- freely available
Sensors 2013, 13(5), 6217-6228; doi:10.3390/s130506217
Abstract: Quorum sensing is a system of stimuli and responses in relation to bacterial cell population density that regulates gene expression, including virulence determinants. Consequently, quorum sensing has been an attractive target for the development of novel anti-infective measures that do not rely on the use of antibiotics. Anti-quorum sensing has been a promising strategy to combat bacterial infections as it is unlikely to develop multidrug resistant pathogens since it does not impose any selection pressure. A number of anti-quorum sensing approaches have been documented and plant-based natural products have been extensively studied in this context. Plant matter is one of the major sources of chemicals in use today in various industries, ranging from the pharmaceutical, cosmetic, and food biotechnology to the textile industries. Just like animals and humans, plants are constantly exposed to bacterial infections, it is therefore logical to expect that plants have developed sophisticated of chemical mechanisms to combat pathogens. In this review, we have surveyed the various types of plant-based natural products that exhibit anti-quorum sensing properties and their anti-quorum sensing mechanisms.
Communication among bacteria is achieved via the production, diffusion, detection and responses to chemical signaling molecules known as autoinducers. When a threshold concentration is reached, the autoinducers are detected and this leads to quorum sensing (QS) gene regulation (Figure 1). This QS process uses autoinducers for the regulation of bacterial behaviors such as formation and release of virulence factors, antibiotic production and also biofilm formation [1,2]. Alternative QS concepts, such as diffusion sensing and efficiency sensing have been previously reported [3,4]. There are several QS systems used by bacteria. For example, Gram-positive bacteria primarily use the oligopeptide signaling systems whereas Gram-negative bacteria primarily uses the LuxR/I-type QS system .
Due to the extensive emergence of antibiotic-resistant bacteria, there is a rising need to control this drug resistance. Many opportunistic pathogenic bacteria depend on QS systems to coordinate their virulence expression. Thus, interference with QS has been regarded as the novel way to control bacterial infections . QS is an evident target to capably block QS signals by inducing attenuation of pathogens' virulence determinants. It is believed that as bacterial growth is not affected, inhibition of QS does not impose selective pressure for the development of resistance [7,8]. However, this point has been challenged on the possibility of resistance to QS disruption might occur . For example, a well studied QS antagonist, brominated furanone C-30, causing rapid bacterial resistance due to mutation has been reported recently .
2. Plants as QS Antagonists?
Natural products were explored initially because of their therapeutic values in traditional medical practice, but recently, there is has been an increasing interest in the biological function and therapeutic roles of natural products and their ecological role in regulating interactions between microorganisms. It is speculated that unlike human and mammals that possess immune systems to defend against invaders, plants are lacking such sophisticated immunity to ward off invading pathogens, so instead of relying on cellular and biochemical defense systems, plants may have evolved to produce anti-QS compounds that can be used to defeat QS pathogens.
To date, biologically active constituents of natural products, especially plant-derived ones, have led to the discovery of new drugs used for treatment of numerous diseases . Various studies showed that eukaryotes have evolved efficiently to manipulate bacterial QS systems and protect themselves from pathogen attack . An important discovery was the fact that the halogenated furanones produced by the marine red alga Delisea pulchra interfere the N-acylated homoserine lactone (AHL) regulatory system in several Gram-negative bacteria. These furanones actually enable the alga to influence the bacterial colonization and fouling on its own surface in the natural marine environment [13,14]. Earlier studies have also reported that certain bacteria possess the ability to quench QS. For example, an N-acylhomoserine (AHL) lactonase enzyme, AiiA from Bacillus sp., was found to hydrolyze the lactone bond of the AHL signalling compound . Interestingly, the paraoxonase (PON) enzymes in human airway epithelial cells also show interference with QS systems .
In this review, we will summarize the QS antagonists derived from plant sources and also provide better understanding of the interference of QS by these antagonists. Although this review represents an evaluation of publicly available data, there may be some important antagonists, especially the non-plant-based compounds that have been excluded.
3. Examples of QS Antagonists
In recent years, the discovery of QS antagonists of bacterial and non-bacterial origin has increased tremendously. There are some chemically synthesized compounds that inhibit QS, but most of the antagonists have been discovered in plants extracts. Since these plants can be consumed by humans, the active compounds that are having QS inhibitory activities from the plants should be deemed as safe and should not cause toxicity towards human cells, but toxicity studies on these compounds are still necessary. Not only to plants produce mimicry molecules that are anti-QS, but certain plant parts such as pea (Pisum sativum) seedlings  also produce exudates that contain compounds that can interfere with QS. These findings provide a better understanding of how the compounds inhibit bacterial QS systems. Biosensors such as Escherichia coli [pSB401], E. coli [pSB1075], Chromobacterium violaceum CV026 are used by researchers to aid the screening for compounds/extracts with anti-QS abilities. These biosensors do not possess the ability to produce any AHLs. External AHLs are supplied exogenously to induce QS traits such as bioluminescence and violacein production which can be quantified. The anti-QS ability of compounds/extracts are measured by the significance of the inhibition. Table 1 shows some of the antagonists discovered in recent studies.
Natural products play a pivotal role for treating and preventing infectious diseases . The plant compounds usually target the bacterial QS system via three different ways, by either stop the signaling molecules from being synthesized by the luxI encoded AHL synthase, degrading the signaling molecules and/or targeting the luxR signal receptor .
AHL biosynthesis typically involves a series of reactions that use S-adenosyl methionine (SAM) as the amino donor to generate the homoserine lactone ring moiety, and an acyl carrier protein (ACP) as the precursor for the N-acyl side chain of the AHL molecules. With this knowledge, several SAM analogues have been synthesized and show anti-QS activity . However, based on our experience on extensive screening of hundreds of plant extracts to specifically look for luxI synthase activity, we did not succeed in finding any suggesting that it is rather rare for plants to possess such anti-luxI synthase activity (unpublished data).
To interfere with signal reception, there can be competitive and non-competitive molecules that can interfere with the binding of AHL to its cognate LuxR receptor. It is logical to imagine that for competitive molecules to bind to AHL receptor, these molecules must be structurally similar to AHLs. For non-competitive binding to the AHL receptor, conceivably, these molecules will bind to the site on the receptor other that than the AHL binding site. Plants can produce molecules that structurally mimic the AHLs , and such competitive binding is effective to block activation of AHL-mediated QS (Figure 2). In addition to that, QS inhibitors can also affect the integrity of biofilms and thus, will make the bacteria more susceptible to conventional antibiotics . This serves as an advantage as it can help to minimize the possibility of the bacteria from becoming resistant .
One of the most extensively studied natural products is the red marine alga known as D. pulchra. This Australian seaweed appears to be able to control bacterial colonization by interfering with the AHL system . Halogenated furanones were found to inhibit the QS regulated behaviors by competitively bind to the LuxR type proteins  and thus, promote their rate of proteolytic degradation without killing the bacteria . Previous research has also shown that furanones are strong inhibitors for both AI-1- and AI-2-mediated QS systems  and such inhibition is partially relieved when the AHL concentration increases . Besides, these particular compounds have been reported to reduce the ability of the E. coli cells to produce biofilms by inhibiting AI-2 activity . Furanones also play a very important role in decreasing the light emission among the Vibrio species, hindering the pigment production in C. violaceum and stop the swarming motility in S. liquefaciens [49,53,54].
Besides D. pulchra, grapefruit extract also contains some bioactive compounds such as furocoumarins, carotenoids, limonoids, pectin and coumarin that have antibacterial and antifungal activities . Furocoumarins were shown to have strong inhibition against both AI-1 and AI-2 activities, as well as hinder the formation of biofilm in E. coli, S. typhimurium and P. aeruginosa . In addition to that, obacunone has been proven to have a strong antagonistic activity against both AHL and AI-2 systems, biofilm formation and EHEC virulence .
Our group has recently reported a non-competitive compound namely malabaricone C whose structure is not similar to AHL but possesses anti-QS activity. Malabaricone C is extracted from nutmeg (Myristica cinnamomea) where it successfully inhibits both the lasR and rhlR systems in P.aeruginosa PA01and also CviR in C. violaceum  and does not inhibit AHL production in P.aeruginosa PA01. Extracts of propolis have also been proven to inhibit the production of violacein in C. violaceum, as well as the LasA and LasB protease activities in P. aeruginosa .
There are also other higher plants such as vegetables that are found to possess anti-QS properties . The examples include carrot, chamomile, and water lily as well as an array of peppers that have been proven to have anti-QS activity against the luxI-gfp reporter strain. Previous research has reported that metabolites such as disulphides and trisulphides which are extracted from garlic can inhibit LuxR-based QSI in P. aeruginosa . Rosmarinic acid extracted from sweet basil can decrease the expression of the elastase and protease, as well as biofilm formation in P. aeruginosa . Pea seedlings and root exudates are also found to inhibit pigment production, exochitinase activity and protease activity in C. violaceum . Medicago truncatula, rice, tomato and soybean can also produce substances that mimic the activities of the AHL [17,61].
In addition to this, research has also proven that plants have the ability to degrade the signaling molecules produced by the bacteria and this will obstruct the bacteria virulence factors by disrupting their communication systems . Plant root-associated fungi such as Phialocephala fortinii and Meliniomyces variabili and an Ascomycete isolate have been found to have the ability to degrade the AHL and have been proposed as an option for diminishing the bacterial virulence .
It is concluded that anti-QS is as important as antibacterial activity as it will unlikely cause resistance problems as it does not pose selection pressure. It is important to establish the modus operandi of the different QS antagonists in the pathogens in order to establish whether the antagonists are narrow or broad spectrum. Most antagonists are reported have narrow spectrum activity which may be used as a shield or sword. A narrow spectrum antagonist will only target specific pathogens where this may be useful to specifically targeting a type of pathogen in a polymicrobial environment such as those in the infection site. But on the other hand, such a narrow action antagonist may have limited clinical value. Also, the anti-QS antagonists may serve as the next generation “magic bullets”, but care must be taken that these molecules that are not bactericidal so they may have limited application for immunocompromised patients. Perhaps, a cocktail therapy involving both antibiotics and anti-QS antagonists may provide synergistic effects.
This work is supported by the High Impact Research Grant (HIR/MOHE A000001-50001) from the University of Malaya to Kok-Gan Chan which is gratefully acknowledged.
Conflict of Interest
The authors declare no conflict of interest.
- Ryan, R.P.; Dow, J.M. Diffusible signals and interspecies communication in bacteria. Microbiology 2008, 154, 1845–1858. [Google Scholar]
- Schauder, S.; Bassler, B.L. The languages of bacteria. Gene. Develop. 2001, 15, 1468–1480. [Google Scholar]
- Redfield, R.J. Is quorum sensing a side effect of diffusion sensing? Trends Microbiol. 2002, 10, 365–370. [Google Scholar]
- Hense, B.A.; Kuttler, C.; Müller, J.; Rothballer, M.; Hartmann, A.; Kreft, J.-U. Does efficiency sensing unify diffusion and quorum sensing? Nat. Rev. Microbiol. 2007, 5, 230–239. [Google Scholar]
- Reading, N.C.; Sperandio, V. Quorum sensing: The many languages of bacteria. FEMS Microbiol. Lett. 2005, 254, 1–11. [Google Scholar]
- Hong, K.W.; Koh, C.L.; Sam, C.K.; Yin, W.F.; Chan, K.G. Quorum quenching revisited—From signal decays to signalling confusion. Sensors 2012, 12, 4661–4696. [Google Scholar]
- Rasmussen, T.B.; Bjarnsholt, T.; Skindersoe, M.E.; Hentzer, M.; Kristoffersen, P.; Köte, M.; Nielsen, J.; Eberl, L.; Givskov, M. Screening for quorum-sensing inhibitors (QSI) by use of a novel genetic system, the QSI selector. J. Bacteriol. 2005, 187, 1799–1814. [Google Scholar]
- Rasmussen, T.B.; Givskov, M. Quorum sensing inhibitors: A bargain of effects. Microbiology 2006, 152, 895–904. [Google Scholar]
- Defoirdt, T.; Boon, N.; Bossier, P. Can bacteria evolve resistance to quorum sensing disruption? PLoS Pathog 2010. [Google Scholar] [CrossRef]
- Maeda, T.; García-Contreras, R.; Pu, M.; Sheng, L.; Garcia, L.R.; Tomás, M.; Wood, T.K. Quorum quenching quandary: Resistance to antivirulence compounds. ISME J. 2011, 6, 493–501. [Google Scholar]
- Hanson, J.R. The Classes of Natural Product and Their Isolation. In Natural Products: The Secondary Metabolites; Royal Society of Chemistry: Cambridge, UK, 2003; pp. 1–34. [Google Scholar]
- González, J.E.; Keshavan, N.D. Messing with bacterial quorum sensing. Microbiol. Mol. Biol. Rev. 2006, 70, 859–875. [Google Scholar]
- Bauer, W.D.; Teplitski, M. Can plants manipulate bacterial quorum sensing? Funct. Plant Biol. 2001, 28, 913–921. [Google Scholar]
- Kjelleberg, S.; Steinberg, P.; Givskov, M.; Gram, L.; Manefield, M.; de Nys, R. Do marine natural products interfere with prokaryotic AHL regulatory systems? Aquat. Microbial. Ecol. 1997, 13, 85–93. [Google Scholar]
- Dong, Y.-H.; Wang, L.-H.; Xu, J.-L.; Zhang, H.B.; Zhang, X.F.; Zhang, L.-H. Quenching quorum-sensing-dependent bacterial infection by an N-acyl homoserine lactonase. Nature 2001, 411, 813–817. [Google Scholar]
- Chun, C.K.; Ozer, E.A.; Welsh, M.J.; Zabner, J.; Greenberg, E.P. Inactivation of a Pseudomonas aeruginosa quorum-sensing signal by human airway epithelia. Proc. Natl. Acad. Sci. USA 2004, 101, 3587–3590. [Google Scholar]
- Teplitski, M.; Robinson, J.B.; Bauer, W.D. Plants secrete substances that mimic bacterial N-acyl homoserine lactone signal activities and affect population density-dependent behaviors in associated bacteria. Mol. Plant Microbe Interaction. 2000, 13, 637–648. [Google Scholar]
- Tan, L.Y.; Yin, W.F.; Chan, K.G. Silencing quorum sensing through extracts of Melicope lunu-ankenda. Sensors 2012, 12, 4339–4351. [Google Scholar]
- Krishnan, T.; Yin, W.F.; Chan, K.G. Inhibition of quorum sensing-controlled virulence factor production in Pseudomonas aeruginosa PA01 by ayurveda spice clove (Syzygium aromaticum) bud extract. Sensors 2012, 12, 4016–4030. [Google Scholar]
- Bjarnsholt, T.; Jensen, P.O.; Rasmussen, T.B.; Christophersen, L.; Calum, H.; Hentzer, M.; Hougen, H.P.; Rygaard, J.; Moser, C.; Eberl, L.; et al. Garlic blocks quorum sensing and promotes rapid clearing of pulmonary Pseudomonas aeruginosa infections. Microbiology 2005, 151, 3873–3880. [Google Scholar]
- Choo, J.H.; Rukayadi, Y.; Hwang, J.K. Inhibition of bacterial quorum sensing by vanilla extract. Lett. Appl. Microbiol. 2006, 42, 637–641. [Google Scholar]
- Zhu, H.; Sun, S.J. Inhibition of bacterial quorum sensing-regulated behaviors by Tremella fuciformis extract. Curr. Microbiol. 2008, 57, 418–422. [Google Scholar]
- Koh, K.H.; Tham, F.Y. Screening of traditional chinese medicinal plants for quorum-sensing inhibitors activity. J. Microbiol. Immunol. Infect. 2011, 44, 144–148. [Google Scholar]
- Song, Z.; Kong, K.F.; Wu, H.; Maricic, N.; Ramalingam, B.; Priestap, H.; Schneper, L.; Quirke, J.M.; Hoiby, N.; Mathee, K. Panax ginseng has anti-infective activity against opportunistic pathogen Pseudomonas aeruginosa by inhibiting quorum sensing, a bacterial communication process critical for establishing infection. Phytomedicine 2010, 17, 1040–1046. [Google Scholar]
- Singh, B.N.; Singh, B.R.; Singh, R.L.; Prakash, D.; Dhakarey, R.; Upadhyay, G.; Singh, H.B. Oxidative DNA damage protective activity, antioxidant and anti-quorum sensing potentials of Moringa oleifera. Food Chem. Toxicol. 2009, 47, 1109–1116. [Google Scholar]
- Issac Abraham, S.V.; Palani, A.; Ramaswamy, B.R.; Shunmugiah, K.P.; Arumugam, V.R. Anti-quorum sensing and antibiofilm potential of Capparis spinosa. Arch. Med. Res. 2011, 42, 658–668. [Google Scholar]
- Al-Hussaini, R.; Mahasneh, A.M. Antimicrobial and antiquorum sensing activity of different parts of Laurus nobilis l. Extracts. Jordan Med. J. 2009, 43, 286–298. [Google Scholar]
- Singh, B.N.; Singh, B.R.; Singh, R.L.; Prakash, D.; Sarma, B.K.; Singh, H.B. Antioxidant and anti-quorum sensing activities of green pod of Acacia nilotica L. Food Chem. Toxicol. 2009, 47, 778–786. [Google Scholar]
- Adonizio, A.L.; Downum, K.; Bennett, B.C.; Mathee, K. Anti-quorum sensing activity of medicinal plants in southern florida. J. Ethnopharmacol. 2006, 105, 427–435. [Google Scholar]
- Vattem, D.A.; Mihalik, K.; Crixell, S.H.; McLean, R.J. Dietary phytochemicals as quorum sensing inhibitors. Fitoterapia 2007, 78, 302–310. [Google Scholar]
- Quave, C.L.; Plano, L.R.; Pantuso, T.; Bennett, B.C. Effects of extracts from italian medicinal plants on planktonic growth, biofilm formation and adherence of methicillin-resistant Staphylococcus aureus. J. Ethnopharmacol. 2008, 118, 418–428. [Google Scholar]
- Musthafa, K.S.; Ravi, A.V.; Annapoorani, A.; Packiavathy, I.S.; Pandian, S.K. Evaluation of anti-quorum-sensing activity of edible plants and fruits through inhibition of the N-acyl-homoserine lactone system in Chromobacterium violaceum and Pseudomonas aeruginosa. Chemotherapy 2010, 56, 333–339. [Google Scholar]
- Song, C.; Ma, H.; Zhao, Q.; Song, S.; Jia, Z. Inhibition of quorum sensing activity by ethanol extract of Scutellaria baicalensis georgi. Plant Pathol. Microbiol. 2012, 7, 1–4. [Google Scholar]
- Bosgelmez-Tinaz, G.; Ulusoy, S.; Ugur, A.; Ceylan, O. Inhibition of quorum sensing-regulated behaviors by Scorzonera sandrasica. Curr. Microbiol. 2007, 55, 114–118. [Google Scholar]
- Truchado, P.; Giménez-Bastida, J.-A.; Larrosa, M.; Castro-Ibáñez, I.; Espín, J.C.; Tomás-Barberán, F.A.; García-Conesa, M.T.; Allende, A. Inhibition of quorum sensing (QS) in Yersinia enterocolitica by an orange extract rich in glycosylated flavanones. J. Agric. Food Chem. 2012, 60, 8885–8894. [Google Scholar]
- Alvarez, M.V.; Moreira, M.R.; Ponce, A. Antiquorum sensing and antimicrobial activity of natural agents with potential use in food. J. Food Safety 2012, 32, 379–387. [Google Scholar]
- Jaramillo-Colorado, B.; Olivero-Verbel, J.; Stashenko, E.E.; Wagner-Dobler, I.; Kunze, B. Anti-quorum sensing activity of essential oils from colombian plants. Nat. Prod. Res. 2012, 26, 1075–1086. [Google Scholar]
- Olivero, J.T.V.; Pajaro, N.P.C.; Stashenko, E. Antiquorum sensing activity of essential oils isolated from different species of the genus Piper. Vitae 2011, 18, 77–82. [Google Scholar]
- Zhu, H.; Liu, W.; Wang, S.; Tian, B.; Zhang, S. Evaluation of anti-quorum-sensing activity of fermentation metabolites from different strains of a medicinal mushroom, Phellinus igniarius. Chemotherapy 2012, 58, 195–199. [Google Scholar]
- Zhu, H.; Liu, W.; Tian, B.; Liu, H.; Ning, S. Inhibition of quorum sensing in the opportunistic pathogenic bacterium Chromobacterium violaceum by an extract from fruiting bodies of lingzhi or reishi medicinal mushroom, Ganoderma lucidum (w.Curt.:Fr.) p. Karst. (higher basidiomycetes). Int. J. Med. Mushrooms 2011, 13, 559–564. [Google Scholar]
- Ganin, H.; Rayo, J.; Amara, N.; Levy, N.; Krief, P.; Meijler, M.M. Sulforaphane and erucin, natural isothiocyanates from broccoli, inhibit bacterial quorum sensing. Med. Chem. Commun. 2013, 4, 175–179. [Google Scholar]
- Chong, Y.M.; Yin, W.F.; Ho, C.Y.; Mustafa, M.R.; Hadi, A.H.; Awang, K.; Narrima, P.; Koh, C.L.; Appleton, D.R.; Chan, K.G. Malabaricone c from Myristica cinnamomea exhibits anti-quorum sensing activity. J. Nat. Prod. 2011, 74, 2261–2264. [Google Scholar]
- Vandeputte, O.M.; Kiendrebeogo, M.; Rajaonson, S.; Diallo, B.; Mol, A.; El Jaziri, M.; Baucher, M. Identification of catechin as one of the flavonoids from Combretum albiflorum bark extract that reduces the production of quorum-sensing-controlled virulence factors in Pseudomonas aeruginosa PA01. Appl. Environ. Microbiol. 2010, 76, 243–253. [Google Scholar]
- Koehn, F.E.; Carter, G.T. The evolving role of natural products in drug discovery. Nat. Rev. Drug Discov. 2005, 4, 206–220. [Google Scholar]
- Suga, H.; Smith, K.M. Molecular mechanisms of bacterial quorum sensing as a new drug target. Curr. Opin. Chem. Biol. 2003, 7, 586–591. [Google Scholar]
- Parsek, M.R.; Val, D.L.; Hanzelka, B.L.; Cronan, J.E., Jr.; Greenberg, E.P. Acyl homoserine lactone quorum-sensing signal generation. Proc. Natl. Acad. Sci. USA 1999, 96, 4360–4365. [Google Scholar]
- Dong, Y.H.; Gusti, A.R.; Zhang, Q.; Xu, J.L.; Zhang, L.H. Identification of quorum-quenching N-acyl homoserine lactonases from Bacillus species. Appl. Environ. Microbiol. 2002, 68, 1754–1759. [Google Scholar]
- Hentzer, M.; Givskov, M. Pharmacological inhibition of quorum sensing for the treatment of chronic bacterial infections. J. Clin. Invest. 2003, 112, 1300–1307. [Google Scholar]
- Givskov, M.; Nys, R.D.; Manefield, M.; Gram, L.; Maximilien, R.; Eberl, L.; Molin, S.; Steinberg, P.D.; Kjelleberg, S. Eukaryotic interference with homoserine lactone-mediated prokaryotic signalling. J. Bacteriol. 1996, 178, 6618–6622. [Google Scholar]
- Manefield, M.; de Nys, R.; Kumar, N.; Read, R.; Givskov, M.; Steinberg, P.; Kjelleberg, S. Evidence that halogenated furanones from Delisea pulchra inhibit acylated homoserine lactone (AHL)-mediated gene expression by displacing the AHL signal from its receptor protein. Microbiology 1999, 145, 283–291. [Google Scholar]
- Manefield, M.; Rasmussen, T.B.; Henzter, M.; Andersen, J.B.; Steinberg, P.; Kjelleberg, S.; Givskov, M. Halogenated furanones inhibit quorum sensing through accelerated LuxR turnover. Microbiology 2002, 148, 1119–1127. [Google Scholar]
- Ren, D.; Sims, J.J.; Wood, T.K. Inhibition of biofilm formation and swarming of Escherichia coli by (5Z)-4-bromo-5-(bromomethylene)-3-butyl-2-(5H)-furanone. Environ. Microbiol. 2001, 3, 731–736. [Google Scholar]
- Martinelli, D.; Grossmann, G.; Sequin, U.; Brandl, H.; Bachofen, R. Effects of natural and chemically synthesized furanones on quorum sensing in Chromobacterium violaceum. BMC Microbiol. 2004, 4, 25–34. [Google Scholar]
- Rasmussen, T.B.; Manefield, M.; Andersen, J.B.; Eberl, L.; Anthoni, U.; Christophersen, C.; Steinberg, P.; Kjelleberg, S.; Givskov, M. How Delisea pulchra furanones affect quorum sensing and swarming motility in Serratia liquefaciens MG1. Microbiology 2000, 146, 3237–3244. [Google Scholar]
- Heggers, J.P.; Cottingham, J.; Gusman, J.; Reagor, L.; McCoy, L.; Carino, E.; Cox, R.; Zhao, J.G. The effectiveness of processed grapefruit-seed extract as an antibacterial agent: II. Mechanism of action and in vitro toxicity. J. Altern. Complement. Med. 2002, 8, 333–340. [Google Scholar]
- Girennavar, B.; Cepeda, M.L.; Soni, K.A.; Vikram, A.; Jesudhasan, P.; Jayaprakasha, G.K.; Pillai, S.D. Grapefruit juice and its furocoumarins inhibits autoinducer signalling and biofilm formation in bacteria. Int. J. Food Microbiol. 2008, 125, 204–208. [Google Scholar]
- Vikram, A.; Jesudhasan, P.R.; Jayaprakasha, G.K.; Pillai, B.S.; Patil, B.S. Grapefruit bioactive limonoids modulate E. coli O157:H7 TTSS and biofilm. Int. J. Food Microbiol. 2010, 140, 109–116. [Google Scholar]
- Lamberte, L.E.; Cabrera, E.C.; Rivera, W.L. Activity of the ethanolic extract of propolis (EEP) as a potential inhibitor of quorum sensing-mediated pigment production in Chromobacterium violaceum and virulence factor production in Pseudomonas aeruginosa. Philipp. Agric. Sci. 2011, 94, 14–22. [Google Scholar]
- Rasmussen, T.B.; Skindersoe, M.E.; Bjarnsholt, T.; Phipps, R.K.; Christensen, K.B.; Jensen, P.O.; Andersen, J.B.; Koch, B.; Larsen, T.O.; Hentzer, M.; et al. Identity and effects of quorum-sensing inhibitors produced by Penicillium species. Microbiology 2005, 151, 1325–1340. [Google Scholar]
- Walker, T.S.; Bais, H.P.; Deziel, E.; Schweizer, H.P.; Rahme, L.G.; Fall, R.; Vivanco, J.M. Pseudomonas aeruginosa-plant root interactions. Pathogenicity, biofilm formation and root exudation. Plant Physiol. 2004, 134, 320–331. [Google Scholar]
- Daniels, R.; de Vos, D.E.; Desair, J.; Raedschelders, G.; Luyten, E.; Rosemeyer, V.; Verreth, C.; Schoeters, E.; Vanderleyden, J.; Michiels, J. The cin quorum sensing locus of Rhizobium etli CNPAF512 affects growth and symbiotic nitrogen fixation. J. Biol. Chem. 2002, 277, 462–468. [Google Scholar]
- Uroz, S.; Heinonsalo, J. Degradation of N-acyl homoserine lactone quorum sensing signal molecules by forest root-associated fungi. FEMS Microbiol. Ecol. 2008, 65, 271–278. [Google Scholar]
|Plant extracts||Melicope lunu-ankenda (leaves)|
Syzygium aromaticum (bud)
|E. coli [pSB401]|
E. coli [pSB1075]
C. violaceum CV026
P. aeruginosa PA01
P. aeruginosa lecA∷lux
|Garlic (bulbs)||P. aeruginosa||[7,20]|
|Vanilla planifolia (beans)||C. violaceum CV026|||
|Tremella fuciformis (whole)||C. violaceum CV026|||
|Panax notoginseng (flowers and roots)|
Areca catechu (seeds)
Prunus armeniaca (kernel of seed)
Prunella vulgaris (whole)
Nelumbo nucifera (leaves)
Punica granatum (bark)
Imperata cylindrical (stem)
P. ginseng (roots)
|C. violaceum CV026|
P. aeruginosa PA01
|Moringa oleifera (leaves and fruits)||C. violaceum ATCC 12472|||
|Capparis spinosa (fruits)||C. violaceum CV026|
|Laurus nobilis (fruits, flowers, leaves, bark)||C. violaceum ATCC 12427|||
|Acacia nilotica (green pod)||C. violaceum ATCC 12472|||
|Quercus virginiana (leaves)|
Chamaesyce hypericifolia (aerial)
Tetrazygia bicolor (leaves)
Conocarpus erectus (leaves)
Bucida burceras (leaves)
Callistemon viminalis (leaves, inflorescence)
|C. violaceum ATCC 12472|
C. violaceum CV026
Agrobacterium tumefaciens NTL4
|C. violaceum CV026|
C. violaceum 31532
P. aeruginosa PA01
E. coli O157:H7
|C. violaceum ATCC 12472|
C. violaceum CV026
P. aeruginosa PA01
|Scutellaria baicalensis||C. violaceum CV026|||
|Scorzonera sandrasica||C. violaceum ATCC 12472|
C. violaceum CV026
|Essential oils||Tea tree|
|C. violaceum CV026|||
|P. putida [pRK-C12)|
E. coli [pJBA132]
|Piper bredemeyeri (leaves)|
P. brachypodom (leaves)
P. bogotence (whole)
|C. violaceum CV026|||
|Bioactive metabolites||Phellinus igniarius||C. violaceum CV026|||
|Plant exudates||Exudates from pea (Pisum sativum)||Serratia liquefaciens MG44|
|Fungal extracts||Ganoderma lucidum||C. violaceum CV026|||
|P. aeruginosa PA01|
C. violaceum CV026
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