expansion, root architecture, or reproduction) and ultimately yield (Hatfield et al., 2011; Gray and Brady, 2016). Amongst climatic risks, global surface temperature is predicted to rise by the end of the century, from 1.0 up to 4.8°C, with higher frequencies and longer periods of heat waves (IPCC, 2014). While an increase of mean temperature constitutes one of the major abiotic stresses that plants have to cope with (Bita and Gerats, 2013; Suzuki et al., 2014), it is also expected to favor the emergence of new pathogens and to increase the occurrence of epidemics (Garrett et al., 2006; Evans et al., 2008; Bebber et al., 2013). For example, recent studies reported that climate change likely increased the emergence of highly aggressive and invasive strains of rust Puccinia graminis, P. striiformis, and of the oomycete Phytophthora infestans (Hovmoller et al., 2008; Singh et al., 2011; Cooke et al., 2012; Bebber et al., 2013). These future outbreaks are a major concern for the maintenance of global food security. Therefore, identifying and studying the genetic and molecular basis of defense mechanisms allowing plants to cope with epidemics under higher temperature conditions is critical.
In their natural habitats, plants have evolved complex defense responses to deal with the simultaneous and/or sequential attacks from various bio-aggressors (e.g., viruses, bacteria, fungi, oomycetes, and herbivores) (Roux and Bergelson, 2016). Defense responses include plant preformed physical or chemical barriers (e.g., rigid cell wall, presence of cuticles or trichomes, production of toxic or repellent compounds) (Osbourn, 1996; Nurnberger and Lipka, 2005) as well as immune signaling responses that are activated upon pathogen recognition. This latter type of resistance mechanism corresponds to a two-level defense system described as the zig-zag model (Jones and Dangl, 2006; Dodds and Rathjen, 2010). In the first level, microbial elicitors, called pathogen- or microbe-associated molecular patterns (PAMPs or MAMPs) are perceived by plant cell surface and transmembrane pattern recognition receptors (PRRs) to initiate a signaling cascade leading to the MAMP- or PAMP-triggered immunity (MTI/PTI), that is efficient against a broad spectrum of pathogens. To overcome PTI, pathogens produce virulence factors called effectors which can promote effector-triggered susceptibility (ETS) by interfering with host defense responses. In turn, effectors can be specifically recognized by plant intracellular resistance proteins, known as nucleotide binding site-leucine rich repeat containing proteins (NLRs), thereby activating a second level of plant defense, the effector-triggered immunity (ETI). ETI results in a strong defense response often associated with a hypersensitive response (HR), characterized by a rapid and local cell death. However, this type of qualitative response is generally specific to a single pathogen species, and even strain-specific, thereby leading to a strong selection of virulent strains that can bypass ETI (Roux et al., 2014). Another form of resistance called Quantitative Disease Resistance (QDR), is characterized by a reduction rather than an absence of disease (St Clair, 2010; Mundt, 2014; Roux et al., 2014; French et al., 2016) and is typically polygenic (Poland et al., 2009). Knowing that QDR provides a durable and a broad-spectrum resistance, this form of resistance appears to be unsurprisingly much more prevalent than ETI in crops and natural plant populations (Young, 1996). The characterization of the main molecular mechanisms underlying PTI and ETI have paved the way to decipher basal and specific immune responses, which is not currently the case of QDR's molecular mechanisms that remain largely unknown (Roux et al., 2014).
Plants are exposed to multiple abiotic and biotic stresses either in crop fields or in natural populations. However, studies deciphering the molecular mechanisms governing plant response to these combined stresses are scarce (Mittler, 2006; Suzuki et al., 2014). Yet, several transcriptome studies recently demonstrated that despite a certain overlap, each combination of stress involves a unique response that could not be easily predicted by the study of each stress individually, and leading to either positive or negative effects on host immunity (Atkinson and Urwin, 2012; Atkinson et al., 2013; Prasch and Sonnewald, 2013; Rasmussen et al., 2013; Suzuki et al., 2014; Onaga et al., 2017). Remarkably, an increase in temperature (3–7°C) was demonstrated (i) to inhibit several major defense mechanisms induced following a pathogen attack, regardless of the pathogen and the plant species considered, or (ii) to suppress ETI-HR related phenotypes. For example, in Arabidopsis thaliana, the expression of two regulators of plant immunity, PAD4 and EDS1, is down-regulated by a rise in temperature from 22 to 28°C (Yang and Hua, 2004). RPS4- or RPM1-mediated resistance responses to Pseudomonas syringae pv. tomato (Pst) DC3000 strains are efficient at 22°C but inhibited at 28°C (Wang et al., 2009). In addition, the HR triggered either by Pst DC3000 strain containing the HopZ1A avirulent effector or by the RPW8 gene conferring resistance against powdery mildew is suppressed by a temperature above 28 and 30°C, respectively (Xiao et al., 2003; Menna et al., 2015). However, for Pst DC3000 strains carrying the AvrRpt2 effector gene, contradictory results were observed. Indeed, elevated temperatures led to either a resistance inhibition (Wang et al., 2009) or a HR suppression without ETI-mediated virulence suppression (Menna et al., 2015). Similar examples of inactivation by an elevated temperature were also reported in other plant species. Resistance conferred by the Mi-1 gene to root-knot nematodes, by the N gene to tobacco mosaic virus (TMV) and by the Cf4 and Cf9 genes to the fungal pathogen Cladosporium fulvum are inactivated in tomato at temperatures above 28, 30, and 33°C, respectively (Whitham et al., 1996; Hwang et al., 2000; de Jong et al., 2002). An elevated temperature also negatively modulated plant defense response linked to Rp1-D21 in maize (Negeri et al., 2013). By contrast, partial or more efficient resistances related to Yr36, Xa7, and Pi54 genes were also described against P. graminis in wheat (Fu et al., 2009), Xanthomonas oryzae pv. oryzae and Magnaporthe oryzae in rice, respectively (Webb et al., 2010; Onaga et al., 2017). Although an increase of temperature can differentially balance host immunity, the molecular mechanisms involved remain elusive.
The Ralstonia solanacearum species complex (RSSC) is responsible for the bacterial wilt, one of the most harmful disease causing tremendous yield losses in more than 200 plant species in tropical, subtropical, and warm temperate areas worldwide (Elphinstone, 2005). The strains composing the RSSC are phylogenetically represented by four phylotypes according to their geographical origin (I: Asia, II: America, III: Africa, IV: Australia-Indonesia-Japan) (Ailloud et al., 2015). The ability of RSSC to quickly adapt to new host plants or to the universal resistant reference Hawaii7996 tomato cultivar (Wicker et al., 2007) is thought to be promoted by (i) many molecular determinants involved in pathogenicity and host-range specificity, (ii) large and variable repertoires of type III effectors (T3Es), and (iii) a high evolutionary ability (Coupat et al., 2008; Remenant et al., 2010; Genin and Denny, 2012). In addition, climate warming has been recently proposed to be involved in the expansion of the potato brown rot disease caused by some RSSC strains in Bolivia (Castillo and Plata, 2016). Host resistance to RSSC, which remains the most efficient strategy of disease control, is generally controlled by a polygenic architecture (Mangin et al., 1999; Wang et al., 2000; Carmeille et al., 2006). In the model plant A. thaliana, the two molecular resistance mechanisms identified so far involve the LRR receptor-like kinase ERECTA (Godiard et al., 2003) and the RPS4/RRS1-R pair of immune receptors (Deslandes et al., 2002; Le Roux et al., 2015), respectively. Recently, Le Roux et al. (2015) demonstrated that RPS4 with RRS1-R represent a DNA-bound immune receptor complex with an integrated effector decoy that directly converts the virulence activity of the PopP2 effector into activation of immunity (Le Roux et al., 2015). Interestingly, this immune-receptor pair also confers resistance to various pathogens including the fungus Colletotrichum higginsianum, Pst DC3000 delivering the AvrRps4 effector, and the strain CFBP6943 of Xanthomonas campestris pv. campestris (Xcc) (Narusaka et al., 2009; Debieu et al., 2016). In addition, in contrast to the well-characterized resistance against R. solanacearum GMI1000 strain identified in the A. thaliana accession Nd-1 (Deslandes et al., 1998, 2002), a tolerant phenotype to R. solanacearum BCCF402 strain in the A. thaliana Kil-0 accession, resulting in the absence of symptom despite a high bacterial multiplication in planta, was demonstrated to be also dependent on the PopP2 effector but with a specific allele of RRS1-R (Van der Linden et al., 2013). Thus, these results suggest that RRS1-R may also be involved in a QDR mechanism in the A. thaliana Kil-0 accession.
Despite the fact that a temperature increase is known to affect host resistance to R. solanacearum in several plant species (Hayward, 1991; Prior et al., 1996), no mechanism of resistance that is efficient under a permanent increase in temperature has been identified yet. Moreover, studies reporting the genetic architecture and the molecular mechanisms underlying the genetic diversity of plant responses to RSSC are still lacking in the context of climate change. Therefore, exploring natural genetic variation can help to identify uncovered sources of resistance to RSSC that are efficient under elevated temperature conditions. Thanks to the development of Next-Generation Sequencing (NGS) technologies and appropriate statistical methods (Bergelson and Roux, 2010), the method of genome-wide association (GWA) mapping recently emerged in plants and has been used so far in 11 species to fine map genomic regions associated with natural variation of response to a range of microbial enemies, including bacteria, fungi, and oomycetes (Bartoli and Roux, 2017). Notably, five quantitative trait loci (QTLs) identified by GWA mapping have been subsequently functionally validated in A. thaliana, demonstrating the power of this method to precisely dissect the intraspecific genetic variation underlying pathogen resistance (Bartoli and Roux, 2017). Therefore, in this study, we adopted a GWA mapping approach to fine map QTLs associated with natural variations of response to the R. solanacearum GMI1000 strain among 176 worldwide natural accessions of A. thaliana. Two inoculation methods were used and root-inoculated plants were incubated at two different temperatures to mimic a permanent increase of temperature. Whatever was the method of inoculation used, GWA mapping confirmed the RPS4/RRS1-R locus as the main QTL of resistance detected at 27°C, demonstrating the power of this approach to functionally fine map important loci for resistance to R. solanacearum. At 30°C, most accessions developed wilting symptoms, confirming the drastic effect of the temperature increase (+3°C) on the mechanisms of resistance triggered by plants at 27°C. Interestingly, we detected several QTLs, underlying natural variation for early plant defense response to R. solanacearum at 30°C. A reverse genetic approach revealed that one of these specific QTLs at 30°C involves a strictosidine synthase-like 4 (SSL4) protein.
Materials and Methods
Bacterial Strain, Plant Material, and Growth Conditions
The wild type R. solanacearum GMI1000 strain used in all inoculation experiments was grown in complete BG medium as described by Plener et al. (2010). A collection of 176 A. thaliana worldwide accessions was used in this study (Table S1). Five to 10 seeds of each accession were directly sown on Jiffy pots (Jiffy Products International AS, Norway) and stratified for 48 h at 4°C in order to release seed dormancy. Accessions were then grown in a growth chamber under controlled conditions for 4 weeks [22°C, 70% relative humidity (RH), 9 h of light] prior to phenotyping experiments. The 38 T-DNA insertion mutants (Ws-0 and Col-0 background) corresponding to 21 genes included in a 80 kb genomic region underlying a QTL of early plant defense response to R. solanacearum were identified using the online Arabidopsis gene mapping tool T-DNA express (http://signal.salk.edu/cgi-bin/tdnaexpress) (Table S2) and ordered from the Nottingham Arabidopsis Stock center (http://arabidopsis.info/). Corresponding seeds were sown and stratified as described above and grown in greenhouse conditions (26.5 ± 1.5°C, 16 h light). Progenies of genotyped homozygous of each mutant were harvested and grown for 4 weeks as described above before inoculation. The Col-0 accession (N60000), susceptible to the R. solanacearum GMI1000 strain, was used as a control in all experiments.
Plant Inoculation and Phenotyping
Four-week-old plants were used in all experiments. Plant response to R. solanacearum GMI1000 strain was assessed at 27 and 30°C using two inoculation conditions: (i) the UNCUT condition previously described (Lohou et al., 2014), where the roots were not wounded thereby mimicking natural infection, and (ii) the CUT condition (Deslandes et al., 1998) where the roots were sectioned with scissors, ~1 cm from the bottom of the Jiffy pot, giving the bacteria a direct access to the xylem vessels. Plants were soaked for 15 min in 2 L per tray of a bacterial suspension at 1.107 bacteria/mL and 1.108 bacteria/mL, for the CUT and the UNCUT conditions, respectively. Inoculated plants were then transferred in growth chambers with controlled conditions at 27 or at 30°C (75% HR, 12 h light, 100 μmol m−2 s−1). The wilting symptoms were scored on an established 0 to 4 disease index scale (Deslandes et al., 1998) with the score 0 and 4 corresponding to healthy and dead plants, respectively. Symptoms were monitored from 3 to 13 days after inoculation (dai), and from 3 to 10 dai for plants incubated at 27 and 30°C, respectively.
Natural Variation of QDR
For each “CUT condition x temperature treatment” combination, an experiment of 1,152 plants was set up using a randomized complete block design (RCBD) of two experimental blocks. Each block was represented by six trays of 96 positions. Each block corresponded to 576 plants with three replicates per accession (n = 528 = 176 accessions * three replicates) and the control accession Col-0 placed in the same five positions within each tray (n = 30 = 6 trays * five replicates). In each block, the remaining 18 positions in the trays were left empty.
For each “UNCUT condition × temperature treatment” combination, an experiment of 570 plants was set up using a RCBD of three experimental blocks. Each block was represented by three trays of 64 positions. Each block corresponded to 192 plants with one replicate per accession (n = 176) and the control accession Col-0 placed in 14 positions across the three trays (n = 14). In each block, the remaining two positions in the trays were left empty.
For each “CUT/UNCUT condition × temperature treatment” combination, we used the following mixed model (MIXED procedure in SAS9.3; SAS Institute Inc., Cary, NC, USA) to explore the natural genetic variation of the disease index at each time point of phenotyping:
where μ is the overall mean of the phenotypic data, “block” accounts for differences in micro-environmental conditions between the two or three experimental blocks; “accession” corresponds to the genetic differences among the natural accessions; “block × accession” accounts for genetic differences among the natural accessions depending on the block; covCol is a covariate accounting for tray effects within blocks (phenotypic mean of the four or five Col-0 replicates per tray was used as a covariate); and “ε” is the residual term. Normality of the residuals was not improved by transformation of the data. The factor “block” was treated as a random factor, whereas the factor “accession” was treated as a fixed factor. Significance of the random effect was tested with likelihood ratio tests of models with and without this effect. Least-square means (LSmeans) were obtained for each natural accession and were subsequently used for GWA mapping analyses. Broad-sense heritabilities (H2) at each time point of phenotyping were estimated from the mean square (MS) of equation (1) using a formula adapted from Gallais (1990). Due to the absence of Col-0 control plants in some trays of the “UNCUT condition × 27°C” combination, the term “covColc” was not modeled in Equation (1).
The 176 natural accessions used in this study have been genotyped for 214,051 SNPs evenly spaced across the genome (Horton et al., 2012). In order to fine map the genomic regions associated with natural disease index variation at each time of phenotyping for each “CUT/UNCUT condition × temperature treatment” combination, we ran a mixed model implemented in the software EMMAX (Efficient Mixed-Model Association eXpedited; Kang et al., 2010). This mixed model includes a genetic kinship matrix K based on the 214,051 SNPs as a covariate to control for population structure in the mapping panel. Because of bias due to rare alleles, we only considered SNPs with minor allele relative frequency (MARF) > 10% (Brachi et al., 2010; Kang et al., 2010). Manhattan plots illustrating the results of phenotype-genotype associations at all stages of infection at 27 and 30°C, in the CUT and UNCUT conditions of inoculation are presented in Figures S1–S4, respectively. Corresponding Q-Q plots and lists of the most significantly associated SNPs (i.e., top SNPs with a –log10 p-value > 4) are depicted in Figures S5, S6 and Table S3.
Gene Ontology and Biological Pathways Enrichment Tests
To determine the biological processes involved in response to R. solanacearum GM1000 strain at 30°C and perform comparisons between the two inoculation methods used, we first tested for each “CUT/UNCUT condition × time point of phenotyping” whether SNPs in the 0.1% upper tail of the –log10 p-value distribution were over-represented in each of 736 Gene Ontology Biological Processes from the GOslim set (Consortium, 2008). A total of 10,000 permutations were run to assess significance using the same methodology as described in Hancock et al. (2011) (Table S4). For each significant enriched biological process at a P < 0.05, we then retrieved the identity of all the genes containing SNPs in the 0.1% upper tail of the –log10 p-value distribution (Table S5). Finally, each list of genes, corresponding to each phenotyping time point, was used after removal of duplicates, to identify biological pathways significantly over-represented (P < 0.01) with the classification superviewer tool on the university of Toronto website (http://bar.utoronto.ca/ntools/cgi-bin/ntools_classification_superviewer.cgi) using the MAPMAN classification (Provart and Zhu, 2003; Tables S6, S7).
T-DNA Insertion Mutants' Validation, Plant Assays, and Statistical Analyses
For each of the 38 T-DNA insertion mutants located in a QTL region of early A. thaliana defense responses to R. solanacearum (see Results section), 12 seedlings were genotyped to check the presence of the T-DNA insertion and to identify homozygous plants. For each seedling, one leaf was collected and used for genomic DNA extraction was adapted from QIAGEN DNeasy kit®as described in Mayjonade et al. (2016). For genotyping, primer pairs were designed using the T-DNA primer design online tool (http://signal.salk.edu/tdnaprimers.2.html). All the primer sequences and corresponding PCR fragment sizes are listed in Table S2. For one PCR reaction, 2 μL of genomic DNA (10 ng/μL) were added to a PCR master mix composed of: 1 μL (10 pM) of each primer composing the LP+RP or RP+BP primer pairs (see Table S2), 0.5 μL (10 mM) dNTPs, 0.2 μL (10 μ/μL) of GoTaq® DNA polymerase (Promega, Madison, WI, USA), 5 μL of 5X GoTaq buffer and 16.2 μL of sterilized water. The PCR cycling conditions were as follow: 95°C for 2 min; 10 cycles at 95°C for 30 s, 62 to 52°C for 30 s (touch-down, 1°C decrease at each cycle) and 72°C for 1 min; 30 cycles at 95°C for 30 s, 52°C for 30 s, and 72°C for 1 min; 72°C for 2 min.
T-DNA insertion mutants were inoculated using the CUT inoculation method with a bacterial suspension of 1.107 bacteria/mL and transferred at 30°C. Three to six independent experiments were made for each T-DNA insertion mutant. In all experiments, plants were organized according to a RCBD. To test whether the disease index was statistically different between the wild type Col-0 and each T-DNA mutant, we used a Kruskal-Wallis analysis under the R environment version 3.3.2 (R_Development_Core_Team, 2013). The dynamics of T-DNA mutant lines response to the R. solanacearum GMI1000 strain was drawn using ggplot2 package (http://ggplot2.org/) showing the confidence interval.
RNA Extractions and RT-qPCR
RNA extractions and RT-qPCR analyses were performed as previously described (Le Roux et al., 2015) using two leaves from healthy plants. Primer pairs used are listed in Table S8.
Extensive Genetic Variation among Worldwide Accessions of A. thaliana for the Response to R. solanacearum: Effects of Temperature and Inoculation Methods
Based on the phenotyping of 176 worldwide accessions of A. thaliana, we detected substantial genetic variation in the response to the GM1000 strain for each “temperature treatment × inoculation method” (Figure 1; Tables 1, 2), with the presence of resistant accessions to R. solanacearum at 30°C (Figures 1B,D). The high broad-sense heritability estimates observed at all stages of infection suggests that plant response to R. solanacearum is genetically controlled even at early stages of infection (Figure 1; Tables 1, 2). In both inoculation methods, accessions were on average more susceptible at 30°C compared to 27°C (CUT – 10 dai, F = 136.9, P < 0.0001; UNCUT – 7 dai, F = 227.1, P < 0.0001) (Figure 1). At 27°C, accessions were on average more susceptible in the CUT condition than in the UNCUT condition (13 dai, F = 17.0, P < 0.0001) (Figure 1). At 30°C, although the accessions had on average a similar disease index at the late stages of infection (6 dai: F = 3.85, P = 0.0509; 7 dai: F = 0.02, P = 0.8889; 10 dai: F = 0.89, P = 0.3472), the dynamics of disease induction was faster in the CUT condition compared to the UNCUT condition at the early stages of infection (3 dai: F = 58.7, P < 0.0001; 4 dai: F = 88.7, P < 0.0001; 5 dai: F = 17.9, P < 0.0001) (Figure 1).
Figure 1. Genetic diversity of plant response to R. solanacearum GMI1000 strain in the CUT and UNCUT conditions of inoculation at 27 and 30°C. The red line represents the mean of disease index over all the accessions. Inoculation was performed at 27°C (A,C) and 30°C (B,D) on 4-week-old plants for which roots have been cut (A,B) or left uncut (C,D). dai, days after inoculation; DI, disease index.
In both methods of inoculation, variation in disease index at 30°C was significantly correlated with variation in disease index at 27°C (Figure 2). However, the correlation coefficient of Pearson was strongly different from 1 (CUT condition, 95% confidence intervals: 0.037–0.357; UNCUT condition, 95% confidence intervals: 0.087–0.383). The observation of crossing reaction norms between 27 and 30°C suggests that the genetic architecture of the response of A. thaliana to the R. solanacearum GMI1000 strain is different between these two temperatures (Figure 2).
Figure 2. Correlations of temperature conditions, 27 and 30°C, in response to R. solanacearum inoculation of the worldwide collection of A. thaliana, at 5 days after inoculation. Inoculation was performed on 4-week-old plants for which roots have been cut (A) or left uncut (B). The red line represents the mean of disease index. dai, days after inoculation; DI, disease index.
A Major QTL Corresponding to the Immune Receptor Pair RPS4/RRS1 Locus Confers QDR to the R. solanacearum GMI1000 Strain at 27°C
In the CUT condition, GWA mapping revealed a unique peak of association on the long arm of chromosome 5 whose significance increased with the stages of infection (Figure S1). Thirteen days post-inoculation, the three most associated SNPs (SNP-5-18325032, P = 5.37 × 10−13, MARF = 0.125; SNP-5-18325565, P = 3.55 × 10−9, MARF = 0.237; SNP-5-18325915, P = 8.65 × 10−9, MARF = 0.151) were located in the RPS4 gene (At5g45250) (Figures 3A–C), that encodes the RPS4 immune receptor. Previously described as cooperating genetically and molecularly with RRS1-R for resistance to R. solanacearum (Narusaka et al., 2009), RPS4 and RRS1 gene are localized near each other and are inserted in opposite directions. Therefore, the identification of the RPS4/RRS1 locus as the major resistance QTL to R. solanacearum confirms the suitability of a GWA mapping approach to investigate the genetic bases of resistance responses to this bacterial pathogen.
Figure 3. The genetics of quantitative disease resistance to R. solanacearum GMI1000 strain at 27°C, identified by GWA mapping at 13 dai in the CUT and UNCUT conditions of inoculation. Whole genome scan of 214,051 single-nucleotide polymorphisms (SNPs) for association with disease index at 13 dai across 152 accessions that have germinated for which roots have been cut (A). Zoom showing the absence of QTLs of resistance in the CUT condition of inoculation on the chromosome IV, compared with the UNCUT condition thereafter (B). Zoom spanning a genomic region on the chromosome V from 17.8 to 18.8 Mb containing the QTL of resistance located in the RPS4/RRS1 locus (C). Whole genome scan of 214,051 single-nucleotide polymorphisms (SNPs) for association with disease index at 13 dai across 163 accessions that have germinated for which roots remained uncut (D) and focus on two genomic regions corresponding to two QTLs of resistance observed on chromosomes IV (D) and chromosome V (E). The red circle indicates the top SNP (SNP-4-5080256, P = 4.93 × 10−7, MARF = 0.429) corresponding to a QTL of resistance detected at the beginning of chromosome IV in the UNCUT condition. The green circles highlight the top SNPs corresponding to the major QTL of resistance detected on the long arm of chromosome V in the UNCUT (SNP-5-18325032, P = 5.37 × 10−13, MARF = 0.125) and CUT (SNP-5-18325565, P = 1.60 × 10−10, MARF = 0.252) conditions.
In the UNCUT condition, we detected two neat peaks of association. The first association peak, at the beginning of chromosome IV, was detected at the late stages of infection (Figure S2), with the top SNP (SNP-4-5080256, P = 4.93 × 10−7, MARF = 0.429) located in a transposable element gene (At4g08100) belonging to the gypsy-like retrotransposon family (Figures 3D,E). The significance of the second association peak located on the chromosome V also increased with the stages of infection (Figure S2). Similarly to the CUT condition, the four most associated SNPs at 13 dai (SNP-5-18325565, P = 1.60 × 10−10, MARF = 0.252; SNP-5-18325032, P = 2.80 × 10−9, MARF = 0.123; SNP-5-18322558, P = 1.19 × 10−8, MARF = 0.301; SNP-5-18323844, P = 4.85 × 10−7, MARF = 0.295) were also found in RPS4 (Figures 3D,F). These results suggest that although the major QTL was common for the two methods of inoculation, medium/minor QTLs can be specific to the inoculation method and/or to the stage of infection.
Different Genetic Architectures at 30°C Highlight Different Plant Defense Response Mechanisms
In agreement with the small correlation coefficients observed at the phenotypic level between 27 and 30°C (Figure 2), GWA mapping revealed a different genetic architecture at 30°C, with no association peak located in the RPS4/RRS1 locus or at its close vicinity (Figures S3, S4). In addition, for each phenotyping time point, less than 2% of the 100 most significant associated SNPs (i.e., top SNPs) were shared between the two inoculation methods at 30°C (Figures S3, S4), suggesting that the genetic basis of response to R. solanacearum largely differs between the CUT and UNCUT conditions. Different significantly over-represented functional classes assigned using the MapMan classification, (supported from >97.5% bootstrap replicate), in which gene lists corresponding to the top SNPs for each “CUT/UNCUT condition × time point of phenotyping” fall in, also support this observation. In the CUT condition, numerous genes involved in RNA processing and RNA regulation were found at 3 and 4 dai, whereas genes related to the perception and the regulation of plant response to biotic or abiotic stresses (i.e., leucine rich repeat protein, NBS-LRR protein, Cystein rich receptor like kinase protein, cytochrome P450) and protein degradation were mostly found at later stages of infection (Table S6, Figure 4A). By contrast, genes retrieved in the UNCUT condition were significantly over-represented in metabolic pathways at 3–5 dai, with genes having a role in hormone metabolism, defense response to biotic and abiotic stresses (CYP450 family 705 subfamily A; flavonoid synthase), cell wall modification and signaling. Genes retrieved at 6 and 7 dai reflect an intense protein metabolism activity with numerous genes involved in protein synthesis and degradation (Table S7, Figure 4B).
Figure 4. Simplified representation of MapMan classification pathways found to be significantly over-represented (P < 0.01). Genes list were retrieved from enrichment tests performed using the SNPs in the 0.1% upper tail of the −log10 p-value distribution for each time point of phenotyping in the CUT (A) and UNCUT (B) conditions at 30°C (Tables S6, S7).
Interestingly, for both inoculation methods, we observed playful dynamics of the association peaks along the infection stages (Figures S3, S4). For example, in the CUT condition, we detected multiple association peaks specific to the 5 dai stage (Figure 5A). In particular, GWA mapping revealed an association peak located at the end of chromosome III supported by 12 SNPs with an association score above 3, embedded in a region of 80 kb (Figure 5B). Similarly, in the UNCUT condition, GWA mapping revealed multiple association peaks specific to the 6 dai stage (Figure 6A). More specifically, two association peaks caught our attention as they are supported by numerous top SNPs, including those the most significantly associated to the plant response to R. solanacearum at the 6 dai stage (Table S3), and overlap with candidate genes known to be involved in plant response to different pathogens. The first one is located at the end of chromosome III, with the top SNP (SNP-3-22-260-125) located in the promoter region of the EIF4G (At3g60240) gene (Figure 6B). The second one is located at the beginning of chromosome V, with the six most associated SNPs all located within the CesA3 (At5g05170) gene (Figure 6C).
Figure 5. The genetics of quantitative disease resistance to R. solanacearum GMI1000 strain at 30°C, identified by GWA mapping at 5 dai in the CUT condition of inoculation. Whole genome scan of 214,051 single-nucleotide polymorphisms (SNPs) for association with disease index at 5 dai across 141 accessions having germinated (A). Zoom spanning a genomic region on the chromosome III from 18.5 to 19.5 Mb containing a QTL of early plant defense response to R. solanacearum (B). Zoom showing the 80 Kb genomic region underlying the QTL of early plant defense response to R. solanacearum, containing 31 annotated genes. Red frames indicate genes coding for AtSSL4 (At3g51420) and AtSSL5 (At3g51430) (C). Dynamics of disease symptoms after inoculation with the GMI1000 strain in wild type Col-0 genetic background and ssl4-1 mutant at 30°C. Means ± SD of the means (ssl4-1 n = 60; Col-0 n = 40) from three independent inoculations (D). Dynamics of disease symptoms after inoculation with the GMI1000 strain in wild type Col-0 genetic background and ssl4-2 mutant at 30°C. Means ± SD of the means (ssl4-2 n = 83; Col-0 n = 59) from four independent inoculations (E). Dynamics of disease symptoms after inoculation with the R. solanacearum GMI1000 strain in wild type Col-0 genetic background and ssl5 mutant at 30°C. Means ± SD of the means (ssl5 n = 124; Col-0 n = 77) from six independent inoculations (F). Symbols *, **, and *** denote significant difference observed between Col-0 and each mutant at P < 0.05, P < 0.01, and P < 0.001 respectively, in Kruskal-Wallis analyses. The red circle indicates the top SNP (SNP-3-18972992, P = 4.70 × 10−6, MARF = 0.142) corresponding to the major QTL of resistance detected at the end of chromosome III.
Figure 6. The genetics of quantitative disease resistance to R. solanacearum GMI1000 strain at 30°C, identified by GWA mapping at 6 dai in the UNCUT condition of inoculation. Whole genome scan of 214,051 single-nucleotide polymorphisms (SNPs) for association with disease index at 6 dai across 158 accessions that have germinated (A) and focus on two genomic regions corresponding to QTLs of early plant defense to R. solanacearum observed at the end of chromosome III (B) and at the beginning of chromosome V (C). The red circle indicates the top SNP (SNP-3-22260125, P = 5.65 × 10−8, MARF = 0.127) corresponding to a QTL of resistance detected at the end of chromosome III. The green circle highlights the top SNP (SNP-5-1530992, P = 4.04 × 10−8, MARF = 0.189) corresponding to a QTL of resistance detected at the beginning of chromosome V.
QDR to the R. solanacearum GMI1000 Strain at 30°C in the Cut Condition Is Conferred by a Gene Encoding for a Strictosidine Synthase-Like Protein 4
Since neat association peaks at the early stages of infection could be detected (Figures 5B, 6B,C), we therefore investigated the molecular mechanisms underlying plant response to R. solanacearum at 30°C. To functionally validate one of those peaks, we focused on the QTL region identified at the bottom of chromosome III at 30°C in the CUT condition (Figure 5B). We screened this 80-kb QTL region (Figure 5C) by genotyping 38 T-DNA insertion mutants publically available and corresponding to 21 candidate genes (Table S2). T-DNA insertions were confirmed by genotyping and sequencing the T-DNA flanking sequences for 24 mutants. Homozygous progenies were produced and their responses to R. solanacearum at 30°C were scored. Out of the 21 mutants tested, two allelic mutants of the At3g51420 gene, named ssl4-1 (N683907), and ssl4-2 (N684981), for which the altered gene expression was confirmed by RT-qPCR (Figure S7), exhibited a significant higher level of resistance from 4 to 7 dai compared to wild-type Col-0 (Figures 5D,E). These data indicate that At3g51420 is a gene that increases the susceptibility to the R. solanacearum GMI1000 strain at 30°C. This gene, that encodes for a strictosidine synthase-like protein 4 (SSL4), belongs to a family of four genes (SSL4, 5, 6, and 7) organized in tandem at this locus. Interestingly, knocking-down of one of the three other genes of the SSL family [ssl5 mutant (N659319)], has also led to a higher level of resistance from 4 to 7 dai (Figures 5C,F). Representative symptoms observed at 5 dai for ssl4-1, ssl4-2, and ssl5 mutants compared to Col-0 accession are shown in Figure S8. Together, our data reveal that both SSL4 and SSL5 can be considered as susceptibility genes since they promote the development of wilting symptoms of Col-0 plants in response to the GMI1000 strain.
In this study, we explored the genetic diversity of responses to R. solanacearum in A. thaliana under elevated temperature conditions (i) to estimate the extent of genetic diversity in response to this combined abiotic-biotic stress, (ii) to describe the genetic architecture of plant response to the bacterial wilt disease, and (iii) to unravel the genetic bases of QDR mechanisms that are efficient under a permanent increase of 3°C. Because R. solanacearum is a soil borne pathogen that penetrates into the plants through the roots, we also aimed at studying how the infection process could modulate the response of A. thaliana to R. solanacearum. For this, two inoculation methods were used: (i) the CUT condition in which the roots were cut allowing the bacteria to access directly to the xylem vessels and (ii) the UNCUT condition, in which the roots were not injured to mimic natural infection.
Significant Natural Genetic Variation Is Observed in A. thaliana Challenged with R. solanacearum, at Both 27 and 30°C
In our study, we observed a drastic effect of elevated temperature on A. thaliana defense response to R. solanacearum. At 30°C, most accessions were on average more susceptible, with wilting disease progression being always faster regardless of the inoculation condition used. These results corroborate several previous studies describing that elevated temperatures generally inhibit resistance responses (Whitham et al., 1996; Hwang et al., 2000; de Jong et al., 2002; Xiao et al., 2003; Wang et al., 2009; Zhu et al., 2010; Menna et al., 2015). At the same time, we also observed an extensive genetic diversity of response among A. thaliana accessions challenged with the GMI1000 strain as well as high estimates of broad-sense heritability across the stages of infection at 30°C, as it was also the case at 27°C. These results reveal the existence of resistant accessions to R. solanacearum with a genetically controlled response at the two temperatures tested. However, the crossing reaction norms observed between 27 and 30°C suggest that the genetic architecture of A. thaliana for the response to R. solanacearum can largely depend on abiotic conditions. Such a temperature-dependent genetic architecture has been previously reported in A. thaliana for diverse phenotypic traits such as flowering time (Lempe et al., 2005) and fertility-related traits (Bac-Molenaar et al., 2015; Thoen et al., 2017).
The Major QTL Associated with Resistance to R. solanacearum at 27°C, Underlying the RPS4/RRS1 Locus, Is Not Detected at 30°C
Whatever was the method of inoculation, GWA mapping revealed a major QTL on the long arm of chromosome V with an increasing temporal significance at 27°C, suggesting that a simple genetic architecture governs the defense response to the R. solanacearum GMI1000 strain. For both inoculation conditions, the most significant SNPs were found in the RPS4/RRS1 locus, known to be involved in one of the best characterized resistance mechanism to R. solanacearum in A. thaliana (Deslandes et al., 2002; Le Roux et al., 2015). Interestingly, a previous GWA study also identified this locus to be responsible for specific QDR in response to the Xcc CFBP6943 strain (race 6) (Debieu et al., 2016). Therefore, our results demonstrate the potential of GWAS to identify major loci associated with natural variation of resistance to R. solanacearum, as previously shown for several other bacterial pathogens, predominantly in A. thaliana (Huard-Chauveau et al., 2013; Debieu et al., 2016; Roux and Bergelson, 2016; Bartoli and Roux, 2017).
By contrast, at all phenotyping time points, no significant association peak underlying the RPS4/RRS1 genomic region was detected at 30°C. This result supports, for the first time, that the resistance mechanism conferred by this immunoreceptor pair is impaired at 30°C. The thermosensitivity of PTI and R-gene-mediated defense for different pathogens in different plant species has been reported in several studies (Whitham et al., 1996; Hwang et al., 2000; de Jong et al., 2002; Xiao et al., 2003; Yang and Hua, 2004; Wang et al., 2009; Menna et al., 2015). In addition, the dwarf phenotype of several autoimmune mutants such as bon1 and snc4-1D or snc2-1D, mkk1 mkk2, and bir1-1 can be totally or partially suppressed above 28°C (van Wersch et al., 2016). This is also the case for the autoimmune response of A. thaliana transgenic lines constitutively expressing the RPS4 immune receptor (Heidrich et al., 2013). To date, the mechanisms involved in such temperature-inhibition of immune responses remain largely uncharacterized. Interestingly, Cheng et al. (2013) proposed that plants preferably activate ETI signaling at low temperatures while they use PTI signaling at elevated temperatures.
In this first GWA study on R. solanacearum, we have identified at 27°C, in both inoculation methods, the RRS1-containing locus, originally mapped by a conventional positional cloning approach (Deslandes et al., 2002). Therefore, we clearly showed that the study of natural diversity of plant response to R. solanacearum is a powerful strategy to fine map genomic regions governing susceptible and resistance responses to bacterial wilt. We also showed that an increase in temperature strongly impacts plant defense responses to R. solanacearum preventing the detection of RSP4/RRS1 locus at 30°C most likely due to a loss of function of this immunoreceptor pair.
GWA Analyses at 30°C Highlight Playful Dynamics in the Genetics of Response to R. solanacearum Depending on the Inoculation Procedure
Owing to GWA analyses carried out on the phenotypic data monitored every day after inoculation, a more pronounced playful dynamics of association peaks along the infection stages was observed at 30°C than at 27°C. Among the multiple peaks identified, comparison of the 100 top SNPs at each phenotyping time point revealed that less than 2% were shared between the CUT and UNCUT conditions, suggesting that the genetic basis of response to R. solanacearum largely depend on the infection process. Enrichment tests performed to determine the most important processes set up by the plant in response to R. solanacearum at 30°C for both inoculation conditions also support these specificities. Indeed, only few genes were found to be significantly over-represented in both conditions and correspond to the same miscellaneous functional class at 3 dai. Interestingly, they mainly encode for CYP450 subfamily 71 and 705 (CYP705) proteins as well as uridine diphosphate glycosyltransferases (UGT) known to be involved in plant response to biotic and abiotic stresses (Ross et al., 2001; Bak et al., 2011). In the CUT condition, at early infection stages, most genes underlying significantly over-represented biological processes correspond to regulatory genes. For instance, many genes encoding transcription factors (TF) were retrieved at 3 and 4 dai, suggesting a rapid transcriptional reprogramming in the early stages of infection. Interestingly, at later infection stages (i.e., from 5 to 7 dai), many genes are involved in calcium-dependent signaling, pathogen perception (TIR-NBS-LRR proteins) and regulation of biotic and abiotic stress responses (LRR- and cystein rich receptor like kinase proteins). For example, CRK28 and its interacting partner CRK29, were recently demonstrated to enhance plant immune responses (Yadeta et al., 2017). By contrast, genes retrieved with the UNCUT condition are predominantly involved in metabolic processes. In particular, genes underlying significantly over-represented biological processes at early infection stages correspond to Brassicaceae-specific CYP705 family and flavonol synthases. Even if the role of the CYP705 family is poorly characterized, the CYP705A1 was described as participating in the formation of a volatile homoterpene, (E)-4,8-dimethyl-1,3,7-nonatriene (DNMT), involved in the A. thaliana resistance to the root-rot pathogen Pythium irregular (Sohrabi et al., 2015). In addition, flavonoids are well-described molecules known to be important for response to other organisms or environmental stresses (Mierziak et al., 2014). At later infection stages (i.e., from 5 to 6 dai), candidate genes have primarily a role in cell wall formation. Interestingly, among virulence factors used by R. solanacearum, cell wall-degrading enzymes such as pectinolytic and cellulytic enzymes, can promote invasion of roots and/or penetration of xylem vessels (Liu et al., 2005). Such specific processes could allow certain accessions to restrict bacterial penetration at the early stages of infection on intact roots. Indeed, through the inoculation of plants with intact or cut roots, Turner et al. (2009) dissected in R. solanacearum the steps involved in root colonization of the model legume plant Medicago truncatula. While two distinct T3Es (Gala7 and AvrA) are involved in the early stages of colonization, suggesting that specific basal defense mechanisms are rapidly manipulated by the bacteria, Gala7 alone was shown to play a major role in the later stages of infection in cut roots (Turner et al., 2009).
In addition to the association peak identified at 5 dai in the CUT condition, GWA analyses revealed two other neat association peaks in the UNCUT condition, with the top SNPs located in the promoter region of the EIF4G gene and within the CesA3 gene. EIF4G is a translation initiation factor that belongs to protein families participating in the eukaryotic translation initiation complex. EIF4G was identified as a recessive resistance gene impairing multiplication of the cucumber mosaic virus (CMV) and of the turnip crinkle virus (TCV) in A. thaliana (Yoshii et al., 2004), or conferring high resistance to the rice yellow mottle virus in rice (Albar et al., 2006). The CesA3 gene belongs to a family of 10 CesA genes identified in A. thaliana of which 9 encode cellulose synthase subunits with known function. CesA1, -2, -3(IXR1), -5, and -6(IXR2) were shown to participate in the cellulose production during the primary cell wall formation, while CesA4 (IRX5), -7 (IRX3), -8(IRX1), and -9 are involved in the secondary cell wall cellulose synthase complex (Endler and Persson, 2011). Hernández-Blanco et al. (2007) demonstrated that mutation in CesA4, -7, and -8, involved in secondary cell wall formation, enhanced tolerance to Botrytis cinerea and Plectosphaerella cucumerina fungi as well as to R. solanacearum. Strikingly, performing inoculation at 27°C with plants for which roots were cut, the authors showed that the ixr1-1/cev1 mutant, altered in CesA3 expression, was susceptible to R. solanacearum. Clearly, further studies are needed to functionally validate the implication of these candidate genes in tolerance to R. solanacearum at elevated temperatures in the early infection stages.
As in many cases in which genetic mapping approaches were developed to identify resistance mechanisms to pathogens (Cook et al., 2012; Roux et al., 2014; Fukuoka et al., 2015), we found in our study that several QTLs control QDR to R. solanacearum at 30°C in a playful manner specific to the inoculation method. Interestingly, the CUT condition highlights different processes that could be related to the perception and regulation pathways, dependent on temperature, of well-conserved microbial signatures such as ubiquitous effectors and PAMPs. On the other hand, the UNCUT condition revealed processes associated to plant development and metabolism which could reflect strategies set up by the plant to limit bacteria penetration and propagation in root tissues at the early stages of infection. As demonstrated by Turner et al. (2009) on the bacterial side and proposed by Roux et al. (2014), these processes could involve host components, sequentially manipulated by effectors during host colonization.
A QDR to R. solanacearum Efficient at 30°C Is Conferred by a Strictosidine Synthase-Like Protein 4
At 5 and 6 dai in the CUT condition, a neat association peak was identified at the end of the chromosome III, corresponding to another QTL involved in early defense response at 30°C. The phenotyping of several T-DNA insertion mutants corresponding to genes underlying this QTL allowed the functional validation of At3g51420 (AtSSL4) as a gene of susceptibility to the R. solanacearum GMI1000 strain. Indeed, two allelic mutants were found to be significantly more resistant compared to wild-type Col-0 susceptible plants. The At3g51420 gene belongs to a subset of four genes (AtSSL4-AtSSL7), arranged in tandem, which shows a strong similarity with genes encoding for hemomucin membrane-anchored immune proteins from Drosophila melanogaster. These proteins contain strictosidine synthase-like (SSL) domain related to plant and Caenorhabditis elegans SSL proteins. Because hemomucin proteins from Drosophila have immune-related functions, Sohani et al. (2009) explored the possible role of AtSSL4-AtSSL7 in plant defense response. Contrary to other AtSSLs genes, AtSSL4 appeared to be slightly up-regulated upon wounding stress but not induced following inoculation with CMV and Alternaria brassicicola (Sohani et al., 2009). Still, these data do not exclude the possibility that AtSSL4 could be regulated by other pathogens, like R. solanacearum. Among the knockout mutants corresponding to the three other AtSSLs genes, the ssl5 mutant was also found to be more resistant to R. solanacearum at 30°C, from 3 to 10 dai. This result also suggests that AtSSL5 could be a gene of susceptibility to R. solanacearum. Interestingly, unlike AtSSL4, AtSSL5 expression is induced by salicylic acid, known to be a defense signaling compound, and is strongly up-regulated upon CMV and A. brassicicola inoculation (Sohani et al., 2009). In tomato, SSL gene expression is also up-regulated following the roots infection by Fusarium oxysporum f.sp. radicis-lycopersici (Manzo et al., 2016). Strictosidine synthase participates in the production of a wide range of monoterpenoid indole alkaloids important for plant defense response (Kibble et al., 2009) and Manzo et al. (2016) proposed that SSL could be involved in the incompatible interaction with the fungus. Thus, our result is the first demonstration of a role of plant SSLs in the resistance response to a bacterial pathogen. The enzymatic activity of proteins encoded by AtSSL4-AtSSL7 has not been demonstrated yet (Kibble et al., 2009). Nonetheless, knowing that SSLs expression is highly regulated in different plant species upon pathogen attack, the resistance spectrum conferred by these mutants to other RSSC strains and other pathogens will be investigated at elevated temperatures.
To our knowledge, this study is the first report of significant genetic variation in A. thaliana in response to R. solanacearum at elevated temperature. Our results also highlight that plant defense responses are strongly impacted at 30°C and differ according to the inoculation procedure. By combining a GWA mapping approach with the response to combined stresses, we identified three neat association peaks underlying QDR to R. solanacearum that are efficient at elevated temperature. Among the most interesting genes underlying the QTLs identified, we functionally validated AtSSL4 as a susceptibility gene that plays a role in R. solanacearum infection at 30°C. Apart from AtSSL4, other genes underlying additional QTLs also constitute good candidates for QDRs that might represent new sources of sustainable resistance to the RSSC in the context of climate warming. In addition, the inhibition of the RPS4/RRS1 resistance signaling at 30°C represents an interesting tool to investigate the impact of elevated temperature on ETI-related processes.
NA, FV, FR, and RB conceived the experiments. NA, LT, FL, FV, and RB performed the experiments. NA and FR performed GWA analyses. NA, FV, and RB analyzed the other data. NA, FR, LD, FV, and RB wrote and corrected the manuscript. All authors approved the manuscript.
NA benefited from a Ph.D. Grant co-financed by the Occitanie Regional Council and the INRA Plant Health and Environment division (SPE). FL was funded by a grant from the French Ministry of National Education and Research. This study was founded by INRA Plant Health and Environment division (SPE). This work was realized at the LIPM belonging to the Laboratoire d'Excellence (LABEX) entitled TULIP (ANR-10-LABX-41).
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
We thank the LIPM greenhouse service for their technical assistance and the Jiffy pots preparation.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/article/10.3389/fpls.2017.01387/full#supplementary-material
Ailloud, F., Lowe, T., Cellier, G., Roche, D., Allen, C., and Prior, P. (2015). Comparative genomic analysis of Ralstonia solanacearum reveals candidate genes for host specificity. BMC Genomics 16:270. doi: 10.1186/s12864-015-1474-8
Albar, L., Bangratz-Reyser, M., Hébrard, E., Ndjiondjop, M. N., Jones, M., and Ghesquière, A. (2006). Mutations in the eIF(iso)4G translation initiation factor confer high resistance of rice to Rice yellow mottle virus. Plant J. 47, 417–426. doi: 10.1111/j.1365-313X.2006.02792.x
Atkinson, N. J., Lilley, C. J., and Urwin, P. E. (2013). Identification of genes involved in the response of Arabidopsis to simultaneous biotic and abiotic stresses. Plant Physiol. 162, 2028–2041. doi: 10.1104/pp.113.222372
Bac-Molenaar, J. A., Fradin, E. F., Becker, F. F., Rienstra, J. A., van der Schoot, J., Vreugdenhil, D., et al. (2015). Genome-wide association mapping of fertility reduction upon heat stress reveals developmental stage-specific QTLs in Arabidopsis thaliana. Plant Cell 27, 1857–1874. doi: 10.1105/tpc.15.00248
Bita, C. E., and Gerats, T. (2013). Plant tolerance to high temperature in a changing environment: scientific fundamentals and production of heat stress-tolerant crops. Front. Plant Sci. 4:273. doi: 10.3389/fpls.2013.00273
Brachi, B., Faure, N., Horton, M., Flahauw, E., Vazquez, A., Nordborg, M., et al. (2010). Linkage and association mapping of Arabidopsis thaliana flowering time in nature. PLoS Genet. 6:e1000940. doi: 10.1371/journal.pgen.1000940
Carmeille, A., Caranta, C., Dintinger, J., Prior, P., Luisetti, J., and Besse, P. (2006). Identification of QTLs for Ralstonia solanacearum race 3-phylotype II resistance in tomato. Theor. Appl. Genet. 113, 110–121. doi: 10.1007/s00122-006-0277-3
Cook, D. E., Lee, T. G., Guo, X., Melito, S., Wang, K., Bayless, A. M., et al. (2012). Copy number variation of multiple genes at Rhg1 mediates nematode resistance in soybean. Science 338, 1206–1209. doi: 10.1126/science.1228746
Cooke, D. E., Cano, L. M., Raffaele, S., Bain, R. A., Cooke, L. R., Etherington, G. J., et al. (2012). Genome analyses of an aggressive and invasive lineage of the Irish potato famine pathogen. PLoS Pathog. 8:e1002940. doi: 10.1371/journal.ppat.1002940
Coupat, B., Chaumeille-Dole, F., Fall, S., Prior, P., Simonet, P., Nesme, X., et al. (2008). Natural transformation in the Ralstonia solanacearum species complex: number and size of DNA that can be transferred. FEMS Microbiol. Ecol. 66, 14–24. doi: 10.1111/j.1574-6941.2008.00552.x
de Jong, C. F., Takken, F. L., Cai, X., de Wit, P. J., and Joosten, M. H. (2002). Attenuation of Cf-mediated defense responses at elevated temperatures correlates with a decrease in elicitor-binding sites. Mol. Plant Microbe Interact. 15, 1040–1049. doi: 10.1094/MPMI.2002.15.10.1040
Debieu, M., Huard-Chauveau, C., Genissel, A., Roux, F., and Roby, D. (2016). Quantitative disease resistance to the bacterial pathogen Xanthomonas campestris involves an Arabidopsis immune receptor pair and a gene of unknown function. Mol. Plant Pathol. 17, 510–520. doi: 10.1111/mpp.12298
Deslandes, L., Olivier, J., Theulieres, F., Hirsch, J., Feng, D. X., Bittner-Eddy, P., et al. (2002). Resistance to Ralstonia solanacearum in Arabidopsis thaliana is conferred by the recessive RRS1-R gene, a member of a novel family of resistance genes. Proc. Natl. Acad. Sci. U.S.A. 99, 2404–2409. doi: 10.1073/pnas.032485099
Deslandes, L., Pileur, F., Liaubet, L., Camut, S., Can, C., Williams, K., et al. (1998). Genetic characterization of RRS1, a recessive locus in Arabidopsis thaliana that confers resistance to the bacterial soilborne pathogen Ralstonia solanacearum. Mol. Plant Microbe Interact. 11, 659–667. doi: 10.1094/MPMI.19220.127.116.119
Evans, N., Baierl, A., Semenov, M. A., Gladders, P., and Fitt, B. D. (2008). Range and severity of a plant disease increased by global warming. J. R. Soc. Interface 5, 525–531. doi: 10.1098/rsif.2007.1136
Fu, D., Uauy, C., Distelfeld, A., Blechl, A., Epstein, L., Chen, X., et al. (2009). A kinase-START gene confers temperature-dependent resistance to wheat stripe rust. Science 323, 1357–1360. doi: 10.1126/science.1166289
Garrett, K. A., Dendy, S. P., Frank, E. E., Rouse, M. N., and Travers, S. E. (2006). Climate change effects on plant disease: genomes to ecosystems. Annu. Rev. Phytopathol. 44, 489–509. doi: 10.1146/annurev.phyto.44.070505.143420
Godiard, L., Sauviac, L., Torii, K. U., Grenon, O., Mangin, B., Grimsley, N. H., et al. (2003). ERECTA, an LRR receptor-like kinase protein controlling development pleiotropically affects resistance to bacterial wilt. Plant J. 36, 353–365. doi: 10.1046/j.1365-313X.2003.01877.x
Hancock, A. M., Brachi, B., Faure, N., Horton, M. W., Jarymowycz, L. B., Sperone, F. G., et al. (2011). Adaptation to climate across the Arabidopsis thaliana genome. Science 334, 83–86. doi: 10.1126/science.1209244
Hatfield, J., Boote, K., Kimball, B., Ziska, L., Izaurralde, R., Ort, D., et al. (2011). Climate impacts on agriculture: implications for crop production. Agron. J. 103, 351–370. doi: 10.2134/agronj2010.0303
Heidrich, K., Tsuda, K., Blanvillain-Baufume, S., Wirthmueller, L., Bautor, J., and Parker, J. E. (2013). Arabidopsis TNL-WRKY domain receptor RRS1 contributes to temperature-conditioned RPS4 auto-immunity. Front. Plant Sci. 4:403. doi: 10.3389/fpls.2013.00403
Hernández-Blanco, C., Feng, D. X., Hu, J., Sánchez-Vallet, A., Deslandes, L., Llorente, F., et al. (2007). Impairment of cellulose synthases required for Arabidopsis secondary cell wall formation enhances disease resistance. Plant Cell 19, 890–903. doi: 10.1105/tpc.106.048058
Horton, M. W., Hancock, A. M., Huang, Y. S., Toomajian, C., Atwell, S., Auton, A., et al. (2012). Genome-wide patterns of genetic variation in worldwide Arabidopsis thaliana accessions from the RegMap panel. Nat. Genet. 44, 212–216. doi: 10.1038/ng.1042
Hovmoller, M. S., Yahyaoui, A. H., Milus, E. A., and Justesen, A. F. (2008). Rapid global spread of two aggressive strains of a wheat rust fungus. Mol. Ecol. 17, 3818–3826. doi: 10.1111/j.1365-294X.2008.03886.x
Huard-Chauveau, C., Perchepied, L., Debieu, M., Rivas, S., Kroj, T., Kars, I., et al. (2013). An atypical kinase under balancing selection confers broad-spectrum disease resistance in Arabidopsis. PLoS Genet. 9:e1003766. doi: 10.1371/journal.pgen.1003766
Hwang, C.-F., Bhakta, A. V., Truesdell, G. M., Pudlo, W. M., and Williamson, V. M. (2000). Evidence for a role of the N terminus and leucine-rich repeat region of the Mi gene product in regulation of localized cell death. Plant Cell 12, 1319–1329. doi: 10.1105/tpc.12.8.1319
IPCC (2014). Climate Change 2014: Synthesis Report. Contribution of Working Groups I, II and III to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change, Core Writing Team, Geneva.
Kang, H. M., Sul, J. H., Service, S. K., Zaitlen, N. A., Kong, S. Y., Freimer, N. B., et al. (2010). Variance component model to account for sample structure in genome-wide association studies. Nat. Genet. 42, 348–354. doi: 10.1038/ng.548
Kibble, N., Sohani, M., Shirley, N., Byrt, C., Cut, R., Antony, B., et al. (2009). Phylogenetic analysis and functional characterization of strictosidine synthase-like genes in Arabidopsis thaliana. Funct. Plant Biol. 36, 1098–1109. doi: 10.1071/FP09104
Le Roux, C., Huet, G., Jauneau, A., Camborde, L., Trémousaygue, D., Kraut, A., et al. (2015). A receptor pair with an integrated decoy converts pathogen disabling of transcription factors to immunity. Cell 161, 1074–1088. doi: 10.1016/j.cell.2015.04.025
Lempe, J., Balasubramanian, S., Sureshkumar, S., Singh, A., Schmid, M., and Weigel, D. (2005). Diversity of flowering responses in wild Arabidopsis thaliana strains. PLoS Genet. 1:e6. doi: 10.1371/journal.pgen.0010006
Liu, H., Zhang, S., Schell, M. A., and Denny, T. P. (2005). Pyramiding unmarked deletions in Ralstonia solanacearum shows that secreted proteins in addition to plant cell-wall-degrading enzymes contribute to virulence. Mol. Plant Microbe Interact. 18, 1296–1305. doi: 10.1094/MPMI-18-1296
Lohou, D., Turner, M., Lonjon, F., Cazalé, A. C., Peeters, N., Genin, S., et al. (2014). HpaP modulates type III effector secretion in Ralstonia solanacearum and harbours a substrate specificity switch domain essential for virulence. Mol. Plant Pathol. 15, 601–614. doi: 10.1111/mpp.12119
Mangin, B., Thoquet, P., Olivier, J., and Grimsley, N. H. (1999). Temporal and multiple quantitative trait loci analyses of resistance to bacterial wilt in tomato permit the resolution of linked loci. Genetics 151, 1165–1172.
Manzo, D., Ferriello, F., Puopolo, G., Zoina, A., D'Esposito, D., Tardella, L., et al. (2016). Fusarium oxysporum f.sp. radicis-lycopersici induces distinct transcriptome reprogramming in resistant and susceptible isogenic tomato lines. BMC Plant Biol 16:53. doi: 10.1186/s12870-016-0740-5
Mayjonade, B., Gouzy, J., Donnadieu, C., Pouilly, N., Marande, W., Callot, C., et al. (2016). Extraction of high-molecular-weight genomic DNA for long-read sequencing of single molecules. BioTechniques 61, 203–205. doi: 10.2144/000114460
Menna, A., Nguyen, D., Guttman, D. S., and Desveaux, D. (2015). Elevated temperature differentially influences effector-triggered immunity outputs in Arabidopsis. Front. Plant Sci. 6:995. doi: 10.3389/fpls.2015.00995
Narusaka, M., Kubo, Y., Shiraishi, T., Iwabuchi, M., and Narusaka, Y. (2009). A dual resistance gene system prevents infection by three distinct pathogens. Plant Signal. Behav. 4, 954–955. doi: 10.1111/j.1365-313X.2009.03949.x
Negeri, A., Wang, G. F., Benavente, L., Kibiti, C. M., Chaikam, V., Johal, G., et al. (2013). Characterization of temperature and light effects on the defense response phenotypes associated with the maize Rp1-D21 autoactive resistance gene. BMC Plant Biol. 13:106. doi: 10.1186/1471-2229-13-106
Onaga, G., Wydra, K., Koopmann, B., Chebotarov, D., Séré, Y., and Von Tiedemann, A. (2017). High temperature effects on Pi54 conferred resistance to Magnaporthe oryzae in two genetic backgrounds of Oryza sativa. J. Plant Physiol. 212, 80–93. doi: 10.1016/j.jplph.2017.02.004
Plener, L., Manfredi, P., Valls, M., and Genin, S. (2010). PrhG, a transcriptional regulator responding to growth conditions, is involved in the control of the type III secretion system regulon in Ralstonia solanacearum. J. Bacteriol. 192, 1011–1019. doi: 10.1128/JB.01189-09
Poland, J. A., Balint-Kurti, P. J., Wisser, R. J., Pratt, R. C., and Nelson, R. J. (2009). Shades of gray: the world of quantitative disease resistance. Trends Plant Sci. 14, 21–29. doi: 10.1016/j.tplants.2008.10.006
Prasch, C. M., and Sonnewald, U. (2013). Simultaneous application of heat, drought, and virus to Arabidopsis plants reveals significant shifts in signaling networks. Plant Physiol. 162, 1849–1866. doi: 10.1104/pp.113.221044
Prior, P., Bart, S., Leclercq, S., Darrasse, A., and Anais, G. (1996). Resistance to bacterial wilt in tomato as discerned by spread of Pseudomonas (Burholderia) solanacearum in the stem tissues. Plant Pathol. 45, 720–726. doi: 10.1046/j.1365-3059.1996.d01-9.x
Rasmussen, S., Barah, P., Suarez-Rodriguez, M. C., Bressendorff, S., Friis, P., Costantino, P., et al. (2013). Transcriptome responses to combinations of stresses in Arabidopsis. Plant Physiol. 161, 1783–1794. doi: 10.1104/pp.112.210773
Remenant, B., Coupat-Goutaland, B., Guidot, A., Cellier, G., Wicker, E., Allen, C., et al. (2010). Genomes of three tomato pathogens within the Ralstonia solanacearum species complex reveal significant evolutionary divergence. BMC Genomics 11:379. doi: 10.1186/1471-2164-11-379
Roux, F., and Bergelson, J. (2016). The genetics underlying natural variation in the biotic interactions of Arabidopsis thaliana: the challenges of linking evolutionary genetics and community ecology. Curr. Top. Dev. Biol. 119, 111–156. doi: 10.1016/bs.ctdb.2016.03.001
Roux, F., Voisin, D., Badet, T., Balague, C., Barlet, X., Huard-Chauveau, C., et al. (2014). Resistance to phytopathogens e tutti quanti: placing plant quantitative disease resistance on the map. Mol. Plant Pathol. 15, 427–432. doi: 10.1111/mpp.12138
Singh, R. P., Hodson, D. P., Huerta-Espino, J., Jin, Y., Bhavani, S., Njau, P., et al. (2011). The emergence of Ug99 races of the stem rust fungus is a threat to world wheat production. Annu. Rev. Phytopathol. 49, 465–481. doi: 10.1146/annurev-phyto-072910-095423
Sohani, M. M., Schenk, P. M., Schultz, C. J., and Schmidt, O. (2009). Phylogenetic and transcriptional analysis of a strictosidine synthase-like gene family in Arabidopsis thaliana reveals involvement in plant defence responses. Plant Biol. 11, 105–117. doi: 10.1111/j.1438-8677.2008.00139.x
Sohrabi, R., Huh, J. H., Badieyan, S., Rakotondraibe, L. H., Kliebenstein, D. J., Sobrado, P., et al. (2015). In planta variation of volatile biosynthesis: an alternative biosynthetic route to the formation of the pathogen-induced volatile homoterpene DMNT via triterpene degradation in Arabidopsis roots. Plant Cell 27, 874–890. doi: 10.1105/tpc.114.132209
Thoen, M. P., Davila Olivas, N. H., Kloth, K. J., Coolen, S., Huang, P. P., Aarts, M. G., et al. (2017). Genetic architecture of plant stress resistance: multi-trait genome-wide association mapping. New Phytol. 213, 1346–1362. doi: 10.1111/nph.14220
Turner, M., Jauneau, A., Genin, S., Tavella, M. J., Vailleau, F., Gentzbittel, L., et al. (2009). Dissection of bacterial Wilt on Medicago truncatula revealed two type III secretion system effectors acting on root infection process and disease development. Plant Physiol. 150, 1713–1722. doi: 10.1104/pp.109.141523
Van der Linden, L., Bredenkamp, J., Naidoo, S., Fouché-Weich, J., Denby, K. J., Genin, S., et al. (2013). Gene-for-gene tolerance to bacterial wilt in Arabidopsis. Mol. Plant Microbe Interact. 26, 398–406. doi: 10.1094/MPMI-07-12-0188-R
van Wersch, R., Li, X., and Zhang, Y. (2016). Mighty dwarfs: Arabidopsis autoimmune mutants and their usages in genetic dissection of plant immunity. Front. Plant Sci. 7:1717. doi: 10.3389/fpls.2016.01717
Wang, J. F., Olivier, J., Thoquet, P., Mangin, B., Sauviac, L., and Grimsley, N. H. (2000). Resistance of tomato line Hawaii7996 to Ralstonia solanacearum Pss4 in Taiwan is controlled mainly by a major strain-specific locus. Mol. Plant Microbe Interact. 13, 6–13. doi: 10.1094/mpmi.2000.13.1.6
Webb, K. M., Oña, I., Bai, J., Garrett, K. A., Mew, T., Vera Cruz, C. M., et al. (2010). A benefit of high temperature: increased effectiveness of a rice bacterial blight disease resistance gene. New Phytol. 185, 568–576. doi: 10.1111/j.1469-8137.2009.03076.x
Wicker, E., Grassart, L., Coranson-Beaudu, R., Mian, D., Guilbaud, C., Fegan, M., et al. (2007). Ralstonia solanacearum strains from Martinique (French West Indies) exhibiting a new pathogenic potential. Appl. Environ. Microbiol. 73, 6790–6801. doi: 10.1128/aem.00841-07
Xiao, S., Brown, S., Patrick, E., Brearley, C., and Turner, J. G. (2003). Enhanced transcription of the Arabidopsis disease resistance genes RPW8.1 and RPW8.2 via a salicylic acid-dependent amplification circuit is required for hypersensitive cell death. Plant Cell 15, 33–45. doi: 10.1105/tpc.006940
Yadeta, K. A., Elmore, J. M., Creer, A. Y., Feng, B., Franco, J. Y., Rufian, J. S., et al. (2017). A cysteine-rich protein kinase associates with a membrane immune complex and the cysteine residues are required for cell death. Plant Physiol. 173, 771–787. doi: 10.1104/pp.16.01404
Yoshii, M., Nishikiori, M., Tomita, K., Yoshioka, N., Kozuka, R., Naito, S., et al. (2004). The Arabidopsis cucumovirus multiplication 1 and 2 loci encode translation initiation factors 4E and 4G. J. Virol. 78, 6102–6111. doi: 10.1128/JVI.78.12.6102-6111.2004
Keywords: climate warming, quantitative disease resistance, Ralstonia solanacearum, Arabidopsis thaliana, natural diversity, genome wide association mapping
Citation: Aoun N, Tauleigne L, Lonjon F, Deslandes L, Vailleau F, Roux F and Berthomé R (2017) Quantitative Disease Resistance under Elevated Temperature: Genetic Basis of New Resistance Mechanisms to Ralstonia solanacearum. Front. Plant Sci. 8:1387. doi: 10.3389/fpls.2017.01387
Received: 10 April 2017; Accepted: 25 July 2017;
Published: 22 August 2017.
Edited by:Pierre Fobert, National Research Council Canada, Canada
Reviewed by:Sanushka Naidoo, University of Pretoria, South Africa
Xiao-Feng Dai, Institute of Food Science and Technology, China
Copyright © 2017 Aoun, Tauleigne, Lonjon, Deslandes, Vailleau, Roux and Berthomé. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Richard Berthomé, email@example.com