Social bacteria use chemical communication to coordinate and synchronize gene expression via the quorum-sensing (QS) regulatory pathway. In Pectobacterium, a causative agent of the blackleg and soft-rot diseases on potato plants and tubers, expression of the virulence factors is collectively controlled by the QS-signals N-acylhomoserine lactones (NAHLs). Several soil bacteria, such as the actinobacterium Rhodococcus erythropolis, are able to degrade NAHLs, hence quench the chemical communication and virulence of Pectobacterium. Here, next-generation sequencing was used to investigate structural and functional genomics of the NAHL-degrading R. erythropolis strain R138. The R. erythropolis R138 genome (6.7 Mbp) contained a single circular chromosome, one linear (250 kbp) and one circular (84 kbp) plasmid. Growth of R. erythropolis and P. atrosepticum was not altered in mixed-cultures as compared with monocultures on potato tuber slices. HiSeq-transcriptomics revealed that no R. erythropolis genes were differentially expressed when R. erythropolis was cultivated in the presence vs absence of the avirulent P. atrosepticum mutant expI, which is defective for QS-signal synthesis. By contrast 50 genes (<1% of the R. erythropolis genome) were differentially expressed when R. erythropolis was cultivated in the presence vs absence of the NAHL-producing virulent P. atrosepticum. Among them, quantitative real-time reverse-transcriptase–PCR confirmed that the expression of some alkyl-sulfatase genes decreased in the presence of a virulent P. atrosepticum, as well as deprivation of organic sulfur such as methionine, which is a key precursor in the synthesis of NAHL by P. atrosepticum.
The plant microbiome encompasses up to thousands of microbial species which interact with each other and with their host, hence affecting health and reproduction of plants, as well as the productivity of crops (Mendes et al., 2013; Berg et al., 2014). Within microbiome, several bacterial species exhibit capacity to coordinate and synchronize gene expression at a population level using diffusible signals. The production, exchange and perception of these signals by bacteria define a gene-regulatory pathway called quorum-sensing (QS; Fuqua et al., 1994). The QS-regulated functions are diverse and have crucial role in microbe–microbe and host-microbe interactions as they are involved in the production of antimicrobial compounds, expression of symbiotic and virulence functions, horizontal gene transfer, as well as formation of biofilms (Boyer and Wisniewski-Dyé, 2009). The plant microbiome also encompasses QS signal-degrading species which may interfere with QS-communication, hence quench the QS-regulated functions of the QS signal-producing species (d'Angelo-Picard et al., 2005; Cirou et al., 2007). Consequently, the interaction between QS signal-producing and -degrading species may directly affect microbiome dynamics and functions, and plant-host health. This paradigm is exemplified by the three-partner interaction involving the QS signal-degrading species Rhodococcus erythropolis, the QS signal-producing species Pectobacterium atrosepticum and their potato plant-host Solanum tuberosum.
P. atrosepticum is a causing agent of the blackleg and soft-rot diseases on potato plants and tubers (Toth et al., 2011). These pathogenic bacteria produce and exchange, N-acylhomoserine lactones (NAHLs) as QS-signal molecules for controlling and coordinating expression of the virulence factors (Jones et al., 1993; Pirhonen et al., 1993). Pectobacterium mutants, which are defective or attenuated in the synthesis, accumulation or perception of the NAHL signals, are unable to express virulence factors and unable to induce disease symptoms on host plants (Pirhonen et al., 1993; Smadja et al., 2004; Liu et al., 2008; Crépin et al., 2012a). Transcriptomics revealed that QS controls expression of 1100 genes in Pectobacterium; hence up to a quarter of its genome, including most of the virulence factors, the plant cell-wall degrading enzymes and their secretion systems, as well as several metabolic pathways (Liu et al., 2008). Because of the key role of QS in virulence, NAHL signals are putative targets for developing anti-virulence strategies against Pectobacterium-induced symptoms (Dong et al., 2007; Faure and Dessaux, 2007; Crépin et al., 2012b). One of these strategies uses particular bacterial strains as biocontrol agents that are able to cleave and degrade NAHL and disrupt QS-signaling of the plant pathogen Pectobacterium.
NAHL-degrading bacterial strains belong to different phyla such as Proteobacteria (e.g., Agrobacterium, Ralstonia, Ochrobactrum), Firmicutes (Bacillus) and Actinobacteria (Rhodococcus). In the plant pathogen Agrobacterium tumefaciens, two cytoplasmic lactonases were shown to be involved in opening of the gamma-butyrolactone ring of NAHLs, and their expression was controlled by plant-derived compounds (Zhang et al., 2002; Carlier et al., 2003; Chevrot et al., 2006; Haudecoeur et al., 2009a, 2009b). R. erythropolis, which is a common inhabitant of the potato plant environment (Cirou et al., 2011; Diallo et al., 2011), efficiently degrades NAHL signals through three intracellular enzymatic activities: lactonase, amidase and reductase (Uroz et al., 2009). The reductase alters ketone function on acyl chain of the NAHL molecules, whereas the lactonase and amidase hydrolyze NAHLs to by products that are proposed to be assimilated through fatty acid oxidation pathways. Regulation of their expression by NAHL or other signals is unknown. Because NAHL molecules diffuse through cell membranes, R. erythropolis is able to degrade NAHL, even its NAHL-degrading enzymes are not secreted. Only the lactonase-encoding gene qsdA was identified in R. erythropolis (Uroz et al., 2008), whereas the genetic determinants coding for the reductase and amidase activities are still unknown. QsdA was showed to be involved in the cleavage of NAHLs and related lactones, such as gamma-heptanolactone and gamma-hexanolactone, which are assimilated as a sole carbon and energy source by R. erythropolis (Uroz et al., 2008; Barbey et al., 2012; Cirou et al., 2012). Because of its ability to cleave NAHLs, R. erythropolis is proposed as a plant-protecting and anti-biofouling agent (Cirou et al., 2007; Faure and Dessaux, 2007; Oh et al., 2012). In addition to NAHL catabolism, R. erythropolis exhibits the capability for degrading hydrocarbons and xenobiotics, hence this bacterium is used as a bioremediation agent for the treatment of polluted soils and waters (de Carvalho and da Fonseca, 2005). Particularly, R. erythropolis may exhibit the capability to cleave C-S bonds in fossil-fuel compounds using four desulfurization enzymes (Ohshiro et al., 1997). Because of the structure of NAHL, consisting in a homoserine lactone linked to an acyl chain, involvement of fatty acid metabolism in NAHL degradation is expected.
Although the capacity of the NAHL-degrading R. erythropolis to obliterate QS-pathway, hence to markedly reduce the virulence gene expression in P. atrosepticum is well documented (Cirou et al., 2007; Barbey et al., 2013), how P. atrosepticum could modify the R. erythropolis transcriptome is not known. In this work, we reported the structural and functional genomics of the NAHL-degrading R. erythropolis strain R138. Specifically, we compared the R. erythropolis transcriptomes when it colonized tuber slices in the presence of either the potato pathogen P. atrosepticum CFBP6276 or its avirulent derivative that is defective for the synthesis of NAHL signals. This work reported a first transcriptome of a NAHL-degrading bacterium in the presence of a NAHL-producing one.
Materials and Methods
R. erythropolis R138 (Cirou et al., 2007) and P. atrosepticum CFBP6276 (Kwasiborski et al., 2013), as well as its expI KmR-derivative, which is defective for producing the NAHL signals and virulence factors (Latour et al., 2007), were routinely cultivated at 28 °C in TY medium (0.5% tryptone, 0.3% yeast extract) supplemented with kanamycin (50 μg ml−1) when appropriate. The NAHL-biosensor Agrobacterium tumefaciens NT1(pZLR4) was cultivated in Agrobacterium Broth (AB) medium supplemented with mannitol (2 g l−1), NH4Cl (1 g l−1) and gentamycin (25 μg ml−1) as described previously (Cha et al., 1998).
Culture conditions with inorganic and organic sulfur sources
Cultures of R. erythropolis R138 in liquid AB medium with gamma caprolactone (2 g l−1) as a carbon source were washed twice in 0.8% NaCl. Bacteria were inoculated at OD600 value of 0.6 in fresh AB medium supplemented with inorganic (MgSO4) and organic (methionine) sulfur sources at 24 and 0.24 mM. After 6 h of incubation at 30 °C, one volume of RNA protect Cell Reagent (Qiagen, Hilden, Germany) was added to the culture and was frozen at −80 °C until use. Each of the four tested culture conditions (two sulfur sources at two concentrations) was replicated three times.
Total DNA of R. erythropolis R138 was extracted from the pellet of a bacterial suspension adjusted to an optical density of 0.6 at 600 nm. The cell lysis was carried out at 37 °C during 2 h in 0.5 ml of TES buffer pH 8 (10 mM Tris, 1 mM EDTA and 150 mM NaCl) supplemented with 20 mg ml−1 lysozyme (Eurobio, Les Ulis, France) and 133 μg ml−1 RNase (Sigma-Aldrich, St-Louis, MO, USA). Then, 100 μl of 20% w/v SDS were added before gentle mixing. One volume of phenol/choroform/isoamylic acid (25:24:1, Sigma-Aldrich) was added, mixed and centrifuged for 15 min at 15 000 g. The aqueous phase was washed twice by addition of one volume of Aquaphenol (MP bio, Santa Ana, California, USA). The genomic DNA was precipitated by one volume of isopropanol. After a centrifugation for 10 min at 15 000 g, the DNA was washed by an addition of a volume of 70% ethanol followed by centrifugation for 10 min at 15 000 g. The pellet was dried before the DNA was solubilized in TE buffer pH 7.5 (10 mM Tris-HCl, 1 mM EDTA). The DNA concentration was estimated using the Nanodrop 1000 spectrophotometer (Thermo Scientific, Whaltham, MA, USA) and frozen until used.
De novo genome assembly of R. erythropolis R138 was performed by combining Illumina and 454-Roche technologies as described by Kwasiborski et al. (2014). Reads were collected from three genomic libraries: two short-fragment libraries (300 bp and 380 bp) used for paired-end 2 × 72 Illumina-sequencing (ImaGif, Paris, France) and single read 454-sequencing (Eurofins MWG, Ebersberg, Germany), and a long-paired end library with an insert size of 8 kbp used for 454-sequencing (Eurofins MWG). Assembly was carried out using the CLC Genomics Workbench v5.1 (CLC bio, Aarhus, Denmark) with read length at 0.5 and similarity at 0.8 as parameters. The coding sequences and their functions of the genome were predicted using the Rapid Annotation using Subsystem Technology v4.0 (RAST) automated pipeline (Aziz et al., 2008). The genome of R. erythropolis R138 was deposited at NCBI (http://www.ncbi.nlm.nih.gov/) under the GenBank reference ASKF00000000.
Inoculation of bacteria on potato tuber slices was adapted from a protocol previously described by Kwasiborski et al., (2012). Bacteria cultivated in TY medium were washed in saline water (0.8% w/v NaCl) and the cell number was adjusted to 109 c.f.u. ml−1. Tuber slices (1 cm) of Solanum tuberosum variety Allians were covered with a membrane (Supor 450, diameter 25 mm, pore size of 0.45 μm, PALL, NY, USA) and inoculated by 300 μl of three cell suspensions: R. erythropolis R138 alone, a mix (ratio 10:1) between R. erythropolis R138 and P. atrosepticum CFBP6276, and a mix (ratio 10:1) between R. erythropolis R138 and the P. atrosepticum expI mutant. The 10:1 ratio between R. erythropolis and P. atrosepticum allowed a reduction of symptoms on potato tuber, as described previously (Cirou et al., 2007). The population dynamics of R. erythropolis and P. atrosepticum on potato tuber slices were measured every 3 hours over a period of 27 h. Bacteria on membranes were recovered by vortexing in saline water (2 ml). Serial dilutions of the bacterial suspensions were plated on TY medium supplemented with X-gal (40 μg ml−1) and incubated at 25 °C for 4 days before counting. R. erythropolis R138 appeared as white colonies, whereas P. atrosepticum CFBP6276 and its expI derivative appeared as blue colonies. Experiments were performed in triplicates.
NAHL extraction and quantification
NAHL extraction and quantification procedures were adapted from Cha et al. (1998) Briefly, bacterial cell suspensions recovered from potato slices, were centrifuged for 10 min at 15 000 g. NAHLs were extracted from the supernatant by addition of one volume of ethyl acetate and air-drying the organic fraction. The extracted NAHLs were dissolved in 20 μl of ethyl acetate, of which 5 μl was spotted on TLC (thin layer chromatography) silica plates (Macherey-Nagel, Düren, Germany). TLCs were overlaid with the NAHL-biosensor strain A. tumefaciens NT1(pZLR4) in AB medium supplemented with agar (15 g l−1) and X-gal (40 μg ml−1). For the quantification of NAHLs, a calibration curve was obtained with pure NAHL, 3-oxo-octanoylhomoserine lactone (Sigma-Aldrich).
After 22-hour incubation of potato slices at 25 °C, bacteria were collected from membranes by vortexing in 1 ml of 50% RNAprotect Cell Reagent. After centrifugation for 10 min at 20 800 g, bacterial pellets were frozen at −80 °C until use. Each of the three conditions, R. erythropolis R138 alone and R. erythropolis R138 in association with either P. atrosepticum CFBP6276 or its expI derivative were replicated three times. The total RNA extraction was carried out using the NucleoSpin RNA II (Macherey-Nagel) according to the manufacturer’s recommendations. The RNAseq analysis was performed using ProfileXpert (University of Lyon I, Lyon, France). RNA control was carried out using the 2100 Bioanalyzer Instrument (Agilent, Santa Clara, CA, USA), then Ribo-Zero rRNA Removal Meta-bacteria kits (tebu-bio, Le Perray en Yvelines, France) was used for rRNA depletion. Directional RNA paired-end libraries were sequenced (2 × 50 bp) on Illumina Hiseq-2500. The number of aligned reads per predicted gene were counted and normalized according to the gene length to calculate for each gene the number of reads per Kilo base per Million mapped reads (RPKM). No interspecies hybridization was observed between the genome of the actinobacterium R. erythropolis R138 and that of the proteobacterium P. atrosepticum CFBP6276 (Kwasiborski et al., 2013).
The differentially expressed genes of R. erythropolis R138 in the presence vs absence of P. atrosepticum CFBP6276 and its expI mutant were identified using DEseq v1.9.6, an R program language package available through the Bioconductor platform (http://www.bioconductor.org/packages/release/bioc/html/DESeq.html). DEseq estimates the variance-mean dependence in count data from high-throughput sequencing assays and tests for differential expression based on a model using the negative binomial distribution (Anders and Huber, 2010). We also listed the highly expressed genes of R. erythropolis when it colonized the potato tuber slices alone. We considered only genes exhibiting a RPKM median value, which was over by three times the RPKM median value of all genes. All predicted genes of which the standard deviation of RPKM was over the RPKM mean value were discarded of the analysis.
Quantitative real-time reverse-transcriptase–PCR (qRT-PCR)
Expression of several genes was quantified by qRT-PCR using biological triplicates. Sequences and characteristics of used primers are presented in the Supplementary Table S1. Reverse transcriptions were carried out using the protocol for high GC content bacteria from the Revert Aid Reverse Transcriptase according to the manufacturer’s recommendations (Fermentas, Whaltham, MA, USA). A Light Cycler 480 (Roche Applied Science, Penzberg, Germany) and Light Cycler 480 SYBR Green I Master (Roche Applied Science) were used for quantitative PCR. The 15 μl final-volume mix contained SYBR Green I Master (1x), forward and reverse primers (1 μM) and 0.01 μg of cDNA samples. After denaturation at 95 °C for 10 min, the amplification and quantification program was repeated 45 times as follows: 95 °C for 15 s, 60 °C for 15 s, 72 °C for 20 s, with a single fluorescence measurement, followed by the melting curve program (65 °C–95 °C with a heating rate of 0.1 °C s−1 and a continuous fluorescence measurement) and a final cooling step at 45 °C. The recombinase A (recA) gene was used as a reference gene.
Genome architecture of R. erythropolis R138
The genome of R. erythropolis R138 consisted of one circular chromosome (6 444 726 bp), a linear plasmid (247 675 bp) and a circular plasmid (84 151 bp). The G+C content was homogenous among the replicons, from 60–62% (Figure 1). The chromosome sequence resulted from the assembly of nine contigs from 5.5 kbp to 2.7 Mbp, which were spaced out by undetermined sequences measuring from 10 to 5500 bp. The linear plasmid sequence was composed of two contigs (22 and 220 kbp), which were separated by a single gap measuring ~3.8 kbp. Finally, the circular plasmid sequence resulted from a single contig of 84 kbp. All characteristics of contigs and gaps are indicated in Supplementary Table S2. Using the GC skew calculation (Perna and Kocher, 1995), replication origins could be located on the chromosome and the circular plasmid and were used for starting the nucleotide numbering. Using the automated annotation RAST software (Table 1), 6562 open reading frames (ORFs) were predicted on the reverse and forward strands (Figure 1). Twelve rRNAs and 50 tRNAs were identified. From 86–94% of R. erythropolis R138 genome sequence in length was shared by genomes of the R. erythropolis strains isolated from different environments: PR4 from ocean, XP and DN1 from oil-contaminated soil, SK121 from human skin and CCM2595 from soil (Sekine et al., 2006; Vesely et al., 2007; Shevtsov et al., 2013). By contrast, number, size and functions of plasmids differed when the R. erythropolis strains were compared.
Among the predicted R. erythropolis R138 ORFs, only 2576 (39.3%) were classified in the RAST-functional categories, showing that the protein annotation was poorly documented in this species. Among them, five categories (metabolism of amino acids, carbohydrates, cofactors, proteins and fatty acids) were the most represented in the genome of R. erythropolis R138. Fatty acid and sulfur metabolism are the most studied pathways in R. erythropolis (de Carvalho and da Fonseca, 2005). Interestingly, in the strain R138, 75 and 268 ORFs are involved in the metabolisms of sulfur and fatty acid, respectively. Especially, the chromosome and linear plasmid harbored a large variety of desulfurating enzymes: five dibenzothiophene desulfurization enzymes that break thioether bonds and six alkylsulfatases, and five arylsulfatases that remove sulfate from diverse carbon skeletons. R. erythropolis R138 also possessed a high number of genes related to acyl-chain degradation and recycling: as an example, the family of long-chain fatty acid-CoA ligases, which are involved in activation of the fatty acids in the course of beta-oxidation, is represented by 66 ORFs.
R. erythropolis R138 and P. atrosepticum CFBP6276 co-exist on potato tubers
On potato slices, R. erythropolis R138 and P. atrosepticum CFBP6276 (or its expI derivative) grew alone and in mixed populations (Figure 2a), confirming that R. erythropolis R138 did not express antibiotic activities against P. atrosepticum CFBP6276 (Uroz et al., 2008). From the inoculation time to the stationary phase (20 h later), the bacterial populations increased by three log. Interestingly, when P. atrosepticum CFBP6276 grew alone, NAHL accumulated up to 6 pmol per membrane, whereas in the presence of the NAHL-degrading strain R. erythropolis R138, NAHL only reached up to 7 fmol per membrane (Figure 2b). As a consequence, NAHL-dependent maceration of the potato tissues decreased dramatically in the presence of the plant-protective R. erythropolis R138 (Figure 2c). Hence, the experimental conditions were appropriate for analyzing transcriptomes of R. erythropolis in response to the presence of P. atrosepticum on potato tubers.
Transcriptome of R. erythropolis was not modified by a NAHL-defective P. atrosepticum
No differentially expressed genes were identified when transcriptomes of R. erythropolis R138 which grew alone on potato tuber slices were compared with those in the presence of the P. atrosepticum expI mutant that is defective for NAHL synthesis. This experiment indicated that R. erythropolis did not modify its gene-expression profile in the presence of an avirulent pathogen. Under this condition, 187 genes were considered as highly expressed in R. erythropolis R138 (Supplementary Table S3). Genes coding for tRNA and rRNA were not considered in this list of unique genes. These highly expressed genes exhibited a homogeneous distribution along the chromosome whereas some gene clusters could be identified on the linear and circular plasmids (Figure 3). The functions of these expressed gene clusters on the plasmids were all unknown. Actually, a functional RAST-category could be assigned to only 29% (55 ORFs) of all the highly expressed genes (Table 1). Interestingly, several genes related to fatty acid and sulfur metabolisms, which are the most studied pathways in R. erythropolis, were highly expressed when R. erythropolis R138 colonized the potato tuber slices. They were 3-ketoacyl-CoA thiolases (ORF1420 and ORF4007), long-chain fatty acid-CoA ligase (ORF2117 and ORF3497) and phosphatidylserine decarboxylase (ORF1766), which all belong to the fatty acid metabolism, and alkylsulfatases (ORF4771 and ORF4816) and thiosulfate sulfur transferase (ORF4081) associated to sulfur metabolism. The identification of these highly expressed genes does not exclude that other genes, which are expressed at a lower level, are involved in potato tuber colonization.
R. erythropolis transcriptome is modified in response to the virulent P. atrosepticum
When the transcriptome of R. erythropolis R138 which grew alone on potato slices was compared with that of R. erythropolis R138 in the presence of the virulent P. atrosepticum CFBP6276, 50 genes were differently expressed: 22 and 31 were down and upregulated, respectively. The localization and expression levels of these genes, their functions according to the RAST annotation and fold change according to the DEseq analysis are given in the Supplementary Data (Supplementary Figure S1 and Supplementary Table S4). Among the downregulated genes, three hypothetical protein genes were localized on the linear plasmid. The others belonged to the chromosome. The downregulated genes were potentially implicated in cofactor metabolism (ORF2389, ORF3251, ORF5957 and ORF5958) and sulfur metabolism (ORF4771, ORF4816 and ORF4877) or exhibited unknown functions (15 ORFs). All the upregulated genes were localized on the chromosome. Twenty genes exhibited unknown functions, whereas the remaining 11 were associated with the metabolism of the carbohydrates (ORF4921), cofactors (ORF1288), DNA (ORF462), iron (ORF2860), transport across membrane (ORF2124), nitrogen (ORF2140), nucleosides and nucleotides (ORF4620), regulation (ORF775), RNA (ORF539 and ORF1958) and response to stress (ORF1552). The qsdA gene (ORF5278) encoding NAHL-degrading lactonase was not differentially expressed, nor highly expressed under the analyzed experimental conditions. Moreover, no putative amidases or reductases were identified among these differentially expressed genes.
Expression of the R. erythropolis alkylsulfatases on potato tuber and in pure culture
Among the differentially expressed genes, the three alkylsulfatases (ORF4771, ORF4816 and ORF4877) retained our attention because their synchronized downregulation could reveal a common response to a particular environmental change, such as a variation in nutrient availability which would be induced by the presence of the virulent P. atrosepticum without any influence on the R. erythropolis R138 growth. Alkyl-sulfatases are expected to be implicated in the sulfur metabolism and/or recycling of sulfured lipid derivatives. They are of special interest in the studied three-partner interaction because (i) potato tuber is known to be a sulfur-limited environment (Subramanian et al., 2011); (ii) sulfur pathways are especially developed in R. erythropolis species (de Carvalho and da Fonseca, 2005); and (iii) organic sulfur (methionine) is a key precursor of NAHL synthesis in Pectobacterium (Crépin et al., 2012c). HiSeq-transcriptomic data showed that, in the absence of the virulent P. atrosepticum CFBP6276, RPKM values were high (between 4370 and 8300), whereas they strongly decreased in its presence (Figure 4a). This differential gene expression was confirmed by qRT-PCR on RNAs extracted from an independent experiment on newly infected potato tubers (Figure 4b). We also investigated whether level and type of the sulfur-source (organic and inorganic) could alter expression of these three alkyl-sulfatase-encoding genes. Although no variation was observed between high and low sulfate concentrations, the expression of the alkylsulfatases ORF4816 and ORF4877 decreased with the level of methionine (Figure 5).
HiSeq-transcriptomics revealed that the NAHL-degrading R. erythropolis responded differentially to virulent and avirulent P. atrosepticum when they were co-cultured on potato slices. Fifty genes were differentially expressed when R. erythropolis was cultivated in the presence vs absence of the NAHL-producing virulent P. atrosepticum. By contrast, no differentially expressed genes were identified when R. erythropolis was cultivated in the presence vs absence of an avirulent P. atrosepticum which is defective for NAHL production. These two different responses are discussed on the light of the NAHL-degrading capability of R. erythropolis and the environmental changes that virulent P. atrosepticum provokes on potato tubers.
When R. erythropolis and avirulent P. atrosepticum were co-cultured, growth curves and transcriptomics showed that the interactions between the two bacteria and especially the response of R. erythropolis were negligible or insignificant. This suggests that under our experimental conditions, the presence of the avirulent P. atrosepticum is neutral for R. erythropolis. This result also indicates that the wounded tuber slices as a growth environment provide enough nutrients to support multiplication of both species without apparent alteration of the plant tissues. This work exemplified a neutral kind of microbe–microbe interaction that is poorly analyzed in the literature. Most of the previous studies focused on competitive and syntrophic interactions between microbes. In these cases, when a microbe enhanced or inhibited the growth of a given bacterium, the transcriptomic analyzes highlighted a shift in the expression of up to hundreds of genes (i.e., more than 10% of the studied genomes) which are implicated in gene regulation, stress responses, metabolic functions and production of antimicrobial compounds (Johnson et al., 2006; Maligoy et al., 2008; Nouaille et al., 2009; Garbeva et al., 2011; Liu et al., 2011). This variation in gene expression was proposed to be a consequence of the presence of other microbes and/or the alteration of the environment.
When R. erythropolis and virulent P. atrosepticum were co-cultured, the growth curves of both bacteria were largely comparable with those of the bacteria grown alone on the potato tubers. Nevertheless, the NAHL-controlled virulence functions were dramatically reduced in P. atrosepticum, strongly reducing the alteration of the plant tissues. Under these conditions, the differentially expressed genes in R. erythropolis represented <1% of its genome; 22 and 31 of them were down and upregulated, respectively. R. erythropolis expresses at least three NAHL-degrading activities that are reductase, amidase and lactonase, but only the lactonase-coding gene qsdA was identified (Uroz et al., 2008 and 2009). Neither qsdA nor the genes encoding putative reductase, amidase and lactonase were present among the differentially expressed genes. In our assays, qsdA remained expressed at a low level in the presence or absence of P. atrosepticum. Recent work reported that a R. erythropolis R138 defective for qsdA was only weakly affected in its capacity to degrade NAHLs and limit the symptoms induced on tubers by P. atrosepticum (Barbey et al., 2013). Thus even if QsdA contributes to NAHLs degradation, other enzymes are expected to have an important role.
When R. erythropolis colonized the potato tuber, a major part of highly expressed genes were related to primary metabolism, probably in order to sustain the observed growth. These genes are potentially involved in metabolism of sugars, amino acids, lipids and ribonucleotides, which are the compounds usually encountered in tubers (Jansky, 2010). Additional genes which exhibit a lower expression level were expected to be also involved in multiplication of R. erythropolis on potato tuber slices. A major characteristic of R. erythropolis species is their capability to assimilate a wide variety of carbon and sulfur sources from natural and xenobiotic compounds (de Carvalho and da Fonseca, 2005; Urai et al., 2007; Aggarwal et al., 2011). This metabolic versatility would contribute to the distribution of R. erythropolis in a wide variety of environments such as oceans and soils, including those polluted by fuels and pesticides. As with soil, potato tuber is considered as a sulfur-limited environment (Subramanian et al., 2011). Noticeably, our results highlighted three alkyl-sulfatase genes (ORF4771, ORF4816 and ORF4877) of which the expression was downregulated in the presence of the plant pathogen P. atrosepticum CFBP6276. Because of their synchronized variation, the alkyl-sulfatase expression could be considered as a signature of the R. erythropolis-P. atrosepticum interaction in the potato environment. These enzymes are implicated in the cleavage of C-OS bond of ester sulfates to release acyl chain and sulfate and could contribute to the recycling and assimilation of carbon and sulfur sources (Kertesz, 2000; Hanson et al., 2004; Sogi et al., 2013). Additional assays revealed that expression of alkylsulfatases ORF4816 and ORF4877 decreased as the level of organic sulfur (methionine) decreased, suggesting that their expression depends on the availability of organic sulfur. We therefore speculate that the virulent pathogen depletes organic sulfur from the potato slices for its use as a precursor of NAHLs or other biomolecules, such as the secreted virulence proteins (plant cell-wall degrading enzymes). This work highlights a novel trait related to sulfur metabolism in a microbe–microbe interaction associating the NAHL-producing and NAHL-degrading bacteria.
When P. atrosepticum interacts with potato plants, two phases can be discerned: an asymptomatic colonization phase, which may occur along the vegetative development of the plant host, followed by a symptomatic phase, in which the blackleg and soft-rot diseases are expressed (Pirhonen et al., 1993; Smadja et al., 2004; Latour et al., 2007; Liu et al., 2008). On the basis of our results on the 3-partner interaction, we postulate a differential response of the biocontrol agent R. erythropolis during both phases of the interaction of P. atrosepticum on potato. Indeed, the R. erythropolis expression profile is not modified in the presence of the avirulent P. atrosepticum expI mutant, which may be considered as a mimic of the pathogen during the asymptomatic phase. In contrast, during the symptomatic phase, R. erythropolis differentially expresses a particular subset of genes and seems to experience some level of methionine deprivation, possibly as a consequence of NAHL synthesis by the virulent P. atrosepticum. Nevertheless, R. erythropolis inactivates part of these NAHLs limiting the disease development. As none of the differentially expressed genes putatively encodes any of the three known NAHL-degrading activities, it is currently unclear how R. erythropolis accomplishes NAHL inactivation. With the limited set of differential genes at hand, the road to address this enigma is wide open. As a conclusion, this work designates sulfur metabolism as a new way to be explored to improve our knowledge of the interaction between the plant pathogen P. atrosepticum and the NAHL-degrading R. erythropolis, as well as to enhance the protective effect of R. erythropolis as a biocontrol agent.
Repository/DataBank Accession: Genbank
Accession ID: ASKF00000000
Databank URL: http://www.ncbi.nlm.nih.gov/nuccore/ASKF00000000
Repository/DataBank Accession: Genbank
Accession ID: ASAB00000000
Databank URL: http://www.ncbi.nlm.nih.gov/nuccore/ASAB00000000.1
This work has been benefited from the facilities and expertise of the high-throughput sequencing platforms of IMAGIF (Gif-sur-Yvette) and ProfileXpert (Lyon). It was supported by the research networks VASI and TERA from the region of Haute-Normandie and ASTREA from the region of Ile-de-France, as well as by the CNRS, French Ministry of Research, ANR (ECORUM 2011) and European Union (FEDER). We thank the High Impact Research Grant (UM.C/625/1/HIR/MOHE/CHAN/01, Grant No A-000001-50001 to KGC) and the French-Malaysian exchange program.
Supplementary Information accompanies this paper on Heredity website (http://www.nature.com/hdy)