Cis-2-dodecenoic acid signal modulates virulence of Pseudomonas aeruginosa through interference with quorum sensing systems and T3SS
© Deng et al.; licensee BioMed Central Ltd. 2013
Received: 1 August 2013
Accepted: 15 October 2013
Published: 18 October 2013
Cis-2-dodecenoic acid (BDSF) is well known for its important functions in intraspecies signaling in Burkholderia cenocepacia. Previous work has also established an important role of BDSF in interspecies and inter-kingdom communications. It was identified that BDSF modulates virulence of Pseudomonas aeruginosa. However, how BDSF interferes with virulence of P. aeruginosa is still not clear.
We report here that BDSF mediates the cross-talk between B. cenocepacia and P. aeruginosa through interference with quorum sensing (QS) systems and type III secretion system (T3SS) of P. aeruginosa. Bioassay results revealed that exogenous addition of BDSF not only reduced the transcriptional expression of the regulator encoding gene of QS systems, i.e., lasR, pqsR, and rhlR, but also simultaneously decreased the production of QS signals including 3-oxo-C12-HSL, Pseudomonas quinolone signal (PQS) and C4-HSL, consequently resulting in the down-regulation of biofilm formation and virulence factor production of P. aeruginosa. Furthermore, BDSF and some of its derivatives are also capable of inhibiting T3SS of P. aeruginosa at a micromolar level. Treatment with BDSF obviously reduced the virulence of P. aeruginosa in both HeLa cell and zebrafish infection models.
These results depict that BDSF modulates virulence of P. aeruginosa through interference with QS systems and T3SS.
Many microorganisms utilize species-specific small signal molecules to coordinate a range of important activities, including virulence factor production, antibiotics biosynthesis and biofilm. This cell-cell communication mechanism is known as quorum sensing (QS) [1–4]. As a ubiquitous environmental organism which infects various animals, plants, and insects, Pseudomonas aeruginosa is also a major source of opportunistic infections in both immunocompromised individuals and cystic fibrosis patients [5, 6]. It has evolved at least three types of quorum sensing (QS) systems, i.e., las, pqs and rhl, which are implicated in regulation of several aspects of pathogenesis, including virulence factor production, biofilm development, and antimicrobial resistance . Besides the QS systems, most clinical isolates of P. aeruginosa also use type III secretion system (T3SS) to evade phagocytosis and facilitate infection [8–13]. T3SS is an important virulence determinant which is conserved in many animal and plant pathogens, including Salmonella spp., Shigella flexneri, Yersinia spp., Escherichia coli, and Chlamydia spp. [14, 15]. Although previous study already revealed that QS controls T3SS in some bacterial species, the relationship between QS systems and T3SS in P. aeruginosa is still not clearly determined [16, 17].
There is a new form of microbe-microbe antagonism interaction designated as signal interference . This type of antagonism acts not by killing, but instead by interfering with the signal-mediated gene expression of the competitors [19, 20]. It has been found that some microorganisms could boost their competitive strength through interfering with QS signaling of their competitors . This interference mechanism has been employed to develop novel drugs as the antagonists of signaling systems of bacterial pathogens. For example, some compounds have been identified or synthesized to act as the antagonists of QS systems of P. aeruginosa, including N-acyl cyclopentylamides, Furanone derivatives, Garlic, Malyngolide, Iberin, Protoanemonin, Norbgugaine and Caffeine [21–28]. Besides the signal interference with QS system, interfering with T3SS system has also been shown as an effective method to treat the bacterial pathogens [29–31]. Given the fact that the anti-QS or anti-T3SS compounds display a significantly inhibitory activity on the virulence of P. aeruginosa, suggesting that interference on QS systems or/and T3SS can be specifically utilized as favorable therapeutic methods on P. aeruginosa infection [32–34].
As a new type of QS signal, the diffusible signal factor (DSF) has been demonstrated to play an important role to control the biological functions such as biofilm formation, motility, virulence and antibiotic resistance [3, 4]. Among DSF-family signals, Cis-2-dodecenoic acid (BDSF) was originally identified in Burkholderia cenocepacia to be involved in regulation of biofilm formation, virulence and motility in B. cenocepacia[35–41]. Furthermore, besides the significance on intraspecies signaling, BDSF also appears its critical importance for maintenance of ecology through interspecies and inter-kingdom communication [35, 37, 42]. Exogenous addition of BDSF from B. cenocepacia restored the biofilm dispersal and virulence factor production of Xanthomonas campestris pv. campestris DSF-deficient mutants. It was also revealed that Candida albicans germ tube formation was strongly inhibited by exogenous addition of physiological relevant level of BDSF . Moreover, BDSF from B. cenocepacia and Stenotrophomonas maltophilia was found to be involved in modulation of virulence, antibiotic resistance and persistence of P. aeruginosa in the cystic fibrosis airway . In combination, these results have well established the role of BDSF play not only in regulation of a range of biological functions through intraspecies signaling, but also in microbial ecology through interspecies and cross-kingdom communication. In this study, we investigate the role of BDSF in the inter-species communication between B. cenocepacia and P. aeruginosa; and discover the inhibitory effect of BDSF on QS systems and T3SS of P. aeruginosa.
BDSF interferes with QS systems of P. aeruginosa
There are at least two AHL-dependent QS systems in P. aeruginosa, las and rhl systems, which control the expression of numerous genes [34, 43, 44]. It was found that the two QS systems are in a hierarchy where las system is dominant over rhl system [45, 46]. Moreover, it was also identified that LasR was required for the production of PQS, which plays a positive effect on rhl system. The three QS systems are interconnected with las system at the top of the QS cascade, which controls rhl and pqs systems [47, 48]. Recently, it was revealed that pqs and rhl systems are under the positive regulation of iqs system (It was named for its role in integrating the QS network in P. aeruginosa), which is tightly controlled by las system in P. aeruginosa.
BDSF inhibits biofilm formation and virulence factor production of P. aeruginosa
P. aeruginosa usually utilizes exoenzyme to induce its pathogenesis [50, 51]. To study the effect of BDSF on the production of exoproteases, which are important virulence factors of P. aeruginosa, BDSF was added to the growth medium of P. aeruginosa PA14 to test its effect on the secretion of proteases in the supernatants. Results demonstrated that addition of BDSF inhibited the production of proteases, treatment with 0.25 mM BDSF caused 30% reduction of the protease activity (Figure 2B). The reduction was increased to 50% when 0.5 mM BDSF was supplemented (Figure 2B).
During the growth process, it was observed that BDSF inhibited the pigment accumulation of P. aeruginosa PA14 in the medium. P. aeruginosa produces a number of colored secondary metabolities; one of them is pyocyanin, which is a virulence factor [52, 53]. To determine whether BDSF affects this virulence factor production, we measured pyocyanin accumulation in LB medium in the absence and presence of BDSF. As shown in Figure 2C, addition of BDSF to the bacterial medium substantially reduced the production of pyocyanin. Compared with the control, addition of 0.1 and 0.5 mM BDSF reduced the pyocyanin production by about 55% and 70%, respectively (Figure 2C).
It was reported that DSF from S. maltophilia influences biofilm formation and polymyxin tolerance in P. aeruginosa through the sensor kinase PA1396 . To test whether PA1396 is also the sensor of BDSF in P. aeruginosa, we then measured the protease activity and pyocyanin production of PA1396 deletion mutant in the absence and presence of BDSF. However, our results showed that disruption of PA1396 was not able to diminish the inhibitory effect of BDSF on the virulence factor production (Additional file 1: Figure S2), suggesting that PA1396 is not BDSF sensor kinase in P. aeruginosa.
Exogenous addition of BDSF represses T3SS of P. aeruginosa
It was previously reported that a long-chain fatty acid (LCFA) negatively modulates the expression of type III exsCEBA operon in P. aeruginosa through the sensor PsrA . To investigate whether BDSF shares the same signaling pathway as LCFA, we then further measured the effect of BDSF on T3SS in P. aeruginosa psrA mutant. Unexpectedly, deletion of psrA displayed no effect on the inhibitory activity of BDSF on T3SS of P. aeruginosa, suggesting that BDSF possibly acts through another sensor different from that of the LCFA molecule (Additional file 1: Figure S3).
BDSF inhibits T3SS of P. aeruginosaat its physiological relevant level
Many BDSF derivatives show inhibitory activity on T3SS of P. aeruginosa
BDSF attenuates the virulence of P. aeruginosa in both in vitro and in vivoassays
Zebrafish was reported to be a good infection model for the test of T3SS-mediated virulence of P. aeruginosa. We then analyzed the effect of BDSF on the virulence of P. aeruginosa PA14 by infecting 6-month-old zebrafish (Danio rerio), which was used as an infection model for B. cenocepacia. As shown in Figure 6B, treatment with 100 μM BDSF significantly reduced the virulence of P. aeruginosa PA14 in zebrafish infection model. While 60% of the fish infected with P. aeruginosa PA14 died within 24 hours post-inoculation, the P. aeruginosa PA14 treated with BDSF was much less virulent and only 10% of the infected fish died (Figure 6B).
This study demonstrated that besides acting as an intraspecies signal, BDSF can also mediate inter-species communication between B. cenocepacia and P. aeruginosa through inhibiting on QS systems and T3SS of P. aeruginosa. Previous studies already found that there is a cross-talk between B. cepacia and P. aeruginosa, which is modulated by AHL QS signal from P. aeruginosa[60, 61]. It was reported that addition of cell-free exoproducts of PAO1 to B. cepacia markedly enhanced its production of siderophore, lipase and protease; while addition of the supernatants of PAO1 with attenuated production of AHL only had slight effect on the production of these virulence factors . Moreover, AHL from PAO1 can also induce the biofilm formation of B. cenocepacia H111, demonstrating that AHL signal plays an important role in the cross-talk between the two bacterial species, which usually share the same niche in cystic fibrosis patients. Recently, the critical role of BDSF in the interspecies communication between B. cenocepacia and P. aeruginosa was also well established by the finding that BDSF modulates virulence, antibiotic resistance and persistence of P. aeruginosa in the cystic fibrosis airway . Our findings not only further confirmed the BDSF role in the complicated interaction between B. cenocepacia and P. aeruginosa, but also depicted how BDSF modulates the virulence of P. aeruginosa.
In P. aeruginosa, there are at least three QS systems, i.e., las, pqs and rhl, consisting of a hierarchy regulatory network. These QS systems regulate a broad range of genes important for the metabolism and virulence of P. aeruginosa. Inhibition on these QS systems will finally attenuate the virulence factor production and virulence of P. aeruginosa. Our study showed that addition of BDSF caused the decreased expression of lasR, which is the regulator of las system (Figure 1B). Consistently with the dominant role of las system over pqs and rhl systems, addition of BDSF also obviously inhibited pqs and rhl systems (Figure 1C-D, Additional file 1: Figure S1), suggesting that the inhibitory activity of BDSF on the QS systems of P. aeruginosa may initial from the inhibition on las system. Recently, a DSF sensor, PA1396 was identified in P. aeruginosa. To determine whether BDSF and DSF share the same sensor in P. aeruginosa, we then tested the BDSF effect on the virulence factor production mediated by QS systems in PA1396 deletion mutant. However, it was revealed that PA1396 is not BDSF sensor kinase, as disruption of PA1396 could not diminish the inhibitory effect of BDSF on the virulence factor production (Additional file 1: Figure S2). How does BDSF interfere with QS systems in P. aeruginosa still needs the further investigation.
T3SS is a key virulence determinant in a wide range of animal and plant pathogens and plays diverse roles in host-pathogen interactions. In P. aeruginosa, the transcriptional expression of effector genes of T3SS is coordinated by ExsA encoded by the exsCEBA operon. Our results showed that BDSF inhibited the expression of exsCEBA, which was confirmed by the results of semi-quantitative RT-PCR analysis and western blotting analysis (Figure 3). It was recently reported that PsrA serves as a sensor for a long chain fatty acid (LCFA) to negatively modulate the expression of T3SS in P. aeruginosa. However, exogenous addition of BDSF still showed a similar inhibition pattern on psrA deletion mutant, suggesting that BDSF may control T3SS through another sensor (Additional file 1: Figure S3). Moreover, the fact that T3SS is more sensitive to the exogenous addition of BDSF than the QS systems indicates that BDSF may interfere with QS systems and T3SS of P. aeruginosa through two independent signaling pathways. Besides the inhibitory effect on the QS systems and T3SS, our microarray analysis data suggests that BDSF also affects many other genes in P. aeruginosa (Data not shown). It was found that treatment with 250 μM of BDSF up-regulated 66 genes more than 2-fold, which is 1.38% to the total number of genes in genome. Meanwhile, a total of 120 genes were down-regulated by more than 2-fold (Data not shown). These genes are classified into the functional groups of metabolism, secretion, motility and cell wall, transcription regulation, protection, enzymes and carbon compound catabolism (Data not shown), suggesting that BDSF plays a global effect on P. aeruginosa.
Antibiotics have been used for a long time to treat the bacterial infection of P. aeruginosa, but resistance to antibiotics could be evolved during clinic treatment. Interestingly, recently studies found that some compounds successfully interfered with N-acyl homoserine lactone of P. aeruginosa and suppressed bacterial QS in lungs, finally caused accelerated lung bacterial clearance and reduced the severity of lung pathology . Furthermore, some other compounds were identified to be the inhibitors of P. aeruginosa T3SS, treatment with these compounds caused the attenuated cytotoxicity of P. aeruginosa on mammalian cells . Combined with our findings, it is suggested that interferences on the QS systems and T3SS can be specifically utilized as favorable therapeutic methods on P. aeruginosa infection [31, 32, 34].
BDSF mediates the cross-talk between B. cenocepacia and P. aeruginosa by interfering with QS systems and T3SS of P. aeruginosa. Biological functions such as biofilm formation and virulence factor production of P. aeruginosa were inhibited by exogenous addition of BDSF. Furthermore, BDSF and some of its derivatives are also able to inhibit T3SS of P. aeruginosa at a micromolar level. Treatment with BDSF obviously reduced the virulence of P. aeruginosa in both in vitro and in vivo models.
Bacterial strains and growth conditions
Bacterial strains and plasmids used in this study
Strain or plasmid
Phenotypes and/or characteristics
Reference or source
J2315 Wild type strain, Genomovars III of B. cepacia complex
BDSF-minus mutant derived from J2315 with Bcam0581 being deleted
Mutant d0581 harboring the expression construct pMLS7-0581
PA14 harboring the T3SS reporter construct mini-CTX-lacZ with the exsCEBA promoter fused to lacZ
PA14 harboring the reporter construct pME2PlasR-lacZ
PA14 harboring the reporter construct pME2PpqsR-lacZ
PA14 harboring the reporter construct pME2PrhlR-lacZ
psrA deletion mutant harboring the T3SS reporter construct mini-CTX-lacZ with the exsCEBA promoter fused to lacZ
PA1396 deletion mutant derived from PA14
Res- pro mod+ integrated copy of RP4, mob+, used for incorporating
The biosensor strain of C4-HSL
AHL reporter strain
Lab of Stephen K. Farrand
mini-CTX-lacZ with the exsCEBA promoter fused to lacZ
pME2-lacZ containing promoter of lasR
pME2-lacZ containing promoter of pqsR
pME2-lacZ containing promoter of rhlR
Bacterial growth analysis
Overnight bacterial cultures grown in LB broth was inoculated in the same medium to an OD600 of 0.025 in the absence and presence of BDSF. Three hundred microliters of inoculated culture were grown in each well at 37°C in a low intensity shaking model using the Bioscreen-C Automated Growth Curves Analysis System (OY Growth Curves AB Ltd, Finland).
Construction of reporter strains and measurement of β-galactosidase activity
The promoters of lasR, rhlR and pqsR were amplified using the primer pairs listed in Additional file 1: Table S2 with HindIII and EcoRI restriction sites attached. The resulting products were digested with HindIII and EcoRI, and ligated at the same enzyme sites in the vector pME2-lacZ. These constructs, verified by DNA sequencing, were introduced into P. aeruginosa by electroporation. Transconjugants were then selected on LB agar plates supplemented with tetracycline. For the construction of reporter strain of T3SS, the promoter of exsCEBA was amplified by PCR using the primer pairs listed in Additional file 1: Table S2, and cloned into the integration vector mini-CTX-lacZ . The construct was introduced into E. coli S17-1(λpir) and then integrated into the chromosome of P. aeruginosa as described previously . The engineered strain was then selected on the LB agar plates containing tetracycline and used as the T3SS reporter strain. Measurement of β-galactosidase activities was assayed following the methods as described previously . Bacteria were grown at 37°C to an OD600 of about 1.5, and the cells were harvested to measure the β-galactosidase activities.
Biofilm formation assays
Biofilm formation in 96-well polypropylene microtitre dishes was assayed as followed. Overnight bacterial cultures grown in LB broth was inoculated in the same medium to an OD600 of 0.01 in the absence and presence of BDSF signal at different concentrations as indicated. One hundred microliters of inoculated culture were grown in each well at 37°C with shaking at 150 rpm for 18 h. The cultures were removed and 200 μl of 1% crystal violet (w/v) was added. Following staining at room temperature for 15 min, the dye was removed and the wells were rinsed three times with water. For quantification of the attached bacterial cells, the stained wells were decolorized with 200 μl of 95% ethanol. The quantity of crystal violet was determined by measuring the absorbance at 595 nm.
Proteolytic activity assay
Protease activity was quantified following the previously described method with minor modifications . Briefly, bacteria were cultured at 37°C for about 12 hours. After measuring the optical density at 600 nm, cultures were centrifuged at 13,000 rpm for 5 min and the supernatants were taken out and filtered through a 0.2 μm pore size cellulose-acetate filter. One hundred microliter of supernatants were incubated at 30°C with equal volume of azocasein dissolved in proteolytic buffer B (5 mg/ml) for 30 min. The reaction was stopped by addition of 400 μl of 10% (w/v) TCA buffer. After incubation for 2 min at room temperature, the mixture was centrifuged at 13,000 rpm for 1 min to remove the remaining azocasein. Supernatants were taken out and mixed with 700 μl of 525 mM NaOH. Absorbance of the azopeptide supernatant was measured at the wavelength of 442 nm. Protease activity was obtained after normalization the absorbance against the corresponding cell density.
After measuring the absorbance at 600 nm, the supernatants of bacterial cultures were collected for extraction of pyocyanin with the method described previously . Briefly, cultures were centrifuged at 13,000 rpm for 1 min and 1.5 ml supernatants were collected and extracted with double volume chloroform with vigorous shaking at room temperature for 30 min. The solvent phase was transferred to a new tube containing 1 ml of 1 N HCl. The mixture was shaken gently to transfer pyocyanin to aqueous phase. The quantity of pyocyanin was determined by measurement of absorbance at 520 nm and normalization against the cell density.
RNA extraction and RT-PCR analysis
P. aeruginosa was grown in LB medium supplemented with NTA till OD600 of 1.5. Total RNA was isolated using the RNeasy mini kit (Qiagen) according to the manufacturer’s instructions. The concentration and purity of RNA were determined by agarose gel electrophoresis and spectrometry. Reverse transcription (RT-PCR) analysis was performed using the One-step RT-PCR kit according to the manufacturer’s instructions (Qiagen).
Protein isolation and western blotting analysis
Bacteria were cultured in LB medium supplemented with NTA to an OD600 of 1.5, 10 ml of each bacterial culture were collected and centrifuged. The supernatants were then filtered with 0.2 μm syringe filter and precipitated with trichloroacetic acid (TCA) at a final concentration of 10%. The precipitates were pelleted by centrifugation, washed twice with acetone, dried, and re-suspended in SDS sampling buffer. The protein samples were denatured by boiling for 5 min and separated by 10% SDS-PAGE. Western blot analysis was performed following the standard protocols .
Cytotoxicity assays in HeLa cell model
BDSF effect on the cytotoxicity of P. aeruginosa 14 was assayed by using HeLa cells. HeLa cells were seeded in 24-well tissue culture plates containing Dulbecco’s Modified Eagle Medium (DMEM) and allowed to grow at 37°C in CO2 for about 18 hours to obtain 80-90% monolayer confluency (5.0×105 cells/well). Culture supernatants were removed and the monolayer was washed once with PBS buffer. Fresh bacterial cells were diluted in DMEM to a concentration about 5×107 CFU per ml. Thereafter, 0.5 ml of bacteria dilutions in the absence and presence of BDSF were applied to the HeLa cell monolayers at a multiplicity of infection (MOI) about 50. Cytotoxicity was determined by measuring the release of the cytosolic enzyme lactate dehydrogenase (LDH) into supernatants using the cytotoxicity detection kit (Roche).
Virulence assays using a zebrafish infection model
P. aeruginosa PA14 virulence was tested by infecting 6-month-old zebrafish (Danio rerio). Firstly, bacterial cultures were grown to an OD600 of 1.0, and washed with phosphate-buffered saline (PBS; pH 7.3), then dissolved in PBS buffer to 5.0 × 109 cfu ml-1 in the presence of 100 μM BDSF or equal volume methanol, respectively. To this end, 30 μl bacterial cultures were injected intraperitoneally into each fish by using a 1-ml tuberculin syringe attached to a 30.5-gauge Precision Glide needle (Becton Dickinson). The experiment was repeated three times, each time using 10 fish of similar body mass per treatment. Mortality was scored daily, and dead fish was removed immediately.
Zebrafish experiments were conducted in accordance with the guidelines of Institutional Biosafety Committee and Institutional Ethics committee (IBC-IEC) of Institute of Molecular and Cell Biology (IMCB) of Singapore. Animal infection experiments were approved by IBC-ITE of IMCB.
The funding for this work was provided by the Biomedical Research Council, Agency of Science, Technology, and Research (A*Star), Singapore.
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