Anti-Quorum Sensing Activity of 12 Essential Oils on chromobacterium violaceum and Specific Action of cis-cis-p-Menthenolide from Corsican Mentha suaveolens ssp. Insularis

Quorum sensing (QS) is a bacterial communication mechanism used to express various survival or virulence traits leading to enhanced resistance. Chromobacterium violaceum is a commonly used strain that highlights anti-QS action of bioactive substances. Here, we wanted to see if 12 selected essential oils (EO) could exert anti-QS activity. We measured the sublethal minimal QS inhibitory concentration (MQSIC) by assessing violacein production of C. violaceum along with bacterial growth. To confirm the QS disruption, we also proceed to surface bacterial observations using scanning electron microscopy (SEM). We showed that cis-cis-p-menthenolide extracted and isolated from a plant endemic to occidental Mediterranean Sea islands, Mentha suaveolens ssp. insularis, acts as an inhibitor of violacein production and biofilm formation. Measured MQSIC was much lower than the minimal inhibitory concentration (MIC): 0.10 mg·mL−1 vs. 3.00 mg·mL−1. Moreover, disturbance of QS-related traits was confirmed by the degradation of C. violaceum biofilm matrix. There is a clear structure–activity relationship between cis-cis-p-menthenolide and anti-QS activity. Indeed, its isomer molecule (mintlactone) exerts a poor anti-QS action. These results indicate that inhibition of violacein production and biofilm formation by cis-cis-p-menthenolide might be related to a disruption in the QS mechanism.


Introduction
Nowadays, bacterial resistance to antibiotics is a major public health issue. Development of new antibiotics with new modes of action is very limited. One potential strategy to override this problem is to restore antibiotic activity. Inhibition of quorum sensing (QS) may be a suitable solution.
QS is a bacterial cell-to-cell communication pathway. This specific signal-response system relies on the synthesis, release, and uptake of specific molecules known as autoinducers [1]. When a specific concentration is reached in the outer medium, which is correlated to population concentration, autoinducers are the starting point to trigger and synchronize QS-related behaviors or traits expression. QS regulation is mainly based on the production of three types of molecules [2]: -N-acyl homoserine lactones, produced by Gram-negative bacteria, used to monitor the population density and thus trigger the process of QS-mediated gene expression;

Inhibition of Violacein Production
Twelve EOs were tested for their anti-QS activity on C. violaceum. Their effects on the production of QS-related violacein pigment were evaluated along with bacterial density counts. We measured their minimal inhibitory concentration (MIC) and the minimal QS inhibiting concentration (MQSIC), which is the minimal EO concentration that inhibits the violacein production of C. violaceum by at least 50% (Table 1). Tested EOs showed a range of antimicrobial activities. According to Djabou et al. [24], EOs can be classified in three categories according to their antimicrobial activity. C. violaceum is not sensitive to Cedrus atlantica EO with a MIC value of 50.00 mg·mL −1 . It is dominated by α-pinene (55%), a hydrocarbon molecule known to be less active than the oxygenated molecules [15]. The strain is moderately sensitive to Helichrysum italicum, Citrus limon and Mentha suaveolens ssp. insularis with respective MIC values of 12.50 mg·mL −1 , 6.00 mg·mL −1 and 3.00 mg·mL −1 . Lastly, C. violaceum appears to be sensitive to Citrus clementina, Lavandula stoechas, Myrtus communis (MIC values 1.50 mg·mL −1 ); Eucalyptus polybractea, Calamintha nepeta ssp. nepeta, Cymbopogon flexosus, Foeniculum vulgare (MIC values 0.80 mg·mL −1 ) and Xanthoxylum armatum (MIC value 0.40 mg·mL −1 ). For this last group, we retrieved EOs from which some major compounds are already known to exert antimicrobial activity, such as 1,8-cineole [26], fenchone [27], citral (geranial and neral) [28], cryptone [29], camphor and linalool [30].
C. violaceum QS was disturbed differently depending on the used EO. The MQSIC for Cedrus atlantica is high (6.00 mg·mL −1 ), thus it is not a relevant anti-QS EO. The EO of Helichrysum italicum, with MQSIC value of 0.80 mg·mL −1 , followed by both Citrus EOs (0.40 mg·mL −1 ) are significantly lower but still a little high in comparison to the upcoming group. Next, there is a larger group of five EOs with MQSIC values of 0.20 mg·mL −1 . Even if EOs action on QS is not widely studied, some essential oils exerted similar effect on C. violaceum QS. For example, the MQSIC values of Rosemary and Tea Tree EOs can be compared to this last group (0.21 mg·mL −1 ) [31]. At these concentrations, they are considered active against QS. Next are Mentha suaveolens ssp. insularis and Myrtus communis with MQSIC values of 0.10 mg·mL −1 . Finally, the lowest MQSIC value was found for Eucalyptus polybractea (0.05 mg·mL −1 ). Colombian Lippia alba EOs, extracted from the whole plants, also had anti-QS activity. MQSIC of the EO from the Santander region is 0.09 mg·mL −1 , which is similar to Mentha suaveolens ssp. insularis and Myrtus communis [32]. However, the isolation methods were different, which may have affected the concentration of the distillated molecules. The most active ones were extracted by microwave-assisted distillation. This method is known to produce a higher ratio of oxygenated compounds [27], but is different from the usual steam distillation method, which was used to produce EOs tested in our work.
We choose to evaluate the MQSIC/MIC ratio using the dilution values ( Table 1). The higher the ratio, the better the anti-QS activity will be. Xanthoxylum armatum appears to be the least efficient EO. The observed reduction of violacein production is more likely to be due to an antimicrobial action than an anti-QS effect. Calamintha nepeta ssp. nepeta and Citrus clementina EOs only have a ratio value of 4, followed by both Cedrus atlantica and Lavandula stoechas with a value of 8. Such low ratio values show, again, that the MQSIC and MIC dilutions are very close. With a MQSIC/MIC value of 16, Citrus limon, Eucalyptus polybractea, Helichrysum italicum and Myrtus communis have an effective action on C. violaceum QS. Major compounds of those EOs have not, to our knowledge, been tested in anti-QS assays. But, as previously seen, Rosemary and Tea Tree EOs seem to exert anti-QS activity. Their major compounds are camphor (≈30%), 1,8-cineole (≈14%) [33] and terpinen-4-ol (≈29%), 1,8-cineole (≈17%) [34]. While 1,8-cineole is one of the major compounds of Eucalyptus polybractea and Myrtus communis, it was not found to be clearly responsible for anti-QS activity.
Only M. suaveolens ssp. insularis EO has an even higher MQSIC/MIC ratio of 32, making this EO the most attractive in terms of anti-QS activity. Since the sublethal anti-QS dilution is very different from the MIC one, this EO has the ability to inhibit preferentially the QS mechanism instead of inhibiting cell growth.
To find molecule(s) that could be responsible for the anti-QS activity of M. suaveolens ssp. insularis EO (Table 2), we tested both its major compounds: pulegone and cis-cis-p-menthenolide. Table 2. Antimicrobial and anti-QS assays of pulegone, cis-cis-p-menthenolide and mintlactone.

Chemical structure
Molecules 2018, 23, x 4 of 11 (≈17%) [34]. While 1,8-cineole is one of the major compounds of Eucalyptus polybractea and Myrtus communis, it was not found to be clearly responsible for anti-QS activity. Only M. suaveolens ssp. insularis EO has an even higher MQSIC/MIC ratio of 32, making this EO the most attractive in terms of anti-QS activity. Since the sublethal anti-QS dilution is very different from the MIC one, this EO has the ability to inhibit preferentially the QS mechanism instead of inhibiting cell growth.
To find molecule(s) that could be responsible for the anti-QS activity of M. suaveolens ssp. insularis EO (Table 2), we tested both its major compounds: pulegone and cis-cis-p-menthenolide. Pulegone is the most abundant compound of this EO, which is already know to exert an antimicrobial activity [35]. Experimentation on the commercial molecule showed that its MQSIC/MIC ratio value is 4, which is lower than the EO value by itself (32) and thus supporting its antibacterial action.
We then evaluated the anti-QS activity of cis-cis-p-menthenolide that we compared to the activity of mintlactone, its commercial isomer. This comparison was done to evaluate the structure-activity relationship of both molecules.
cis-cis-p-menthenolide((3aS,6S,7aS)-6-methyl-3-methylidenehexahydro-1-benzofuran-2(3H)-one)), a methylidene lactone bearing the menthane skeleton, is the second major component of this essential oil (27.3%). Nonetheless, this molecule is found in higher concentrations in the hydrolate extract (67.3%) [36]. As a water-soluble molecule, it is more likely to be found in this fraction of the plant hydrolate. For this reason, the hydrolate extract was used to isolate the molecule. cis-cis-pmenthenolide has a MQSIC/MIC ratio of 64, which is the highest found in our study, proving the anti-QS effect of that molecule. On the other hand, the mintlactone MQSIC/MIC ratio (8) is only slightly higher than pulegone (Table 2). Thus, its action can be considered more as antimicrobial than anti-QS. cis-cis-p-menthenolide and mintlactone exhibit the α,β unsaturated lactone substructure. However, they only differ by the double bond position (intracyclic or exocyclic), which is probably responsible for the difference in anti-QS activity between cis-cis-p-menthenolide and mintlactone.
Since Gram-negative bacteria use acyl-homoserine lactone as diffusible signal molecules for QS, we can suppose that the lactone skeleton of those molecules could be responsible for interfering with and disrupting the QS mechanism in C. violaceum. These results highlight the disruptive role of ciscis-p-menthenolide on violacein production and possibly on the QS system.
As this study was about the primary anti-QS mode of action of tested EOs, it'll be interesting, in the future, to discover how cis-cis-p-menthenolide is interfering with QS. We could think about three main targets, acyl-homoserine-lactone synthase (CviI), the lactone itself (N-Hexanoyl-L-homoserine), or the transcriptional regulator (CviR). Knowing the homology found between lactone structure of cis-cis-p-menthenolide and N-Hexanoyl-L-homoserine, we might think to a competition between those two compounds. This could lead to a blocking in the process of gene expression normally induced by the CviR-N-Hexanoyl-L-homoserine binding process, but this will need to be tested through the use of fluorescent quenching. (≈17%) [34]. While 1,8-cineole is one of the major compounds of Eucalyptus polybractea and Myrtus communis, it was not found to be clearly responsible for anti-QS activity. Only M. suaveolens ssp. insularis EO has an even higher MQSIC/MIC ratio of 32, making this EO the most attractive in terms of anti-QS activity. Since the sublethal anti-QS dilution is very different from the MIC one, this EO has the ability to inhibit preferentially the QS mechanism instead of inhibiting cell growth.
To find molecule(s) that could be responsible for the anti-QS activity of M. suaveolens ssp. insularis EO (Table 2), we tested both its major compounds: pulegone and cis-cis-p-menthenolide. Pulegone is the most abundant compound of this EO, which is already know to exert an antimicrobial activity [35]. Experimentation on the commercial molecule showed that its MQSIC/MIC ratio value is 4, which is lower than the EO value by itself (32) and thus supporting its antibacterial action.
We then evaluated the anti-QS activity of cis-cis-p-menthenolide that we compared to the activity of mintlactone, its commercial isomer. This comparison was done to evaluate the structure-activity relationship of both molecules.
cis-cis-p-menthenolide((3aS,6S,7aS)-6-methyl-3-methylidenehexahydro-1-benzofuran-2(3H)-one)), a methylidene lactone bearing the menthane skeleton, is the second major component of this essential oil (27.3%). Nonetheless, this molecule is found in higher concentrations in the hydrolate extract (67.3%) [36]. As a water-soluble molecule, it is more likely to be found in this fraction of the plant hydrolate. For this reason, the hydrolate extract was used to isolate the molecule. cis-cis-pmenthenolide has a MQSIC/MIC ratio of 64, which is the highest found in our study, proving the anti-QS effect of that molecule. On the other hand, the mintlactone MQSIC/MIC ratio (8) is only slightly higher than pulegone (Table 2). Thus, its action can be considered more as antimicrobial than anti-QS. cis-cis-p-menthenolide and mintlactone exhibit the α,β unsaturated lactone substructure. However, they only differ by the double bond position (intracyclic or exocyclic), which is probably responsible for the difference in anti-QS activity between cis-cis-p-menthenolide and mintlactone.
Since Gram-negative bacteria use acyl-homoserine lactone as diffusible signal molecules for QS, we can suppose that the lactone skeleton of those molecules could be responsible for interfering with and disrupting the QS mechanism in C. violaceum. These results highlight the disruptive role of ciscis-p-menthenolide on violacein production and possibly on the QS system.
As this study was about the primary anti-QS mode of action of tested EOs, it'll be interesting, in the future, to discover how cis-cis-p-menthenolide is interfering with QS. We could think about three main targets, acyl-homoserine-lactone synthase (CviI), the lactone itself (N-Hexanoyl-L-homoserine), or the transcriptional regulator (CviR). Knowing the homology found between lactone structure of cis-cis-p-menthenolide and N-Hexanoyl-L-homoserine, we might think to a competition between those two compounds. This could lead to a blocking in the process of gene expression normally induced by the CviR-N-Hexanoyl-L-homoserine binding process, but this will need to be tested through the use of fluorescent quenching. (≈17%) [34]. While 1,8-cineole is one of the major compounds of Eucalyptus polybractea and Myrtus communis, it was not found to be clearly responsible for anti-QS activity. Only M. suaveolens ssp. insularis EO has an even higher MQSIC/MIC ratio of 32, making this EO the most attractive in terms of anti-QS activity. Since the sublethal anti-QS dilution is very different from the MIC one, this EO has the ability to inhibit preferentially the QS mechanism instead of inhibiting cell growth.
To find molecule(s) that could be responsible for the anti-QS activity of M. suaveolens ssp. insularis EO (Table 2), we tested both its major compounds: pulegone and cis-cis-p-menthenolide. Table 2. Antimicrobial and anti-QS assays of pulegone, cis-cis-p-menthenolide and mintlactone.
We then evaluated the anti-QS activity of cis-cis-p-menthenolide that we compared to the activity of mintlactone, its commercial isomer. This comparison was done to evaluate the structure-activity relationship of both molecules.
cis-cis-p-menthenolide((3aS,6S,7aS)-6-methyl-3-methylidenehexahydro-1-benzofuran-2(3H)-one)), a methylidene lactone bearing the menthane skeleton, is the second major component of this essential oil (27.3%). Nonetheless, this molecule is found in higher concentrations in the hydrolate extract (67.3%) [36]. As a water-soluble molecule, it is more likely to be found in this fraction of the plant hydrolate. For this reason, the hydrolate extract was used to isolate the molecule. cis-cis-pmenthenolide has a MQSIC/MIC ratio of 64, which is the highest found in our study, proving the anti-QS effect of that molecule. On the other hand, the mintlactone MQSIC/MIC ratio (8) is only slightly higher than pulegone (Table 2). Thus, its action can be considered more as antimicrobial than anti-QS. cis-cis-p-menthenolide and mintlactone exhibit the α,β unsaturated lactone substructure. However, they only differ by the double bond position (intracyclic or exocyclic), which is probably responsible for the difference in anti-QS activity between cis-cis-p-menthenolide and mintlactone.
Since Gram-negative bacteria use acyl-homoserine lactone as diffusible signal molecules for QS, we can suppose that the lactone skeleton of those molecules could be responsible for interfering with and disrupting the QS mechanism in C. violaceum. These results highlight the disruptive role of ciscis-p-menthenolide on violacein production and possibly on the QS system.
As this study was about the primary anti-QS mode of action of tested EOs, it'll be interesting, in the future, to discover how cis-cis-p-menthenolide is interfering with QS. We could think about three main targets, acyl-homoserine-lactone synthase (CviI), the lactone itself (N-Hexanoyl-L-homoserine), or the transcriptional regulator (CviR). Knowing the homology found between lactone structure of cis-cis-p-menthenolide and N-Hexanoyl-L-homoserine, we might think to a competition between those two compounds. This could lead to a blocking in the process of gene expression normally induced by the CviR-N-Hexanoyl-L-homoserine binding process, but this will need to be tested through the use of fluorescent quenching. (128) 3.00 (16) 3.00 (16) MQSIC value (mg·mL −1 )/MQSIC dilution 0.10 (512) 0.05 (1024) 0.40 (128) MQSIC/MIC ratio 4 64 8 Pulegone is the most abundant compound of this EO, which is already know to exert an antimicrobial activity [35]. Experimentation on the commercial molecule showed that its MQSIC/MIC ratio value is 4, which is lower than the EO value by itself (32) and thus supporting its antibacterial action.
We then evaluated the anti-QS activity of cis-cis-p-menthenolide that we compared to the activity of mintlactone, its commercial isomer. This comparison was done to evaluate the structure-activity relationship of both molecules.
cis-cis-p-menthenolide((3aS,6S,7aS)-6-methyl-3-methylidenehexahydro-1-benzofuran-2(3H)-one)), a methylidene lactone bearing the menthane skeleton, is the second major component of this essential oil (27.3%). Nonetheless, this molecule is found in higher concentrations in the hydrolate extract (67.3%) [36]. As a water-soluble molecule, it is more likely to be found in this fraction of the plant hydrolate. For this reason, the hydrolate extract was used to isolate the molecule. cis-cis-p-menthenolide has a MQSIC/MIC ratio of 64, which is the highest found in our study, proving the anti-QS effect of that molecule. On the other hand, the mintlactone MQSIC/MIC ratio (8) is only slightly higher than pulegone (Table 2). Thus, its action can be considered more as antimicrobial than anti-QS. cis-cis-p-menthenolide and mintlactone exhibit the α,β unsaturated lactone substructure. However, they only differ by the double bond position (intracyclic or exocyclic), which is probably responsible for the difference in anti-QS activity between cis-cis-p-menthenolide and mintlactone.
Since Gram-negative bacteria use acyl-homoserine lactone as diffusible signal molecules for QS, we can suppose that the lactone skeleton of those molecules could be responsible for interfering with and disrupting the QS mechanism in C. violaceum. These results highlight the disruptive role of cis-cis-p-menthenolide on violacein production and possibly on the QS system.
As this study was about the primary anti-QS mode of action of tested EOs, it'll be interesting, in the future, to discover how cis-cis-p-menthenolide is interfering with QS. We could think about three main targets, acyl-homoserine-lactone synthase (CviI), the lactone itself (N-Hexanoyl-L-homoserine), or the transcriptional regulator (CviR). Knowing the homology found between lactone structure of cis-cis-p-menthenolide and N-Hexanoyl-L-homoserine, we might think to a competition between those two compounds. This could lead to a blocking in the process of gene expression normally induced by the CviR-N-Hexanoyl-L-homoserine binding process, but this will need to be tested through the use of fluorescent quenching.

Anti-Biofilm Action
To confirm the anti-QS activity of cis-cis-p-menthenolide, we choose to evaluate the inhibition of biofilm formation by scanning electron microscopy because it is mediated by QS in C. violaceum. Biofilm formation is a multistage process that starts with bacterial adhesion to a surface followed by the production and accumulation of an extracellular polymeric matrix [37]. The action of M. suaveolens ssp. insularis EO, cis-cis-p-menthenolide and mintlactone on biofilm formation are shown in Figure 1.

Anti-Biofilm Action
To confirm the anti-QS activity of cis-cis-p-menthenolide, we choose to evaluate the inhibition of biofilm formation by scanning electron microscopy because it is mediated by QS in C. violaceum. Biofilm formation is a multistage process that starts with bacterial adhesion to a surface followed by the production and accumulation of an extracellular polymeric matrix [37]. The action of M. suaveolens ssp. insularis EO, cis-cis-p-menthenolide and mintlactone on biofilm formation are shown in Figure 1. In standard conditions, C. violaceum grows in a very dense and homogenous biofilm (Figure  1a,b). When M. suaveolens ssp. insularis EO (Figure 1c,d) is used at its MQSIC, bacterial density is similar to the control condition, but the matrix seems to be degraded and fragmented as shown in the Figure 1d. The same can be said when assessing cis-cis-p-menthenolide (Figure 1e,f), with even more disaggregation of the matrix. On the contrary, when mintlactone is used at its MQSIC (Figure 1g,h), In standard conditions, C. violaceum grows in a very dense and homogenous biofilm (Figure 1a,b). When M. suaveolens ssp. insularis EO (Figure 1c,d) is used at its MQSIC, bacterial density is similar to the control condition, but the matrix seems to be degraded and fragmented as shown in the Figure 1d. The same can be said when assessing cis-cis-p-menthenolide (Figure 1e,f), with even more disaggregation of the matrix. On the contrary, when mintlactone is used at its MQSIC (Figure 1g,h), there is visible reduction of the population density. This observation seems to be in agreement with the MQSIC/MIC ratios in Table 2, where we show this molecule has no influence on the QS but rather exerts a direct action on the bacterial cell.
We clearly showed, in the first part of the study, that cis-cis-p-menthenolide action lead to a strong decrease in violacein production, thus without impacting bacterial density which is implying a disruption of the QS. So, visible results of its action on C. violaceum biofilm matrix appear as one other proof of the implied action against QS.
Further investigations could be undertaken in the future to confirm this hypothesis. For example, we could determine the chitinolytic activity of C. violaceum. Indeed, when in presence of chitin in a low nutrient environment, C. violaceum can, under QS control, induce chitinase production [8].

Bioactive Substances
Twelve EOs were tested. Hydro-distillations were made from various parts of the plants of interest: the leaves for Mentha suaveolens ssp. insularis and Eucalyptus polybractea, young leaves and green twigs for Citrus clementina and Citrus limon, aerial parts for Myrtus communis, Cedrus atlantica, Calamintha nepeta ssp. nepeta and Cymbopogon citratus, flowering tops for Helichrysum italicum, Lavandula stoechas, seeds for Foeniculum vulgare and dried fruits for Xanthoxylum armatum. They were mainly supplied by U Mandriolu Sarrola Carcopino (Corsica, France). Essential oil of Mentha suaveolens ssp. insularis was isolated from aerial part (leaves) of the plant by hydro-distillation in our laboratory.
Plant materials were dried one day at room temperature, away from direct sunlight, and submitted to water-distillation (3 h) using a Clevenger-type apparatus (yields: 0.14% w/w). The combined EO (10 mL) and the hydrolate (10 L) from the same distillation were stored in the dark at 4 • C. Three portions (3.3 L each) of the hydrolate were extracted with diethyl oxide (3 × 1 L) and the combined organic layer was dried over MgSO 4 . The solvent was removed under reduced pressure yielding the hydrolate extract (HE, 3.8 g).
Mintlactone and pulegone were purchased from Sigma-Adrich™ (St. Louis, MO, USA). All products were solubilized in dimethyl sulfoxide (DMSO, Sigma-Aldrich™). Antimicrobial activity of the DMSO solvent was tested beforehand and showed no effect on bacterial growth at the tested concentrations.

Gas Chromatography (GC) Analyses
Analyses were performed on a Clarus 500 PerkinElmer (PerkinElmer, Courtaboeuf, France) system equipped with a FID and two fused-silica capillary columns (50 m × 0.22 mm, film thickness 0.25 µm), BP-1 (polydimethylsiloxane) and BP-20 (polyethylene glycol). The oven temperature was programmed from 60 • C to 220 • C at 2 • C/min and then held isothermal at 220 • C for 20 min; injector temperature: 250 • C; detector temperature: 250 • C; carrier gas: hydrogen (1 mL/min); split: 1/60; injected volume: 0.5 µL. The relative proportions of the oil constituents were expressed as percentages obtained by peak-area normalization, without using correction factors. Retention indices were determined relative to the retention times of a series of n-alkanes (C 7 -C 28 ) with linear interpolation (Target Compounds software from PerkinElmer).

Bacterial Strains and Growth Conditions
Chromobacterium violaceum wild-type strain (CIP 103350T) was obtained from the Institut Pasteur's Biological Resource Center (Paris, France). The strain was grown under aerobic condition in trypticasein soy (TS) broth and agar (Conda™, Torrejón de Ardoz, Spain), incubated at 30 • C for 24 h.

Anti-QS Assay: Violacein Quantification and Measurement of Cell Growth
The anti-QS activity of Corsican EOs was assessed on C. violaceum (10 6 CFU·mL −1 ). Their concentrations ranged from 50.00 mg·mL −1 (dilution: 1) to 1.25 × 10 −2 mg·mL −1 (dilution: 4096) and were obtained by a two-fold serial dilution method. C. violaceum was incubated in culture tubes containing TS broth at 30 • C on an orbital shaker (Stuart™, Stone, UK). Violacein production was quantified using the Choo, Rukayadi, & Hwang protocol [18]. Briefly, 1 mL of overnight culture of each culture tube was centrifuged at 13,000 rpm for 10 minutes to precipitate the pigment. The pellet was resuspended in 1 mL of DMSO and homogenized by pipetting. Violacein absorbance at 585 nm was measured by an UV-visible spectrophotometer (Jasco™, Oklahoma City, CA, USA). The control samples consisted of incubating C. violaceum in TS broth without the addition of bioactive substances. Each test was performed in triplicate. Percentages of violacein production were expressed using the following formula: (absorbance of tested concentration at 585 nm/absorbance of the control at 585 nm) × 100 (1) Since a reduction of violacein production can be due to either blocking the QS mechanism or inhibiting bacterial growth [40], the bacterial concentration was evaluated in parallel: 10-fold serial dilutions were performed from each culture tube; 100 µL of each dilution was then plated on TS agar dishes and incubated at 30 • C for 24 h. Colonies were then counted and expressed as Log CFU·mL −1 . This assay also allows us to determine the minimal inhibitory concentration (MIC), which is the minimal dilution where at least 90% of the bacterial population has not grown compared to the control (when growth is <2 Log CFU·mL −1 according to method sensitivity). According to Djabou et al. (2013) [24], a strain is considered as not sensitive for MIC value between 50.00 or above to 25.00 mg·mL −1 , moderately sensitive for value between 12.50 and 3.00 mg·mL −1 and sensitive for value between 2.00 and 0.40 mg·mL −1 . Finally, the minimum QS inhibitory concentration (MQSIC) was defined as the effective concentration of EOs or bioactive agents which for at least 50% of the violacein production was reduced [41] in absence of significant effect on cell growth (Figure 2). Each test was performed in triplicate. 2) for 2 to 3 h at 4 °C. They were washed in two successive 10 min baths of sodium cacodylate buffer, dried for 120 h, and then coated with gold/palladium sputter coating (Quorum Technologies SC7640, Lewes, UK). The pegs were then examined under a scanning electron microscope (Hitachi™ S3400N, Tokyo, Japan) with an accelerating voltage of 5 or 10 kV. Each test was performed in triplicate and the images are representative of the bacterial distribution on the whole peg surface.

Conclusions
In summary, cis-cis-p-menthenolide, a p-menthane exhibiting a characteristic exocyclic α,β unsaturated lactone substructure is of specific interest because it is only found in the endemic to the occidental Mediterranean Sea islands Mentha suaveolens ssp. insularis. In this study, it appears that ciscis-p-menthenolide, extracted from Corsican Mentha suaveolens ssp. insularis, seems to act as a quencher of the QS signaling pathway. Its sublethal MQSIC dilution of 1024 (0.05 mg·mL −1 ) had no bactericidal effect, but considerably reduced violacein production. Moreover, anti-QS action was enlightened by scanning electron micrographies where biofilm matrix appears to be altered without affecting bacterial density.  2) for 2 to 3 h at 4 °C. They were washed in two successive 10 min baths of sodium cacodylate buffer, dried for 120 h, and then coated with gold/palladium sputter coating (Quorum Technologies SC7640, Lewes, UK). The pegs were then examined under a scanning electron microscope (Hitachi™ S3400N, Tokyo, Japan) with an accelerating voltage of 5 or 10 kV. Each test was performed in triplicate and the images are representative of the bacterial distribution on the whole peg surface.

Conclusions
In summary, cis-cis-p-menthenolide, a p-menthane exhibiting a characteristic exocyclic α,β unsaturated lactone substructure is of specific interest because it is only found in the endemic to the occidental Mediterranean Sea islands Mentha suaveolens ssp. insularis. In this study, it appears that ciscis-p-menthenolide, extracted from Corsican Mentha suaveolens ssp. insularis, seems to act as a quencher of the QS signaling pathway. Its sublethal MQSIC dilution of 1024 (0.05 mg·mL −1 ) had no bactericidal effect, but considerably reduced violacein production. Moreover, anti-QS action was enlightened by scanning electron micrographies where biofilm matrix appears to be altered without affecting bacterial density.

Conclusions
In summary, cis-cis-p-menthenolide, a p-menthane exhibiting a characteristic exocyclic α,β unsaturated lactone substructure is of specific interest because it is only found in the endemic to the occidental Mediterranean Sea islands Mentha suaveolens ssp. insularis. In this study, it appears that ciscis-p-menthenolide, extracted from Corsican Mentha suaveolens ssp. insularis, seems to act as a quencher of the QS signaling pathway. Its sublethal MQSIC dilution of 1024 (0.05 mg·mL −1 ) had no bactericidal effect, but considerably reduced violacein production. Moreover, anti-QS action was enlightened by scanning electron micrographies where biofilm matrix appears to be altered without affecting bacterial density. 2) for 2 to 3 h at 4 °C. They were washed in two successive 10 min baths of sodium cacodylate buffer, dried for 120 h, and then coated with gold/palladium sputter coating (Quorum Technologies SC7640, Lewes, UK). The pegs were then examined under a scanning electron microscope (Hitachi™ S3400N, Tokyo, Japan) with an accelerating voltage of 5 or 10 kV. Each test was performed in triplicate and the images are representative of the bacterial distribution on the whole peg surface.

Conclusions
In summary, cis-cis-p-menthenolide, a p-menthane exhibiting a characteristic exocyclic α,β unsaturated lactone substructure is of specific interest because it is only found in the endemic to the occidental Mediterranean Sea islands Mentha suaveolens ssp. insularis. In this study, it appears that ciscis-p-menthenolide, extracted from Corsican Mentha suaveolens ssp. insularis, seems to act as a quencher of the QS signaling pathway. Its sublethal MQSIC dilution of 1024 (0.05 mg·mL −1 ) had no bactericidal effect, but considerably reduced violacein production. Moreover, anti-QS action was enlightened by scanning electron micrographies where biofilm matrix appears to be altered without affecting bacterial density.  2) for 2 to 3 h at 4 °C. They were washed in two successive 10 min baths of sodium cacodylate buffer, dried for 120 h, and then coated with gold/palladium sputter coating (Quorum Technologies SC7640, Lewes, UK). The pegs were then examined under a scanning electron microscope (Hitachi™ S3400N, Tokyo, Japan) with an accelerating voltage of 5 or 10 kV. Each test was performed in triplicate and the images are representative of the bacterial distribution on the whole peg surface.

Conclusions
In summary, cis-cis-p-menthenolide, a p-menthane exhibiting a characteristic exocyclic α,β unsaturated lactone substructure is of specific interest because it is only found in the endemic to the occidental Mediterranean Sea islands Mentha suaveolens ssp. insularis. In this study, it appears that ciscis-p-menthenolide, extracted from Corsican Mentha suaveolens ssp. insularis, seems to act as a quencher of the QS signaling pathway. Its sublethal MQSIC dilution of 1024 (0.05 mg·mL −1 ) had no bactericidal effect, but considerably reduced violacein production. Moreover, anti-QS action was enlightened by scanning electron micrographies where biofilm matrix appears to be altered without affecting bacterial density. They were washed in two successive 10 min baths of sodium cacodylate buffer, dried for 120 h, and then coated with gold/palladium sputter coating (Quorum Technologies SC7640, Lewes, UK). The pegs were then examined under a scanning electron microscope (Hitachi™ S3400N, Tokyo, Japan) with an accelerating voltage of 5 or 10 kV. Each test was performed in triplicate and the images are representative of the bacterial distribution on the whole peg surface.

Conclusions
In summary, cis-cis-p-menthenolide, a p-menthane exhibiting a characteristic exocyclic α,β unsaturated lactone substructure is of specific interest because it is only found in the endemic to the occidental Mediterranean Sea islands Mentha suaveolens ssp. insularis. In this study, it appears that cis-cis-p-menthenolide, extracted from Corsican Mentha suaveolens ssp. insularis, seems to act as a quencher of the QS signaling pathway. Its sublethal MQSIC dilution of 1024 (0.05 mg·mL −1 ) had no bactericidal effect, but considerably reduced violacein production. Moreover, anti-QS action was enlightened by scanning electron micrographies where biofilm matrix appears to be altered without affecting bacterial density.