Abstract
Drug resistance and tolerance greatly diminish the therapeutic potential of antibiotics against pathogens. Antibiotic tolerance by bacterial biofilms often leads to persistent infections, but its mechanisms are unclear. Here we use a proteomics approach, pulsed stable isotope labelling with amino acids (pulsed-SILAC), to quantify newly expressed proteins in colistin-tolerant subpopulations of Pseudomonas aeruginosa biofilms (colistin is a ‘last-resort’ antibiotic against multidrug-resistant Gram-negative pathogens). Migration is essential for the formation of colistin-tolerant biofilm subpopulations, with colistin-tolerant cells using type IV pili to migrate onto the top of the colistin-killed biofilm. The colistin-tolerant cells employ quorum sensing (QS) to initiate the formation of new colistin-tolerant subpopulations, highlighting multicellular behaviour in antibiotic tolerance development. The macrolide erythromycin, which has been previously shown to inhibit the motility and QS of P. aeruginosa, boosts biofilm eradication by colistin. Our work provides insights on the mechanisms underlying the formation of antibiotic-tolerant populations in bacterial biofilms and indicates research avenues for designing more efficient treatments against biofilm-associated infections.
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Introduction
The therapeutic efficacy of antibiotics can be severely crippled by two major bacterial defence strategies. ‘Resistance’ occurs when bacteria acquire genetic mutations or mobile genetic elements that enable growth under conditions of constant antibiotic exposure1, while ‘tolerance’ is mediated by transient phenotypic variations (based on protein expression) that enable bacteria to survive exposures to the highest deliverable doses of antibiotics2,3.
While the current view is that development of tolerance is intrinsically linked to the biofilm lifestyle, early experiments conducted on bacteria in the planktonic lifestyle revealed that tolerance can develop to a number of stresses including antibiotics4,5. However, in contrast to the planktonic mode of life, biofilms are sessile, densely populated multicellular communities embedded in biopolymeric matrix components6. A major advantage for bacteria that aggregate into biofilms is that a multitude of matrix components and physiological states offers additional levels of protection against immune defences and antibiotics, which cannot be obtained in the planktonic growth mode7,8,9. It is widely accepted that pathogenic bacteria in the biofilm mode significantly contribute to the development of nosocomial infections as they are colonizing hospital settings and chronic infection sites, where they represent a serious threat to public health6. Bacterial cells differentiate into several physiologically distinct subpopulations within a biofilm10. Antibiotic treatment often eradicates sensitive subpopulations, but leaves small antibiotic-tolerant subpopulations behind, resulting in recurring infections after antibiotic treatment has been stopped10. Antibiotic-tolerant bacterial cells are variants of wild-type cells that can revert back to the wild type when antimicrobial treatment has ceased11. Their transient nature and low abundance make it difficult to investigate their tolerance-related physiology.
With only a few studies that have investigated planktonic antibiotic-tolerant cells by pre-isolating them using flow cytometry12,13,14,15, the mechanisms underlying the formation of antibiotic-tolerant subpopulation in biofilms have remained elusive. Moreover, these pre-isolation-based strategies are destructive and not feasible for studying the antibiotic-tolerant subpopulations in biofilms. This prompted us to develop an alternative, high-resolution ‘-omics’ approach to simultaneously characterize the physiologies of sensitive and antibiotic-tolerant subpopulations in biofilms.
Pseudomonas aeruginosa forms biofilm with extreme tolerance to antibiotics in nosocomial infections, such as pneumonia and surgical site infections, prompting the Centers for Disease Control and Prevention to classify P. aeruginosa under ‘serious’-threat level (http://www.cdc.gov/drugresistance/threat-report-2013/) and the Infectious Diseases Society of America to declare it as one of the six ‘top-priority dangerous, drug-resistant microbes’16. Colistin is a last-resort polymyxin antibiotic available for treatment of infections caused by drug-resistant Gram-negative bacteria17. P. aeruginosa biofilms in flow chambers develop colistin-tolerant cells rapidly and these cells feature high expression levels of the pmr operon18.
Here we observe the dynamic development of drug-tolerant subpopulations in P. aeruginosa biofilms after treatment with colistin. To obtain knowledge about the physiology of the colistin-tolerant biofilm cells, we apply pulsed stable isotope labelling with amino acids (pulsed-SILAC) proteomics method to selectively quantify the newly expressed proteins that incorporate and are thus labelled with heavy C13 lysine, to promote understanding of the colistin-tolerant subpopulation physiology. The colistin-tolerant populations are able to migrate to the top of the dead biofilm by employing type IV pili-dependent motility and initiate formation of new biofilm via quorum sensing (QS)-regulated group activity. Synergistic treatment by use of erythromycin, which can inhibit QS and motility with colistin, is able to boost the elimination of P. aeruginosa biofilms. Hence, our study provides key insights in developing novel treatments against biofilm-associated infections, which otherwise prove hard to eradicate.
Results and Discussion
Development of colistin-tolerant subpopulations in biofilms
We monitored the development of live and dead subpopulations of P. aeruginosa biofilms after exposure to colistin in real-time by using time series confocal image acquisition as well as enumeration of viable cells with colony forming units (c.f.u. per ml). Colistin exposure of P. aeruginosa wild-type biofilms tagged with green fluorescent protein (GFP) led to a sudden reduction in cell viability according to the propidium iodide (PI) dead staining (Fig. 1a and Supplementary Movies 1 and 2) and c.f.u. per ml counting (Fig. 1b). However, we noticed that a few P. aeruginosa cells localized at the substratum of the biofilms remained alive even after 24 h of colistin treatment (Fig. 1a), which might result from the heterogeneous compositions/structures of the exopolymeric matrix materials19,20. Certain exopolymeric matrix components might act as physical barriers and reduce the penetration of colistin into deep part of biofilms21, which allows a few biofilm cells at the substratum to survive and acquire colistin tolerance.
Interestingly, we observed that colistin-tolerant subpopulations were able to migrate towards the top of the large microcolonies of dead P. aeruginosa biofilm cells (Fig. 1a,b and Supplementary Movies 3 and 4). Tracking of colistin-tolerant cell aggregates close to the large microcolonies revealed that those aggregates moved towards the dead microcolonies (Fig. 1c and Supplementary Movies 3 and 4)—a migration that was unrelated to the flow direction of the culture medium (from top to bottom of the image). In contrast, single colistin-tolerant cells far away from the large microcolonies appeared randomly distributed (Fig. 1c and Supplementary Movies 3 and 4). These results suggested that migration of colistin-tolerant cell aggregates towards large microcolonies of dead biofilm cells was a coordinated process that might involve specific signals.
Colistin-tolerant cells obtained from biofilms only showed transient expression of the pmr operon (Supplementary Fig. 1a) and lost their colistin tolerance after overnight culturing in ABTGC medium containing no colistin (Supplementary Fig. 1b,c), supporting our view that the colistin-tolerant cells were the result of phenotypic variation and not per se resistant cells. DNA sequencing of the biofilms with and without colistin treatment showed that there was no convergent non-synonymous mutation gained by the three colistin-treated biofilm populations compared with the control biofilm populations (Supplementary Data 1). The development of motile colistin-tolerant subpopulations in biofilms has major clinical implications as they can result in persistent infections.
Using pulsed-SILAC to study colistin-tolerant subpopulations
To further understand the process that caused the directed motility and formation of colistin-tolerant biofilm subpopulations, we further used the pulsed-SILAC quantitative proteomic approach, with the aim of studying new proteins’ abundance in the colistin-tolerant subpopulations formed by P. aeruginosa biofilms after a high-dose colistin treatment (Fig. 2a). We hypothesized that the actively expressed proteins in the colistin-tolerant subpopulations provided the survival advantages to the bacteria. SILAC is a simple and fast but powerful in vivo method, commonly used for eukaryotes to label proteins for mass spectrometry (MS)-based quantitative proteomics22. Although this method had been used in labelling prokaryotes to compare biofilm and planktonic cells23,24, pulsed-SILAC had never been employed to determine new proteins’ abundance in the antibiotic-sensitive and -tolerant subpopulations coexisting in the same bacterial biofilm.
A P. aeruginosa mutant that cannot synthesize lysine, mPAO1ΔlysA, was employed to form biofilms in medium supplemented with C12 L-lysine. Although this mPAO1ΔlysA mutant could only grow in the presence of L-lysine (Supplementary Fig. 2), it formed biofilms similar to wild-type mPAO1 when lysine was added to the culture medium (Supplementary Fig. 3). Biofilms were treated with high doses of colistin at 10 μg ml−1 (10-fold higher than the minimum bactericidal concentration) in minimal medium supplemented with C12 L-lysine for 8 h. After killing the antibiotic-sensitive population, the remaining surviving antibiotic-tolerant cells were then treated with fresh medium containing colistin and C13 L-lysine for 48 h to incorporate C13 L-lysine into the newly expressed proteins of only live cells (Fig. 2a).
This pulsed-labelling approach allowed for selective tagging of newly expressed proteins in the antibiotic-tolerant subpopulations, with C13 L-lysine without prior physical isolation. The level of new protein abundance could be normalized by dividing the relative abundances of C13 L-lysine-tagged proteins (proteins expressed after colistin treatment) with the relative abundances of C12 L-lysine-tagged proteins (proteins expressed before colistin treatment).
We used Q Exactive MS to analyse the pulsed-SILAC labelled samples, followed by the MaxQuant and Andromeda software25,26 to identify 4,250 P. aeruginosa proteins with <1% false discovery rate (FDR). Only proteins that were significantly and consistently changed/regulated in three biological replicates (variability <30%) were shortlisted for further analysis (Supplementary Data 2). Lowly and highly expressed proteins in the colistin-tolerant subpopulation as compared with the colistin-sensitive population are functionally grouped in Fig. 2b,c, respectively, while the complete list of lowly and highly expressed proteins are listed in Supplementary Data 3 and 4, respectively.
Our initial analysis of the data showed that some of the actively expressed proteins were subunits of ribosomes (Supplementary Data 4), supporting the notion that colistin-tolerant cells are metabolically active27. We also found that the bifunctional polymyxin-resistance proteins ArnA and PmrA were expressed at a high level in antibiotic-tolerant cells (Supplementary Data 2, markers intensity sheet: ArnA (intensity L:H=1.51E+10:4.58E+10); PmrA (intensity L:H=5.26E+09:1.12E+10)). The arnBCADTEF lipopolysaccharide-modification operon had been shown to be controlled by the upstream pmr operon and contribute to the tolerance to polymyxin B and colistin in P. aeruginosa28. Hence, both proteins served as positive controls and showed that pulsed-SILAC was highly reliable in detecting proteins important in colistin tolerance. These two markers were consistently detected with high abundance level in the heavy C13 lysine-labelled proteins in seven out of eight technical replicates of the three biological replicates except in BR1:R2, where ArnA was not detected in the light C12 condition, and PmrA was not detected in both H and L conditions due to technical variation (Supplementary Data 2, markers intensity sheet). The missing detection of marker proteins in BR1:R2 might be attributed to growth variations during biofilm cultivation as biofilm experiments normally require a long cultivation period (5 days).
Pili and QS led to colistin tolerance
Interestingly, we found that antibiotic-tolerant subpopulations also expressed proteins required for type IV pili assembly, such as PilF (ref. 29, at high levels (Supplementary Data 4). Hence, we hypothesized that type IV pili are required for the migration of colistin-tolerant cell aggregates onto the dead microcolonies. Migration of colistin-tolerant subpopulations was decreased in biofilms formed by the type IV pili mutant, ΔpilA (Fig. 3a,b). Complementation of ΔpilA with pDA2, a plasmid containing the pilA gene in a pUCP18 vector, restored the antibiotic-tolerant phenotype (Fig. 3a,b).
Furthermore, we found that QS-regulated proteins, including LasB, chitinase and phenazine/pyocyanin-synthesis (Phz) proteins, were highly expressed in colistin-tolerant antibiotic-tolerant subpopulations (Supplementary Data 4). Because QS coordinates group behaviour in biofilms30, we thus hypothesized that QS coordinates the development of antibiotic-tolerant microcolonies within biofilms. The QS null mutant, ΔlasIΔrhlI, developed less antibiotic-tolerant subpopulations in response to colistin treatment than the wild type (Fig. 3a,b). Chemical complementation by the addition of 1 μM N-3-(oxododecanoyl)-L-homoserine lactone (OdDHL) (a QS signalling molecule) to ΔlasIΔrhlI biofilms allowed ΔlasIΔrhlI to regain the development of colistin-tolerant subpopulations (Fig. 3a,b). We further showed that biofilms formed by a QS and type IV pili-defective triple mutant, ΔpilAΔlasRΔrhlR, could only develop a negligible amount of antibiotic-tolerant subpopulations in response to colistin treatment as compared with the wild type (Fig. 3a,b).
We found that type IV pili-mediated migration preceded induction of QS activity in the colistin-tolerant subpopulations. The QS reporter lasB-gfp translational fusion31 was highly expressed in antibiotic-tolerant subpopulations of wild-type biofilms but not in the antibiotic-tolerant subpopulations of ΔpilA biofilms in response to colistin exposure (Fig. 4a). Colistin-tolerant biofilms produced more OdDHL, the QS autoinducer, than wild-type biofilms (Fig. 4b). In response to colistin treatment, colistin-tolerant wild-type biofilms also secreted more elastase and pyocyanin than untreated biofilms, which correlates with our proteomic data that LasB and pyocyanin-synthesis proteins were highly expressed in colistin-tolerant biofilm cells (Fig. 4c,d).
Given the active expression of virulence factors in the colistin-tolerant subpopulations, we evaluated the macrophage-killing capacity of supernatants from wild-type biofilms with and without colistin treatment by using the mouse RAW264.7 cell line. After staining the dead macrophages with 20 μM PI, we observed that the supernatant from colistin-treated biofilms was more cytotoxic to macrophages than that of control biofilms (Supplementary Fig. 4). Induction of QS-regulated virulence factors in colistin-tolerant microcolonies is clinically relevant because they are detrimental to the host immune system32,33,34,35,36.
It is unclear why the colistin-tolerant cell aggregates migrate to the top of dead biofilms. Our previous work demonstrated that the motile subpopulation of the wild-type P. aeruginosa biofilms migrate towards the non-motile subpopulation to seek iron source37. We hypothesized that the tolerant cells migrate to acquire iron. To test this hypothesis, we added the iron chelator 2,2-dipyridyl (DIPY)38 together with colistin to treat P. aeruginosa wild-type biofilms. We found that DIPY was able to interfere with the development of colistin-tolerant subpopulations associated with the dead microcolonies (Supplementary Fig. 5).
Hence, in addition to mechanisms directly involved in antibiotic tolerance, we showed that multicellular behaviours such as migration and cell–cell signalling (QS) are important in the recovery of pathogenic biofilms that can survive the otherwise lethal antibiotic treatments. Since clinical departments only test for resistance (growth versus no growth on medium supplemented with antibiotics) before the commencement of antibiotic treatments of the patient, the development of antibiotic-tolerant subpopulations in response to exposures can be considered a concealed mechanism of antibiotic recalcitrance.
Chemical Approach to combat colistin-tolerant subpopulations
Given that both type IV pili-mediated migration and QS are required for establishing antibiotic-tolerant subpopulations in developing P. aeruginosa biofilm, we employed a chemical biology approach to disable these activities. Macrolides, which can inhibit type IV pili assembly and QS in P. aeruginosa39, were used in combination with colistin to treat P. aeruginosa biofilms.
Treatment with erythromycin had a mild killing effect on biofilm cells and planktonic cells (Fig. 5a–c, respectively), implying that erythromycin was unable to kill the biofilms. However, combination treatments with erythromycin and colistin lead to complete eradication and repression of the development of antibiotic-tolerant subpopulations (Fig. 5a,b). Supporting that our combination treatment was specific to the colistin-tolerant cells present in the biofilm mode of life, we did not observe the synergistic effect of colistin and erythromycin against planktonic P. aeruginosa at concentrations equivalent to that of the biofilm treatment (Fig. 5c).
To verify the functional eradication of antibiotic-tolerant cells by both antibiotics in vivo, we used a murine model for implant-associated infection40. As opportunistic infections on the host could occur when biofilm is formed on implants such as catheters and heart valves, treatments that prevent the rise of antimicrobial-tolerant or -resistant populations are essential41,42. Implants coated with P. aeruginosa biofilms were surgically inserted into the peritoneum of mice. The mice were treated locally with antibiotics to emulate the treatment given to patients with infections from implants. The concentration of antibiotics (1 mg kg−1 colistin and 10 mg kg−1 erythromycin) used for each mouse was well below the median lethal dose of each antibiotic (86 mg kg−1 colistin and 280 mg kg−1 erythromycin), ensuring the non-lethal treatment of P. aeruginosa biofilm in the mouse.
The c.f.u. per ml count of P. aeruginosa from the implant and spleen after 24 h incubation in the mouse revealed that administration of colistin or erythromycin alone did not eradicate the infection. However, synergistic treatments with colistin and erythromycin eradicated the biofilm to the limit of detection by c.f.u. per ml (Fig. 5d). Since we were unable to detect live bacterial cells in the spleen samples, we concluded that the spread of infection was also halted (Fig. 5e). Hence, supplementing conventional antibiotic treatment with a tolerance-interfering compound appears to be a promising therapy for eradicating biofilm-associated infections.
The association between type IV pili and the colistin-tolerant subpopulations in developing P. aeruginosa biofilm has been presented previously18, whereas the position in a nutrient-rich microenvironment seems to be important for the development of colistin-tolerant subpopulations in more mature P. aeruginosa biofilms27. We here tracked the formation of antibiotic-tolerant subpopulations in developing P. aeruginosa biofilms and used pulsed-SILAC to selectively label their proteome to determine new protein abundance in the antibiotic-tolerant subpopulations, which led to the identification of multiple genes/proteins essential for the development of antibiotic-tolerant biofilm.
We propose the following model for the development of colistin-tolerant subpopulations in developing P. aeruginosa biofilm, which links it to the ‘phoenix effect’ (Fig. 6): (a) the majority of the biofilm is killed by colistin treatment; (b) surviving antibiotic-tolerant cell aggregates overexpress type IV pili for targeted migration to the top of the dead biofilm; (c) and produce QS-regulated factors for promoting the formation of new antibiotic-tolerant microcolonies. The microcolony size in our in vitro P. aeruginosa biofilms is around 50 μm, which is within the range of microcolony sizes identified from in vivo43,44 and ex vivo45,46 P. aeruginosa biofilms. This suggested that colistin might have similar effects on in vivo P. aeruginosa biofilms as those observed on our in vitro P. aeruginosa biofilms.
Furthermore, our study showed that targeting mechanisms important to antibiotic-tolerant cells greatly improved conventional biofilm treatment strategies. It highlighted the importance of developing QS and motility inhibitors that can be given to chronically infected patients, with the aim of constituting functional anti-biofilm chemotherapies. This strategy might also be applied to other complex differentiated communities, such as cancer, as a recent study revealed the presence of motile drug-tolerant cells in chemotherapy-treated cancer cell populations47.
Methods
Bacterial strains and growth conditions
The bacterial strains and plasmids used in this study are listed in Supplementary Table 1. P. aeruginosa strains were grown at 37 °C in ABT minimal medium48 supplemented with 5 g l–1 glucose (ABTG) or 2 g l−1 glucose and 2 g l–1 casamino acids (ABTGC). For marker selection in P. aeruginosa, 30 μg ml−1 gentamicin and 200 μg ml−1 carbenicillin were used as appropriate.
Cultivation of biofilms in flow chambers
MiniTn7-gfp-tagged P. aeruginosa biofilms were cultivated in ABTG medium at 37 °C using 40 mm × 4 mm × 1 mm three-channel flow chambers. Flow chambers were assembled as described previously, consisting of a flow cell that acted as a chamber for the growth of biofilms49. The flow cell was supplied with a flow of medium and oxygen, while waste medium was removed into a waste flask, by using a peristaltic pump. Each flow channel was inoculated with 300 μl of a 1:1,000 dilution of an overnight culture using a syringe and was incubated without flow for 1 h. Medium flow was started and maintained at a velocity of 0.2 mm s−1 by the A Cole-Palmer peristaltic pump. After 72 h of growth, PAO1 biofilms were treated with 10 μg ml−1 colistin. After 48 h of treatment, 300 μl of 20 μM PI was injected into each flow channel to stain dead cells in the biofilm. Experiments were performed in triplicate, and results are shown as the mean±s.d.
Reversion of antibiotic-tolerant phenotype in biofilms
MiniTn7-gfp-tagged and pmr-gfp-tagged P. aeruginosa biofilms were cultivated and treated with colistin as described above. Colistin-containing ABTG medium was switched to antibiotic-free ABTG to allow the reversion of antibiotic-tolerant phenotype back to normal biofilm for 48 h. To examine whether the antibiotic-tolerant phenotype can be re-induced, the biofilms were challenged with 10 μg ml−1 colistin for the second cycle. A volume of 300 μl of 20 μM PI was injected into each flow channel to stain dead cells in the biofilm. Biofilms were observed at 0 and 4 h after the second challenge of colistin.
Reversion of antibiotic-tolerant cells in planktonic cultures
PAO1 and PAO1/pmr-gfp biofilm containing the live colistin-tolerant subpopulations and dead colistin-sensitive subpopulations were obtained from the flow chamber biofilm by flushing out the entire biofilm with 5 ml of 0.9% NaCl. The biofilm was homogenized by vortexing for 30 s and the cells were washed twice with 1 ml 0.9% NaCl. The antibiotic-tolerant cells were grown in 2 ml ABTGC to revert to normal phenotype and 2 ml ABTGC with 10 μg ml−1 colistin to maintain the colistin-tolerance phenotype, at 37 °C, 200 r.p.m. for 16 h. The cells were then washed twice in 2 ml 0.9% NaCl. PAO1 cells were serially diluted, plated on Luria–Bertani (LB) agar and incubated at 37 °C overnight. C.f.u. per ml was calculated by multiplying the average number of colonies by the dilution factor and dividing by the volume. For PAO1/pmr-gfp cells, fluorescence from pmr-gfp expression (expressed in relative fluorescence units, r.f.u.) was measured for each well using a microplate reader (Tecan Infinite 2000) and was normalized to the OD600 of each well. Experiments were performed with three replicates, and the results are shown as the mean±s.d.
Viable colony counts of biofilms with colistin treatment
PAO1 biofilms were cultivated as described above. After 72 h of growth, PAO1 biofilms were treated with 10 μg ml−1 colistin. Biofilms were collected from flow chamber by mechanical disruption with syringes at 0, 6, 24 and 48 h of colistin treatment. The biofilms were resuspended in 0.9% NaCl and further homogenized by vortexing. PAO1 cells were serially diluted, plated on LB agar and incubated at 37 °C overnight. C.f.u. per ml was calculated by multiplying the average number of colonies by the dilution factor and dividing by the volume. Experiments were performed with three replicates, and the results are shown as the mean±s.d.
Microscopy and image acquisition of biofilms
All microscopy images were captured and acquired using an LSM confocal laser scanning microscope (CLSM; Carl Zeiss, Germany). The × 20 objective was used to monitor GFP and PI fluorescence. IMARIS software (Bitplane AG, Zurich, Switzerland) was used to process the images. Experiments were performed in triplicate, and representative images are shown.
Video of antibiotic-tolerant cell migration in biofilms
MiniTn7-gfp-tagged PAO1 biofilms were treated with 10 μg ml−1 colistin and 4 μg ml−1 PI. From 24 to 32 h of colistin treatment, videos were captured and acquire using a CLSM with a × 40 objective lens. GFP and PI fluorescence were observed. IMARIS software (Bitplane AG, Zurich, Switzerland) was used to process the videos. Experiments were performed in triplicate, and representative videos are shown.
Tracking antibiotic-tolerant cells migration in biofilms
After acquiring videos as described in previous section, IMARIS software (Bitplane AG) was used to process the particle tracking of antibiotic-tolerant cells migrating, according to the manufacturer’s instructions.
DNA sequencing analysis
Genomic DNA of the P. aeruginosa biofilms with and without 48 h colistin treatment was purified using QIAamp DNA Mini Kit (Qiagen, Germany) and sequenced on an Illumina MiSeq V3 platform generating 300 bp long paired-end reads. The experiment was performed in three biological replicates: three colistin-treated biofilms and three control biofilms. The average insert sizes are 490–544 nucleotides and the average genomic coverage depths are 63–167 folds. Nucleotide differences were generated from the CLC Genomics Workbench 8.0 (CLC Bio, Aarhus, Denmark), and all of the used parameters were listed in Supplementary Methods. Briefly, adapters and low-quality reads were trimmed off. Paired-end reads in FASTQ format of colistin-treated and control biofilm genomes were first mapped against the P. aeruginosa PAO1 genome (NC_002516). Variants were detected using the low-frequency variant detection method with the required significance of 1%. Convergent non-synonymous variants of colistin-treated biofilm genomes compared with the P. aeruginosa PAO1 reference genome were obtained with the following criterions: (i) Parallel variants were found in the same gene in all of the three colistin-treated biofilm samples; and (ii) no variant was found in the same gene in any of the control biofilm samples.
Pulsed-SILAC
Three independent biological replicates (BR1, BR2 and BR3) were performed. Biofilms treated with colistin were grown and prepared for pulsed-SILAC analysis22. PAO1 ΔlysA biofilms were cultivated in 25 cm × 5 mm Ø flow tubes as described previously49, using ABTG medium, 500 μM C12 L-lysine and 192 mg l−1 Amino acid Drop-out Mix Minus Lysine without Yeast Nitrogen Base (United States Biological, MA) at 37 °C. Flow channels were inoculated with 1 ml of a 1:1,000 dilution of an overnight culture using a syringe and were incubated without flow for 1 h. A Cole–Palmer peristaltic pump was used to supply medium at a velocity of 0.2 mm s−1, which corresponds to a laminar flow with a Reynolds number of 0.02. After culturing for 72 h, biofilms were treated with 10 μg ml−1 colistin for 6 h to kill the antibiotic-sensitive cells in biofilms. Biofilms were then treated with fresh ABTG supplemented with 500 μM C13 L-lysine and 192 mg l−1 Amino acid Drop-out Mix minus Lysine without Yeast Nitrogen Base for 48 h to tag new synthesized proteins in live antibiotic-tolerant cells with C13 L-lysine. Biofilms were washed with PBS and sonicated by probe sonicator (5 s on, 5 s off for 5 min in ice slurry, amplitude 30%) for cell lysis.
Protein samples were separated on a SDS–PAGE gel. Protein bands were washed with ddH2O mixed with 50% acetonitrile (ACN)/50% 25 mM NH4HCO3 via vigorous vortexing for 30 min, and dehydrated with 100% ACN until the gel particles became white. They were then reduced with 10 mM dithiothreitol at 56 °C for 1 h and alkylated with 55 mM iodoacetamide (IAA) for 45 min in the dark. The proteins were then washed with 25 mM NH4HCO3 and 50% ACN/50% 25 mM NH4HCO3. Gel particles were then dehydrated with 100% ACN and dried under vacuum. Trypsin (V5111, Promega, Madison, WI) was added to the gel particles at a ratio of 1:30, and allowed to be completely adsorbed by the gel particles. A unit of 25 mM NH4HCO3 was then added to completely cover the particles for incubation at 37 °C overnight. Peptides were extracted from the gel particles by two 20-min sonications in the presence of 50% ACN containing 0.1% Trifluoroacetic acid (TFA). Extracts were combined, vacuum-dried and resuspended in 0.1% FA for liquid chromatography (LC)–MS/MS analysis.
Peptides were separated and analysed on a Dionex Ultimate 3000 RSLCnano system coupled to a Q Exactive (Thermo Fisher, MA) as previously described50. Approximately 1 μg of peptide from each pooled fraction was injected into an Acclaim peptide trap column (Thermo Fisher, MA, USA) via the Dionex RSLCnano auto-sampler. Peptides were separated in a Dionex EASY-Spray 75 μm × 10 cm column packed with PepMap C18 3 μm, 100 Å (Thermo-Scientific, MA, USA) at room temperature. The flow rate was 300 nl min−1. Mobile phase A (0.1% formic acid in 5% ACN) and mobile phase B (0.1% formic acid in 90% ACN) were used to establish a 60-min gradient. Peptides were then analysed on Q Exactive with an EASY nanospray source (Thermo Fisher, MA) at an electrospray potential of 1.5 kV. A full MS scan (350–1,600 m/z range) was acquired at a resolution of 70,000 at m/z 200 and a maximum ion accumulation time of 100 ms. Dynamic exclusion was set as 15 s. The resolution of the higher energy collisional dissociation (HCD) spectra was set to 17,500 at m/z 200. The automatic gain control (AGC) settings of the full MS scan and the MS2 scan were 3E6 and 2E5, respectively. The 10 most intense ions above the 2,000 count threshold were selected for fragmentation in HCD, with a maximum ion accumulation time of 100 ms. An isolation width of 2 was used for MS2. Single and unassigned charged ions were excluded from MS/MS. For HCD, the normalized collision energy was set to 28%. The underfill ratio was defined as 0.2%.
Two injections have been performed for the first biological replicates and three injections have been performed for the second and third biological replicates, respectively, to evaluate the technical reproducibility of the instrument and workflow. Raw data files of the eight technical replicates were processed and searched as eight experiments using MaxQuant (v1.5.2.8) (refs 25, 26) and the Genebank P. aeruginosa protein database (downloaded on 21 May 2015, 55,063 sequences, 17,906,244 residues) together with the common contaminant proteins. Standard search type with 2 multiplicity, 3 maximum labelled AAs and heavy labelled Lys6 were used for the pulsed-SILAC quantitation. The database search was performed using the Andromeda search engine bundled with MaxQuant using the MaxQuant default parameters for Q Exactive Orbitrap mass spectrometer. The first and main searches peptide mass tolerance for were 20 and 4.5 parts per million (p.p.m.) respectively, while the MS/MS match tolerance was 20 p.p.m. with FTMS de-isotoping enabled. The absence of two trypsin cleavage sites per protein was allowed. Carbamidomethylation (C) was set as a fixed modification. Oxidation (M) and deamidation (NQ) were set as variable modifications. The search was performed in the Revert decoy mode with PSM FDR, protein FDR and site decoy fraction set to 0.01.
A total of 4,382 proteins including 4,250 P. aeruginosa proteins were identified by Andromeda in MaxQuant with FDR <1% (Supplementary Data 2). The scatter plots of inter-technical replicates of each biological replicate were used to evaluate the technical reproducibility of the results (Supplementary Data 2). The technical reproducibility is good and follows the order of BR2(R2=∼0.95)>BR3(R2=∼0.9)>BR1(R2=0.86). To evaluate the repeatability of the biological replicates, all LC–MS/MS raw data files of BR1, BR2 or BR3 were grouped and searched, respectively, using MaxQuant to obtain the pulsed-SILAC protein abundance levels in the three biological replicates. The scatter plots of inter-biological replicates were all included in Supplementary Data 2.
Relative quantification of OdDHL
Effluents from flow chambers were collected, filtered through 0.2-μm filters and the filtrates were collected. Overnight cultures of the reporter strain ΔlasIΔrhlI/lasB-gfp (ref. 51) were adjusted to OD600=0.15 using ABTGC medium. A volume of 100 μl of filtrate was added to 100 μl of ΔlasIΔrhlI/lasB-gfp in a 96-well plate (Nunc, Denmark). Because ΔlasIΔrhlI cannot produce its own OdDHL, lasB-gfp is induced by the addition of filtrates containing OdDHL. Fluorescence from lasB-gfp expression (expressed in r.f.u.) was measured for each well using a microplate reader (Tecan Infinite 2000) and was normalized to the OD600 of each well. Experiments were performed in triplicate, and results are shown as the mean±s.d.
Elastase assay
Effluents from flow chambers were collected, centrifuged to remove bacterial cells and filtered through 0.2-μm filters. An Elastase Assay Kit (EnzChek) was used according to the manufacturer’s instructions. ABTG medium was used as the negative control and elastase was used as the positive control. The fluorescence from each reaction (expressed in r.f.u.) was measured using a microplate reader (Tecan Infinite 2000) and was normalized to the OD600 for each well of the 96-well microplate. Experiments were performed in triplicate, and results are shown as the mean±s.d.
Pyocyanin assay
Relative pyocyanin concentrations were quantified as described previously52. Effluents from flow chambers were collected, centrifuged to remove bacterial cells and filtered through 0.2-μm filters. ABTG medium was used as the negative control. A volume of 10 ml of filtrate was mixed with 1 ml of chloroform by vortexing. The lower chloroform phase was transferred to a new tube containing 200 μl of 0.2 M hydrochloric acid and vortexed. The top phase was then carefully transferred to a 96-well plate to measure OD520 using a microplate reader (Tecan Infinite 2000). Experiments were performed in triplicate, and the results are shown as the mean±s.d.
Cytotoxicity assay for macrophages
In all, 5 × 105 RAW264.7 (ATCC TIB-71) murine macrophages were grown in 24-well culture plate as previously described38. The effluent from the flow chamber biofilms with or without colistin treatment were collected and filtered through a 0.2-μm filter to remove bacterial cells. ABTG media was used as negative control, while ABTG media+10 μg ml−1 colistin was used to show that colistin had no side effects on macrophages. The resultant supernatant was mixed at equal volumes with fresh DMEM and added to the macrophages. Macrophages were incubated for 4 h in 37 °C, 5% CO2. The cytotoxicity of the supernatants on macrophages was determined by adding 20 μM PI to monitor cell integrity. Macrophages stained red by PI under epifluorescent microscopy ( × 20 objective) were counted as dead, leaving the live ones unstained. Cells from five images of each samples were enumerated and the ratio of dead cells to live cells was calculated. Experiments were performed in triplicate, and the results are shown as the mean±s.d.
Eradication of biofilms with colistin and DIPY iron chelator
Fluorescent-tagged P. aeruginosa biofilms were cultivated as described above. After 72 h of growth, PAO1 biofilms were treated with 10 μg ml−1 colistin or 100 μg ml−1 DIPY plus 10 μg ml−1 colistin. After 48 h of treatment, 300 μl of 20 μM PI was injected into each flow channel to stain dead cells in the biofilm. Biofilm were observed under the CLSM as described above. As pyoverdine is a fluorescent metabolite53, its presence and localization in the biofilm was observed by CLSM with Ex 358 nm/Em 461 nm. Experiments were performed in triplicate, and results are shown as the mean±s.d.
Eradication of biofilms by colistin and erythromycin
Fluorescent-tagged P. aeruginosa biofilms were cultivated as described above. After 72 h of growth, PAO1 biofilms were treated with 10 μg ml−1 colistin or 100 μg ml−1 erythromycin plus 10 μg ml−1 colistin. After 48 h of treatment, 300 μl of 20 μM PI was injected into each flow channel to stain dead cells in the biofilm. Biofilm were observed under the CLSM as described above. Experiments were performed in triplicate, and results are shown as the mean±s.d.
Time-dependent killing of planktonic PAO1 with erythromycin and colistin
The minimal inhibitory concentration (MIC) of erythromycin is 2,000 μg ml−1, while the MIC for colistin is 1 μg ml−1 in PAO1 strains. Planktonic P. aeruginosa strains were grown at 37 °C in ABTGC with 100 μg ml−1 of erythromycin, 10 μg ml−1 of colistin and 100 μg ml−1 of erythromycin+10 μg ml−1 of colistin. Cells were collected at 0, 1 and 3 h. PAO1 cells were serially diluted, plated on LB agar and incubated at 37 °C overnight. C.f.u. per ml was calculated by multiplying the average number of colonies by the dilution factor and dividing by the volume.
Mouse implant infection model
The animals used in this study were 7-week-old female BALB/c mice (Taconic M&B A/S). The animal experiments were performed in accordance to the NACLAR Guidelines and Animal and Birds (Care and Use of Animals for Scientific Purposes) Rules by Agri-Food & Authority of Singapore (AVA), with authorization and approval by the Institutional Care and Use Committee (IACUC) and Nanyang Technological University, under the permit number A-0191 AZ. PAO1 biofilms were grown on cylindrical implants (3 mm × 5 mm Ø) in 0.9% NaCl at 37 °C with shaking at 110 r.p.m. for 20 h, as described previously40,54. The biofilm-coated implants were washed three times with 0.9% NaCl and transplanted into the peritoneum of the mice after they were anesthetized with 100 mg kg−1 ketamine and 10 mg kg−1 xylene. Antibiotics were injected at the site of implantation. No antibiotics, 1 mg kg−1 colistin, 10 mg kg−1 erythromycin, or 1 mg kg−1 colistin and 10 mg kg−1 erythromycin were used on groups of five mice. Mice were killed after 24 h of treatment. Implants were collected, sonicated in 0.9% NaCl in an ice water bath using an Elmasonic P120H (Elma, Germany; power=50% and frequency=37 KHz) for 10 min and vortexed three times for 10 s to disrupt the biofilms. Spleens were also collected and completely homogenized using the Bio-Gen PRO200 Homogenizer (Pro Scientific, US) at maximum power on ice. Samples were serially diluted, plated on LB agar and incubated at 37 °C overnight. C.f.u. per ml was calculated by multiplying the average number of colonies by the dilution factor and multiplying by the volume. Experiments were performed with five replicates, and the results are shown as the mean±s.d.
Additional information
Accession codes: Whole-genome sequence data for P. aeruginosa biofilms have been deposited in the NCBI Short Read Archive (SRA) database with accession code SRP058610. LC–MS/MS raw data of the eight replicates and results for protein and peptide identification and quantification from MaxQuant have been submitted to the ProteomeXchange Consortium via the PRIDE data repository with the dataset identifier PXD002369.
How to cite this article: Chua, S. L. et al. Selective labelling and eradication of antibiotic-tolerant bacterial populations in Pseudomonas aeruginosa biofilms. Nat. Commun. 7:10750 doi: 10.1038/ncomms10750 (2016).
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Acknowledgements
We thank Dr Daniela Drautz-Moses, Mr Yap Zhei Hwee and Mr Rikky Wenang Purbojati for help with the DNA sequencing experiments. We thank Mr Bryan Giin Chyuan Tan for his help with the flow cell biofilm experiments. This research was supported by the National Research Foundation and the Ministry of Education of Singapore under its Research Centre of Excellence Programme, the Start-up Grant (M4330002.C70) from Nanyang Technological University and AcRF Tier 2 (MOE2014-T2-2-172) from Ministry of Education, Singapore.
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S.L.C. and J.K.H.Y. designed methods and experiments, carried out the laboratory experiments, analysed the data and interpreted the results; Y.L. co-designed the DNA sequencing experiments and worked on associated data collection and its interpretation; P.H., S.S.A. and S.K.S. performed pulse-SILAC experiment and data interpretation; M.M.S. co-designed and conducted animal experiments; M.G. and T.T.-N. discussed analyses, interpretation and presentation; S.L.C., S.K.S. and L.Y. wrote the paper; all authors have contributed to, seen and approved the manuscript.
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Supplementary Information
Supplementary Figures 1-5, Supplementary Table 1, Supplementary Methods and Supplementary References (PDF 616 kb)
Supplementary Movie 1
Killing of biofilms by colistin. Top view of 72 h old wild-type P. aeruginosa biofilms were treated with colistin and observed from 2 to 20 h. Scale bars, 10 μm. (MOV 2056 kb)
Supplementary Movie 2
Killing of biofilms by colistin. Side view of 72 h old wild-type P. aeruginosa biofilms were treated with colistin and observed from 2 to 20 h. Scale bars, 10 μm. (MOV 509 kb)
Supplementary Movie 3
Migration and formation of colistin tolerant subpopulation in biofilm. Top view of 72 h old wild-type P. aeruginosa biofilms were treated with colistin and observed from 24 to 34 h of treatment. Scale bars, 10 μm. (MOV 1407 kb)
Supplementary Movie 4
Migration and formation of colistin tolerant subpopulation in biofilm. Side view of 72 h old wild-type P. aeruginosa biofilms were treated with colistin and observed from 24 to 34 h of treatment. Scale bars, 10 μm. (MOV 638 kb)
Supplementary Data 1
Comparing the variants of colistin-treated biofilms samples with untreated biofilm samples. (XLSX 33 kb)
Supplementary Data 2
Total list of P. aeruginosa proteins identifed by SILAC. (XLSX 11708 kb)
Supplementary Data 3
Proteins that were of lower abundance in P. aeruginosa PAO1 tolerant cells than in non-tolerant biofilm cells. (XLSX 19 kb)
Supplementary Data 4
Proteins that were of higher abundance in P. aeruginosa PAO1 tolerant cells than in non-tolerant biofilm cells. (XLSX 25 kb)
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Chua, S., Yam, J., Hao, P. et al. Selective labelling and eradication of antibiotic-tolerant bacterial populations in Pseudomonas aeruginosa biofilms. Nat Commun 7, 10750 (2016). https://doi.org/10.1038/ncomms10750
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DOI: https://doi.org/10.1038/ncomms10750
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