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Inhaled Lactonase Reduces Pseudomonas aeruginosa Quorum Sensing and Mortality in Rat Pneumonia

  • Sami Hraiech ,

    Contributed equally to this work with: Sami Hraiech, Julien Hiblot

    Affiliations Unité de Recherche sur les Maladies Infectieuses et Tropicales Emergentes, UMR CNRS-IRD 6236, IFR48, Aix-Marseille Université, Marseille, France, Réanimation - Détresses Respiratoires et Infections Sévères, APHM, CHU Nord, Marseille, France

  • Julien Hiblot ,

    Contributed equally to this work with: Sami Hraiech, Julien Hiblot

    Affiliation Unité de Recherche sur les Maladies Infectieuses et Tropicales Emergentes, UMR CNRS-IRD 6236, IFR48, Aix-Marseille Université, Marseille, France

  • John Lafleur,

    Affiliations Department of Biology, University of Massachusetts Dartmouth, Dartmouth, Massachusetts, United States of America, Department of Emergency Medicine, Alpert School of Medicine, Providence, Rhode Island, United States of America

  • Hubert Lepidi,

    Affiliation Unité de Recherche sur les Maladies Infectieuses et Tropicales Emergentes, UMR CNRS-IRD 6236, IFR48, Aix-Marseille Université, Marseille, France

  • Laurent Papazian,

    Affiliations Unité de Recherche sur les Maladies Infectieuses et Tropicales Emergentes, UMR CNRS-IRD 6236, IFR48, Aix-Marseille Université, Marseille, France, Réanimation - Détresses Respiratoires et Infections Sévères, APHM, CHU Nord, Marseille, France

  • Jean-Marc Rolain,

    Affiliation Unité de Recherche sur les Maladies Infectieuses et Tropicales Emergentes, UMR CNRS-IRD 6236, IFR48, Aix-Marseille Université, Marseille, France

  • Didier Raoult,

    Affiliation Unité de Recherche sur les Maladies Infectieuses et Tropicales Emergentes, UMR CNRS-IRD 6236, IFR48, Aix-Marseille Université, Marseille, France

  • Mikael Elias,

    Affiliation Weizmann Institute of Science, Biological Chemistry, Rehovot, Israel

  • Mark W. Silby,

    Affiliation Department of Biology, University of Massachusetts Dartmouth, Dartmouth, Massachusetts, United States of America

  • Janek Bzdrenga,

    Affiliation Unité de Recherche sur les Maladies Infectieuses et Tropicales Emergentes, UMR CNRS-IRD 6236, IFR48, Aix-Marseille Université, Marseille, France

  • Fabienne Bregeon , (FB); (EC)

    Affiliation Unité de Recherche sur les Maladies Infectieuses et Tropicales Emergentes, UMR CNRS-IRD 6236, IFR48, Aix-Marseille Université, Marseille, France

  • Eric Chabriere (FB); (EC)

    Affiliation Unité de Recherche sur les Maladies Infectieuses et Tropicales Emergentes, UMR CNRS-IRD 6236, IFR48, Aix-Marseille Université, Marseille, France



The effectiveness of antibiotic molecules in treating Pseudomonas aeruginosa pneumonia is reduced as a result of the dissemination of bacterial resistance. The existence of bacterial communication systems, such as quorum sensing, has provided new opportunities of treatment. Lactonases efficiently quench acyl-homoserine lactone-based bacterial quorum sensing, implicating these enzymes as potential new anti-Pseudomonas drugs that might be evaluated in pneumonia.


The aim of the present study was to evaluate the ability of a lactonase called SsoPox-I to reduce the mortality of a rat P. aeruginosa pneumonia.


To assess SsoPox-I-mediated quorum quenching, we first measured the activity of the virulence gene lasB, the synthesis of pyocianin, the proteolytic activity of a bacterial suspension and the formation of biofilm of a PAO1 strain grown in the presence of lactonase. In an acute lethal model of P. aeruginosa pneumonia in rats, we evaluated the effects of an early or deferred intra-tracheal treatment with SsoPox-I on the mortality, lung bacterial count and lung damage.

Measurements and Primary Results

SsoPox-I decreased PAO1 lasB virulence gene activity, pyocianin synthesis, proteolytic activity and biofilm formation. The early use of SsoPox-I reduced the mortality of rats with acute pneumonia from 75% to 20%. Histological lung damage was significantly reduced but the lung bacterial count was not modified by the treatment. A delayed treatment was associated with a non-significant reduction of mortality.


These results demonstrate the protective effects of lactonase SsoPox-I in P. aeruginosa pneumonia and open the way for a future therapeutic use.


The dramatic increase of antibiotic resistance in bacterial isolates from intensive care unit (ICU) patients leads to an important reduction of therapeutic arsenal [1],[2], [3],[4], [5]. Alternative approaches to combat multidrug-resistant strains are under extensive research, especially using molecules that can reduce bacterial expression of virulence factors [1][3],[6].

Expression of virulent phenotypes of numerous pathogenic bacteria is activated when the pathogen senses that a critical population density has been reached. This ability relates to the quorum sensing (QS) by which bacteria can sense messenger molecules thus virulence genes are activated [7]. This communication ability enables the bacteria to coordinate bacterial population behavior during the invasion of a host [8],[9].

Acyl-Homoserine Lactones (AHLs) are QS molecule messengers used by a large number of Gram-negative bacteria, including Pseudomonas aeruginosa [10]. These bacteria are able to form biofilms whose maturation is regulated through QS [11]. Biofilms have been implicated in antibiotic resistance in chronic P. aeruginosa infections, primarily through the limitation of the diffusion of antibiotics into the bacterial colonies [12]. P. aeruginosa possesses two different AHL-based QS systems: the LasI/R and RhlI/R with their respective cognate 3-oxo-C12 AHLs and C4 AHLs messenger molecules [13].

The inhibition of bacterial virulence by targeting QS mechanism can be mediated by (i) the inhibition of the messenger production, (ii) inhibition of its detection, both known as QS inhibition/inhibitors [14], [15],[16], or (iii) the elimination of the messenger known as quorum quencher (QQ) [17], [18] thus alteration of the P. aeruginosa QS system can attenuate its virulence. In pneumonia, the efficacy of QS modulation has been tested at the genomic level with reduction in lethality of infected animals [9]. Therapeutic management of animals with pneumonia has been tested with QS inhibitors such as furanones and patulin showing that these molecules can increase the clearance of bacteria in mice infected with P. aeruginosa [19], [20],[21]. Because some in vitro studies suggest toxicity of furanones and patulin [22],[23], other QS inhibition options are under investigation [24] among which the use of lactonases or acylases enzymes [10],[25]. Lactonases efficiently decrease the production of virulence factors and biofilm by P. aeruginosa in vitro [26],[27], and may therefore represent an alternative and promising strategy for reducing bacterial virulence. The efficacy of lactonases to decrease bacterial virulence has been reported in several hosts [28], [29],[30]. In a recent in vivo study on mice with pneumonia [31], the use of a lactonase-producing P. aeruginosa mutant showed reduced lung injury and increased survival as compared to the wild strain. These encouraging results would suggest that the use of lactonases as a topic therapeutic agent could be effective in improving outcome in P. aeruginosa pneumonia.

The aim of our work was to test the efficacy of inhaled lactonase in improving survival of rats with acute P. aeruginosa pneumonia. To do this, we used an engineered variant of the hyperthermostable lactonase SsoPox (first isolated from the extremophilic archaea Sulfolobus solfataricus) [32], SsoPox-I, exhibiting a high stability and an improved ability to hydrolyze 3-oxo-C12 AHLs. We first tested in vitro the ability of our molecule to reduce, in a P.aeruginosa PAO1 strain, the virulence gene lasB activity, the pyocianin synthesis, the proteolytic activity and the biofilm formation. Thus, we evaluated the effect of SsoPox-I when delivered early or late intra-tracheally to animals with lungs infected with P. aeruginosa.

Material and Methods

Protein production & purification

The plasmid encoding SsoPox-I protein was commercially obtained (GeneArt, Invitrogen; Germany). SsoPox-I protein was synthesized in E. coli strain BL21(DE3)-pGro7/GroEL (TaKaRa) in ZYP medium [33] containing 100 µg/ml ampicillin and 34 µg/ml chloramphenicol as previously described [22]. The proteins were purified as previously described [34]. Briefly, the culture was incubated at 70°C for 30 minutes, followed by differential ammonium sulfate precipitation, dialysis and exclusion size chromatography. The proteins were quantified using a nanospectrophotometer (Nanodrop, ThermoFisher Scientific, France) and the protein molar extinction coefficient was determined using the protein primary sequence in PROT-PARAM (ExPASy tool software) [35]. The protein yield was approximately 10 mg/L for SsoPox-I, and the identity and purity of the purified protein was assessed through sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and mass spectrometry (Plateforme Timone, Marseille, France). The enzymes were stored and used in phosphate-buffered saline (PBS) (Biomerieux; France).

In vitro experiments

P. aeruginosa culture.

P. aeruginosa (strain PA01 ATCC 15692) was grown at 37°C in Luria-Bertani (LB) medium (BD, France) with shaking (200 rpm). When required, 1.5% bacto agar was added to solidify the LB.

For in vivo experiments [36], aliquots containing P. aeruginosa PAO1 strain were thawed and cultured on COS (Biomerieux, France) (Columbia with 5% Sheep blood) agar plates. Ten fresh PAO1 colonies were sampled and cultured at 37°C in tryptic soy broth (TSB, Biomerieux, France) with continuous shaking until the OD600 nm = 1. Serial dilutions were subsequently performed to adjust the bacterial amount, and the precise concentrations were confirmed after plating serial dilutions on the appropriate culture medium and counting the resulting colonies.

LasB reporter system.

A 50-µl aliquot from an 18-hour culture of P. aeruginosa PAO1 carrying PlasB-luxCDABE (QS reporter) was added to the wells of a 96-well plate. A ten-fold dilution series from 50 µg to 0.05 µg of SsoPox-I was added to the wells containing the P. aeruginosa reporter strain. LB was added to each well to generate a final volume of 100 µl. The plates were incubated at 37°C for 90 minutes, with shaking every 10 minutes, and subsequently analyzed using a Varioskan Flash multimode plate reader. The luminescence was measured every 10 minutes to determine the QS reporter activity.

Quantification of pyocianin synthesis.

Quantification of pyocyanin was performed as previously described [37]. Briefly, P. aeruginosa PAO1 strain was grown in 1 mL of Glycerol-alanine (GA) minimum medium (10 mL.L−1 glycerol, 6 g.L−1 L-alanine, 2 g.L−1 MgSO4, 0.1 g.L−1 K2HPO4, 0.018 g.L−1 FeSO4) with and without 14 µM of filtered (0.2 µm pore) SsoPox-I enzyme during 24 h at 37°C and 450 rpm shaking in 48-well plate (Greiner Bio-One, Germany). Cells were centrifuged 15 min at 12.000 g and the supernatant was filtered (0.2 µm pore). Extraction of pyocyanin was performed on 500 µL of supernatant using 0.5× volume of chloroform and absorbance was subsequently measured at 690 nm. Blank assay was realized using 500 µL of culture medium with and without 14 µM of filtered (0.2 µm pore) SsoPox-I enzyme.

Proteolytic activity.

Measurement of the proteolytic activity was made using azocasein enzymatic assay as previously described [38]. Briefly, P. aeruginosa PAO1 strain was grown in 200 µL of LB medium with and without 14 µM of filtered (0.2 µm) SsoPox-I enzyme during 24 h at 37°C and 450 rpm shaking in 96-well plate. The SsoPox-I enzyme stock solution being in PBS buffer, control cultures were supplemented with equivalent PBS quantity. Cells were centrifuged 15 min at 12.000 g. The reaction was performed in 0.3 M TrisHCl buffer (pH 7.5) with 50 µL of azocasein (Sigma, St. Louis, USA) (30 mg.mL−1 dissolved in water) and with 50 µL of culture's supernatant for a final volume of 1.5 mL. The reaction was incubated at 37°C for 1 h and subsequently stopped by addition of 250 µL of 20% (w/v) trichloroacetic acid (TCA). The blank assay was realized using 50 µL of culture medium with and without 14 µM of filtered (0.2 µm pore) SsoPox-I enzyme. After centrifugation at 12.000 g for 10 min, optical density was measured at 366 nm. The proteolytic activity was defined as the increase in absorbance at 366 nm.h−1 per number of cells (OD600).

Biofilm formation assays.

Liquid cultures of P. aeruginosa PAO1 were grown for 18 hours, and subsequently diluted 1∶50 in 10% TSB. To examine biofilm susceptibility to SsoPox-I, 100 µl aliquots were dispensed onto Calgary Biofilm Device 96-well plates (MBEC Assay for Physiology & Genetics, Innovotech Inc., Edmonton, Alberta, Canada). A three-fold dilution series from 50 µg to 0.5 µg of SsoPox-I was added to the wells containing P. aeruginosa. The plates were incubated for 4 hours with rocking at 120 Hz at 37°C, and subsequently, the MBEC device with adherent P. aeruginosa biofilms was placed on a fresh 96-well plate containing 100 µl of 1% crystal violet dye in each well for 15 minutes. The MBEC device was subsequently washed three times with 100 µl of water to remove excess dye and allowed to dry. Crystal violet stain was solubilized from the biofilms after placing the MBEC device on a 96-well plate with 100 µl of 100% ethanol in each well. The solubilized crystal violet dye was measured at 600 nm using a Varioskan Flash multimode plate reader (Thermo). The optical density at 600 nm was also used to assess P. aeruginosa PAO1 planktonic growth on the original 96-well plate to determine the effect of SsoPox-I on P. aeruginosa planktonic growth.

In vivo experiments

Ethics statement.

The experiments and protocols were performed in accordance with the European law and the French version of this law details the statutory requirements for the live animal experiments (articles R214-87 to R215-10 of Code Rural, law #76–629 from July 10th, 1976/law #2001-464 from May 29th, 2001 (published in JORF on May 31st, 2001)). Consistent with these laws, the experiments were performed under the direct control of the researcher authorized through the Préfecture-des-Bouches-du-Rhone Administration (authorization number: 13–437). The animal experiments were performed in accordance with ‘Animal Research: Reporting In Vivo Experiments’ (ARRIVE Guidelines and the guidelines of the Guide for the Care and Use of Laboratory Animals. All animal experiments were authorized through the National Animal Ethics Committee («Comité National de Réflexion Ethique sur l′Expérimentation Animale (Comité d′éthique de Marseille)»). The experiments were performed in the Faculté de Pharmacie-Aix-Marseille University.

The animals were euthanized with an intra-peritoneal injection of a lethal dose of thiopental (Panpharma, France).

General procedures.

Adult Sprague-Dawley male pathogen-free rats, weighing 250 to 300 g, were obtained from SAS Janvier (Le-Genest-St-Isle, France) and housed in individual plastic cages (4 animals per cage) in a ventilated pressurized cabinet (A-BOX 160, Noroit, Rezé, France) with free access to water and standard diet food. The rats were anesthetized with 5% Sévoflurane (Abbott, Rungis, France) in 100% oxygen (anesthetizing box, Harvard Apparatus, Les Ulis, France). The trachea was exposed, and they were intubated using a 16-gauge catheter for drug and/or bacterial administration. The awakened rats were housed under the same conditions and weighed daily. At the end of each experiment, the rats were euthanized with an intra-peritoneal injection of a lethal dose of thiopental (Panpharma, France).

Rat tolerance of inhaled SsoPox-I.

The tolerance to intra-tracheal treatment with SsoPox-I was examined in a preliminary study on 3 groups of animals (n = 3 per group) receiving 250 µl of SsoPox-I at a concentration of 0.1, 1 or 10 mg/ml and compared with 5 control animals receiving 250 µl of PBS. After the treatment, signs of bad tolerance of the molecule were investigated i.e. shortness of breathing, prostration and atony or weight loss above 10% from baseline. Spontaneous mortality was also recorded. One animal from each group was sacrificed after 6, 24 and 48 hours. The remaining animals were sacrificed after 48 hours. Subsequently, the lungs were removed, macroscopically examined, and preserved in formaldehyde for histological assessment of lung damage.

Rat respiratory infection model and SsoPox-I treatment.

Three groups of 20 animals were infected through intra-tracheal inoculation with 250 µl of a PBS solution containing 108 CFU/ml of P. aeruginosa PAO1.

Among the 3 groups of infected rats, one group received immediately after infection 250 µl of PBS (non-treated group: NT), while another group was treated with 250 µl of SsoPox-I at a concentration of 1 mg/ml (immediate treatment group: IT). The last group received 250 µl of 1 mg/ml SsoPox-I at 3 hours after infection (deferred treatment group: DT). SsoPox-I and additional PBS were delivered intra-tracheally using the same anesthetic procedure as used for the infection.

Lung processing and blood or spleen samples.

After infection, the animals were observed for 2 days, and spontaneous mortality was examined. Animals' conditions and clinical status were checked every 2 hours. Humane endpoints were used during the survival study. If animals had one of the following signs, they were anesthetized and euthanized with an intra-peritoneal injection of a lethal dose of thiopental (Panpharma, France) to avoid suffering:

  1. Major dyspnea with noisy breathing and head or neck movements associated with breathing
  2. Prostration and atony
  3. Weight loss>20% of initial body weight.

The remaining rats were euthanized after 48 hours. Subsequently, the lungs were removed aseptically. The right lung was homogenized in PBS for bacterial culture, and the left lung was preserved for histological analysis. The blood and spleen were sampled and cultured on agar plates to assess systemic diffusion of the bacteria.

Histological severity score (HSS).

Sections (3 mm thick) were obtained from the upper, mid and lower parts of the lungs, including the entire circumference. The sections were stained with hematoxylin and eosin. A pathologist blinded to the group identity (H. L.) examined the samples. The HSS was calculated based on the number of bronchopneumonia lesions (0, no lesions; 1, 30 lesions/lung; 2, ≥30 lesions/lung; 3, confluent lesions of bronchopneumonia), as previously reported [39], [40].


The number of studied animals (20 animals per group) was calculated based on a mortality reduction from 80% in the NT group infected with PAO1 to an expected mortality rate of 50% in the treated groups, with 90% statistical power and a two-sided alpha value of 0.05. The data were expressed as the means ± standard deviation (SD) or median [inter-quartile range, IQR] according to the distribution of the data. Student's t-test or the Mann-Whitney rank-sum test were used for inter-group comparisons. Kaplan-Meier analysis was performed to evaluate 48-h mortality. Intergroup differences were evaluated using the log rank test. The data analysis was performed with SPSS for Windows (Chicago, IL), version 12.0. A value of p≤0.05 was considered statistically significant.


Protein production & purification

See Fig. S1 in supplementary material.

In vitro experiments

We monitored the lasB activity in a P. aeruginosa PAO1 strain carrying the PlasB-luxCDABE plasmid. We showed that the addition of SsoPox-I significantly reduced the levels of lasB activity (Fig. 1A). Moreover, this inhibition exhibited a dose-dependent profile with a half inhibition concentration ([C1/2]) of the enzyme of approximately 0.5 µg/ml (Fig. 1A).

Figure 1. Effects of SsoPox-I on PAO1 virulence factors expression and biofilm formation. 1A: lasB activity.

The chart shows the lasB activity in treated cultures, expressed as the percentage of that in untreated controls (no SsoPox-I), and these data represent the average of three independent experiments, each with three technical replicates. The error bars represent 95% confidence intervals. Student's t test p<0.05 for SsoPox-I. T tests were used for the comparison of baseline with the highest dose of enzyme. 1B: pyocianin synthesis. Pyocyanin quantification of P. aeruginosa PAO1 strain after 24 h growth in GA medium was assessed in presence (black) or absence (gray) of 14 µM of SsoPox-I lactonase. Pyocyanin quantity was followed at A690 as per number of cells (A600). 1C: proteolytic activity. Proteolytic activity of P. aeruginosa PAO1 strain after 24 h growth in LB medium was assessed in presence (black) or absence (grey) of 14 µM of SsoPox-I lactonase. Proteolytic activity was measured by the azocasein assay (A366.h−1) as per number of cells (A600). ND stands for non-detected activity. 1D: biofilm formation. Biofilms were grown in an MBEC device as described in the methods section. The dose-dependent inhibition of P. aeruginosa biofilm formation through SsoPox-I was observed and analyzed using Student's t test p = 0.05 for SsoPox-I.

Pyocyanin secretion was affected by the presence of SsoPox-I and presented a 4 fold drop in quantity as compared to the control (Fig. 1B).

Cultures of PAO1 made in presence of 14 µM SsoPox-I showed after 24 h a clear drop of protease activity followed using azocasein assay. Protease activity in presence of SsoPox-I was beyond detection limit (Fig. 1C).

The biofilm assay showed that SsoPox-I reduced biofilm formation in a dose-dependent manner with a [C1/2]∼170 µg/ml (Fig. 1D).

Interestingly, SsoPox-I did not significantly affect the rate of P. aeruginosa growth. Indeed, even at the highest enzyme dose (5 mg/ml), the optical density of the cell culture did not significantly differ from that of the control experiment with no treatment (Fig. S2).

In vivo experiments

Rat tolerance to inhaled SsoPox-I.

The effects of SsoPox-I treatment on rat tissues were investigated. On the 9 rats that received SsoPox-I into the trachea, none exhibited any sign of bad tolerance including in the group that received the highest dose. The weight curve of treated rats was not different to control animals and no animal loosed weight. There was no spontaneous mortality after 48-hours observation in the treated group as well as in the control group. After sacrifice, the lungs were harvested and the macroscopic examination showed no signs of injury. Histological assessment showed that there was no sign of lung damage 6, 24 or 48 hours after the treatment including in the group receiving the highest dose of SsoPox-I.

Rat respiratory infection model and SsoPox-I treatment.

The influence of SsoPox-I on pulmonary P. aeruginosa infection was monitored in 3 groups of 20 rats. The spontaneous mortality rate was 75% (15/20) in the non-treated group (NT). When the rats were treated with SsoPox-I (1 mg/ml) immediately after infection (IT), the mortality rate was significantly reduced to 20% (4/20) (p = 0.0001 vs. NT). The protective effect of lactonase on mortality was less significant in the deferred treatment (DT) group, where the treatment was administered at 3 hours after the infection (mortality rate of 50% (10/20) (p = ns vs. NT) (Fig. 2). However, in the DT group, the mean delay of mortality was significantly longer than that in the control group (respectively 26±9.5 vs. 17±9.2 hours; p = 0.04).

Figure 2. Forty-eight-hour survival curves for the 3 groups of animals after infection.

The animals were infected with 108 CFU/ml (2.5×107 CFU/rat) of P. aeruginosa PAO1 in the following treatment groups: non-treated (NT), immediate-treatment (IT) or deferred treatment (DT) who received treatment with SsoPox-I at 3 hours after infection.

In addition to death, other parameters were monitored during the infection, including the weight of the animals. We observed that the loss of body weight, measured from the day of infection until the day of death, was significantly less important in the IT group than in the NT group (11.3±12 g vs. 20.4±9.3 g respectively; p = 0.01). The DT group lost 25.6±1.82 g of body weight (p = ns vs. NT group).

Notably, consistent with the increased survival rate observed in the IT group, we also observed that compared with the NT group, the damage to the lungs of the animals in the IT group was less significant (Fig. 3), as revealed by a significantly lower HSS (HSS IT group vs. NT group: 1.27±0.6 vs. 2.64±0.4; p = 0.005). In the DT group, the mean HSS was not significantly different from that in the NT group.

Figure 3. Lung histological examination after infection.

Pathological mapping of the lungs of non-treated (NT) (A), deferred-treatment (DT) (B) and immediate-treatment (IT) (C) groups. Photomicrographs of the pathological Giemsa staining of the lung sections (100X). Mean histological severity score (HSS) was 2.64±0.4 (mean ± SD) for the NT group, 1.27±0.6 for the IT group (p = 0.005 vs. NT) and 2.32±0.4 for the DT group (p = NS vs. NT).

Moreover, we also investigated the potential effects of lactonase treatment on the lung bacterial count, associated with the increased survival observed in the IT group. We observed that the lung bacterial count did not significantly differ between the 3 groups (CFU/g of lung in median [inter-quartile range]: 3.3×105 [5.6×103−1.3×106] in the NT group; 1.3×105 [9.2×103−106] in the IT group; and 105 [8.4×104−7.8×105] in the DT group) (Fig. 4).

Figure 4. Lung bacterial count after infection.

The lung bacterial count was adjusted according to the lung weight. The box plots limits represent the 25th and 75th percentiles, and the bars represent the 5th and 95th percentiles. The median is represented as a horizontal line. NT =  non-treated group; IT =  immediate treatment group; DT =  deferred treatment group.

Finally, there was no difference concerning the number of animals with positive blood or spleen culture at the time of death between the 3 groups (n/tot (%): 8/20 (40%) in the NT group; 7/20 (35%) in the IT group; 10/20 (50%) in the DT group; p = NS).

Discussion and Conclusions

In the present study, we used both in vitro and in vivo experiments to show that the lactonase SsoPox-I was able to decrease the activity of lasB virulence gene, the synthesis of pyocianin, the proteolytic activity and the biofilm formation of the P. aeruginosa PAO1 strain. In addition, the treatment with SsoPox-I was associated with an important improve in survival in a rat model of highly lethal acute pneumonia.

Originally, this work focuses on the lactonase SsoPox-I QQ activity with a design trying to approach clinical settings by giving the enzyme as a therapeutic drug. Similarly, QS inhibitor molecules such as furanones have been shown to increase the bacterial clearance in animal models of P. aeruginosa pneumonia but data on reduction of mortality are lacking [16] [19], [20]. In one study in mice using indirect demonstration of QQ effects of lactonases in animal models of pneumonia [31], Migiyama et al. showed a decrease in mortality and lung damage when animals were infected with a lactonase-producing P. aeruginosa strain. The main difference between Migiyama's study and ours is that we used a wild strain of P. aeruginosa for infections and we treated the animals with a synthetic lactonase given after infection as a therapeutic drug.

The catalytic efficiency and quenching activity of the QS lactonase SsoPox-I against 3-oxo-C12 AHLs has been previously improved through protein engineering [32]. While the QS activity of the wild-type enzyme has been previously demonstrated in vitro [26], the efficiency of this enzyme in vivo has not been explored. SsoPox-I inhibits the lasB gene activity, a classical virulence factor [41], at concentrations as low as 0.5 µg/ml. SsoPox-I is also able to decrease the pyocianin synthesis as well as the proteolytic activity of a P.aeruginosa PAO1 strain. Moreover, the effect of SsoPox-I on P. aeruginosa goes beyond the inhibition of virulence-associated genes. Indeed, SsoPox-I also inhibited biofilm formation, albeit at much higher concentrations (170 µg/ml). This discrepancy in the active dose of the enzyme might reflect the distinct regulation of biofilm formation and maturation [12] [42]. Indeed, multiple quorum sensing-regulated genes are modulated without affecting lasRI, rhlRI or the production of N-acyl-L-homoserine lactones. In particular, the transcriptional regulator MvfR may contribute more to biofilm formation of P. aeruginosa. This could explain why in our experiments SsoPox-I seemed to have a better efficacy on lasB gene down regulation than on decrease in biofilm formation [43], [44].

We further investigated the potential consequences of the observed in vitro effects. For this, we used an acute lethal model of P. aeruginosa pneumonia. Our model was consistent with previous ones showing a high and early lethality within the 24–48 first hours [45][47]. On histological analysis, the lungs of untreated animals exhibited important and confluent lesions of broncho-pneumonia arguing for the correlation between death and severity of pneumonia. In addition, nearly one half of the animals had bacteremia which probably contributed to the high mortality rate. In this model, SsoPox-I significantly decreased the mortality rate from 75% in the non-treated group to 20% in the group treated immediately after infection. This observation is consistent with the dramatic reduction in the lung damage observed in the treated group. The results are also consistent with previous studies showing that infections with QS-deleted strains of P. aeruginosa were less severe in several infection models [48],[49].

SsoPox-I did not significantly reduce lung lesions and rat mortality when administrated at 3 hours after the onset of infection. This ineffectiveness might be due to the use of a highly lethal model of infection (death in 48 hours). The preventive action of SsoPox-I might be higher than its curative effect as previously observed for QSI [22]. QS is indeed under a positive retro-control regulation [50]: when the bacterial quorum is reached, the inhibition of QS is more difficult because of the self-stimulating properties of bacteria.

In our study, the innovative molecule SsoPox-I was administered intra-tracheally within the 3 first hours of infection. This design was chosen to approach clinical preventive therapeutic methods used in patients at risk for P. aeruginosa infections, such as ICU patients. However, our model did not totally mimic clinical settings primarily because of the high amount of bacteria given in one inoculation.

No difference in the lung bacterial burden was observed between the control group and the 2 treated groups regardless the time of administration of the molecule. While surprising, these results are consistent with our in vitro findings on bacterial cultures in which lactonase adjunction to the media did not influence P. aeruginosa growth. These results agree with those of Migiyama et al. [31] who showed similar bacterial count with animals infected with wild-type P. aeruginosa and their lactonase-producing mutant strain. It remains however unknown whether the improved survival could be due to a less invasive activity of the microorganism towards the lung parenchyma and/or to change in the host-pathogen interaction regardless the bacterial load.

In summary, SsoPox-I presents several properties that could increase the therapeutic arsenal, particularly in the field of nosocomial pneumonia. In contrast to antibiotics, quorum-quenching strategies do not impose drastic selection pressure on bacterial survival. Therefore, treatments with lactonases such as SsoPox-I might not or only slightly, promote the emergence of resistance [7],[51]. Interestingly, due to their ability to reduce biofilm formation, lactonases could restore susceptibility to antibiotics in drug-resistant strains as previously observed with tobramycin in animal models [52]. Because of its mechanisms of action involving a modulation of the QS, azythromycin has been recently shown in a randomized controlled trial to reduce the incidence of ventilator-acquired pneumonia in pseudomonas colonized patients [53] showing the growing interest of QS inhibitors in clinics.

To conclude, our results open the way to further investigations assessing SsoPox-I as a possible tool in antimicrobial strategy.

Supporting Information

Figure S1.

SDS-PAGE of SsoPox-I. Twenty-five µg of SsoPox-I (left band) were deposited next to a Molecular weight Marker (MwM, right panel) (Mulicolor broad range protein ladder, Euromedex).


Figure S2.

The growth of P. aeruginosa in the presence of SsoPox-I. A small decrease in P. aeruginosa growth was observed at the highest concentration of SsoPox-I; however, this effect was not significant (Student's t test p = 0.67). The chart shows percentage of controls (no SsoPox-I) and represents the data obtained from four independent experiments, each performed with three technical replicates. The error bars represent 95% confidence intervals.



We acknowledge Dr JM Brunel and Mr Janek Bzdrenga for their contribution to this work.

Author Contributions

Conceived and designed the experiments: SH JH FB EC LP MS ME JL. Performed the experiments: SH JH FB MS ME JL HL. Analyzed the data: SH JH FB EC MS ME JL. Contributed reagents/materials/analysis tools: LP JMR DR. Wrote the paper: SH JH FB EC MS ME JL HL.


  1. 1. Stanton TB (2013) A call for antibiotic alternatives research. Trends Microbiol 21: 111–113 S0966-842X(12)00199-0 [pii];10.1016/j.tim.2012.11.002 [doi].
  2. 2. Garcia-Quintanilla M, Pulido MR, Lopez-Rojas R, Pachon J, McConnell MJ (2013) Emerging therapies for multidrug resistant Acinetobacter baumannii. Trends Microbiol 21: 157–163 S0966-842X(12)00225-9 [pii];10.1016/j.tim.2012.12.002 [doi].
  3. 3. Breidenstein EB, Fuente-Nunez C, Hancock RE (2011) Pseudomonas aeruginosa: all roads lead to resistance. Trends Microbiol 19: 419–426 S0966-842X(11)00086-2 [pii];10.1016/j.tim.2011.04.005 [doi].
  4. 4. Agodi A, Barchitta M, Cipresso R, Giaquinta L, Romeo MA, et al. (2007) Pseudomonas aeruginosa carriage, colonization, and infection in ICU patients. Intensive Care Med 33: 1155–1161 10.1007/s00134-007-0671-6 [doi].
  5. 5. Adair CG, Gorman SP, Feron BM, Byers LM, Jones DS, et al. (1999) Implications of endotracheal tube biofilm for ventilator-associated pneumonia. Intensive Care Med 25: 1072–1076 90251072.134 [pii].
  6. 6. Hoiby N, Bjarnsholt T, Givskov M, Molin S, Ciofu O (2010) Antibiotic resistance of bacterial biofilms. Int J Antimicrob Agents 35: 322–332 S0924-8579(10)00009-9 [pii];10.1016/j.ijantimicag.2009.12.011 [doi].
  7. 7. Schuster M, Sexton DJ, Diggle SP, Greenberg EP (2013) Acyl-homoserine lactone quorum sensing: from evolution to application. Annu Rev Microbiol 67: 43–63 10.1146/annurev-micro-092412-155635 [doi].
  8. 8. Wagner VE, Frelinger JG, Barth RK, Iglewski BH (2006) Quorum sensing: dynamic response of Pseudomonas aeruginosa to external signals. Trends Microbiol 14: 55–58 S0966-842X(05)00333-1 [pii];10.1016/j.tim.2005.12.002 [doi].
  9. 9. Lesprit P, Faurisson F, Join-Lambert O, Roudot-Thoraval F, Foglino M, et al. (2003) Role of the quorum-sensing system in experimental pneumonia due to Pseudomonas aeruginosa in rats. Am J Respir Crit Care Med 167: 1478–1482 10.1164/rccm.200207-736BC [doi];200207-736BC [pii].
  10. 10. Grabiner MA, Fu Z, Wu T, Barry KC, Schwarzer C, et al. (2014) Pseudomonas aeruginosa Quorum-Sensing Molecule Homoserine Lactone Modulates Inflammatory Signaling through PERK and eI-F2alpha. J Immunol. jimmunol.1303437 [pii];10.4049/jimmunol.1303437 [doi].
  11. 11. Parsek MR, Greenberg EP (2005) Sociomicrobiology: the connections between quorum sensing and biofilms. Trends Microbiol 13: 27–33 S0966-842X(04)00261-6 [pii];10.1016/j.tim.2004.11.007 [doi].
  12. 12. Costerton JW, Stewart PS, Greenberg EP (1999) Bacterial biofilms: a common cause of persistent infections. Science 284: 1318–1322.
  13. 13. Williams P, Camara M (2009) Quorum sensing and environmental adaptation in Pseudomonas aeruginosa: a tale of regulatory networks and multifunctional signal molecules. Curr Opin Microbiol 12: 182–191 S1369-5274(09)00008-3 [pii];10.1016/j.mib.2009.01.005 [doi].
  14. 14. Galloway WR, Hodgkinson JT, Bowden S, Welch M, Spring DR (2012) Applications of small molecule activators and inhibitors of quorum sensing in Gram-negative bacteria. Trends Microbiol 20: 449–458 S0966-842X(12)00113-8 [pii];10.1016/j.tim.2012.06.003 [doi].
  15. 15. Kalia VC (2013) Quorum sensing inhibitors: an overview. Biotechnol Adv 31: 224–245 S0734-9750(12)00185-1 [pii];10.1016/j.biotechadv.2012.10.004 [doi].
  16. 16. Rasmussen TB, Givskov M (2006) Quorum-sensing inhibitors as anti-pathogenic drugs. Int J Med Microbiol 296: 149–161 S1438-4221(06)00078-6 [pii];10.1016/j.ijmm.2006.02.005 [doi].
  17. 17. Dong YH, Wang LH, Xu JL, Zhang HB, Zhang XF, et al. (2001) Quenching quorum-sensing-dependent bacterial infection by an N-acyl homoserine lactonase. Nature 411: 813–817 10.1038/35081101 [doi].
  18. 18. Amara N, Krom BP, Kaufmann GF, Meijler MM (2011) Macromolecular inhibition of quorum sensing: enzymes, antibodies, and beyond. Chem Rev 111: 195–208 10.1021/cr100101c [doi].
  19. 19. Hentzer M, Wu H, Andersen JB, Riedel K, Rasmussen TB, et al. (2003) Attenuation of Pseudomonas aeruginosa virulence by quorum sensing inhibitors. EMBO J 22: 3803–3815 10.1093/emboj/cdg366 [doi].
  20. 20. Rasmussen TB, Skindersoe ME, Bjarnsholt T, Phipps RK, Christensen KB, et al. (2005) Identity and effects of quorum-sensing inhibitors produced by Penicillium species. Microbiology 151: 1325–1340 151/5/1325 [pii];10.1099/mic.0.27715-0 [doi].
  21. 21. Jakobsen TH, van GM, Phipps RK, Shanmugham MS, Christensen LD, et al. (2012) Ajoene, a sulfur-rich molecule from garlic, inhibits genes controlled by quorum sensing. Antimicrob Agents Chemother 56: 2314–2325 AAC.05919-11 [pii];10.1128/AAC.05919-11 [doi].
  22. 22. O′Loughlin CT, Miller LC, Siryaporn A, Drescher K, Semmelhack MF, et al. (2013) A quorum-sensing inhibitor blocks Pseudomonas aeruginosa virulence and biofilm formation. Proc Natl Acad Sci U S A 110: 17981–17986 1316981110 [pii];10.1073/pnas.1316981110 [doi].
  23. 23. Baveja JK, Willcox MD, Hume EB, Kumar N, Odell R, et al. (2004) Furanones as potential anti-bacterial coatings on biomaterials. Biomaterials 25: 5003–5012 10.1016/j.biomaterials.2004.02.051 [doi];S0142961204002005 [pii].
  24. 24. Bjarnsholt T, Tolker-Nielsen T, Hoiby N, Givskov M (2010) Interference of Pseudomonas aeruginosa signalling and biofilm formation for infection control. Expert Rev Mol Med 12: e11 S1462399410001420 [pii];10.1017/S1462399410001420 [doi].
  25. 25. Uroz S, Oger PM, Chapelle E, Adeline MT, Faure D, et al. (2008) A Rhodococcus qsdA-encoded enzyme defines a novel class of large-spectrum quorum-quenching lactonases. Appl Environ Microbiol 74: 1357–1366 AEM.02014-07 [pii];10.1128/AEM.02014-07 [doi].
  26. 26. Ng FS, Wright DM, Seah SY (2011) Characterization of a phosphotriesterase-like lactonase from Sulfolobus solfataricus and its immobilization for disruption of quorum sensing. Appl Environ Microbiol 77: 1181–1186 AEM.01642-10 [pii];10.1128/AEM.01642-10 [doi].
  27. 27. Pei R, Lamas-Samanamud GR (2014) Inhibition of biofilm formation by T7 bacteriophages producing quorum quenching enzymes. Appl Environ Microbiol. AEM.01434-14 [pii];10.1128/AEM.01434-14 [doi].
  28. 28. Dong YH, Xu JL, Li XZ, Zhang LH (2000) AiiA, an enzyme that inactivates the acylhomoserine lactone quorum-sensing signal and attenuates the virulence of Erwinia carotovora. Proc Natl Acad Sci U S A 97: 3526–3531 10.1073/pnas.060023897 [doi];060023897 [pii].
  29. 29. Stoltz DA, Ozer EA, Taft PJ, Barry M, Liu L, et al. (2008) Drosophila are protected from Pseudomonas aeruginosa lethality by transgenic expression of paraoxonase-1. J Clin Invest 118: 3123–3131 10.1172/JCI35147 [doi].
  30. 30. Papaioannou E, Wahjudi M, Nadal-Jimenez P, Koch G, Setroikromo R, et al. (2009) Quorum-quenching acylase reduces the virulence of Pseudomonas aeruginosa in a Caenorhabditis elegans infection model. Antimicrob Agents Chemother 53: 4891–4897 AAC.00380-09 [pii];10.1128/AAC.00380-09 [doi].
  31. 31. Migiyama Y, Kaneko Y, Yanagihara K, Morohoshi T, Morinaga Y, et al. (2013) Efficacy of AiiM, an N-acylhomoserine lactonase, against Pseudomonas aeruginosa in a mouse model of acute pneumonia. Antimicrob Agents Chemother 57: 3653–3658 AAC.00456-13 [pii];10.1128/AAC.00456-13 [doi].
  32. 32. Hiblot J, Gotthard G, Elias M, Chabriere E (2013) Differential active site loop conformations mediate promiscuous activities in the lactonase SsoPox. PLoS One 8: e75272 10.1371/journal.pone.0075272 [doi];PONE-D-13-20233 [pii].
  33. 33. Studier FW (2005) Protein production by auto-induction in high density shaking cultures. Protein Expr Purif 41: 207–234.
  34. 34. Hiblot J, Gotthard G, Chabriere E, Elias M (2012) Characterisation of the organophosphate hydrolase catalytic activity of SsoPox. Sci Rep 2: 779 10.1038/srep00779 [doi].
  35. 35. Wilkins MR, Gasteiger E, Bairoch A, Sanchez JC, Williams KL, et al. (1999) Protein identification and analysis tools in the ExPASy server. Methods Mol Biol 112: 531–552.
  36. 36. Hraiech S, Roch A, Lepidi H, Atieh T, Audoly G, et al. (2013) Impaired virulence and fitness of a colistin-resistant clinical isolate of Acinetobacter baumannii in a rat model of pneumonia. Antimicrob Agents Chemother 57: 5120–5121 AAC.00700-13 [pii];10.1128/AAC.00700-13 [doi].
  37. 37. Price-Whelan A, Dietrich LE, Newman DK (2007) Pyocyanin alters redox homeostasis and carbon flux through central metabolic pathways in Pseudomonas aeruginosa PA14. J Bacteriol 189: 6372–6381 JB.00505-07 [pii];10.1128/JB.00505-07 [doi].
  38. 38. Nicodeme M, Grill JP, Humbert G, Gaillard JL (2005) Extracellular protease activity of different Pseudomonas strains: dependence of proteolytic activity on culture conditions. J Appl Microbiol 99: 641–648 JAM2634 [pii];10.1111/j.1365-2672.2005.02634.x [doi].
  39. 39. Marquette CH, Wermert D, Wallet F, Copin MC, Tonnel AB (1999) Characterization of an animal model of ventilator-acquired pneumonia. Chest 115: 200–209.
  40. 40. Hraiech S, Bregeon F, Brunel JM, Rolain JM, Lepidi H, et al. (2012) Antibacterial efficacy of inhaled squalamine in a rat model of chronic Pseudomonas aeruginosa pneumonia. J Antimicrob Chemother 67: 2452–2458 dks230 [pii];10.1093/jac/dks230 [doi].
  41. 41. Wagner VE, Gillis RJ, Iglewski BH (2004) Transcriptome analysis of quorum-sensing regulation and virulence factor expression in Pseudomonas aeruginosa. Vaccine 22 Suppl 1S15–S20 S0264-410X(04)00613-9 [pii];10.1016/j.vaccine.2004.08.011 [doi].
  42. 42. Dickschat JS (2010) Quorum sensing and bacterial biofilms. Nat Prod Rep 27: 343–369 10.1039/b804469b [doi].
  43. 43. Deziel E, Gopalan S, Tampakaki AP, Lepine F, Padfield KE, et al. (2005) The contribution of MvfR to Pseudomonas aeruginosa pathogenesis and quorum sensing circuitry regulation: multiple quorum sensing-regulated genes are modulated without affecting lasRI, rhlRI or the production of N-acyl-L-homoserine lactones. Mol Microbiol 55: 998–1014 MMI4448 [pii];10.1111/j.1365-2958.2004.04448.x [doi].
  44. 44. Ilangovan A, Fletcher M, Rampioni G, Pustelny C, Rumbaugh K, et al. (2013) Structural basis for native agonist and synthetic inhibitor recognition by the Pseudomonas aeruginosa quorum sensing regulator PqsR (MvfR). PLoS Pathog 9: e1003508 10.1371/journal.ppat.1003508 [doi];PPATHOGENS-D-12-03063 [pii].
  45. 45. Bakker-Woudenberg IA, ten Kate MT, Guo L, Working P, Mouton JW (2002) Ciprofloxacin in polyethylene glycol-coated liposomes: efficacy in rat models of acute or chronic Pseudomonas aeruginosa infection. Antimicrob Agents Chemother 46: 2575–2581.
  46. 46. Rezaiguia S, Garat C, Delclaux C, Meignan M, Fleury J, et al. (1997) Acute bacterial pneumonia in rats increases alveolar epithelial fluid clearance by a tumor necrosis factor-alpha-dependent mechanism. J Clin Invest 99: 325–335 10.1172/JCI119161 [doi].
  47. 47. Wen J, Li CM, Gu L, Yin SJ, Li W, et al. (2014) Aging reduces the expression of lung CINC and MCP-1 mRNA in a P. aeruginosa rat model of infection. Inflammation 37: 933–941 10.1007/s10753-014-9813-5 [doi].
  48. 48. Pearson JP, Feldman M, Iglewski BH, Prince A (2000) Pseudomonas aeruginosa cell-to-cell signaling is required for virulence in a model of acute pulmonary infection. Infect Immun 68: 4331–4334.
  49. 49. Smith RS, Harris SG, Phipps R, Iglewski B (2002) The Pseudomonas aeruginosa quorum-sensing molecule N-(3-oxododecanoyl)homoserine lactone contributes to virulence and induces inflammation in vivo. J Bacteriol 184: 1132–1139.
  50. 50. Seed PC, Passador L, Iglewski BH (1995) Activation of the Pseudomonas aeruginosa lasI gene by LasR and the Pseudomonas autoinducer PAI: an autoinduction regulatory hierarchy. J Bacteriol 177: 654–659.
  51. 51. Rutherford ST, Bassler BL (2012) Bacterial quorum sensing: its role in virulence and possibilities for its control. Cold Spring Harb Perspect Med 2 2/11/a012427 [pii];10.1101/cshperspect.a012427 [doi].
  52. 52. Christensen LD, van GM, Jakobsen TH, Alhede M, Hougen HP, et al. (2012) Synergistic antibacterial efficacy of early combination treatment with tobramycin and quorum-sensing inhibitors against Pseudomonas aeruginosa in an intraperitoneal foreign-body infection mouse model. J Antimicrob Chemother 67: 1198–1206 dks002 [pii];10.1093/jac/dks002 [doi].
  53. 53. van DC, Kohler T, Brunner-Ferber F, Francois B, Carlet J, et al. (2012) Azithromycin to prevent Pseudomonas aeruginosa ventilator-associated pneumonia by inhibition of quorum sensing: a randomized controlled trial. Intensive Care Med 38: 1118–1125 10.1007/s00134-012-2559-3 [doi].