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  • Research article
  • Open Access

Transcriptome analysis revealed that a quorum sensing system regulates the transfer of the pAt megaplasmid in Agrobacterium tumefaciens

  • 1,
  • 1, 3,
  • 1, 4,
  • 2,
  • 2,
  • 1 and
  • 1Email author
BMC Genomics201617:661

https://doi.org/10.1186/s12864-016-3007-5

©  The Author(s). 2016

  • Received: 20 May 2016
  • Accepted: 10 August 2016
  • Published:

Abstract

Background

Agrobacterium tumefaciens strain P4 is atypical, as the strain is not pathogenic and produces a for this species unusual quorum sensing signal, identified as N-(3-hydroxy-octanoyl)-homoserine lactone (3OH,C8-HSL).

Results

By sequence analysis and cloning, a functional luxI-like gene, named cinI, has been identified on the At plasmid of A. tumefaciens strain P4. Insertion mutagenesis in the cinI gene and transcriptome analyses permitted the identification of 32 cinI-regulated genes in this strain, most of them encoding proteins responsible for the conjugative transfer of pAtP4. Among these genes were the avhB genes that encode a type 4 secretion system (T4SS) involved in the formation of the conjugation apparatus, the tra genes that encode the DNA transfer and replication (Dtr) machinery and cinI and two luxR orthologs. These last two genes, cinR and cinX, exhibit an unusual organization, with the cinI gene surrounded by the two luxR orthologs. Conjugation experiments confirmed that the conjugative transfer of pAtP4 is regulated by 3OH,C8-HSL. Root colonization experiments indicated that the quorum sensing regulation of the conjugation of the pAtP4 does not confer a gain or a loss of fitness to the bacterial host in the tomato plant rhizosphere.

Conclusion

This work is the first identification of the occurrence of a quorum sensing regulation of the pAt conjugation phenomenon in Agrobacterium.

Keywords

  • Agrobacterium
  • At plasmid
  • Transcriptomics
  • Conjugation
  • T4SS
  • Dtr system
  • Acylhomoserine lactone
  • Quorum sensing

Background

Members of the species Agrobacterium tumefaciens are plant pathogens, inducing the formation of tumors mostly at the crown of dicotyledonous plant species. The main pathogenic element of the bacteria is the tumor-inducing (Ti) plasmid, a fragment of which, the T-DNA, is transferred from the bacteria to the plant cell upon infection (for reviews, see [1–4]). The expression of T-DNA genes in the plant leads to the formation of the tumor and to the synthesis, by the tumor cells, of specific molecules, the opines. Opines are instrumental in the ecological niche constituted by the tumor [5]. First, they are used as growth substrates by the tumor-inducing Agrobacterium strains via the products of genes located on the Ti plasmid. Second, some of them also induce the conjugative transfer of the Ti plasmid (for reviews, see [6, 7]).

In the A. tumefaciens reference strain C58 (genomospecies G8), the genome consists of two chromosomes, a circular one (ca. 2.8 Mbp) and a linear one (ca. 2.1 Mbp), plus an At plasmid (ca. 540 kbp) and a Ti plasmid (ca. 214 kbp [8, 9]). This latter plasmid bears most of the genetic determinants involved in the induction of plant tumors that are characterized by the presence of opines of the nopaline and agrocinopine families. Nopaline is an arginine derivative while the agrocinopines (A and B) are arabinose phosphate derivatives (for a review, see [6]). These last two opines induce the conjugative transfer of the C58 Ti plasmid in conjunction with a quorum sensing (QS) regulatory pathway [10–14] (for reviews, see [7, 15]). In bacteria, QS couples gene expression with bacterial cell concentration. It involves the production and sensing, by members of a bacterial population, of diffusible signals, the concentration of which mimics that of the bacterial cells. Once a threshold cell density is reached (i.e. a quorum), the concentration of the signals permits their perception and the subsequent activation or repression of the transcription of QS-regulated genes (for reviews, see [16–18]). In A. tumefaciens, the QS signal molecule that controls the conjugative transfer of the Ti plasmid belongs to the most common signal class in Proteobacteria, i.e. the N-acyl homoserine lactone (AHL) class; it is N-(3-oxo-octanoyl)-L-homoserine lactone (3O,C8-HSL; [10, 12]). AHLs are generally synthesized by the prodcucts of luxI and luxI-like genes (for reviews, see [16–18]).

In strain C58, the genetic determinants involved in the conjugative transfer of Ti plasmid are induced by the agrocinopines, which bind the AccR regulator encoded by the accR gene (Additional file 1). This releases the repression of transcription of the accABCDEFG operon encoding the transport and degradation of the agrocinopines A and B. Bound to agrocinopines, the AccR regulator also derepresses the expression of the arc operon. Among the arc genes is traR, a member of the luxR family that encodes the QS regulator TraR. This latter regulator binds the QS signal molecule 3O,C8-HSL, dimerizes, and activates the transcription of the tra and trb operons involved in the conjugative transfer of the Ti plasmid, and to a lesser extent that of the rep operon involved in the replication of the Ti plasmid [19] (for reviews, see [7, 20, 21]). This complex regulatory system implies that C58 Ti plasmid conjugation can only occur at high donor cell density and in agrocinopine-rich environments, allowing the efficient dissemination of the main pathogenic element of the bacteria in tumors.

In contrast with the wealth of data dealing with the Ti plasmid, little is known about the At plasmid in spite of the fact that it is often found in natural isolates of Agrobacterium spp. and can represent up to ca. 10 % of the bacterial genome. The At plasmid can sustain some large deletions (25 to 30 % of the plasmid size) that are associated with a significantly reduced carrying cost to the cell [22]. Known functions of this plasmid are scarce. One is the utilization of gamma-butyrolactone and gamma hydroxy-butyrate via the products of the blcABC (also known as attKLM) operon [23]. The last gene of this operon, blcC (aka attM) encodes the lactonase that hydrolyses gamma butyrolactone, as well as numerous QS signal molecules of the AHL class [24]. The At plasmid also harbor genes involved in the degradation of Amadori compounds such as deoxyfructosyl-glutamate and deoxyfructosyl-glutamine, that are commonly found in decaying plant material [25]. At plasmids are also conjugative plasmids. Sequence analyses of the C58 genome have revealed the occurrence of a type 4 secretion system (T4SS), termed AvhB, on pAtC58 that is highly similar to the VirB system of Bartonella henselae [26]. The pAtC58 T4SS (T4SSpAt) also shares some common traits with two previously identified T4SS of Agrobacterium, i.e. the one encoded by the virulence (vir) genes of the Ti plasmid (involved in T-DNA transfer to the plant cells and thus in disease induction) and the one encoded by the trb genes (T4SSpTi, involved in the conjugative transfer of this plasmid [27]). Interestingly, a recent study revealed that also the T4SSpAt of strain C58 is regulated by the master regulator AccR encoded by the Ti plasmid accR gene [28], a feature that favors the co-transfer of both Agrobacterium megaplasmids in the agrocinopine-rich environment of the tumor.

Agrobacterium strain P4 was previously isolated from a plant rhizosphere [29]. This strain exhibited the capacity to synthesize a QS signal of the AHL class. Strain P4 is non-pathogenic and in agreement with this, no Ti plasmid was observed following the complete sequencing of its genome [30]. We report here the structure of the AHL produced by P4, we investigated the possibility that this AHL is indeed a QS signal and we identified the relevant determinants in QS. Moreover, we report the occurrence of a QS regulation of the expression of the T4SSpAt in strain P4.

Methods

Bacterial strains and growth conditions

The bacterial strains and plasmids used in this study are described in Table 1. Agrobacterium strains were routinely cultivated at 28 °C in modified Luria Bertani medium (LBm [31]), tryptone-yeast medium (TY: bactotryptone 5 g/L, yeast extract 3 g/L) or in Agrobacterium broth (AB) minimal medium [32] supplemented with ammonium chloride (1 g/L) and a carbon source (mannitol or glucose 2 g/L, for AB mannitol and AB glucose, respectively). When necessary, media were solidified using bacto-agar (Becton-Dickinson), 15 g/L. Escherichia coli cells were routinely cultivated at 37 °C in LBm. Media were supplemented with appropriate antibiotics that were added at the following final concentrations: rifampicin 100 mg/L, streptomycin 250 mg/L, gentamicin 25 mg/L, carbenicillin 100 mg/L and ampicillin 50 mg/L.
Table 1

Bacterial strains and plasmids used in this study

Strain or Plasmid

Relevant genotype or characteristics

Reference or source

Strains

 P4

Agrobacterium tumefaciens. Isolated from tobacco rhizosphere (La Côte Saint André, France)

Mondy et al., 2013

 P4cinI

A. tumefaciens; Gmr a, pAtcinI::Gm

This study

 P4Rif

A. tumefaciens; Rifr

Laboratory collection

 P4RifcinI

A. tumefaciens; Rifr, Gmr, pAtcinI::Gm

This study

 P4RifNC

A. tumefaciens; Rifr, Gmr, pAt::Gm

This study

 P4RifRIX

A. tumefaciens; Rifr, Gmr, pAtΔcinRcinIcinX::Gm

This study

 C58.00

A. tumefaciens; Rifr, Smr, cured of the At and Ti plasmids

Laboratory collection

 NT1(pZLR4)

A. tumefaciens b Gmr, NT1 derived from strain C58, carrying plasmid ZLR4; OC8-HSL biosensor

Cha et al., 1998 ; Pipper et al., 1993

 DH5α

Escherichia coli; F, Φ 980dlacZ : M15, recA1, endA1, gyrA96, thi-1, hsdR17(rK–, mK+), supE44,relA1, deoR:(lacZYA–argF)U169

Hanahan, 1983

Plasmids

 pGEM®-T Easy

Ampr, high copy number

Promega Crop., Madison, WI

aabbreviations are as follows: Rifr, Smr, Gmr, Ampr, resistant to rifampicin, streptomycin, gentamicin, and ampicillin, respectively

bThis strain is also a derivative of strain C58

Identification, extraction and determination of the structure of acyl-homoserine lactones

Preliminary tests to evaluate the production of AHLs were performed essentially as described earlier [33]. Aliquots of overnight culture supernatants, or 10 fold concentrated ethyl acetate extracts of culture supernatants of the assayed strains, were spotted onto TLC silica plate (Whatman ref. 4801-800). Both Chromobacterium violaceum strain CVO26 [34] and Agrobacterium strain NT1(pZLR4) [33] were used as bio-indicators. When necessary, TLC plates were first submitted to chromatography in a methanol/water solvent system (55/45; v/v).

For the determination of the structure of AHL, 500 mL of LBm medium inoculated with the P4 strain were centrifuged (10 min., 4000 g, 4 °C) and the supernatant serially filtered on 1.8, 1.2 and 0.45 μm ultrafilters under vacuum. The filtered supernatant was extracted with ethyl acetate (v/v). Ethyl acetate was rotary evaporated to dryness at 30 °C, and the extract resuspended in 100 % acetonitrile prior to UPLC MS/MS analysis. UPLC MS/MS was performed on a Waters Aquity UPLC-TQD apparatus driven by a MassLynx 4.1 software, and fitted with an Acquity HSS C18 column (2.1 mm × 50 mm; 1.8 μm). The temperature was set at 20 °C and the solvent flow at 0.6 mL/min. The solvent composition is provided in Additional file 2. Mass spectrometry was performed by electrospay ionization. The triple quadrupole analyzer was used in both MS and MS/MS modes with a m/z mass ranging from 50 to 800. The most sensitive analytical conditions were first determined using synthetic N-(octanoyl)-L-homoserine lactone (C8-HSL) and 3O,C8-HSL. Synthetic N-(3-hydroxy-octanoyl)-homoserine lactone (3OH,C8-HSL) was used as a standard in UPLC MS/MS analyses.

Gene sequence analyses

Identification of ORFs, determination of gene organization and comparative genomic analyses of plasmids and chromosomal regions were performed at the NCBI web site (http://blast.ncbi.nlm.nih.gov/Blast.cgi), MicroScope plateform (https://www.genoscope.cns.fr/agc/microscope/home/index.php) and INRA AGMIAL [35] plateform (http://maiage.jouy.inra.fr/?q=fr/logiciels). In this latter case, the Artemis program was used. Sequence comparisons were performed using BLAST tools (blastn, blastp and tblastn) with default parameters. BLAST analyses were achieved on both the non-redundant nucleotide sequence collection (nr/nt) and whole-genome shotgun contigs (WGS) databases. Prediction of functional domains was achieved using InterPro [36]. Protein sequences were aligned using ClustalW [37]. Phylogenetic trees based on protein sequence analysis were constructed using the Neighbor-Joining method implemented in MEGA program version 5 [38]. Bootstrapping was performed with 1,000 replicates to assess confidence on the nodes.

Cloning and mutagenesis

Plasmid extractions were performed with the QIAprep® Spin Miniprep Kit (Qiagen, GmbH). Restriction enzymes, T4 DNA ligase (Thermo Scientific, GmbH), and T4 DNA polymerase (Eurobio, France) were used according to manufacturer’s recommendations. PCR assays were performed in a final volume of 25 μL containing 1 X DNA polymerase buffer (provided by the manufacturer), dNTPs 2.5 mM, MgCl2 2 mM, primers (Table 2) 1 μM each, DNA polymerase 0.5 unit, and 1 μL of boiled bacterial suspensions. PCR conditions were 5 min at 94 °C, followed by 35 cycles of 1 min at 94 °C, 1.5 min at 58 °C, and 2 min at 94 °C, and a final 10 min incubation at 75 °C phase.
Table 2

PCR primers used in this study

Targeted gene or region

 

Primer sequencea

P4 cinI

F :

GGCGCAATACCTCAATTGATTG

R :

CATCATGGACGTCGTATCGATC

P4 pAt non coding-region (coord. 36817–37590b)

F :

CATCTCGTTGATCGCAACATGGTCGTT

R :

GATTTGGATGCTTCAACCGAAGATTTATTTGC

P4 pAt non encoding-region (coord. 36950–37353b)

F :

CCGAAAGTAACATTTGATGCCCCAACTGAATTTT

R :

ATAACTGACAGGCATGCGAAAGCCGTC

P4 cinR cinI cinX

F :

TGCTTGTCGTCTGCGCCGTGAGA

R :

CTCAAACACCGCTGGAGCGAACTCA

P4 avhB5 RT-qPCR

F:

CCAAGCAGATCGAGAGCAT

R:

TTGTTGAGCGAGCCATAAAG

P4 avhB11 RT-qPCR

F:

ACGCTTTCCAAAGCATTGAT

R:

CGTGGTTCGGTTGTGAGATA

P4 AGROTU_05920 RT-qPCR

F:

TTGTTGAATGTATGCGGGTT

R:

TATGCGCTGTGGAGATATGG

P4 traA RT-qPCR

F:

CGAGCTGTTCCTCACTACAGT

R:

TTCAATCTTTCCGACAGCACC

P4 cinR RT-qPCR

F:

CGTCGGAGAGTTCGGTTATT

R:

CCTGCAACAAGTCTGTCCC

P4 cinI (internal) RT-qPCR

F:

ATATGGGAAGGCACACGAAT

R:

AAAGGAACCCAAACGCTCTA

P4 cinX RT-qPCR

F:

AATATCGGCAGGAGCATTTC

R:

GCTCATGCTCAAGGTCAAAG

P4 traG RT-qPCR

F:

GATTTCGATTCGACCCACAT

R:

AGCGGGCCTGTATATCTGAG

P4 gyrB RT-qPCR

F:

GATGGCAAGGCCTATGAAAC

R:

CACTTCCAGAAGATCGGACA

P4 blcR RT-qPCR

F:

CGACATTCAACGACCATCTC

R:

CAGCCGATGTAAACGACTTC

aall primer sequences are given in the 5′- > 3 orientations. F forward primer, R reverse primer

bcoordinates on pAt P4 with respect to the position of the first and last base amplified by the primer couples

To mutagenize cinI, the Gm cassette from plasmid p34S-Gm [39] was inserted at the unique XbaI restriction site of a pGEM®-T Easy vector (Promega France) harboring a ca. 800 bp region of the cinI gene obtained by PCR amplification (Additional file 3). The same cassette was also inserted at the unique SphI restriction site found in a 1240 bp non-coding region of plasmid At (located in between 36783 bp and 38021 bp coordinates), previously amplified and cloned into pGEM®-T Easy. The resulting plasmids, which are not replicative in Agrobacterium, were electroporated (2500 V, 125 Ω, 50 μF) into P4 and P4Rif strains. Double crossing-overs that led to a marker exchange were identified by carbenicillin sensivity and gentamicin resistance assays and verified by PCR using the appropriate primers. The cinI mutants and the pAt non-coding control mutant were named P4cinI and P4RifcinI (depending on the background) and P4RifNC, respectively.

Another mutant harboring a deletion in the region cinR cinI cinX was generated by homologous recombination of a DNA fragment that consisted of a Gm-cassette surrounded by 375 bp of the 3′ end of the cinR gene and 336 bp of the 5′ end of the cinX gene (Additional file 3). This DNA fragment was synthesized and cloned into the pMA-T vector at the unique SfiI restriction site by the provider (Life Technologies, Carlsbad, USA). The resulting plasmid which is not replicative in Agrobacterium was electroporated (2500 V, 125 Ω, 50 μF) into the P4Rif strain. Double crossing-overs that led to a marker exchange were identified by carbenicillin sensitivity and gentamicin resistance assays and verified by PCR using appropriate primers. This mutant was named P4RifRIX.

Transcriptomic and RT-PCR analyses

Overnight cultures of A. tumefaciens strains P4 and P4cinI were diluted to an OD600nm = 0.1 in 50 mL AB mannitol. Cells were grown at 28 °C up to an OD600nm = 0.7 and harvested by centrifugation (15 min, 3500 g, 4 °C). RNA was extracted using the NucleoSpin RNA II kit (Macherey-Nagel Ltd., Oensingen, Switzerland) and further treated using RNase-free DNAse (Ambion, Austin, TX, USA) according to manufacturer’s instructions to ensure the absence of any contaminating DNA. RNA concentration and purity were assessed using a nanodrop ND-100. RNA samples were used in transcriptomics, RT-PCR and RT-qPCR experiments.

For transcriptomic analyses (performed at the high throughput sequencing platform of the Institute for Integrative Biology of the Cell, Gif-sur-Yvette, France), RNA quality was re-evaluated on an Agilent Bioanalyzer 2100, using an RNA 6000 pico kit (Agilent Technologies, Santa Clara, USA). Total mRNA were purified from 1 μg total RNA using Ribo-Zero rRNA (bacteria) removal kit (Epicentre, Madison, USA), according to the manufacturer recommendations. Directionnal RNA-seq libraries were constructed using ScriptSeq V2 RNA-seq library preparation kit (Epicentre, Madison, USA), according to the manufacturer’s recommendations (with 14 PCR cycles). Library quality was assessed on an Agilent Bioanalyzer 2100, using an Agilent High Sensitivity DNA Kit. Libraries were sequenced on an Illumina Hiseq 1000 instrument, with a TruSeq SR Cluster Kit v3-cBot-HS (Illumina, San Diego, USA) and a TruSeq SBS v3-HS - 50 cycles Kit (Illumina, San Diego, USA), using a Single Read 50 bp recipe. Libraries were pooled in equimolar proportions and diluted to a final concentration of 12pM, according to Illumina recommandations. The generated data were demultiplexed by the high throughput sequencing platform of the Institute for Integrative Biology of the Cell (Gif-sur-Yvette, France) using CASAVA software suite (CASAVA-1.8.2; Illumina, San Diego, USA). The quality of the data was checked with the software FastQC 0.10.1 from Babraham Bioinformatics, Cambridge, UK). The Illumina 3′-adapter was trimmed using Cutadapt-1.2.1 (Python community), and only reads with a minimal length of 10 nucleotides were kept. After the trimming step, the data were mapped using TopHat2 (Center for Computational Biology, John Hopkins University, Baltimore, USA) with a seed length of 8 (default value) to the appropriate reference genome of P4 (including 3 scaffolds). Only unique reads were analyzed. Bam output files were sorted with Samtools (http://www.htslib.org/). HTSeq-count (EMBL, Heidelberg, Germany) was used to evaluate the number of reads by gene or by CDS. The DESEQ package [40] was used to analyze the differential expression of genes between the reference strain P4 and the cinI mutant.

Standard RT reactions were performed with 1 μg total RNA obtained as indicated above, using random hexamers as primers and the Revert Aid TM HM Inis First Strand cDNA Synthesis Kit (Fermentas) according to the manufacturer’s instructions. RT-qPCRs were performed in a Lightcycler® 480 II (Roche) apparatus. The data were processed using the 2-ΔΔCT method. For all primer sets (Table 2), the similarities of amplification efficiencies were controlled. The expression of the following 8 pAtP4 genes was investigated: avhB11, avhB5, traA, traG, cinR, cinI, cinX, and AGROTU_05920. The internal control used was the regulator gene blcR (Atu5136), also located on the At plasmid.

Measurement of bacterial doubling time

Strains P4Rif and P4RifcinI were cultivated at 28 °C during 40 h in AB mannitol and AB glucose and in the rich media LBm and TY. For each condition, five independent repeats were set up per strain. Bacterial growth was estimated by measuring the OD600nm every 30 min using a Biosreen C microplate reader and according to the manufacturer’s recommendations (Growth Curves USA, Piscataway, NJ, USA). Generation times were calculated based on the OD600nm from graphical plots of the growth curves. The experiment was repeated 5 times.

Conjugation assays

Conjugation assays were performed under in vitro conditions. Overnight cultures in LBm of donor and recipient cells were mixed at an equal cell density (i.e. ratio 1:1). Twenty μL of the mix were subcultured into 180 μL of AB mannitol and incubated in microplates at 28 °C for 72 to 96 h with no shaking, if necessary in the presence of 100 nM AHL. Dilutions of these mixed cultures were spotted onto LBm agar media supplemented with the appropriate antibiotics to enumerate the different bacterial populations, i.e the donor, recipient, and At plasmid transconjugants. The verification of the presence of the At plasmid in a subset of randomly picked, putative transconjugants was performed by PCR with appropriate primers (Table 2). For each experiment, at least 8 independent repeat assays were performed, and the conjugation frequencies expressed per recipient cells.

Plant colonization under bacterial competition assays

Tomato plants (Solanum lycopersicum cv. F1 hybrid Dona, Vilmorin, France) were grown in a greenhouse under long day conditions (16 hours light), controlled temperature (24 to 25 °C night and day), in an unsterilized horticultural soil and daily watered with unsterilized tap water. At the zero time point, the pots containing three-week old plants were soaked with the bacterial suspensions (strains P4RifNC and P4RifRIX mixed at an equal cell density, i.e. ratio 1:1; final OD600nm = 0.1) until the maximum water retention capacity of the soils was reached. Nine plants were inoculated with the bacteria mixture and 3 samples consisting of 10 g of rhizospheric soil (defined as the soil fraction strongly adherent to the roots) were obtained at each time point, i.e. 1 day post inoculation (dpi), 7 dpi, and 21 dpi. The soil samples were resuspended in 30 mL sterile NaCl 0.8 % and vigorously vortexed for 30 s. Dilutions of these suspensions were plated onto AB mannitol agar supplemented with rifampicin and gentamicin to enumerate CFU after a 2 day incubation. PCR amplifications were performed using the appropriate primers (Table 2) to discriminate strain P4RifNC from P4RifRIX on a subset of 150 randomly picked, enumerated colonies per time point.

Results

Agrobacterium strain P4 produced N-(3-hydroxy-octanoyl)-homoserine lactone (3OH,C8-HSL) but not 3O,C8-HSL

Strain P4 was identified as one of the environmental strains that activates a beta-galactosidase activity in A. tumefaciens strain NT1(pZLR4) [29], a QS bioindicator that responds to long chain AHLs [41]. The production of short chain AHLs was assessed using the C. violaceum bio-indicator strain CVO26 and found to be undetectable. Ethyl acetate supernatant extracts were obtained from spent culture media of strain P4 and analyzed by TLC using synthetic AHL migration standards and the above mentioned bio-indicator NT1(pZLR4). Strain P4 produced a single AHL molecule spot as judged from the TLC plate, the Rf and shape of which suggested that it might be N-(3-hydroxy-octanoyl)-homoserine lactone (3OH,C8-HSL). The presence, in the ethyl acetate extract of the only 3OH,C8-HSL signal molecule, that is not the common signal detected in other Agrobacterium strains [33], was confirmed (Fig. 1) using ultra-performance liquid chromatography - tandem mass spectrometer (UPLC-MS/MS) analysis.
Fig. 1
Fig. 1

Identification of N-(3-hydroxy-octanoyl)-homoserine lactone (3OH,C8-HSL) in culture supernatants of strain P4. An ethyl acetate extract of a spend culture supernatant was concentrated, resuspended in 100 % acetonitrile and analyzed by UPLC MS/MS. Panel a: elution profile of synthetic 3OH,C8-HSL. Panel b: mass spectra of synthetic 3OH,C8-HSL. The m/z values 244, 226 and 102 correspond to the protonated forms of 3OH,C8-HSL (243 + 1), the dehydrated 3OH,C8-HSL (225 + 1) and the characteristic amine substituted lactone cycle (101 + 1), respectively. Panel c: elution profile of the concentrated culture supernatant of strain P4. The major peak migrates as the one of synthetic 3OH,C8-HSL. Panel d: mass spectrum of the major peak observed in the concentrated culture supernatant of strain P4. The m/z values and species are identical to those observed for synthetic 3OH,C8-HSL

Strain P4 displayed a functional luxI-like gene (cinI) bordered by two luxR-like genes (cinR and cinX)

Blast analysis of the genome of strain P4 revealed the occurrence of a single luxI-like gene that exhibited a 783 bp ORF and encoded a deduced 29.6 kDa protein. This protein consisted of 260 amino acids. The P4 luxI-like gene, that we termed cinI (see below), was PCR-amplified, cloned into pGEM®-T easy and the production of AHL by the resulting strain was evaluated. The presence of the cloned cinI gene in E. coli conferred the ability to produce 3OH,C8-HSL.

The proteins most related to the P4 LuxI-like protein were other deduced LuxI proteins from four Agrobacterium strains, namely A. tumefaciens strains 5A, RV3, and NCPPB 1641, and A. radiobacter strain DSM 30147 (Fig. 2a, b). The P4 CinI protein was also related to the TraI protein of Agrobacterium strain C58 (32 % identity and 45 % similarity). Outside the Agrobacterium genus, the closest deduced protein was CinI from Rhizobium leguminosarum (57 % identity and 71 % similarity; Fig. 2b), hence the name cinI for the P4 luxI homologue. It is located on the At plasmid of strain P4 at coordinates 292 921 to 293 703.
Fig. 2
Fig. 2

Genetic determinants of the quorum sensing regulation on pAtP4 and related regions of other plasmids. Panel a: genetic organization of the cinI region on the pAt plasmid of A. tumefaciens strains P4 and 5A, A. radiobacter DSM 30147 and in the genome of R. leguminosarum strain 3841. Gene sizes are drawn to scale (scale at the left bottom part of panel a). Panel b: Phylogenetic relatedness of the deduced CinI protein of strain P4. The tree has been constructed using the Neighbor-Joining method and bootstrap values calculated from 1,000 re-samplings technique. Panel c: Phylogenetic relatedness of the deduced CinR and CinX proteins of strain P4. The tree has been constructed as indicated above

The Blast analysis was expanded to the right and left side of cinI to search for other possible component(s) of a QS regulatory system as their coding sequences are often located in the vicinity of luxI-like genes [42]. This analysis revealed the presence to the left and right regions of cinI of two luxR-like determinants (AGROTU_05922 and AGROTU_05924; Fig. 2a) that were termed cinR and cinX, respectively. The putative protein CinR (ca. 30 kDa) consisted of 239 amino acids, while the putative CinX protein (27.8 kDa) consisted of 247 amino acids. Both CinR and CinX proteins exhibited the characteristic AHL-binding and DNA-binding domains [43, 44]. The proteins most related to the P4 CinR protein were again the deduced LuxR proteins from A. radiobacter DSM 30147 and A. tumefaciens 5A, RV3, and NCPPB 1641. Outside the Agrobacterium clade, the proteins most related to the P4 CinR protein were those from Ochrobactrum rhizosphaerae SJY1 and Rhizobium etli with which P4 CinR shared 55 and 54 % identity and 73 and 69 % similarity, respectively (Fig. 2c). The P4 CinR protein was also related to the TraR protein of Agrobacterium strain C58 (22 % identity and 44 % similarity). The proteins most related to CinX were the LuxR-like proteins from the above mentioned Agrobacterium strains and, outside this clade, CinR from Sinorhizobium meliloti GVPV12 with which P4 CinX shared 39 % identity and 59 % similarity (Fig. 2c). CinR and CinX displayed only 29 % identity and 49 % similarity with each other and were therefore only distantly related.

The exact same organization of the cinR cinI cinX region was found in data bases only in the four above mentioned Agrobacterium strains (i.e. 5A, RV3, NCPPB 1641, and DSM 30147; Fig. 2a). A related gene organization was observed in R. leguminosarum strain 3841. However in this later strain, cinX was absent and replaced by cinS [45, 46].

Transcriptome analysis revealed that cinI regulated the expression of genes involved in the transfer of the At plasmid in strain P4

The identification of a luxI-like gene involved in the synthesis of an AHL molecule and the presence of luxR-like genes that encode proteins with characteristic AHL-binding and DNA-binding domains on pAtP4, are clear indications that they most likely constitute QS regulatory elements. To identify genes potentially regulated by these QS elements, a cinI mutant was generated via the insertion of a gentamicin resistance cassette within cinI by homologous recombination (Additional file 3). The resulting strain, termed P4cinI, lost the ability to produce any detectable AHL signal, as judged from the analyses of spent culture supernatant and ethyl acetate extracts.

RNA was extracted from both P4 and P4cinI strains during the exponential phase of growth, and used to perform transcriptome analyses. Only fold changes above 3 with a p-value lower than 5 10 −2 were considered significant. Using these parameters, 32 differentially expressed genes were identified (Additional file 4), all of them being upregulated in P4 when compared to P4cinI. Most of the genes, i.e. 29 out of 32, were located on the At plasmid of strain P4 (Fig. 3). The remaining 3 genes were located on the circular (AGROTU_03028) and linear (AGROTU_05377 and AGROTU_05378) chromosomes. Gene AGROTU_03028 encodes a conserved hypothetical protein, AGROTU_05377 a hypothetical protein, and AGROTU_05378 a putative nucleotidyl transferase.
Fig. 3
Fig. 3

Comparison of three pAtP4 regions displaying upregulated genes. Fold change of pAtP4 genes obtained from the transcriptome experiments are shown above each panel. Upregulated genes of the pAtP4 are shown by arrows with different backgrounds while the non-regulated genes are shown by open arrows. Gene sizes are drawn to scale (scale at the left bottom part of panel c). Panel a: the avhB cluster of pAtP4 with genes upregulated or not. The avhB cluster of pAtP4 was aligned with the avhB cluster of pAtC58 and compared with the trb cluster of pTiC58. C58 genes displaying significant similarity to avhB genes are marked with the same background pattern as used for the corresponding avhB gene of pAtP4. Panel b: the tra cluster of pAtP4 with genes upregulated or not. The tra cluster of pAtP4 was aligned with tra cluster of pAtC58. Up regulated and non-regulated genes are represented as indicated above. Panel c: the cinR cinI cinX genomic region with upregulated genes of the pAtP4. The cinR cinI cinX genomic region was aligned with the corresponding pAt region of A. radiobacter strain DSM 30147 and compared to the one of R. leguminosarum bv. viciae strain 3841. Up regulated and non-regulated genes are represented as indicated above

On pAtP4, a first group of upregulated genes comprised the avhB genes plus the genes AGROTU_05875, AGROTU_05881 and atsE. This cluster was located between coordinates 241 317 and 252 681 (Fig. 3a). It encompasses another gene, rctA, which did not appear to be differentially expressed in strains P4 and P4cinI. The pAt avhB genes of strain P4 were orthologs to those of pAtC58 that encode the T4SSpAt involved in the conjugative transfer of this plasmid [26]. AGROTU_05875 encoded a partly deleted avhB5 gene. The two other genes, AGROTU_05881 and atsE, encoded a hypothetical protein and a hypothetical host attachment protein, respectively.

A second group of upregulated genes was located between coordinates 314 321 and 325 085. It comprised the traA, traC, traD, traG gene cluster, plus four neighboring genes, namely AGROTU_05943, AGROTU_05944, AGROTU_05953 and riorf105 (Fig. 3b). The four tra genes of strain pAtP4 are orthologs to the tra genes of pAtC58. These genes encode components of the DNA transfer and replication (Dtr) system that recognizes and cleaves at the origin of transfer (oriT) of plasmids [26, 47]. The genes AGROTU_05943, AGROTU_05953 and riorf105 encoded hypothetical proteins with no predicted functional domains, whereas AGROTU_05944 encoded a putative plasmid stabilization protein. Two other genes, namely hipA2 and hipB2, located downstream of traA on pAtP4, were orthologous to respectively Atu5112 (hipA) and Atu5113 (hipB encoding a transcriptional regulator) of pAtC58. These genes were not overexpressed in P4 compared to P4cinI.

The third group of upregulated genes was located between coordinates 285 182 and 294 410 (Fig. 3c). Remarkably, this group of genes encompassed cinR, cinI and cinX, cinI being the most upregulated gene within this set of three. The other genes, sus and msi250, encoded hypothetical proteins, while AGROTU_05920 encoded a hypothetical protein with a metal-dependent hydrolase domain and msi287 a phosphate regulatory protein.

The upregulation of a subset of 8 of the above mentioned pAtP4 genes (i.e. avhB11, avhB5, traA, traG, cinR, cinI, cinX, and AGROTU_05920) was confirmed in strains P4 and P4cinI by RT-qPCR (Additional file 4).

CinI and 3OH,C8-HSL regulated the conjugative transfer of the pAt in strain P4

The above data strongly support the view that cinI and the associated 3OH,C8-HSL molecule controlled the conjugative transfer of the At plasmid of strain P4. To validate this hypothesis, two P4 mutant strains were used as pAt donor strains in conjugation experiments: P4RifcinI that harbored a cinI gene disrupted by a gentamicin resistance cassette and P4RifNC that harbored the same gentamicin resistance cassette inserted in a noncoding region of the At plasmid (see Methods). Conjugations were performed with strain C58.00 as a recipient. The average pAt transfer frequencies (expressed per recipient cell) were 1.24 10−4 in the cross P4RifNC x C58.00 and 8.9 10−6 in the cross P4RifcinI x C58.00. These two values statistically differed (Kruskal-Wallis and post hoc Tuckey; p < 0.05; Fig. 4). The transfer frequency of the At plasmid was therefore ca. 14 times higher for the strain carrying an intact cinI gene than it was for the strain with a mutated cinI gene. When 100 nM synthetic 3OH,C8-HSL were added in the media that supported the cross P4RifcinI x C58.00, the conjugation frequency was comparable to that observed in the cross P4RifNC x C58.00 (Kruskal-Wallis and post hoc Tuckey; p < 0.05; Fig. 4). These results unambiguously demonstrated that cinI and the associated 3OH,C8-HSL signal control the transfer of the At plasmid in strain P4.
Fig. 4
Fig. 4

pAt conjugation efficiencies of strain P4 and related mutants. Crosses involved the pAt donor indicated on the x axis and strain C58.00 as a recipient. Conjugation frequencies (y axis) were expressed per recipient cells. A Kruskal-Wallis non parametric test and a post-hoc Tukey test were used to evaluate whether the observed differences were significant (p ≤ 0.05) or not (p > 0.05). Results are shown by the letters displayed above the graph

The role of CinR and CinX was assessed using another mutant, P4RifRIX that carried a deletion of the cinR cinI cinX region replaced by the same gentamicin resistance cassette used to generate P4RifcinI and P4RifNC (see Additional file 3). This mutant was used as a pAt donor strains in conjugation experiments that involved strain C58.00 as a recipient. Crosses were performed either in the absence or in the presence of 100 nM synthetic 3OH,C8-HSL. The average pAt transfer frequencies (expressed per recipient cell) were 2.75 10−6 in the cross performed in the absence of the AHL, and 2.91 10−6 in the cross performed in the presence of the AHL, two values that do not statistically differ from each other (Kruskal-Wallis and post hoc Tuckey; p > 0.05; Fig. 4). These results indicated that either CinR or CinX, or both, are essential for the detection of the AHL signal molecule.

Quorum sensing regulation of the conjugation of the At plasmid did not confer a selective advantage in tomato plant rhizosphere

To investigate whether the QS regulated transfer of the At plasmid may provide the host bacteria with a selective advantage, a series of experiments that involved various P4 mutant strains were performed. First, the consequences on bacterial growth of the mutation of the P4 gene cinI was evaluated in vitro, by comparing the generation time of strain P4Rif and P4RifcinI. In AB mannitol, generation times were 2.57 and 2.55 h, respectively. In AB glucose, they were 2.61 and 2.71 h, in LBm 1.74 and 1.96 h, and in TY broth 1.92 and 1.92 h, respectively. These experiments were repeated 5 times independently and the differences observed for each culture media were not significant (Mann and Whitney, p > 0.05).

The relative fitness of strain P4 derivatives producing or not 3OH,C8-HSL was next evaluated in a competition experiment in a more ecologically-significant environment. To do so, and because P4 produces large amount of 3OH,C8HSL that can still be sensed by P4RifcinI, we used the cinR cinI cinX mutant described earlier. Tomato rhizospheres were inoculated by Agrobacterium strains P4RifRIX and P4RifNC at equal cell density and the colonization of the root system assessed at various times by enumeration from soil suspensions of the inoculated bacteria on AB mannitol supplemented by rifampicin and gentamicin. The results (Fig. 5) did not revealed any fitness differences of the two competing strains.
Fig. 5
Fig. 5

Fitness of P4 and the P4 cinR cinI cinX mutant in the tomato rhizosphere. Cell densities (CFU/g of soil) of strains P4RifNC and P4RifRIX inoculated simultaneously on tomato plants cultivated in an unsterilized horticultural soil were assessed by dilution and plating onto the appropriate media (see Methods). Panel a: cell density of both co-inoculated P4RifNC and P4RifRIX. Panel b: ratio of the cell densities of each strain. At each time point (but not between time points), the values generated by the 3 repeats were statistically analyzed by a Mann and Whitney non parametric test which indicated that the proportion of the cell densities of the two strains were not statistically different (p-values > 0.05)

Discussion

This study led to the identification of the AHL molecule 3OH,C8-HSL produced by the avirulent Agrobacterium strain P4. The 3OH,C8-HSL signal is unusual among Agrobacteria but has been described as a QS signal in other systems (e.g. Burkholderia mallei [48]). In strain P4, several elements indicate that a QS system controlled the conjugative transfer of pAtP4. These are: (i), the production of 3OH,C8-HSL in P4 culture supernatants, a molecule that belongs to the AHL class of QS signals; (ii), the presence of cinI, a luxI ortholog in strain P4 involved in the synthesis of the 3OH,C8-HSL signal; (iii), the occurrence of luxR orthologs that encoded proteins that possess characteristic AHL- and DNA-binding domains; and, (iv) the results of the transcriptome analysis and conjugation activities. Indeed, from the differential transcriptome analysis of strains P4 and a P4 mutant unable to synthesize the signal molecule, it appears that the wild type P4 strain expressed sets of pAtP4 genes involved in the conjugative transfer of this plasmid at a much higher level than the mutant did. In support of this, the conjugation frequency of the At plasmid of strain P4 was ca. 14 times higher in the wild type strain than it was in the mutant. As a whole, this work is the first identification of the occurrence of QS regulation in the conjugation of an At plasmid in Agrobacterium. A possibility exists, however, that a similar system has been identified, but not characterized, by other authors on a transmissible genetic element of Agrobacterium [49].

Three sets of genes were upregulated in the wild type strain P4 (when compared with the mutant unable to produce the signal). The first set encoded the T4SSpAt involved in the formation of the conjugation apparatus in the donor bacteria, also termed the mating pair formation (Mpf) complex [50]. The genes and deduced proteins that encode or determine the T4SSpAt of strain P4 were highly related to those present on the At plasmid of strain C58. T4SS are indeed widespread among bacteria, where they ensure the transfer of protein(s) or nucleoprotein complexes outside the bacterial cell (for reviews, see [51, 52]). This is the case of the T4SS of A. tumefaciens, known as the Vir system, that promotes the transfer of a single strand copy of T-DNA from the bacteria to the plant cell [53] (for review, see [2]) and that of several plasmid conjugation systems such as those of the above mentioned pAt and pTi in strain C58 (for review, see [52]).

The second set of upregulated genes encoded the DNA transfer and replication (Dtr) system, a protein complex also known as the relaxosome. The relaxosome recognizes and cleaves the nic site at the origin of transfer (oriT) of plasmids [26, 47]. The oriT of pAt strain P4 has not been formally identified, but on pAtC58 the origin of transfer was previously located between the traA and traC genes [26]. Considering the high relatedness of the sequences of traA, traC and their intergenic region, it is tempting to speculate that the oriT of pAtP4 may be located also here. Based on the similarity of the deduced protein sequences, pAtP4 traA, traC, traD might encode the relaxosome, while traG may encode the so-called coupling protein that bridges the relaxosome and its cognate T4SS [54]. In the Rhizobiaceae, three Dtr systems have been identified among all species. The types I and II Dtr systems are found to be encoded by autotransferable plasmids, and the type III by mobilizable ones [55]. It has been proposed that class I Dtr systems such as the one encoded by the pTiC58 tra genes, are regulated by QS while class II Dtr sytems, including the one encoded by the pAtC58 tra genes, are regulated by an RctA repressor associated with an RctB anti-activator [55, 56]. Interestingly, the organization of the four tra genes of pAtP4 did not reveal the presence of traF and traB orthologs downstream of traA, a key feature of type I Dtr systems. The absence of traF and traB orthologs on pAtP4 would therefore place the pAtP4 Dtr system amongst type II systems regulated by RctA, especially considering that a rctA ortholog, but no rctB ortholog, is present on pAtP4 (Fig. 3). The present study however demonstrated that the pAtP4 type II Dtr system was regulated in a luxI/luxR dependent fashion. This finding therefore indicated that type II Dtr systems could also be regulated by QS, contrarily to what has been suggested earlier [55]. We propose that two subclasses of type II Dtr systems exist: a first one regulated by RctA and RctB (e.g. on pAtC58), and a second by RctA and QS (e.g. on pAtP4). In agreement with this, a similar situation (presence of the QS genes, presence of the repressor gene rctA and absence of the rctB gene) was found on the At plasmid of Agrobacterium strain 5A (not shown) that could therefore also belong to the second class of Type II Dtr systems.

In relation with the above, genes encoding components of a QS regulatory system have been detected on pAtP4 among those upregulated in the wild type P4 strain with respect to the mutant. The gene cluster structure is quite unusual, as it consisted of a single luxI-like gene surrounded by two luxR-like genes. This organization appears to be unique in the bacterial world, and found only in Agrobacterium strains (P4, 5A, RV3, NCPPB 1641 and DSM 30147). Interestingly, strains P4 and 5A belong to the same A. tumefaciens genomospecies 1 and have been isolated in different experiments performed with a soil of the same origin (X. Nesme, personal communication).

Besides the molecular genetics of pAt conjugation, the reported data tackled some ecological aspects of the phenomenon. A recent report indicated that the At plasmid confers a competitive advantage upon the host strain in the rhizosphere but exhibits a high cost under carbon-limiting conditions [22]. Therefore, we investigated whether the ability to transfer the plasmid also favors or hampers bacterial growth in the rhizosphere environment. No fitness differences were observed under the experimental conditions we used between strains P4RifRIX and P4RifNC (Fig. 5). From the above, it is reasonable to conclude that the QS-regulation of the conjugative transfer of pAtP4 did not confer a selective advantage upon the plasmid host in the tomato rhizosphere, at least under our experimental conditions.

Conclusion

This study led to the identification of novel conjugation system in which QS regulates plasmid transfer. However, contrary to what is observed for the conjugation of the Ti plasmid, the QS regulation of pAt transfer was not stringent (i.e. it was not a “on/off switch”), a feature that suggests that additional regulatory components may exist. The ecological and evolutionary relevance of the QS control of plasmid conjugation is still open to debate [21]. Although such a regulatory process might be necessary to prevent a futile mobilization of the donor metabolic resources required for the conjugative transfer of a replicon (that can represent, in the case of the At plasmid, ca. 10 % of its genome) when the donor population is low, QS regulation does not allow the donor to sense whether putative recipients are present. In relation to this, it has been suggested that QS regulation of plasmid conjugation may serve as a way to detect a presence of a biofilm rather than to evaluate a cell density [57]. This suggestion can be related to the diffusion sensing concept described by Redfield [58]. Both hypotheses propose that QS would permit the biological phenomenon, here the conjugative transfer of Ti and At plasmids, to occur only or preferentially in confined environments. Another report suggested that QS regulation of plasmid conjugation may be a way to switch the bacterial behavior from plasmid donor at high cell density to recipient at low cell density [59]. This elegant proposal is based on the existence of genes encoding a plasmid exclusion entry system that relies upon two Trb proteins (TrbJ and TrbK) encoded by the corresponding trb genes of Ti plasmids. Interestingly pAtP4, as well as pAtC58, do not harbor trbJ and trbK orthologs. The ecological relevance of QS regulation of the pAtP4 conjugative transfer therefore remains, to some extent, unclear.

Abbreviations

3O,C8-HSL: 

N-(3-oxo-octanoyl)-L-homoserine lactone

3OH,C8-HSL: 

N-(3-hydroxy-octanoyl)-homoserine lactone

AB: 

Agrobacterium broth

AHL: 

N-acyl homoserine lactone

C8-HSL: 

N-(octanoyl)-L-homoserine lactone

Ca.: 

Circa (about)

Dtr: 

DNA transfer and replication

LBm: 

Luria Bertani medium, modified

Mpf: 

Mating pair formation

QS: 

Quorum sensing

T-DNA: 

Transferred DNA

TY: 

Tryptone-yeast medium

UPLC: 

Ultra-performance liquid chromatography

Declarations

Acknowledgments

The authors wish to thank Dr. Xavier Nesme (University of Lyon I) for helpful discussions on Agrobacterium taxonomy and pAt occurrence in nature, Almudena González-Mula and Dr. Julien Lang (I2BC, Gif-sur-Yvette, France) for advice on mutagenesis, RT-qPCR and plasmid conjugation, and Pr. Mike DuBow and Dr. Peter Mergaert (I2BC, Gif-sur-Yvette, France) for correction of the language in the manuscript. This work has benefited from the facilities and expertise of the high throughput sequencing platform of the Institute for Integrative Biology of the Cell (I2BC, Gif-sur-Yvette, France) for RNA-seq analyses. The authors are also very grateful to Odile Thoison (ICSN-CNRS, Gif sur Yvette, France) for her advice on chromatography analyses.

Funding

The Institut for integrative biology of the cell benefits from the support of the LabEx Saclay Plant Sciences-SPS (ANR-10-LABX-0040-SPS). This work was made possible by a grant from Agence Nationale de la Recherche (ANR) via the ECORUM project (ANR project 11-BSV7-019). The financial support of NMH through this grant is hereby acknowledged.

Availability of data and material

Agrobacterium strain P4 is available from the authors upon request. The A. tumefaciens P4 genome sequence has been deposited at DDBJ/EMBL/GenBank under the accession number APJV00000000 (http://www.ncbi.nlm.nih.gov/nuccore/APJV00000000). Transcriptome data obtained from the high throughput sequencing platform of the Institute for Integrative Biology of the Cell are given in Additional file 5.

Authors’ contributions

NMH performed most of the experiments described in the manuscript with the exception of the chemical identification of the AHL molecules, that was performed by NH and FP. NY, in association with NMH, generated the mutants and performed the conjugation experiments. SM analyzed the P4 genome and identified the luxI and luxR orthologs. DF and YD conceived the experiments and obtained the financial supports. YD analyzed the transcriptome and conjugation data with NMH. YD and NMH wrote the manuscript that was approved by all authors.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

Not applicable.

Ethics approval and consent to participate

Not applicable.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Institut for integrative biology of the cell, CEA, CNRS, Université Paris-sud, Université Paris-Saclay, 91198 Gif sur Yvette, CEDEX, France
(2)
Institut de chimie des substances naturelles, CNRS, Avenue de la terrasse, 91198 Gif sur Yvette, France
(3)
Present address: CIRAD, 7 chemin de l’IRAT, ligne Paradis, 97410 Saint Pierre de la Réunion, France
(4)
Present address: UMR1347 Agroécologie, INRA, Centre de Dijon, 17 rue Sully, BP 86510, 21065 Dijon, CEDEX, France

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