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The Gram-negative bacillus Stenotrophomonas maltophilia (SM) is an emerging MDR opportunistic pathogen. Recent studies identify a potentially relevant activity of azithromycin against Gram-negative bacteria overlooked in standard bacteriological testing. We investigated azithromycin activity against SM in testing conditions incorporating mammalian tissue culture medium and host defence factors.
MIC testing, chequerboard assays, time–kill assays and fluorescence microscopy were performed for azithromycin, the cationic peptide antibiotic colistin and the human defence peptide cathelicidin LL-37 alone or in combination in cation-adjusted Mueller–Hinton broth or mammalian tissue culture media. Azithromycin sensitization of SM to host immune clearance was tested in a human neutrophil killing assay and a murine pneumonia model.
We observed potent bactericidal activity of azithromycin against SM in mammalian tissue culture medium absent in bacteriological medium. Colistin and LL-37 strongly potentiated azithromycin killing of SM by increasing drug entry. Additionally, azithromycin sensitized SM to neutrophil killing and increased SM clearance in the murine pneumonia model.
Despite lack of activity in standard MIC testing, azithromycin synergizes with cationic peptide antibiotics to kill SM in medium mimicking tissue fluid conditions. Azithromycin, alone or in combination with colistin, merits further exploration in therapy of drug-resistant SM infections.
Stenotrophomonas maltophilia (SM) is a ubiquitous MDR Gram-negative bacillus and opportunistic pathogen. Risk factors for infection include malignancy, neutropenia, HIV, cystic fibrosis, mechanical ventilation, ICU admission, long-term central venous catheter use, recent surgery, trauma and prior broad-spectrum antibiotic administration. Common SM infections are pneumonia and bacteraemia, with reported mortality of 18%–69%.1 The incidence of SM infections ranges from 7.1 to 14.1 per 10000 inpatients and is increasing, with intrinsic or acquired antibiotic resistance presenting great therapeutic challenges in severe infection.2,3 Trimethoprim/sulfamethoxazole and ticarcillin/clavulanic acid (no longer manufactured in the USA) are first- and second-line treatments for serious SM infections, but recent studies have found in vitro resistance to these agents to be as high as 30% and 41%, respectively.4,5
Clinical data regarding optimal therapy for SM infection are limited. Moreover, in vitro antimicrobial susceptibility testing results may not correctly predict SM clinical treatment response with reported discrepancies among testing methods (e.g. Etest, disc diffusion versus agar dilution) and differing guidelines (e.g. EUCAST versus CLSI). Consequently, SM MIC results vary according to the conditions and methods implemented.3 There is a great need to identify innovative treatment strategies for SM infection and a consistent antimicrobial susceptibility scheme to guide such therapy.
Macrolides are never recommended for SM therapy based on high MIC values in standard assays. However, recent studies have indicated that conventional antimicrobial susceptibility testing conditions may overlook macrolide activity and antibiotic synergies against other MDR Gram-negative bacteria including Pseudomonas aeruginosa, Klebsiella pneumoniae and Acinetobacter baumannii.6,7 Here, we examine the potential of the commonly prescribed macrolide azithromycin to combat SM under more physiological medium conditions, in synergy with colistin or endogenous host defence factors (cathelicidin LL-37 and neutrophils) in vitro, and in vivo using a murine pneumonia model.
MDR SM isolate K279a (ATCC BAA-2423) was utilized in all experiments. Additional MDR SM clinical isolates were obtained from the University of California, San Diego (UCSD) Center for Advanced Laboratory Medicine (three strains) and the Laboratory of Bacterial Drug Resistance, Gunma University Graduate School of Medicine (five strains). Isolates were stored in LB broth+50% glycerol at −80°C until use. Azithromycin and colistin were purchased from Sigma–Aldrich and cathelicidin LL-37 from American Peptide. Bacteriological medium Mueller–Hinton broth (Spectrum Chemicals) was supplemented with 20–25 mg/L Ca2+ and 10–12.5 mg/L Mg2+ (CA-MHB). Tissue culture medium Roswell Park Memorial Institute 1640 (RPMI) (ThermoFisher Scientific) was supplemented with 10% LB broth (Hardy Diagnostics) (RPMI+10%LB).
Broth microdilution antimicrobial susceptibility testing was performed in CA-MHB according to CLSI guidelines and in RPMI+10%LB. Chequerboard panels were likewise performed in both media.8,9 Synergy, indifference and antagonism were defined by the fractional inhibitory concentration index (FICI): FICI≤0.5=synergy, FICI>0.5 to ≤4=indifference and FICI>4=antagonism. Time–kill assays were performed in CA-MHB and RPMI+10%LB as previously described, with bactericidal activity defined as a reduction in viable bacteria by ≥3 log10 cfu/mL; synergy, ≥2 log10 cfu/mL reduction; indifference, <2 log10 cfu/mL reduction; and antagonism, >2 log10 cfu/mL increase.10
Fluorescence microscopy was performed as previously described with the following modifications.11 For ready visualization, SM was used at a 2 log10 cfu/mL higher concentration than in MIC testing, along with higher, but pharmacologically achievable, concentrations of antibiotics [NBD-tagged azithromycin (20× MIC), colistin (8× 1/4 MIC) and LL-37 (10× 1/4 MIC)].12 Bacteria were labelled with 1 μg/mL FM4-64 (membrane) and 2 μg/mL DAPI (nucleic acid) (Molecular Probes) prior to transfer onto a 1.2% agarose pad containing 20% LB broth for microscopy and image analysis using ImageJ software v1.48f and CellProfiler 2.0.
Human neutrophils were isolated from healthy donors using the PolymorphPrep system (Axis-Shield) under protocols approved by the UCSD Human Subjects Institutional Review Board for use in established bacterial killing assays with minor modifications.13 Neutrophils were resuspended in RPMI to 2×106 cells/mL, stimulated with 25 nM phorbol-12-myristate-13-acetate for 2 h at 37°C, washed and used to seed a 96-well plate (2×105 cells/well). Cells were infected at an moi equal to 50 with SM that were untreated or exposed overnight to a sub-bacteriostatic concentration (0.03 mg/L) of azithromycin.
Adapting a published pneumonia model, A/J mice (8–10 weeks old, Jackson Laboratory) were infected intratracheally with 2×106 cfu (low inoculum) or 2×107 cfu (high inoculum) of SM (K279a) and treated with PBS control or 50 mg/kg azithromycin subcutaneously (sc) every 24 h for one dose (low inoculum) or two doses (high inoculum).14 Animals were euthanized and lungs harvested, weighed, homogenized, serially diluted and plated onto LB agar to enumerate cfu after 24 h of incubation at 37°C. In a subset of mice infected at the high inoculum, bronchoalveolar lavage fluid (BALF) was collected at 48 h by exposing the trachea, injecting 0.8 mL of cold PBS and retrieving BALF using an 18 gauge needle connected to a 1 mL syringe. BALF was centrifuged at 500 g for 10 min and supernatants frozen at −80°C for later cytokine analysis using commercial ELISA kits for IL-1β (R&D Systems) and macrophage inflammatory protein 2 (MIP-2) (BD Biosciences). Pelleted BALF cells were resuspended in 0.25 mL cold PBS and enumerated utilizing a haemocytometer, light microscopy and Wright–Giemsa staining to determine the differential leucocyte count. Excised lungs from four mice in each group were fixed using 4% formalin, embedded in paraffin, sectioned and stained with haematoxylin–eosin for blinded analysis by a pathologist. A graded scale of 0 (absent) to 3 (extensive) was used to assess overall airspace involvement, perivascular/peribronchial inflammation, evidence of inflammation and oedema/debris or macrophages in the intra-alveolar space. All procedures were performed by a protocol approved by the UCSD Institutional Animal Care and Use Committee.
Statistical analyses were performed using GraphPad Prism 6.0f (GraphPad Software). One-way ANOVA, two-way ANOVA or unpaired Student's t-test were utilized where appropriate. P values <0.05 were regarded to be statistically significant.
Supplementary methods (growth curve analysis, electron microscopy, neutrophil extracellular trap and oxidative burst studies) are available as Supplementary data at JAC Online.
Azithromycin MICs for several MDR SM strains were determined by CLSI broth microdilution methodology using either the recommended bacteriological medium, CA-MHB, or the common mammalian tissue culture medium RPMI supplemented with 10% LB broth to support equivalent bacterial growth (Figure S1). A >500-fold reduction in MIC (≤0.25 versus ≥128 mg/L) was observed for nearly all isolates tested with RPMI+10%LB compared with CA-MHB (Table 1). Transmission electron microscopy of SM K279a cells treated with azithromycin, a ribosomal protein synthesis inhibitor, in RPMI+10%LB revealed ribosomal clustering consistent with its known target of action (Figure S2). In a kinetic killing assay, 0.25 mg/L azithromycin had no effect on SM K279a growth in CA-MHB, but reduced bacterial cfu below detectable levels within 24 h in RPMI+10%LB (Figure 1a).
We recently observed synergy of azithromycin with cationic antimicrobial peptides against other Gram-negative bacilli.7 The cationic peptide antibiotic colistin, a drug of last resort for certain MDR pathogens, is bacteriostatic against SM in RPMI+10%LB, but not in CA-MHB (Figure 1a). At 1/4 MIC of both drugs, azithromycin showed potent bactericidal synergy with colistin in RPMI+10%LB, but not CA-MHB (Figure 1b). The human cathelicidin LL-37 is a cationic endogenous host defence peptide abundantly produced by neutrophils and epithelial cells. Once again, at 1/4 MIC of each agent, azithromycin showed bactericidal synergy with LL-37 in RPMI+10%LB, but not CA-MHB (Figure 1c). Using fluorescence microscopy-based bacterial cytological profiling, both colistin and LL-37, which are known to form pores and disrupt bacterial membranes, markedly enhanced entry of fluorescently labelled (NBD-tagged) azithromycin into bacterial cells (Figure 2a and b), facilitating azithromycin access to the 50S ribosomal subunit.
Azithromycin synergizes with LL-37 against SM, suggesting it could sensitize the opportunistic pathogen to killing by neutrophils, which produce the defence peptide as part of their antimicrobial arsenal. SM induced oxidative burst and the formation of neutrophil extracellular traps (in which LL-37 is deployed) from freshly isolated human neutrophils (Figure S3). Overnight pretreatment of SM with a sub-bacteriostatic concentration of azithromycin sensitized the bacterium to human neutrophil killing (Figure 3a). We next assessed the efficacy of azithromycin monotherapy in an adapted murine model of SM pneumonia, using immune susceptible A/J mice that have functional C5 complement deficiency. Under the experimental conditions, azithromycin treatment did not affect the acute histopathological features of inflammatory pneumonia (Figure 3b and Figure S4A), the amount or composition of BALF leucocyte infiltration (Figure 3c) nor BALF levels of pro-inflammatory cytokines MIP-2 or IL-1β (Figure S4B) at 48 h post-infection. However, the recovered cfu of SM from the lungs was markedly reduced by 58% in azithromycin-treated mice (1629±123 cfu/g) versus PBS controls (3898±1154 cfu/g) at 24 h in a lower inoculum challenge and reduced by 95% in azithromycin-treated mice (824±184 cfu/g) versus PBS controls (17915±11186 cfu/g) at 48 h in a higher inoculum challenge (Figure 3d).
Using SM K279a, a strain with several genes conferring resistance to heavy metals and antimicrobials (including nine resistance–nodulation–division-type efflux pump genes), and several contemporary clinical SM isolates, this study demonstrated a striking difference of azithromycin potency in standard bacteriological testing medium (negligible activity, MIC as high as 256 mg/L) compared with mammalian tissue culture medium (MIC ≤0.25 mg/L) supplemented with 10% LB broth.15 While there is no current clinical MIC breakpoint of azithromycin for SM, the EUCAST breakpoint used for the Gram-negative bacillus Campylobacter jejuni is 4 mg/L. Azithromycin also showed potent synergy with colistin, an antibiotic of last resort for MDR Gram-negative bacilli infections, and LL-37, an endogenous cationic antimicrobial peptide. As disruptors of bacterial membranes, colistin and LL-37 potentiate azithromycin entry into bacterial cells and enhance azithromycin access to its ribosomal target.
Recent studies suggest different antibiotics may work in concert or at odds with our innate immune system in the setting of infection.13,16 However, our understanding of the interactions between common antibiotics prescribed in clinical practice and endogenous antimicrobials such as LL-37 and the cells that produce them (e.g. neutrophils) remains limited. Whereas SM was impervious to human neutrophil killing in our ex vivo assay, it was sensitized to neutrophil killing by azithromycin pretreatment. Moreover, azithromycin showed the ability to significantly reduce SM bacterial counts in an in vivo murine pneumonia challenge model in which a predominantly neutrophilic inflammatory infiltrate was elicited in the lungs.
Traditional SM antimicrobial susceptibility testing can be problematic given inconsistencies between the results of different methods, the lack of a gold standard or universal reference method and the inability of testing results to reliably and appropriately translate to clinical efficacy. Conventional in vitro studies also inadequately account for the dynamic interactions between conventional antibiotics and the host immune response. Our study and others suggest that current standardized susceptibility testing in bacteriological medium may fail to adequately detect the bactericidal activity of azithromycin and its interactions with the innate immune system against various MDR Gram-negative bacilli, including SM.6,7
Limitations of our study include the modest number of SM isolates tested and the reliance on a murine pneumonia model for in vivo azithromycin activity against SM without human clinical data. Nevertheless, this preliminary investigation highlights a potential utility of azithromycin, a safe and established antibiotic, used alone or in combination with colistin, in SM infection. The work also emphasizes the importance of accounting for the dynamic interaction between conventional antibiotics and host immunity in the setting of infection. Future randomized clinical trials in humans with azithromycin will be required to determine the true utility of this finding.
This work was supported by National Institutes of Health grants T32-AI007036 (to M. K.), HD071600 (to G. S. and V. N.), AI052453 and AR052728 (to V. N.) and AI113295 (to J. P.).
None to declare.
We thank Dr Sharon Reed (University of California, San Diego), Dr Nicholas P. Cianciotto (Northwestern University Medical School) and Dr Koichi Tanimoto (Gunma University Graduate Medical School) for providing bacterial isolates. We also thank Ying Jones, Timo Meerloo and Dr Marilyn G. Farquhar of the UCSD Electron Microscopy Core Facility for their assistance with electron microscopy studies.