Quorum-sensing regulates biofilm formation in Vibrio scophthalmi
© Garcia-Aljaro et al.; licensee BioMed Central Ltd. 2012
Received: 11 May 2012
Accepted: 23 November 2012
Published: 3 December 2012
In a previous study, we demonstrated that Vibrio scophthalmi, the most abundant Vibrio species among the marine aerobic or facultatively anaerobic bacteria inhabiting the intestinal tract of healthy cultured turbot (Scophthalmus maximus), contains at least two quorum-sensing circuits involving two types of signal molecules (a 3-hydroxy-dodecanoyl-homoserine lactone and the universal autoinducer 2 encoded by luxS). The purpose of this study was to investigate the functions regulated by these quorum sensing circuits in this vibrio by constructing mutants for the genes involved in these circuits.
The presence of a homologue to the Vibrio harveyi luxR gene encoding a main transcriptional regulator, whose expression is modulated by quorum–sensing signal molecules in other vibrios, was detected and sequenced. The V. scophthalmi LuxR protein displayed a maximum amino acid identity of 82% with SmcR, the LuxR homologue found in Vibrio vulnificus. luxR and luxS null mutants were constructed and their phenotype analysed. Both mutants displayed reduced biofilm formation in vitro as well as differences in membrane protein expression by mass-spectrometry analysis. Additionally, a recombinant strain of V. scophthalmi carrying the lactonase AiiA from Bacillus cereus, which causes hydrolysis of acyl homoserine lactones, was included in the study.
V. scophthalmi shares two quorum sensing circuits, including the main transcriptional regulator luxR, with some pathogenic vibrios such as V. harveyi and V. anguillarum. However, contrary to these pathogenic vibrios no virulence factors (such as protease production) were found to be quorum sensing regulated in this bacterium. Noteworthy, biofilm formation was altered in luxS and luxR mutants. In these mutants a different expression profile of membrane proteins were observed with respect to the wild type strain suggesting that quorum sensing could play a role in the regulation of the adhesion mechanisms of this bacterium.
KeywordsVibrio scophthalmi Biofilm formation Quorum-sensing AiiA LuxS Acyl homoserine lactone
V. scophthalmi is the most abundant species among the marine aerobic or facultatively anaerobic bacteria present in the intestinal tract of cultured turbot (Scophthalmus maximus) even though it is not the most abundant Vibrio species in the surrounding water [1, 2]. However, the possible benefits of turbot colonization by this bacterium are not well understood.
Bacteria communicate with members of their own species and even with bacteria outside of the species boundary to coordinate their behaviour in response to the density of the bacterial population, which is known as quorum-sensing . This communication relies on the production and sensing of one or more secreted low-molecular-mass signalling molecules, such as N-acylhomoserine lactones (AHLs), the extracellular concentration of which is related to the population density of the producing organism. Once the signalling molecule has reached a critical concentration, the quorum-sensing regulon is activated and the bacteria elicit a particular response as a population.
The first quorum-sensing system identified was shown to control bioluminescence in Vibrio fischeri through the LuxI-LuxR system [4, 5]. LuxI synthesizes a diffusible signal molecule, N-(3-oxohexanoyl)-L-homoserine lactone (3-oxo-C6-HSL), which increases in concentration as the cell density increases. LuxR, the transcriptional activator of the bioluminescence lux operon, binds 3-oxo-C6-HSL, which increases its stability. This complex binds the promoter of the lux operon activating the production of light. The LuxI-LuxR quorum-sensing circuit is found in many Gram-negative bacteria and has been shown to regulate a variety of genes; for instance, it has been shown to regulate virulence in Pseudomonas aeruginosa. However, this quorum-sensing circuit initially described in V. fischeri is not present in all Vibrio spp.
In Vibrio harveyi three additional quorum-sensing circuits were characterized that respond to three different signal molecules (see , for review). The first quorum-sensing system is composed of an AHL synthase, LuxM, which is responsible for the synthesis of 3-hydroxy-C4-HSL, and the receptor LuxN, a hybrid sensor kinase (present in V. harveyi, Vibrio anguillarum and Vibrio parahaemolyticus, among others). The second is composed of LuxS, LuxP and LuxQ. LuxS is responsible for the synthesis of the autoinducer 2 (AI-2), a universal signaling molecule used both by Gram-negative and Gram-positive bacteria for interspecies communication , LuxP is a periplasmic protein that binds AI-2 and LuxQ is a hybrid sensor kinase. The third system is composed of CqsA and CqsS. CqsA is responsible for the synthesis of a different autoinducer, the cholerae autoinducer CAI-I , and CqsS is the hybrid sensor kinase. These three quorum-sensing systems converge via phosphorelay signal transduction to a single regulator LuxO, which is activated upon phosphorylation at low cell density. LuxR, a regulatory protein that shares no homology to the V. fischeri LuxR, activates bioluminescence, biofilm formation, and metalloprotease and siderophore production at high cell density, is at the end of this cascade . This regulatory protein is repressed at low cell density and derepressed at high cell density in the presence of autoinducers which, after binding, activate the phosphatase activity of the sensor kinases. This more complex quorum-sensing system is found predominately in Vibrio species and components of the network vary between species .
In a previous work, we demonstrated the presence of two quorum-sensing signal molecules in the supernatants of V. scophthalmi: N-(3-hydroxydodecanoyl)-L-homoserine lactone (3-hydroxy-C12-HSL) and AI-2, encoded by a luxS gene . However, there is still a lack of knowledge of the bacterial activities that are regulated by quorum-sensing in this bacterium. In this study, we identified a homologue of the V. harveyi luxR transcriptional regulator and analyzed the functions regulated by LuxR and the previously identified quorum-sensing signaling molecules by constructing mutants for the coding genes.
Results and discussion
Detection and sequencing of luxRhomologue
Primers used in this study
luxR null mutant
Over expression luxR
Sequencing luxR and
Detection of luxR
Detection of luxR and
luxS null mutant
Over expression luxS
Cloning of luxS into pACYC184
Percentage of nucleotide and amino acid identity and similarity of V. scophthalmi A089 LuxR with previously reported V. harveyi -like LuxR regulators
% nt id (% aa id/% aa sim)
V. alginolyticus (AF204737.1)
V. anguillarum (AF457643.2)
V. cholerae (EU523726.1)
V. harveyi (M55260.1)
V. mimicus (AB539839.1)
V. parahaemolyticus (AF035967.1)
V. vulnificus (EF596781.1)
Functions regulated by luxR, luxSand AHLs
In order to uncover the functions regulated by quorum-sensing in V. scophthalmi null mutants for luxR and luxS were constructed. Additionally, a recombinant strain generated in a previous study that carries a gene coding for a lactonase from Bacillus cereus (AiiA) which was previously shown to hydrolyse AHLs  was included in the assays to study the functions regulated by AHLs.
Positive and negative regulation of biofilm formation has been reported in other vibrio such as V. anguillarum and V. cholerae, respectively [16, 17]. Interestingly, in a recent study on quorum-sensing in V. ichthyoenteri (the most closely related species to V. scophthalmi), its luxS homologue was sequenced and a mutant for this gene constructed, but no functions were reported to be regulated by this gene . It has to be noted that neither the V. ichthyoenteri wild type, nor the luxS mutant formed biofilms in the microwell plates. Our results showed that luxS is involved in biofilm formation at least in vitro in V. scophthalmi. However, it is important to highlight that in our study the V. scophthalmi wild-type strain was only able to form significant biofilm when grown in MB, while TSB inhibited biofilm formation in vitro. Therefore, it would be interesting to assess if V. ichthyoenteri and the luxS mutant behave similarly to V. scophthalmi since they are so closely related. In V. scophthalmi, these two quorum-sensing systems may play a role in the colonization and establishment of this bacterium in the fish intestine, since it is a normal inhabitant of the turbot intestine . In fact most vibrio species form biofilms on different structures, which is believed to be beneficial for the populations against different environmental stresses . Work is currently being done to test these hypotheses.
Extracellular protease activity was not detected in either the wild-type strain or any of the luxR and/or luxS mutants as determined by a qualitative milk plate assay as well as a quantitative detection method using azocasein. On the other hand, siderophore production, which has been shown to be regulated by quorum-sensing in other vibrios was evaluated using the siderophore CAS assay. In addition, the ability to grow in iron depleted medium (EDDA assay) was assessed. A minor positive signal indicating the presence of siderophore activity was detected in all the mutants and wild type strains with the same intensity. However, neither the wild-type strain nor the mutants grew in the EDDA-supplemented medium suggesting that this species is not able to grow in iron-depleted medium, at least under the conditions used in the assay. Extracellular proteases and siderophores are often produced by pathogenic vibrios [20–22], although some vibrios that are not pathogenic have been shown to produce siderophores in an iron-limited host environment, such as V. fischeri.
The Vibrio harveyi-like LuxR family of regulators is a diverse family with different associated functions depending on the Vibrio species. For example, in V. harveyi, luxR is expressed at high cell densities and regulates different functions including siderophores, colony morphology, activates bioluminescence, activates metalloprotease production, represses the type III secretion system [21, 24, 25]. Apart from this diversity, all the V. harveyi-like quorum-sensing systems converge to a phosphorelay circuit that regulates the expression of luxR. However, in V. anguillarum, contrary to other members of the LuxR family, this gene is expressed at low densities. This gene represses exopolysaccharide production, and regulates biofilm formation, metalloprotease, pigment production and serine biosynthesis . In the case of V. scophthalmi, which is a non-pathogenic vibrio, no virulence factors are shown to be regulated by this transcriptional regulator. At this moment, genome sequencing of the two V. scophthalmi strains used in this study is under process in our laboratory. Future work will involve transcriptome analysis of these mutants.
V. scophthalmi shares two quorum sensing circuits, including the main transcriptional regulator LuxR, with some pathogenic vibrios such as V. harveyi and V. anguillarum. However, contrary to these pathogenic vibrios no virulence factors (such as protease or siderophore production) were found to be quorum sensing regulated in this bacterium. Noteworthy, biofilm formation was altered in luxS and luxR mutants. In these mutants a different expression profile of membrane proteins were observed with respect to the wild type strain suggesting that quorum sensing could play a role in the adhesion and subsequent colonization of the fish by this bacterium. Further studies are needed in order to ascertain a similar behaviour of these mutants in vivo.
Bacterial strains, culture media and growth conditions
Bacterial strains and plasmids used in this study
Strain or plasmid
Genotype and feature(s)
V. scophthalmi strains
Wild type, turbot isolate (CECT 4638T)
Wild type, turbot isolate (CECT 5965)
A089 ΔluxR mutant
A089_23 (pMMB207::luxR) mutant
A089 ΔluxS mutant
A089_68 (pMMB207::luxS) mutant
A102 ΔluxR mutant
A102_56 (pMMB207::luxR) mutant
A102 ΔluxS mutant
A102_73 (pMMB207::luxS) mutant
E. coli strains
E. coli used for transformation: λpir
E. coli used for conjugation: λpir mob
Cmr Kanr SacBR; suicide vector
Cmr,Ptac, broad host range expression vector
Tetr, Cmr, broad host range expression vector
Ampr Kanr; TA cloning vector for sequencing
Detection of luxRhomologues by PCR
Primers luxRI-F2 and luxRI-R2 (Table 1) were designed based on V. harveyi luxR and luxR homologue sequences from other vibrios retrieved from GenBank. Genomic DNA was used as template. Genomic DNA was isolated from single colonies by inoculating them in 20 μl of double distilled H2O and boiling for 10 min. The samples where then chilled and centrifuged for 5 min at 16,000 g and 5 μl of the supernatant was used as template for the PCR. The primers and reagents for PCR were purchased from Roche Diagnostics (Barcelona, Spain). The conditions used for the PCR are described elsewhere . A 636-bp fragment containing part of the luxR gene was obtained.
Cloning and sequencing of luxRgene and its flanking DNA
The DNA sequence of the entire luxR gene of the two strains of V. scophthalmi together with the 5’- and 3’- flanking regions was obtained by inverted PCR . To prepare template for the inverted PCR, genomic DNA was digested with the restriction enzyme HincII and the linear HincII fragments were circularized by ligation with T4 DNA ligase (Invitrogen). The ligated DNA molecules were used as template to amplify a DNA fragment on which the 5’- and 3’-ends of the luxR gene have been joined at a HincII site. To amplify this fragment, primers (LuxRI-R4 and LuxRI-F4, Table 1) were designed to polymerize DNA out from either end of the 636-bp fragment that contains part of the luxR gene. A single amplimer was generated and sequenced to identify the flanking ends of the luxR gene. Using this sequence data, primers (LuxR-1 and LuxR-2, Table 1) were designed to amplify the entire luxR gene plus the 5’- and 3’-flanking DNA (a total of 944 bp). This fragment was cloned and sequenced using the LuxR-1 and LuxR-2 primers. These sequences were submitted to the GenBank database under the accession number JN684209 and JN684210, for V. scophthalmi A089 and A102, respectively.
Sequencing of DNA that flanks the luxSgene
The flanking regions of the previously sequenced luxS gene (accession number EF363481) were obtained as described above for luxR, except that the restriction enzyme DraI and the primers LuxS-F6 and LuxS-R7 were used (Table 1).
DNA sequencing was performed with the Big Dye Terminator Cycle Sequencing Ready Reaction Kit 3.1 (Applied Biosystems), according to the manufacturer’s instructions.
Construction of ΔluxR and ΔluxSmutants by allelic exchange
In-frame deletions of the luxR and luxS genes were generated by allelic exchange as previously described . Briefly, an altered allele for both the luxR and the luxS genes was created by overlap PCR that encodes the first 12 amino acids fused to the last 9 amino acids, for luxR and the first 9 amino acids fused to the last 9 amino acids for luxS. The PCR primers LuxR-A, LuxR-B and LuxR-C, LuxR-D (Table 1) were used to create the luxR mutant allele and primers LuxS-A, LuxS-B, LuxS-C, and LuxS-D (Table 1) were used to create the luxS mutant allele. Both alleles were cloned into the R6K-origin based suicide vector pDM4 creating pDM4-luxR-AD and pDM4-luxS-AD, respectively. These plasmids were transferred to the V. scophthalmi A089 and A102 parental strains by bacterial conjugation as stated below, generating the V. scophthalmi A089_23 and A102_56 mutant, which carry a luxR in-frame deletion, and the V. scophthalmi A089_68 and A102_73 mutants, which carry a luxS in-frame deletion.
Construction of mutants over-expressing luxR and luxSgenes
In order to determine the effect of over-expressing the luxR gene, the luxR and luxS genes were cloned into pMMB207 and fused to the tac promoter, which was induced using 0.5 mM IPTG. To clone into this vector, primers LuxR-G and LuxR-H were used for luxR and LuxS-PMMBF and LuxS-PMMBR for luxS. In order to tranfer the pMMB207 plasmid alone or the pMMB207 plasmid carrying the luxS or luxR genes to V. scophthalmi luxR and luxS null mutants, the plasmid constructions were electroporated into E. coli S17-1. The plasmids were later transferred to V. scophthalmi by bacterial conjugation as stated below.
Complementation of luxSnull mutant
Complementation of the A102_73 luxS mutant was performed by amplification of luxS gene with primers LuxS-AI and LuxS-BI (Table 1), followed by digestion with BamHI and SalI and ligation to the pACYC plasmid digested with the same strains (Table 3). The pACYC plasmid carrying the luxS gene was then electroporated into E. coli S17-1 (Table 3) and the transformants selected using 20 μg/ml chloramphenicol LB plates. This plasmid was later transferred to V. scophthalmi by bacterial conjugation and selected in TCBS with 5 μg/ml as stated below.
Plasmids pMMB207, pMMB207::luxR, pMMB207::luxS and pACYC::luxS cloned into E. coli S17-1 were mobilized into V. scophthalmi by bacterial conjugation. Briefly, the E. coli S17-1 carrying the corresponding plasmid and the V. scophthalmi receptor strain were grown to mid-logarithmic growth phase. A total of 0.5 ml of the E. coli culture was pelleted in a microfuge, the supernatant was removed, and the cells were mixed with 1 ml of V. scophthalmi. The cell mixture was centrifuged and suspended in 50 μl of TSB2. The 50 μl were spotted onto a TSA2 plate and incubated at 30°C for 24 h. Following incubation, the bacterial cells were resuspended in TSB2 and serial dilutions were plated onto TCBS medium (Oxoid) containing 5 μg/ml chloramphenicol to select for the V. scophthalmi containing the plasmids.
In order to construct the V. scophthalmi luxR and luxS null mutants, the E. coli S17-1 strains carrying either pDM4-luxR-AD and pDM4-luxS-AD were mated with V. scophthalmi A089 and A102 wild type strains. The selection for the strains carrying the suicide plasmid was performed in TCBS containing 5 μg/ml chloramphenicol as stated above. Afterwards, the null mutants were further selected after induction of sacBR in TSB2 agar plates supplemented with 5% sucrose. The in-frame deletions were confirmed by sequencing a PCR-amplified DNA fragment containing each mutation.
The effect of the mutations on the growth rate of these bacteria was analysed. Briefly, ON cultures were prepared on TSB2 and diluted to an initial density of approximately 0.01 and incubated for 10 h at 30°C with continuous agitation. Bacterial growth was estimated from OD readings at 600 nm taken at different intervals.
Extracellular protease activity was evaluated both qualitatively and quantitatively. For qualitative assay the parental as well as the mutant strains were streaked onto TSA2 and MA supplemented with 1%, 1.5% or 2% skimmed milk and incubated for a maximum of 48 h. The presence of a casein degradation halus was considered a positive result. The quantitative assay was performed as previously described using the azocasein assay as previously described , using O/N supernatants of the strains to be tested.
Biofilm formation was evaluated using 96-well polystyrene cell-culture treated microtiter plates after 48 h incubation using the crystal violet staining method, as previously described . Briefly, O/N cultures of the corresponding strain to be tested were diluted into fresh TSB2 or MB media to get approximately an optical density of 0.01 OD600 nm units. A total of 200 μl were dispensed in each well and incubated statically in a wet chamber for 48 h at 30°C. A minimum of four replicates in three independent assays were measured.
MA and TSA2 swimming plates containing 0.25% agar were used to assess the effect of LuxS and LuxR in motility. An overnight culture of the corresponding strain to be analysed was diluted 1:100 and a drop containing 10 μl of the sample was inoculated in the middle of the plate and the movement of the strains was monitored up to 48 h by measuring the diameter reached by the bacteria.
Detection of siderophores
The chrome azure assay (CAS) was used to detect the production of siderophores in both the mutants and wild type strains, as described in  with minor modifications. Briefly, the nutrient medium used for the growth of the bacteria was TSA supplemented with 0.5% NaCl. Additionally, the ability of these strains to grow on iron depleted media was assessed using MA and TSA2 plates containing 0.2 mM ethylenediamine di(o-hydroxyphenylacetic acid) (EDDA) chelating agent.
Membrane protein profiling by mass spectrometry
Membrane proteins from the mutants and wild type strains were extracted from 500 ml ON cultures. Briefly, the cultures were centrifuged for 10 min at 16,000 g and washed with PBS. The cells were suspended in 10 ml Tris 50 mM pH 8.0 and the suspension was frozen at −80°C. Successive rounds of freezing and thawing were performed. The suspension was then centrifuged for 2 min at 16,000 g. The supernatant was centrifuged at 16,000 g for 1 hour at 4°C and the pellet enriched in membrane proteins was suspended in 10 μl of 50% acetonitrile-2.5% trifluoroacetic acid. One microliter of the supernatant was placed onto a spot of a ground steel plate and air dried at room temperature. Each sample was overlaid with 1 μl of matrix solution (saturated solution of α-cyno-4-hydroxy-cinnamic acid in 50% acetonitrile-2.5% trifluoroacetic acid) and air dried at room temperature.
Measurements were performed on an Autoflex III MALDI-TOF/TOF mass spectrometer (Bruker Daltonics, Leipzig, Germany) equipped with a 200-Hz Smartbeam laser. Spectra were recorded in the linear, positive mode at a laser frequency of 200 Hz within a mass range from 2,000 to 20,000 Da. The IS1 voltage was 20 kV, the IS2 voltage was maintained at 18.7 kV, the lens voltage was 6.50 kV, and the extraction delay time was 120 ns.
For each spectrum approximately 500 shots from different positions of the target spot were collected and analyzed. The spectra were calibrated externally using the Bruker Bacterial Test Standard (Escherichia coli extract including the additional proteins RNase A and myoglobin). Calibration masses were as follows: RL29 3637.8 Da; RS32, 5096.8 Da; RS34, 5381.4 Da; RL33meth, 6255.4 Da; RL29, 7274.5 Da; RS19, 10300.1 Da; RNase A, 13683.2 Da; myoglobin, 16952.3 Da). The analyses were performed in triplicate.
We would like to thank Barbara Weber, Ramon Rosselló-Mora, Ana Cifuentes and Rosa Maria Gomila for the technical assistance. This work was supported by the FEMS research grant ES-SEM2010-1Garcia-Aljaro, the Xarxa de Referència en Biotecnologia (XRB) and the Government of Catalonia’s research program 2009SGR1043.
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