Detection of Quorum Sensing Signal Molecules and Identification of an Autoinducer Synthase Gene among Biofilm Forming Clinical Isolates of Acinetobacter spp.

Background Quorum sensing is a term that describes an environmental sensing system that allows bacteria to monitor their own population density which contributes significantly to the size and development of the biofilm. Many gram negative bacteria use N-acyl-homoserine lactones as quorum sensing signal molecules. In this study, we sought to find out if the biofilm formation among clinical isolates of Acinetobacter spp. is under the control of autoinducing quorum sensing molecules. Methodology/Principal Findings Biofilm formation among clinical isolates of Acinetobacter spp. was assessed and the production of signal molecules were detected with Chromobacterium violaceum CV026 biosensor system. Characterisation of autoinducers was carried out by mass spectrometric analysis. We have also reported the identification of an autoinducer synthase gene, abaΙ among the isolates that produce quorum sensing signal molecules and have reported that the mutation in the abaI gene influences their biofilm forming capabilities. Using a microtitre-plate assay it was shown that 60% of the 50 Acinetobacter spp. isolates significantly formed biofilms. Further detection with the biosensor strain showed that some of these isolates produced long chain signal molecules. Mass spectrometric analysis revealed that five of these isolates produced N-decanoyl homoserine lactone and two isolates produced acyl-homoserine lactone with a chain length equal to C12. The abaΙ gene was identified and a tetracycline mutant of the abaΙ gene was created and the inhibition in biofilm formation in the mutant was shown. Conclusions/Significance These data are of great significance as the signal molecules aid in biofilm formation which in turn confer various properties of pathogenicity to the clinical isolates including drug resistance. The use of quorum sensing signal blockers to attenuate bacterial pathogenicity is therefore highly attractive, particularly with respect to the emergence of multi antibiotic resistant bacteria.


Introduction
Acinetobacter spp. are gram negative aerobic coccobacilli that are ubiquitous in nature, persistent in the hospital environment, and cause a variety of opportunistic nosocomial infections [1]. Among the Acinetobacter genomic species, Acinetobacter baumannii is recognized as the species most frequently isolated from patients. Acinetobacter spp. have been isolated from various types of opportunistic infections, including septicemia, pneumonia, endocarditis, meningitis, skin and wound infection, and urinary tract infection [1]. The distribution by site of Acinetobacter infection does not differ from that of other nosocomial Gram-negative bacteria. Often, Acinetobacter spp. emerged as important pathogens in the intensive care unit (ICU) setting, and this is probably due to the increasingly invasive diagnostic and therapeutic procedures used in hospital ICUs [2]. As it is a multi-drug resistant organism, infections are difficult to treat [3], resulting in mortalities of 23% for hospitalised patients and 43% for patients under intensive care [4]. The Antimicrobial Availability Task Force of the infectious Diseases Society of America recently identified A. baumannii, along with Aspergillus spp., extended-spectrum b-lactamase producing Enterobacteriaceae, Vancomycin-resistant Enterococcus faecium, Pseudomonas aeruginosa and methicillin-resistant Staphylococcus aureus, as 'particularly problematic pathogens' for which there is a desperate need for new drug development [5]. Similarly, the SENTRY Antimicrobial Surveillance Program lists Acinetobacter spp. as the causative agent in 2.3 to 3.0% of health care-associated pneumonia and as the eighth most common pathogen (4.0%) isolated from ICU patients worldwide [6]. Thus, Acinetobacter spp. is emerging as an increasingly important multidrug resistant pathogen, spreading in hospitals, and causing severe adverse outcomes. Besides that, Acinetobacter spp. seems to be spreading from hospital to hospital, and it has caused endemic infections in various geographical areas through multiple hospital outbreaks. It has become a leading nosocomial pathogen in many hospitals as compared to other non-fermenting Gram-negative bacilli. Therefore, a new strategy in the successful treatment of Acinetobacter infections is an absolute necessity.
Most Acinetobacter spp. research to date has focused on cataloguing and understanding the variety of antimicrobial resistance genes and mechanisms found within the species [7,8,9,10]. It has been shown that A. baumannii forms biofilm with enhanced antibiotic resistance [11,12]. Biofilm formation is a trait closely related to pathogenicity. Bacteria form multicellular biofilm communities on most surfaces. Formation of these sessile communities and their inherent resistance to antimicrobial agents are at the root of many persistent and chronic bacterial infections. Biofilms represent microbial societies with their own defense and communication systems. According to a public announcement from the US National Institutes of Health more than 80% of all microbial infections involve biofilms [13,14].
Very little is known regarding factors required for biofilm formation in A. baumannii. A chaperone and a protein that are required for this process has been identified [15,16]. The expression of an operon, pgaABCD, encoding a poly N-acetyl glucosamine (PGA) extracellular matrix has been shown to have a role in biofilm formation [17,18].
There are reports suggesting that the autoinducer (AI), quorum sensing (QS) signal molecules play an important role in biofilm formation [19,20]. Studies on two fundamental bacterial smallmolecule signaling pathways: extracellular quorum-sensing signaling and intracellular cyclic dinucleotide signalling suggested how these two pathways may converge to control complex processes including multicellularity, biofilm formation, and virulence [19].
Cell-to-cell signalling is often mediated by the production of N-acyl-homoserine lactone (AHL) signalling molecules [21]. These are synthesized by the family of homologue proteins. They use the appropriately charged acyl carrier protein as the major acyl chain donor and S-adenosyl methionine, which provides the homoserine moiety [22]. To detect these signals, various biosensor strains have been constructed [23,24,25]. These biosensors have been used previously to show AHL productions in Acinetobacter spp. By using an Agrobacterium tumefaciens reporter strain it was shown that all the cultures produced two to four detectable signal molecules with different chromatographic patterns. In A. calcoaceticus BD413 supernatants four compounds were detected in a time-dependent manner, and maximal activity was reached at stationary phase [26]. There is a previous report on the AHLs produced by Acinetobacter baumanii and it has been shown that mutations in autoinducer synthesis lead to the formation of biofilms with abnormal structures in Acinetobacter baumannii [27].
In this study, we report the detection of AHL signal molecules among the 50 biofilm forming clinical isolates of Acinetobacter spp. from University of Malaya Medical Centre, Malaysia using the Chromobacterium violaceum CV026 biosensor monitor system. Mass spectrometry was used to identify the AHL signals produced by these isolates. An autoinducer synthase designated abaI has also been identified among these clinical isolates producing QS signal molecules, a mutant of this gene has been created and has been shown to influence the biofilm forming capabilities. The impairment in the biofilm formation was rescued by ethyl acetate extracts of the culture supernatants from the wildtype strain. These findings could allow further investigations into the antagonists of the QS signal molecules, which could inhibit biofilm formation among the clinical pathogens.

Quantification of Biofilm Formation Using Microtiter Plate Method
Quantification of biofilm produced by the 50 clinical isolates of Acinetobacter spp. revealed that 30(60%) isolates significantly formed biofilms under prolonged period of incubation (p value ,0.05). Figure 1 shows the graphical representation of the biofilm formation among all the 50 isolates. Quantification of biofilm formation after prolonged incubation periods showed that in all the 50 isolates 48 hrs incubation showed higher biofilm formation compared to 24 hrs of incubation (Fig. 1). Isolates with no change in OD over the control were classified as non-biofilm formers. The microtitre plate assay was done in triplicates and the data were pooled from these experiments. Thus the graph also shows the standard deviation.

Screening for AHLs Among the Isolates
When CV026 induction test was carried out for the detection of short chain AHLs, all the 50 isolates produced colourless colonies. This showed that none of these Acinetobacter spp. clinical isolates produced short chain AHL molecules. In CV026 inhibition test, 7 of the isolates marked as S1, S11, S53, S54, S93, S102, S117 tested positive for long-chain AHL production. They produced colourless colonies in the induced chromoplate, while the negative isolates produced purple colonies (Fig. 2). The CV026 induction test was done on the chromoplate and the positive colonies producing the AHLs are expected to produce purple colonies. None of the tested isolates were positive for the induction test. CV026 inhibition test was carried in a chromoplate to which the synthetic AHL was previously added. Here long-chain AHLs are expected to inhibit the induced CV026 and thus produce colourless colonies in the purple background. Seven isolates tested positive for long-chain AHLs.

Quantification of the AHLs by Well-diffusion Assay
AHLs were extracted and quantified by the well diffusion assay. Increasing amounts of AHL added to the wells in the well-diffusion assay caused increase in the size of induced and inhibited zones surrounding the wells in Chromobacterium violaceum CV026 (Fig. 3A). Standard curves were created by comparing log (amount of AHL) to surface area of the zones (Fig. 3A). Based on the standard curves, extraction efficiencies were calculated using DHL (Decanyl Homoserine Lactone) in case of long-chain AHLs and HHL (3-N-Hexanoyl homoserine lactone) in case of short-chain AHLs, using both acidified and nonacidified ethyl acetate. Approximately twice as much AHL was extracted when using acidified ethyl acetate as compared to non-acidified. Extraction efficiencies were tested on supernatants from Acinetobacter strains and it was observed that acidified extractions gave better yields as compared to the non-acidified extractions. Yields obtained were in the range of 1610 29 moles to 6610 29 moles of AHLs (Fig. 3B). These were later confirmed by quantification through mass spectrometry.

Mass Spectrometry and Structural Identification of the AHLs
Mass spectrometric analysis revealed the presence of C 10 AHLs in the tested 5 isolates (S1, S11, S54, S93 and S117) and other 2 isolates (S53, S102) produced AHLs with chain lengths C 12. Of the masses that were reported the only ones that seem to make sense are 284 and 282 as an AHL with a 12 carbon acyl chain, with the lower mass (282) containing a single alkene (Table 1). An alkene could be anywhere along the chain length, however it can be rationalized that it could be a dehydration product from a betahydroxy derivative. The retention time at a later time than the decanoyl standard fits well. These masses were found in samples 53 and 102, which well confirms the presence of chain lengths C 12 . The TIC trace of each sample (1,11,53,54,93,102,117) with overlaid common precursor ions are shown in Fig. 4.
Identification of abaI Gene in Acinetobacter spp.
Organisation of the abaI Region in Acinetobacter spp. (S117) The amplicon of the abaI gene from isolate S117 was further sequenced and analysed. Isolate S117 showed the maximum differences in the nucleotides and thus the aminoacid sequence of the autoinducer synthase protein when compared with the already reported abaI gene sequences. Hence this protein was chosen for all subsequent experiments. The BLAST analysis program revealed that the abaI gene identified in Acinetobacter spp. isolate S117 is 92% identical to the corresponding protein reported in recently published A. baumannii ATCC 17978 genome [28]. The AbaI protein shared 91% identity and 97% similarity with the already reported AbaI protein of A. baumannii M2 strain [27]. Further, the BLAST analysis also revealed that the AbaI protein exhibited 61% identity and 79% similarity to the acyl homoserine lactone synthase of Halothiobacillus neapolitanus c2, 65% identity and 75% similarity to the autoinducer synthesis protein of Acidithiobacillus ferrooxidans ATCC 53993, 47% identity and 67% similarity with autoinducer synthatase family protein of Burkholderia mallei ATCC 23344 and 49% identity and 63% similarity with N-acyl homoserine lactone synthase from Pseudomonas fluorescens. This sequence has already been submitted to the NCBI Genbank (Accession number HQ013310).

Mutation in the abaI Gene
The abaI gene from isolate S117 cloned into plasmid vector pCR 2.1-TOPO and transformed into chemically competenet E.coli cells. These cells carrying the wild type abaI gene was found to produce the same kind of AHL signal produced by S117 in the thin layer chromatography bioassay overlay (results not shown). The abaI::Tc mutant was further constructed which failed to produce any detectable signals using the biosensor strain (results not shown). The examination of the ability of the wild type and the abaI::Tc mutant to form biofilms showed that there was inhibition in the biofilm formation in the abaI::Tc mutant when compared to the wild type (Fig. 6A). The mutation complementation experiment with the ethyl-acetate extracts of the culture supernatants from wild type and the abaI::Tc mutants showed that the addition of ethyl-acetate extracts from the wild type cells restored the ability of the abaI::Tc mutants to form normal biofilms. But, the ethyl-acetate extracts from the abaI::Tc mutants failed to restore the biofilm forming capabilities in the abaI::Tc mutant (Fig. 6B).

Discussion
The current view of biofilm infections leads to the realization that their effective control will require a concerted effort to develop therapeutic agents that target the biofilm phenotype and community signalling-based agents that prevent the formation, or promote the detachment, of biofilms [29]. Several molecules have been associated with the coordination of activities of microorganisms within a community. These include AHL, oligopeptides, amino acids such as glutamate and aspartate, and fatty methyl esters. It is conceivable that one or more of these molecular signals may impact biofilm physiology [15,30].
QS is a regulatory mechanism which enables bacteria to make collective decisions with respect to the expression of a specific set of genes. These may include genes involved in biofilm formation and virulence. They play a key role in orchestrating the expression of exoproteases, siderophores, exotoxins and several secondary metabolites, and participate in the development of biofilms. It has been shown that in contrast to the other QS systems, the AHL-mediated QS signalling system appears to control genes essential for colonisation of eukaryotes across a large number of bacterial species. This process is facilitated by bacterial biofilms [29]. The high density of bacteria within biofilms has led to the speculation that quorum-sensing genes and AHL production may be fundamentally associated with biofilm physiology. It has been shown that mutations in autoinducer synthesis lead to the formation of biofilms with abnormal structures in Acinetobacter baumannii [27].
In our study, it is observed that about 60% of our clinical isolates of Acinetobacter spp. significantly formed biofilms under prolonged period of incubation. When investigations on the sources of isolation of these isolates were done, they were equally from the upper and lower respiratory tracts. All these isolates were also screened for the QS signal molecule production and 7 of these isolates effectively produced long chain AHL molecules by using the CV026 biosensor monitor system. On analysis of the biofilm forming capabilities of the 7 isolates that produced the long chain AHls, they all form biofilms significantly. The method presented here for screening pure cultures of Acinetobacter spp. for AHL production using the Chromobacterium violaceum CV026 monitor system has not been used previously. It is rapid and does not require sterile supernatants or AHL extractions from cultures. It also has the advantages of only requiring monitor strains and the ability of the strains tested to grow on LB media. Also about 6 strains can be tested on the same plate. The only limitation of this assay is that the detection limit lies within the scope of the signal monitor system CV026 that was used and this monitor system is poor in sensing some of the signal molecules.
In this study, it has been shown that among the 30 biofilm forming isolates, only 7 produced long-chain AHLs. This may be due to the fact that biofilm formation is a multifactorial event and QS signals are one of such factors. Genetic analysis of biofilm formation has led to the proposal that extracellular signals and quorum sensing regulatory systems are essential for differentiated biofilms. Hence, differentiated biofilms may also be the net result of many independent interactions, rather than being determined by a particular global Quorum Sensing system [31].
Further mass spectrometric analysis confirmed the presence of C 10 AHLs in the tested 5 isolates and other 2 isolates produced AHLs with chain lengths C 12. Of the masses that were reported the only ones that seem to make sense are 284 and 282 as an AHL with a 12 carbon acyl chain, with the lower mass (282) containing a single alkene (Table 1). An alkene could be anywhere along the chain length, however it can be rationalized that it could be a dehydration product from a beta-hydroxy derivative. The retention time at a later time than the decanoyl standard fits well. These masses were found in samples 53 and 102. In Table 1, it is shown that some strains produce a signal with an m/z of 274 that gives rise to a MS/MS product of 102 suggesting it is likely comprised of an HSL moiety. This could be due to the presence of minor quantity of 3-oxo-C11 HSLs. However, none of the clinical isolates tested produced 3-OH-C12 seen in the M2 strain described by Niu et al [27].
Further quantification of the QS molecules by well diffusion assay revealed that a minimum of approximately 2610 29 moles and a maximum of 6610 29 moles of AHLs were detected among the clinical isolates of Acinetobacter. Quantifications done by mass spectrometric analysis also confirms these values.
An autoinducer synthase gene in A. baumannii that was designated as abaI has already been identified and characterised. The deduced AbaI protein was highly similar to the members of the LuxI family. It has been shown that this autoinducer synthase was required for normal biofilm development [27]. In our study we have identified and analysed abaI gene which encodes a similar protein. The BLAST analysis revealed that the abaI protein has only 91% identity with the already reported protein, but still retains its function as a quorum sensing autoinducer synthase. Further, the similarity of the identified AbaI protein from S117 to various species of Burkholderia, Pseudomonas fluorescens and Acidithiobacillus ferrooxidans suggests a common origin of these genes.
In this study we have further cloned the abaI gene. The cloned gene was further mutated and a abaI::Tc mutant of the gene was created and the mutant was shown to have inhibition in the biofilm formation. This shows that the abaI gene product was required for biofilm formation (Fig. 6). The differences between the wild type and the abaI::Tc mutant clearly showed that abaI directed AHL pathway is required for efficient biofilm formation. The mutation complementation experiments reveal that the wild type phenotype can be restored.
This study has revealed that it is likely that QS regulation is important for biofilm development, but there is no reason to assume that this type of regulation is the only important effector. In a given setting, the biofilm associated community will exploit all available adaptive mechanisms and the corresponding network of regulatory activities (including QS) and it is not possible to unequivocally assign a specific determining regulatory factor for the structure/function relationship of the community. In conclusion, the use of simple methods for detection of AHLs and their involvement in biofilm formation have been presented. These methods can be used to determine to certain extent the type of AHLs produced as well as to study the increase in AHL concentration over time. Mass spectrometric analysis revealed the exact structure of these AHL molecules to be C10 and C12.
The identification of the abaI and the AHL signals will allow the identification of the antagonists that inhibit biofilm development. These antagonists may reduce the ability of Acinetobacter spp. to survive on environmental surfaces for extended periods, a key component of its ability to form biofilms and persistence in intensive care wards.

Bacterial Strains and Culture Conditions
Fifty strains that were identified as Acinetobacter spp. were obtained from the Diagnostic Bacteriology Laboratory, University Malaya Medical Centre (UMMC) between August 2003 to March 2004. The strains were obtained from invasive and non-invasive sites which include blood, tracheal secretion, sputum, throat swab, peritoneal fluid, wound, bronchial lavage, and urine. The details of the source of isolation of all these isolates have been listed ( Table 2). The identity of the isolates was confirmed using standard laboratory methods which include Gram-stain, colony morphology, lactose fermention, and reaction to the oxidase test [32]. The isolates were further reconfirmed to belong to the Acinetobacter baumannii/calcoaceticus complex using API20NE kit (bioMerieux, France). These isolates were all screened for the production of quorum sensing signal molecules. The test isolates were grown on LB (Difco).
The biosensor strains detect AHL signals by the activation of a reporter gene such as lacZ or lux or by the production of or inhibition of a purple pigment in Chromobacterium violaceum.  Chromobacterium violaceum, a Gram-negative bacterium commonly found in soil and water, produces the characteristic purple pigment violacein. Previously the authors described a violaceinnegative, mini-Tn5 mutant of Chromobacterium violaceum (CV026) in which pigment production can be restored by incubation with supernatants from the wild-type strain. This mutant was developed to be used as a general biosensor for AHLs. In CV026, violacein is inducible by all the AHL compounds evaluated with N-acyl side chains from C 4 to C 8 in length, with varying degrees of sensitivity. Although AHL compounds with N-acyl side chains from C 10 to C 14 are unable to induce violacein production, if an activating AHL is incorporated into the agar, these long-chain AHLs can be detected by their ability to inhibit violacein production. Chromobacterium violaceum strain CV026 was the monitor strain used to screen for AHL-producing Acinetobacter strains. The CviR (Chromobacterium violaceum Repressor) of Chromobacterium violaceum strain CV026 (Throup et al., 1995) [33] regulates the production of a purple pigment when induced by AHL. Certain long-chained AHLs reversibly inhibit the induced CviR resulting in a lack of pigment when compared to a control. The CV026 strain was routinely grown in a shaker incubator in Luria Bertani broth (LB) (1% peptone, 0.5% yeast extract, 0.5% NaCl; PH 7.00) (Bertani, 1951) [34] solidified with 1.25% agar when required and supplemented with 20 mg/ml of kanamycin. For screening AHLs, TY medium containing (per liter) 8 g of Bacto Tryptone (Difco Laboratories), 5 g of yeast extract, and 5 g of NaCl (pH 7) was used.

Quantification of Biofilm Formation Using Microtiter Plate Method
Biofilm formation was determined by the ability of cells to adhere to the base of 96-well polystyrene plate using the method of Boddey et al [35] with modification. Briefly, 100ml of LB broth was added into each well of sterile 96-well polystyrene plate followed by the addition of 1ml of bacterial culture that was grown at 37uC overnight with shaking at 150 rpm. The plate was incubated without shaking at 37uC for 18 hours. Thereafter, 1 ml from each well was transferred into triplicate wells of a fresh 96-well plate containing 100 ml of fresh LB and the plates incubated without shaking for 24 hours at 37uC. Following incubation the supernatant was discarded carefully and the wells were stained with 150ml of 1% crystal violet at room temperature for 30 minutes. The stain was then removed and the wells were washed twice with 175 ml sterile deionized water, before the addition of 175 ml of dimethyl sulfoxide (DMSO) to solubilize the crystal violet. The plate was then read spectrophotometrically at an absorbance wavelength of 570 nm. For each strain the assay was run in triplicate wells and in three independent experiments. Wells containing only the medium was used as control. The same protocol was followed to quantify the biofilm after prolonged incubation at 37uC for 48 hours and then they were compared to the biofilms formed after incubation for 24 hours.

Statistical Analysis
The significance of the biolfilms formed by the 50 isolates were statistically analysed by using a one-way analysis of variance (ANOVA) with post hoc multiple comparisons. The P value was less than 0.05. All the statistical tests were performed by SPSS software.

Screening for AHL
Screening for AHL production among the 50 isolates was done as follows: A fresh plate of C.violaceum CV026 was prepared on LB agar plates containing 20 mg/ml kanamycin. This plate was incubated overnight at 37uC. A loopful of cells was taken and resuspended in 10 ml of sterile water and adjusted to an OD 600 nm of approximately 0.4. Then 5 ml of this culture was added to 200 ml of cooled TY agar and poured as a thin plate. The test strains were grown separately in 5 ml of TY broth for 24 hours and then diluted to an OD 600 nm of 1.0. About 5 ml drops of the test strains were then added to the previously prepared chromoplate and allowed to dry. The tests are done in duplicate and incubated for 2-3 days at 28uC. This test can detect the presence of short chain AHL producing test strains. For detecting the long chain AHLs producing test strains a variant of this test was carried out in which the chromoplate was prepared along with 75 nM concentration of N-Hexanoyl Homoserine lactone (HHL) incorporated in the medium. Monitor strains themselves served as negative control and monitor strains in plate containing 75 nM HHL served as positive control. The basic concept of this method was adopted from McClean et al 1997 [23]. This method was previously not used for directly screening AHL producing bacteria. Figure 5. The electrophoretic banding patterns of the PCR products using the primers for the abaI gene. Lane 1-100bp DNA ladder, lane 2, 3, 4, 5, 6, 7, 8-amplicons from isolates S1, S11, S53, S54, S93, S102 and S117 respectively, lane 9-Negative control. doi:10.1371/journal.pone.0036696.g005

Extraction of Culture Supernatants for Mass Spectrometry
Extractions for Mass Spectrometry (MS) were prepared as described by Shaw et al 1997 [24] with minor modifications. Tenmilliliter volumes of the bacterial cultures were centrifuged and the supernatants were extracted with an equivalent volume of ethyl acetate acidified by supplementing with 0.5% formic acid. The mixture was shaken vigorously for 30 seconds and the two phases were allowed to separate. The shaking was repeated three times before the ethyl acetate containing fraction was removed and another 10 ml fraction was added. The whole extraction process was repeated three times. The combined extracts were dried filtered and evaporated to dryness. Residues were dissolved in 50-100 ml of HPLC-grade ethyl acetate. Comparisons were made of

Well-diffusion Assays
Quantifications of the AHLs produced by the test strains can be done by well-diffusion assays. This was done as described by Ravn et al 2001 [36] with some modifications. The agar plates were prepared as follows: a preculture of Chromobacterium violaceum CV026 was grown in LB for 24 hours at 25uC with aeration and 2 ml of the preculture was used to inoculate 100 ml of LB broth. The culture was grown for 24 hours at 25uC with aeration and was poured into 200 ml of LB agar (1.2% agar) containing 20 mg/ml kanamycin maintained at 46uC. The agar culture solution was immediately poured as 20 ml portions in petri dishes. Fifty ml volumes of AHL containing solutions (either the standard or the extraction from culture supernatants) were pipetted into wells (6 mm) punched in the solidified agar. The plates were incubated at 25uC for 48 hours before the diameter of the AHL induced zones surrounding the wells was measured. For the inhibition of the induced CV026, the LB-agar was supplemented with 75 nM Nhexanoyl L-homoserine lactone (HHL, Sigma-Aldrich).

Mass Spectrometry
Extracts were also subjected to Mass Spectrometric analysis. Sample pellets were re-suspended in a mixture of 50% acetonitrile:distilled water 0.1% formic acid (200 mL) initially using a pipette, then sonicated for several minutes. The samples were centrifuged for 5 minutes at maximum rpm and then the supernatant was carefully removed and transferred to a new vial. 10 mL of each sample was transferred to a sample vial with insert and diluted 1 in 5 by addition of 50% acetonitrile, 0.1% formic acid (40 mL). An Agilent 6420 LC-ESI-QQQ using a dynamic multiple reaction monitor (DMRM) was used for quantification. Instrument conditions were: Gas Temperature: 300uC, Gas Flow:   spectra/s with a maximum of 5 precursors selected and fragmented using collision energy of 25V. Precursors were excluded after 1 spectra for a period of 30 seconds. The standards of beta-ketocaproyl, hexanoyl, heptanoyl, octanoyl and decanoyl were diluted using 100% acetonitrile. The diluted standards were mixed to provide a stock solution containing all standards with the following concentrations: 0.1, 0.5, 1, 5, 10, 50, 100, 500, 1000, 5000 and 10,000 micromolar (mM). A standard curve was run between the concentrations and in each case a curve was fit over the appropriate range, with a linear curve attempted in all cases, except where high concentration points were required. For the experiment where concentrated samples were tested a limited concentration range 0.1 mM -100 mM was used, this significantly reduced signal suppression and turnover of the standard curve. Quantification of AHLs in the sample was done using these standard curves.
Identification of abaI Gene in Acinetobacter spp.

Producing the QS Signal Molecules
The presence of abaI gene encoding an autoinducer synthase was identified by polymerase chain reaction (PCR) using already published primers [27], F-59-GTACAGTCGACGTATTTGTT-GAATATTTGGG-39 and R-59-CGTACGTCTAGAGTAAT-GAGTTGTTTTGCGCC-39. The final PCR amplification reaction mixture contained 5.0 mM PCR buffer, 8.3 mM MgCl 2 , 200 nM dNTP (MBI, Fermentas, Vilnius, Lithuania), 0.3 mM of each primer pair, 2 units of Taq DNA polymerase (MBI, Fermentas) and 3 ml of DNA template in a final volume of 25 ml. The PCR amplification was performed with mycyler thermocycler (BioRad laboratires, Hercules, CA) with the following PCR temperature cycling parameters: Initial denaturation at 94uC for 10 minutes followed by 30 cycles of denaturation at 94uC for 30 seconds, Primer annealing at 66.5uC for 30 seconds, primer extension at 72uC for 1 minute and the final extension at 72uC for 5 minutes. The resulting amplicons of the isolate S117 has been sequenced and it's organisation in the genome was analysed.

Mutation in the abaI Gene
The abaI gene from isolate S117 was further cloned into plasmid vector pCR 2.1-TOPO using the TOPO TA cloning kit (Invitrogen Corporation, California) following the manufacturer's instructions. The PCR purification of the abaI gene was done using the Expin PCR purification kit (GeneAll Biotechnology, Korea) before cloning. The cloned abaI gene was disrupted by insertional inactivation using tetracycline gene cassette at the SspI site (blunt end ligation) within the abaI gene. The insertion of tetracycline gene in the coding region of the abaI gene that prevented the production of the AHL signal was identified using the biosensor strain. To inactivate the abaI gene in the chromosome of the Acinetobacter spp. S117, the insertion that disrupted the abaI gene in the middle along with the flanking chromosomal DNA was cloned into pUC18-based suicide delivery vector. This plasmid pUC18.abaI::Tc was introduced into Acinetobacter spp. S117 by conjugation. E.coli K12 carrying the pUC18.abaI::Tc plasmid was the donor. Matings were performed on filter membrane. Following conjugation, the suicide vector pUC18.abaI::Tc would be integrated at the wildtype abaI gene, that results in the wildtype copy of the abaI gene and second copy with the abaI::Tc disruption. These exconjugants with both the wildtype and the mutant copy of the abaI gene (single crossover event) were selected based on their tetracycline and ampicillin resistance (tetracycline marker was present on the disrupted abaI gene and ampicillin marker was on the pUC18 vector). Following this, the exconjugants were grown without the antibiotic pressure. This removes the pressure to maintain the plasmid integration. Then the exconjugants that carry only the mutant abaI gene (double crossover event) were selected by eliminating any bacteria that have maintained the plasmid integration and selecting the bacteria that does not grow in the presence of the vector marker (ampicillin). The mutation was confirmed by PCR to get wildtype PCR products followed by sequencing. The abaI::Tc mutants failed to produce any AHL signals and were further evaluated for their biofilm forming capabilities and compared with the biofilm formation in the wild type abaI gene. The biofilm formation was done as described previously in microtiter plate. To demonstrate that the biofilm inhibition in the mutant was due to the loss of the AHL signal, mutation complementation experiment with the exogenously added AHLs as the ethyl-acetate extracts of the culture supernatants from the wildtype and the mutants was performed. Only ethyl-acetate was added in the negative control samples.