Extracellular DNA-induced antimicrobial peptide resistance in Salmonella enterica serovar Typhimurium
- Lori Johnson†1,
- Shawn R Horsman1,
- Laetitia Charron-Mazenod1,
- Amy L Turnbull1,
- Heidi Mulcahy1,
- Michael G Surette1, 2 and
- Shawn Lewenza1Email author
© Johnson et al.; licensee BioMed Central Ltd. 2013
Received: 23 January 2013
Accepted: 17 May 2013
Published: 24 May 2013
The Salmonella enterica serovar Typhimurium PhoPQ two component system (TCS) is activated by low Mg2+ levels, low pH and by antimicrobial peptides (AP). Under Mg2+ limitation, the PhoPQ system induces pmrD expression, which post-translationally activates the PmrAB TCS. PhoPQ and PmrAB control many genes required for intracellular survival and pathogenesis. These include the polymyxin resistance (pmr) operon, which is required for aminoarabinose modification of LPS and protecting the outer membrane from antimicrobial peptide disruption and killing. Extracellular DNA is a ubiquitous polymer in the matrix of biofilms and accumulates in some infection sites. Extracellular DNA chelates cations and thus activates the Pseudomonas aeruginosa PhoPQ/PmrAB systems, leading to expression of the orthologous arn (pmr) operon.
Here we show that extracellular DNA induces expression of the S. Typhimurium pmr antimicrobial peptide resistance operon in a PhoPQ and PmrAB-dependent manner. Induction of the pmr genes by DNA was blocked when present with excess Mg2+. Exogenous DNA led to increased resistance of planktonic cultures to aminoglycosides, antimicrobial peptides (AP) and ciprofloxacin, but only AP resistance was PhoPQ/PmrAB-dependent. Extracellular DNA was shown to be a matrix component of S. Typhimurium biofilms cultivated in flow chambers and on glass surfaces. A pmrH-gfp fusion was highly expressed in flow chamber biofilms cultivated in medium with repressing levels of 10 mM Mg2+ and co-localized with eDNA. Expression of pmrH-lux was monitored in plastic peg biofilms and shown to require PhoPQ and PmrAB. Biofilms had higher levels of pmrH expression compared to planktonic cultures. We propose that DNA accumulation in biofilms contributes to the increased pmrH-lux expression in biofilms.
The Salmonella PhoPQ/PmrAB systems and antimicrobial peptide resistance are activated by the cation chelating properties of extracellular DNA. DNA-induced AP resistance may allow immune evasion and increased survival of S. Typhimurium biofilms formed during extracellular growth stages of an infection or outside the host.
KeywordsSalmonella phoPQ pmrAB Antimicrobial peptides Antibiotic resistance Extracellular DNA Biofilms Immune evasion
Salmonella enterica serovar Typhimurium is an enteroinvasive bacterial pathogen typically encountered by ingesting contaminated food or water. S. Typhimurium causes self-limiting gastroenteritis in humans and typhoid-like fever in mice [1, 2]. Greater than 99% of the bacteria in murine salmonellosis are killed in the stomach or passed out of the gut , but S. Typhimurium that survive passage through the acidic stomach environment enter into the small intestine, where upon they transverse the intestinal epithelial barrier. The bacteria are then phagocytosed by macrophages or they can actively invade both phagocytic and non-phagocytic cells using a type III secretion system . Following invasion, Salmonella disseminates throughout the body leading to a systemic typhoid-like infection .
Salmonella forms biofilms on abiotic surfaces such as plastic and egg conveyer belts, which may have a role in environmental survival of this organism [3, 4]. Biofilm formation and aggregation in S. enterica serovar Typhimurium is exemplified by the rdar colony morphology, where colonies grown on media containing Congo red are red, dry, and rough [5, 6]. This morphology requires the production of curli fimbriae and multiple exopolysaccharides [7, 8]. S. Typhimurium also grows enmeshed in EPS rich biofilms on the surface of gallstones, which may contribute to inefficient antibiotic treatment and facilitates typhoid carriage [9, 10]. Biofilm shedding from colonized gallstones is likely a source of recurring infections .
The PhoPQ two-component system is important for intracellular survival within macrophages. Limiting Mg2+, low pH and the presence of antimicrobial peptides are PhoPQ-activating signals in culture [12, 13] but low pH and antimicrobial peptides are important activating signals during intracellular macrophage growth . The PmrAB two component system responds to Fe3+ and low pH, and is activated under Mg2+ limiting conditions by a post-translational mechanism involving PmrD, a PhoPQ-regulated protein. PmrD prevents the dephosphorylation of PmrA by PmrB, thus activating the expression of PmrA-regulated genes . The pmrHFIJKLM operon is directly regulated by PmrAB, is induced during phagocytosis and is required for survival from host antimicrobial peptide production . The pmr operon encodes an LPS modification system that is responsible for aminoarabinose modification of the lipid A moiety of LPS. Reducing the negative charge of the bacterial surface with aminoarabinose is critical for reducing the membrane damaging effects of cationic antimicrobial peptides.
We recently demonstrated that DNA is a cation chelator that induces expression of the Pseudomonas aeruginosa arnBCADTEF-ugd (PA3552-PA3559; pmr) operon in DNA-enriched planktonic cultures and biofilms . DNA sequesters cations and creates a condition that resembles a Mg2+-limited environment, similar to known chelators like EDTA. Expression of this operon was required for very high levels of biofilm resistance to antimicrobial peptides and partially contributed to aminoglycoside resistance . During Mg2+ limiting growth conditions, the P. aeruginosa PhoPQ and PmrAB systems are both required for expression of the arn operon [18, 19]. Both the PhoPQ and PmrAB systems respond to Mg2+ limitation in P. aeruginosa, and there is no PmrD ortholog to connect the two pathways. In addition, the P. aeruginosa PhoQ sensor does not directly detect antimicrobial peptides, and the PmrB sensor does not respond to trivalent metals . Extracellular DNA also induces the expression of PmrAB-regulated spermidine synthesis genes, which results in the production of the polycation spermidine on the surface and protection of the outer membrane from antimicrobial peptide treatment . Both the arn and spermidine synthesis (PA4773-PA4775) clusters were induced in biofilms formed by a bfmR mutant of P. aeruginosa that accumulated more eDNA than wild-type biofilms . When sufficient DNA accumulates in P. aeruginosa biofilms, or in the cystic fibrosis (CF) lung where the concentration of DNA is very high and leads to viscous sputum production in CF patients [22, 23], the expression of these DNA-induced surface modifications likely protect from host antimicrobial peptide killing. Therefore, we wanted to determine if extracellular DNA plays a general role in antimicrobial peptide resistance by imposing a cation limitation on S. Typhimurium biofilms and activating the PhoPQ/PmrAB systems, similar to P. aeruginosa.
Results and discussion
Extracellular DNA induces expression of the Salmonella pmroperon
Next, we monitored pmrH-lux expression in wild type, phoPQ, ΔpmrAB and phoPQ/ΔpmrAB mutant backgrounds. DNA-induced expression did not occur in ΔpmrAB or phoPQ/ΔpmrAB double mutants, indicating an absolute requirement for pmrAB in responding to extracellular DNA (Figure 1D). A phoPQ mutant was still able to partially respond to extracellular DNA, which was likely due to the presence of PmrAB (Figure 1D). In summary, extracellular DNA imposes a cation limitation on S. Typhimurium, leading to induction of the pmrH promoter in a PhoP and PmrA-dependent manner.
Extracellular DNA is a matrix component S.Typhimurium biofilms
DNA-enriched planktonic cultures show increased antibiotic resistance
Extracellular DNA induces antibiotic resistance in S. Typhimurium
Minimal inhibitory concentration (MIC)
The observation that phoPQ and pmrAB mutants showed an increased susceptibility to colistin and polymyxin B, in the presence of eDNA, indicated a role for PhoPQ/PmrAB-regulated phenotypes in resistance to membrane acting antimicrobial peptides, likely through the aminoarabinose modification of LPS via the pmr operon.
The pmroperon is highly expressed in biofilms
We measured pmrH-lux expression in conditions with repressing levels of Mg2+ (1 mM), and showed that pmrH expression was dependent on both PhoPQ and PmrAB in biofilms (Figure 4B). Lastly, we calculated the fold induction values of pmrH between inducing (100 μM) and repressing Mg2+ levels (10 mM), simultaneously for both peg-adhered biofilms and the planktonic cultures that served as the inoculum for the biofilms. Interestingly, pmrH was more highly expressed in biofilms when compared to planktonic cultures (27-fold higher), and expression under all conditions required PhoPQ and PmrAB (Figure 4C). We propose that the higher pmrH expression levels in biofilms may be due to the accumulation of eDNA, which increases pmrH expression in biofilms but not planktonic cultures.
We showed evidence that extracellular DNA is a component of the S. Typhimurium extracellular matrix when grown in biofilms. When added to planktonic cultures, eDNA chelates cations resulting in a Mg2+ limited environment and increased expression of the pmr operon. The pmr operon was more highly expressed in biofilms, when compared to planktonic cultures. Expression of pmr in biofilms and DNA-induced expression in planktonic conditions is dependent on the PhoPQ/PmrAB systems. The addition of eDNA to planktonic cultures also led to increased antimicrobial peptide resistance in a PhoPQ/PmrAB-dependent manner. Combined with our previous observations of DNA-induced antibiotic resistance mechanisms in P. aeruginosa , we propose that extracellular DNA has a general role as a cation chelator that induces antimicrobial peptide resistance in biofilms. DNA-induced resistance to antibiotics and antimicrobial peptides from the innate immune system may promote long-term survival of S. Typhimurium biofilms in the environment, on the surface of gallstones, or possibly in the extracellular phases of growth during intestinal infection.
Bacterial strains and growth conditions
S. enterica serovar Typhimurium strain ATCC 14028 was used as the reference strain in this study. The phoPQ::Tn10-Tc R mutant was previously described , ΔpmrAB::cat was constructed as previously described , and the phoPQ ΔpmrAB mutant strain was constructed by P22-mediated transduction  of both mutations into the same background. Cultures were routinely grown overnight at 37°C with agitation in Luria Broth base (LB) supplemented with 50 μg/ml kanamycin, if necessary. Gene expression experiments were performed in NM2 defined minimal media with either high (7.4) or low (5.5) pH. NM2 growth medium includes the following components: 5 mM potassium chloride, 7.5 mM ammonium sulfate, 0.5 mM potassium sulfate, 1 mM monopotassium phosphate, 38 mM glycerol, 0.1% casamino acids, and 100 mM Tris (pH 7.4 or 5.5), supplemented with magnesium sulfate when indicated. When added, the source of extracellular DNA was fish sperm DNA-sodium salt (MJS BioLynx).
Gene expression assays in planktonic cultures
Gene expression was performed in high throughput format using 96-well microplates as previously describe . Briefly, overnight cultures were grown in LB supplemented with 50 μg/ml kanamycin as required, diluted 1/1000 into 150 μl of NM2 defined culture medium with MgSO4, DNA or both, in 96-well black plates with a transparent bottom (9520 Costar; Corning Inc.) and overlaid with 50 μl of mineral oil to prevent evaporation. Microplate planktonic cultures were incubated at 37°C in a Wallac Victor3 luminescence plate reader (Perkin-Elmer) and optical density (growth, OD600) and luminescence (gene expression, counts per second (CPS)) readings were taken every 20 minutes throughout growth.
Biofilm and gene expression assays on pegs
Biofilms were cultivated on 96-well format, polystyrene pegs (Nunc-TSP) that were immersed in 150 μl of NM2 growth medium, as previously described . After biofilm cultivation, non-adherent cells were removed by rinsing the pegs once in 20 mM Tris buffer (pH 7.4). Gene expression (CPS) from peg-adhered biofilms was measured by luminescence readings in the Wallac MicroBeta Trilux multi-detector (Perkin-Elmer). Biofilm formation on the pegs was quantitated by crystal violet (CV) staining as previously described . Gene expression (CPS) on pegs was divided by the biofilm biomass (CV) to normalize gene expression to cell number (CPS/CV), and gene expression in planktonic culture was divided by the OD600 value of cells in suspension to normalize for cell number (CPS/OD600). Biofilms were cultivated in NM2 with limiting Mg2+ (100 μM) or high levels of Mg2+ (1–10 mM).
Minimal inhibitory concentration (MIC) assay
The MIC values were determined using the broth microdilution procedure in 96-well microplates. Briefly, all strains were grown overnight in LB medium, sub-cultured into NM2 medium (1 mM Mg2+) (1/100 dilution) and grown to mid-log phase. All cultures were normalized to a common OD600 value and 10 μl of mid-log culture (~6 × 105 cfu) was inoculated into 90 μl of NM2 media containing repressing levels Mg2+ (1 mM), with or without 5 mg/ml DNA-sodium salt. Microtitre plates containing the antibiotic dilution series and bacteria were incubated for 18 hours at 37°C. The MIC was determined as the concentration of antibiotic that reduced growth to an OD600 value less than 0.1. The median MIC values from three experiments are shown.
Flow chamber biofilm cultivation and imaging
Biofilms were grown in flow chambers with channel dimensions of 1 × 4 × 40 mm as previously described but with minor modifications . Autoclaved silicone tubing (VWR, .062 ID x .125 OD x .032 wall) was assembled and sterilized by pumping 0.5% hypochlorite solution through the flow chamber for 2 hours. For rinsing, sterile water was pumped though for 30 minutes followed by LB media for 30 minutes. Flow chambers were inoculated by injecting with a syringe, 400 μl of mid-log culture diluted to an OD600 of 0.02. After inoculation, chambers were left without flow for two hours to allow the bacteria to adhere, after which media was pumped though the system at a constant rate of 0.75 rpm (3.6 ml/hour). Biofilms were cultivated for 48 hours at 37°C in LB medium and stained with the membrane staining dye FM 4–64 (Invitrogen), the extracellular DNA stains TOTO-1 or Sytox Red (Invitrogen), or an EPS stain fluorescent brightener 28 (Sigma). Biofilms were imaged using a Leica DMI 4000 B widefield fluorescence microscope equipped with filter sets for blue (Ex 390/40, Em 455/50), green (Ex 490/20, Em 525/36) and red (Ex 555/25, Em 605/52) fluorescence using the Quorum Angstrom Optigrid (MetaMorph) acquisition software. Images were obtained with a 63 × 1.4 objective. Deconvolution was performed with Huygens Essential (Scientific Volume Imaging B.V.) and 3D reconstructions were generated using the Imaris software package (Bitplane AG).
Monitoring pmrH-gfpexpression in flow chamber biofilms
The promoter of pmrH was amplified from genomic DNA of S. typhimurium 14028 using the primer pair pmrF-1 (AGTCCTCGAGACTACCGGATGCTGCTTC) and pmrF-2 (AGTCGGATCCATTGCCAGTTAGCCGACA), digested with BamHI-XhoI and cloned into BamHI-XhoI-digested pCS21 upstream of a gfpmut3 reporter . The pmrH-gfp vector was moved into S. Typhimurium 14028 by electroporation. Flow chamber biofilms were cultivated in NM2 containing 0.1 mM Mg2+ for 28 hours and then 10 mM Mg2+ was introduced into the growth media for an additional 16 hours of biofilm cultivation prior to imaging.
This work is dedicated to the memory of our colleague Dmitry Apel. This research was supported by Cystic Fibrosis Canada, the Canadian Institutes of Health Research the Westaim Corporation, and the Alberta Science and Research Authority (ASRA). We thank Dmitry Apel for strain construction. HM was the recipient of a Cystic Fibrosis Canada fellowship. SL holds the Westaim-ASRA Chair in Biofilm Research. MGS holds a Canada Research Chair in Microbial Gene Expression.
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