ANTI-QUORUM SENSING ACTIVITY OF SOME MEDICINAL PLANTS

Collection of Plant Materials and Preparation of the Extracts

The fresh materials of Mentha longifolia, Senna italica, Valantia hispida, Tephrosia purpurea, Teucrium polium, Tribulus arabicus, and Commophora molmol were collected from Abyar Al-Mashy and Gabal Al-aquiq, Al Madinah Al Munawwarah, Saudi Arabia in March 2015. The other plant materials were purchased at the markets in Al-Madinah Al-Munawwarah, Saudi Arabia (Table 1). Authentication of the plant samples was established by Prof. Dr. A. Fayed (Professor of Plant Taxonomy, Faculty of Science, Assiut University, Egypt). The plants were shade dried for 7 days and ground to powder, using mortar and grinder of the electric mixer. Voucher specimens have been deposited at the Department of Pharmacognosy and Pharmaceutical Chemistry, Faculty of Pharmacy, Taibah University, Al Madinah Al Munawwarah, Saudi Arabia. Powdered samples (100 g each) were separately extracted using 95% methanol (5 x 250 mL). The extracts were concentrated under reduced pressure using rotary evaporator (Heidolph, Schwabach, Germany) and re-dissolved in dimethyl sulfoxide (DMSO 2.5%) for the assay of QSI activity. The solvent DMSO (1.5%) would not inhibit growth of the microorganisms (Zgoda and Porter 2001).

Bacterial Strains and Growth Conditions

The anti-quorum sensing assay was performed using Chromobacterium violaceum ATCC 12472. It was grown in Luria-Bertani (LB) media (1% peptone, 0.5% yeast extract (Bactoagar, BD Difco), and 1% NaCl (pH 7.4) solidified using 0.5 or 1.5% agar) (Bertani, 2004) and incubated at 28 °C for 48 h. C. violaceum ATCC 12472 was cultivated every 7 days on fresh LB agar slant and kept at 28 °C. P. aeruginosa PA14 was cultivated in LB media, incubated at 37 °C, and preserved as glycerol stocks at -20 °C.

Reporter Strain Assay of QSI Potential of Plant Extracts

Quorum sensing inhibitory effect of the tested extracts was estimated by agar cup diffusion assay using C. violaceum strain ATCC 12472 (McClean et al., 1997). Cultures were prepared by cultivating the bacteria in LB broth for 24 h at 28 °C. Luria-Bertani agar plates (1.5% agar) were prepared 15 mL/plate. C. violaceum was inoculated (100 μL/plate) in LB soft agar (0.5% agar) and poured on the solidified LB plates. Cups were made in LB agar medium of 10 mm diameter. A volume of 100 μL of each extract was placed in the corresponding cup and the assay plates were incubated at 28 °C for 48 h. Inhibition of quorum sensing was calculated using the equation (r₂-r₁) in mm; where r2 is the total growth and the QS inhibition zone radius and r₁ is the clear zone radius. Quorum sensing inhibition zone <10 mm was considered moderate activity and when QSI zone >10 mm designated potent effect (Zaki et al., 2013).

Assay of Some Virulence Factors of P. aeruginosa PA14

Formation of Biofilm

The activity of various plant extracts on biofilm assembly by P. aeruginosa PA14 was measured using tube assay method (Christensen et al., 1982). Overnight culture of P. aeruginosa PA14 (500 μL) was inoculated into fresh LB broth (5 mL) with and without plant extracts (200 μL), then tubes were incubated overnight at 37 °C. Free unbound cells were discarded and biofilm layer was washed 3-4 times with water. The formed biofilm was stained by crystal violet (5% w/v) for 10 min, unbound stain was discarded. The tubes were washed and dried in opposite position. The formed biofilm on sides and bottom of the tubes was assigned.

Motility Assay

P. aeruginosa is capable of swimming on soft surfaces, twitching on hard surfaces, and swarming on semi-solid surfaces. The tested plants extracts were added to the motility plates. An overnight culture of PA14 was diluted to 0.1-0.2 nm at OD₆₀₀. Twitching motility was performed through stab-inoculation 1% LB plates with and without plant extracts using 2 μL of the diluted Pseudomonas culture and inoculated at 37 °C for 48 h. The diameter of Pseudomonas twitching at the interface between plastic and agar was measured (Murray et al., 2010). Flagellum-dependent swimming was performed using swimming media (1% tryptone, 0.5% NaCl, and 0.5% agar). The plates were inoculated with 2 μL of diluted PA14 and incubated for 18 h at 37 °C. The diameter of the turbid zone (mm) was measured (Murray et al., 2010). Swarming motility was assayed using swarming media (0.5% agar, 0.5% peptone, 0.2% yeast extract, and 1.0 % glucose). Two micro-liters of the diluted PA14 culture were inoculated at the middle of the plate and the plates were incubated for 18 h at 37 °C (Krishnan et al., 2012). Motility assay was performed in triplicate and the mean of the diameter was assigned.

Statistical Analysis

The mean of three separate experiments ± standard deviation was calculated using Excel data sheet. Statistical analysis was estimated using GraphPad Instate software package (version3.05), Tukey-Kramer multiple-comparison test and the significant difference was assigned when P <0.05.

Quorum Sensing Inhibitory Effect

Assay of QSI activity of the alcohol extracts of 20 medicinal plants was performed using Chromobacterium violaceum ATCC12472 reporter strain (McClean et al., 1997). Most of the tested extracts exhibited potent antibacterial activity against the reporter strain. Inhibition of purple pigmentation of C. violaceum provided a readily and easily observable phenotype that simplified and facilitated screening for QSI effect. In the following work, seven of the screened extracts demonstrated QS antagonistic activity. The extracts of C. sinensis, L. nobilis, E. cardamomum, A. cepa, and C. sativum showed a pronounced quorum quenching effect with violacein inhibitory actions (Table 1). They showed clearly visible white halo in the violacin bioassay (20, 10, 10, 20, and 10 mm), respectively compared to garlic extract (A. sativa) (positive control). It was reported that A. sativa inhibited LuxR-based QSI in P. aeruginosa due to the presence of ajoene a sulfur-rich molecule (Jakobsen et al., 2012), while the extracts of P. guajava and M. longifolia showed moderate QSI effect.

Inhibition of Pyocyanin

P. aeruginosa produces green characterized pigment called pyocyanin after 24-48 h of growth. The disappearance of the green coloring of the P. aeruginosa PA14 culture indicated the lower produced levels of pyocyanin or no pyocyanin is present in the supernatant. The effect of C. sinensis, L. nobilis, E. cardamomum, A. cepa, and C. sativum extracts on the production pyocyanin was performed. In this study, pyocyanin level in Pseudomonas culture treated with these five plant extracts was significantly reduced (P<0.05) without affecting bacterial growth in contrast to the green pigment of untreated cultures (Figure 1). This could be explicated as quorum-control of pyocyanin pigment production (Dietrich et al., 2006). Moreover, quorum quenching agents have a great impact on pyocyanin release from P. aeruginosa (Morkunas et al., 2012; El-Mowafy et al., 2014).

Figure 1

Influence of plant extracts on pyocyanin production by PA14: Extracts of C. sinensis, C. sativum, L. nobilis, A. cepa, and E. cardamomum significantly (*; P <.0.05) inhibited pyocyanin compared to control.

Effect on Biofilm Development

Furthermore, QS controls bacterial adhesion, biofilm formation, and production of alginates and polysaccharides required for biofilm development (Schuster and Greenberg, 2007). The first discovered natural products inhibited QS and biofilm maturation in Gram-negative bacteria are the halogenated furanones from Delisea pulchra (Givskov et al., 1997) and other QSI compounds such as cyclic sulfur derivatives obtained from garlic (Persson et al., 2005) and patulin produced by Penicillium sp. (O’Loughlin et al., 2013).

The extracts of C. sinensis, L. nobilis, E. cardamomum, A. cepa, and C. sativum were tested for Pseudomonas biofilm formation using tube assay method. All these plants extracts showed discriminative effect on biofilm formed by P. aeruginosa PA14 compared to the untreated control (Figure 2).

Figure 2

Effect of plant extracts on biofilm formation by PA14; Citrus sinensis, Coriandrum sativum, Laurus nobilis, Allium cepa, and Elettaria cardamomum (5, 9, 11, 14, and 20, respectively) compared to control untreated Pseudomonas PA14.

Motility Assay

Normal bacterial motility is important for proliferation of burn and colonization of wounds (Arora et al., 2005). P. aeruginosa has three types of bacterial motility: swimming, twitching, and swarming which are propagated by flagella and pili IV. The extracts of C. sinensis, L. nobilis, E. cardamomum, A. cepa, and C. sativum were tested for their influence on the motility of P. aeruginosa PA14. They manifested a distinct influence on swarming and twitching motility (Table 2). C. sinensis, L. nobilis, and A. cepa extracts reduced twitching in PA14 by 88, 77, and 85%, respectively (P<0.01). Previous studies verified that QS systems control Pseudomonas motilities and inhibition of QS signals affects the motilities (Glessner et al., 1999; Juhas et al., 2005). Although C. sativum and E. cardamomum extracts substantially inhibited biofilm and pyocyanin production in PA14, it was noticed that they did not significantly affect bacteria motility. It appears that these extracts contain compounds; some of them are agonist of the motility, while others may affect the different signaling pathways in P. aeruginosa PA14. Motility is a complex phenotype that involves various regulatory components (Overhage et al., 2008). Elimination of Pseudomonas motility confirmed the potential effect of C. sinensis, L. nobilis, and A. cepa on biofilm formation as modulation of bacterial motilities is associated with thin and dispersed biofilm (Shrout et al., 2006).