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Pharmacodynamics of a polymyxin B, meropenem, and rifampin triple combination were examined against Klebsiella pneumoniae carbapenemase-producing Klebsiella pneumoniae (KPC-Kp) ST258. In time-kill experiments against three KPC-Kp isolates, triple combination generated 8.14, 8.19, and 8.29 log10 CFU/ml reductions within 24 h. In the hollow-fiber infection model, the triple combination caused maximal killing of 5.16 log10 CFU/ml at 78 h and the time required for regrowth was more than doubled versus the 2-drug combinations. Remarkably, combinations with a high single-dose polymyxin B burst plus rifampin preserved KPC-Kp polymyxin susceptibility (MIC240 h = 0.5 mg/liter) versus the same combination with traditionally dosed polymyxin B, where resistance was amplified (MIC240 h = 32 mg/liter).
Klebsiella pneumoniae carbapenemase-producing Klebsiella pneumoniae (KPC-Kp) strains have spread worldwide and are associated with unacceptable mortality rates of up to 50% in the hospital setting (1, 2). The ST258 lineage of KPC-Kp is the most common clone globally and in the United States (3). The genes encoding KPC enzymes are commonly found on plasmids or transposons that contain additional antibiotic resistance determinants, resulting in multidrug-resistant (MDR) isolates susceptible to only a few preserved antimicrobial agents (4).
Although the polymyxin antibiotics (polymyxin E [colistin] and polymyxin B) fell out of favor after their introduction in the 1950s due to concerns over dose-limiting toxicities, their clinical use has seen a recent resurgence given the sharp rise in infections caused by MDR Gram-negative pathogens. In many clinical scenarios, polymyxin B is favored over colistin due its more favorable pharmacological properties that can be attributed to its administration as an active antibiotic. The polymyxins are among the only remaining classes of antibiotics that consistently maintain activity against KPC-Kp, with susceptibility rates of >85% (5). Despite sustained in vitro activity, treatment with polymyxin monotherapy frequently results in clinical failure, probably due to rapid proliferation of resistant subpopulations (6, 7). Polymyxin-carbapenem combination regimens have been associated with improved clinical outcomes and reduced mortality in KPC-Kp infections, providing a viable alternative to polymyxin monotherapy (8, 9). However, the clinical benefit of adding a carbapenem to the polymyxin is not apparent in infections due to KPC-Kp with elevated carbapenem MICs (≥16 mg/liter) (10). Interestingly, rifampin-containing combination regimens to combat KPC-Kp have shown promise in preclinical animal models and some in vitro studies (11,–13). However, optimized combination regimens involving polymyxins, carbapenems, and rifampin have yet to be fully elucidated. Here, we describe the pharmacodynamic activity of single-drug regimens and double- and triple-drug combination regimens containing polymyxin B, meropenem, and rifampin against KPC-2-producing K. pneumoniae ST258 isolates with elevated meropenem MICs. To our knowledge, this study represents the first to have examined humanized polymyxin and polymyxin-based combination regimens over 10 days in the hollow-fiber infection model (HFIM) against KPC-Kp with high meropenem MICs.
Polymyxin B (Sigma-Aldrich, St. Louis, MO; lot WXBB4470V), meropenem (AK Scientific, Union City, CA; lot LC24337), and rifampin (Sigma-Aldrich, St. Louis, MO; lot 109K1417) were utilized in all experiments, and MICs were determined in duplicate using broth microdilution according to CLSI guidelines (14). The KPC-2-producing K. pneumoniae ST258 bloodstream isolates used in the present study (KPC-Kp 9A, KPC-Kp 24A, and KPC-Kp 27A) were obtained from cultures of blood from three different patients with hematologic malignancies, all of whom developed septic shock and died within 1 week of bacteremia onset (15). The KPC-Kp isolates were subjected to PCR with previously published primers for detection of blaSHV, blaTEM, blaCTX-M, blaNDM, blaVIM, blaIMP, and blaOXA-48 genes, followed by sequencing of positive results (16, 17). The presence and type of blaKPC gene were determined by a multiplex molecular-beacon real-time PCR assay (18), and PCR was performed for detection of mutations in K. pneumoniae outer membrane porin genes ompK35 and ompK36, as described previously (19). KPC-Kp 9A, KPC-Kp 24A, and KPC-Kp 27A were used in time-kill experiments at an ~108 CFU/ml inoculum to initially assess the combinatorial pharmacodynamics over 24 h, as described previously (20). Time-kill experiments were carried out in duplicate with polymyxin B (2.41 and 6 mg/liter) (21), meropenem (49.6 mg/liter) (22), and rifampin (3.5 mg/liter) (23, 24) at concentrations representing the HFIM projected maximum free drug concentration (fCmax). The lower limit of quantification was 102 CFU/ml.
To build upon the time-kill data, HFIM experiments (cartridge C3008; FiberCell Systems Inc., Frederick, MD) were performed over 10 days, as previously described (7), to evaluate the effectiveness of dosing regimens of polymyxin B alone or combined with meropenem and rifampin. KPC-Kp 9A and KPC-Kp 27A were selected as representative isolates to use in the HFIM at an ~108 CFU/ml inoculum for a proof-of-concept evaluation of the drug regimens described below. Population analysis profiles (PAPs) were also determined during the HFIM by plating a 50-μl aliquot of a bacterial sample onto an agar plate embedded with polymyxin B (0.5, 1, 4, or 10 mg/liter) or meropenem (4, 16, or 64 mg/liter) to simultaneously track the polymyxin- and meropenem-heteroresistant subpopulations that are often present in K. pneumoniae (25, 26). HFIM polymyxin B dosage regimens were based on the population pharmacokinetic model described by Sandri et al. from 24 critically ill patients who received intravenous polymyxin B doses ranging from 0.45 to 3.38 mg/kg of body weight/day (7, 21). The following polymyxin B (half-life [t1/2] = 8 h), meropenem (t1/2 = 2.5 h), and rifampin (t1/2 = 2.5 h) regimens were simulated using each drug alone or in double or triple combinations in the HFIM based on human pharmacokinetic data in critically ill patients (22,–24):
During combination experiments where the HFIM system was set to a 2.5-h half-life, polymyxin B was supplemented into the central reservoir every 80 min to maintain a pharmacokinetic profile consistent with an 8-h half-life (27). Samples for validation of the antimicrobial pharmacokinetics were obtained from monotherapy HFIM runs over a 48-h period prior to the addition of bacteria. Polymyxin B concentrations were determined by a liquid chromatography single-quadrupole mass spectrometry (LC-MS) method (28). Meropenem concentrations were quantified using a liquid chromatography tandem mass spectrometry method (LC-MS/MS) that utilized an Agilent 1200 system and an Agilent 6430 system (Santa Clara, CA) (29). Rifampin concentrations were validated using a microbiological assay that utilized Staphylococcus aureus (ATCC 29213) as an indicator organism embedded in Mueller-Hinton agar (MHA) at 107 CFU/ml (30). Using 35 ml of agar, rifampin concentrations ranging from 0.0625 to 10 mg/liter were used to generate a logarithmic standard curve (R2 = >0.99). There was satisfactory agreement between the observed and targeted pharmacokinetic profiles for polymyxin B (R2 = 0.98, slope = 0.83, and intercept = −0.10), meropenem (R2 = 0.97, slope = 0.85, and intercept = 1.67), and rifampin (R2 = 0.99, slope = 1.15, and intercept = 0.08).
In time-kill experiments against KPC-Kp 9A, KPC-Kp 24A, and KPC-Kp 27A, monotherapies were unable to sustain bacterial killing through 24 h (Table 1). A double combination with polymyxin B at 6 mg/liter and rifampin was bactericidal (≥3 log10 CFU/ml reduction in viable colony count from the initial inoculum) and synergistic at 24 h against all three isolates, whereas polymyxin B at 6 mg/liter combined with meropenem was bactericidal and synergistic only against isolate KPC-Kp 27A at 24 h. Triple combination therapy with polymyxin B at 6 mg/liter yielded synergistic killing and undetectable bacterial counts at 24 h against all isolates.
In the HFIM, neither meropenem nor rifampin as monotherapy was able to cause bacterial killing of KPC-Kp 9A at any time point (Fig. 1). Polymyxin B monotherapy administered as either a loading dose or a burst regimen caused >3 log10 CFU/ml bacterial reductions throughout the first 6 h. The polymyxin B loading dose achieved bactericidal activity and a maximal bacterial reduction of 3.57 log10 CFU/ml after 3 h, while the burst regimen provided bactericidal activity within 2 h and a maximal bacterial reduction of 5.56 log10 CFU/ml at 4 h. Bacterial killing with each polymyxin B monotherapy regimen was not maintained, and the total population regrew to growth control levels by 24 h. The polymyxin B burst regimen, which displayed greater killing than the loading dose, was essentially unaided by the addition of meropenem, where maximal log10 CFU/ml reductions of 5.41 were also achieved after 4 h. However, the addition of rifampin to the polymyxin B burst regimen enabled prolonged killing with bactericidal activity detected out to 30 h and synergy from 24 to 30 h before the total population began to regrow.
Triple antimicrobial therapy combining polymyxin B, meropenem, and rifampin against KPC-Kp 9A in the HFIM substantially potentiated the activity of the individual agents. This triple combination using a polymyxin B loading dose maintained bactericidal activity until 54 h (3.81 log10 CFU/ml reduction) and doubled the time during which the combination could prevent bacterial regrowth compared to polymyxin B with rifampin. Despite administration of only a single polymyxin B dose, the burst in combination with meropenem and rifampin displayed the most bacterial killing of any regimen by tripling the time to bacterial regrowth over two-antibiotic combinations and causing maximal reductions of 5.16 log10 CFU/ml after 78 h. Against KPC-Kp 27A in the HFIM, the triple combination using a polymyxin B burst caused a 3.05 log10 CFU/ml reduction by 2 h and a maximal reduction of 6.95 log10 CFU/ml by 6 h. The triple combination maintained bactericidal activity through at least 30 h before the bacterial population completely regrew to the level seen with the growth control by 72 h.
The levels of growth of KPC-Kp 9A and KPC-Kp 27A subpopulations resistant to polymyxin B and meropenem were tracked using PAPs over 240 h in the HFIM (Fig. 2). Irrespective of the administered antibiotic regimen, meropenem PAPs remained proportional to that seen with the growth control; there was not an appreciable expansion of any meropenem subpopulation, even after exposure to meropenem. Growth on plates containing polymyxin B at up to 10 mg/liter was noted for KPC-Kp 9A after exposure to polymyxin B without rifampin, including exposure to the burst and loading-dose monotherapies and the burst plus meropenem combination. In agreement with the PAPs, the KPC-Kp polymyxin B MICs following 240 h of exposure to these three antimicrobial regimens in the HFIM were >32 mg/liter. Conversely, when polymyxin B was administered as a burst in combination with rifampin against KPC-Kp 9A or KPC-Kp 27A, polymyxin B-resistant subpopulations displayed growth profiles similar to that of the growth control and, at 240 h postexposure, polymyxin B MICs remained 0.5 mg/liter. Further, the polymyxin B burst, meropenem, and rifampin triple combination suppressed the polymyxin B- and meropenem-resistant subpopulations to below baseline levels until at least 96 h for KPC-Kp 9A and 48 h for KPC-Kp 27A. In comparison to the polymyxin B burst triple combination, the three-drug regimen based on the polymyxin B loading dose caused ~3 log10 CFU/ml more growth on plates treated with 4 or 10 mg/liter polymyxin B at 240 h and resulted in a postexposure polymyxin B MIC of 32 mg/liter.
Nontraditional combinations involving the polymyxin antibiotics are frequently employed in the fight against KPC-Kp because therapeutic options are extremely limited. However, it is unclear how the polymyxins should be dosed, especially when used in combination with other agents, such as carbapenems and rifampin. In the present investigation, against KPC-Kp isolates with meropenem MICs of ≥16 mg/liter (stop codons at amino acid [aa] 89 of the ompK35 porin gene), administration of polymyxin B with meropenem 2-drug combinations did not result in consistent bacterial killing. Unlike KPC-Kp 9A and KPC-Kp 24A, which harbored wild-type ompK36 genes, KPC-Kp 27A had an IS5 insertion in the promoter region of ompK36. Interestingly, synergy for the polymyxin B and meropenem combination was detected only against KPC-Kp 27A. The variations in meropenem MICs observed between KPC-Kp 9A, 24A, and 27A were likely due to these differing combinations of porin channel mutations in addition to fluctuations in expression of porin channels and the KPC-2 enzyme (31, 32). Similarly to polymyxin B with meropenem, polymyxin B and rifampin 2-drug combinations caused undetectable counts of only one KPC-Kp strain (isolate 24A) through 24 h; therefore, 3-drug regimens with rifampin were explored.
The addition of rifampin to polymyxin B and meropenem may enable prolonged bactericidal activity and may improve upon the potentially unreliable activity of 2-drug combinations against KPC-Kp with higher meropenem MICs. Administration of a polymyxin with a carbapenem and rifampin is a promising combination that was previously shown to be bactericidal (against 8/9 strains) in static time-kill experiments against carbapenemase-producing K. pneumoniae (33, 34) and was further validated in the present study. In the current investigation, rifampin added to a polymyxin B burst preserved polymyxin susceptibility through 10 days (polymyxin B MIC240 h = 0.5 mg/liter) for both KPC-Kp isolates. Contrastingly, polymyxin B monotherapy or polymyxin B plus meropenem or traditionally dosed polymyxin B plus meropenem and rifampin regimens resulted in amplified polymyxin resistance where KPC-Kp polymyxin B MICs were ≥32 mg/liter at 10 days postexposure. The benefit of coadministration of rifampin with the polymyxin B burst and meropenem may be multifactorial as a consequence of (i) directly reducing K. pneumoniae total population counts and (ii) suppressing polymyxin B resistance. Recurrent ~1 to 2 log10 CFU/ml drops in bacterial density seen during administration of a polymyxin B-rifampin combination, but not rifampin monotherapy, in the HFIM support the concept that killing caused by rifampin is potentiated by polymyxin B, possibly via damage to the outer membrane of K. pneumoniae (35). Suppression of polymyxin B resistance by rifampin could be explained by an ability to inhibit the expression of lipopolysaccharide regulators such as phoP plus phoQ and pmrA plus pmrB, which can lower the negative charge of the K. pneumoniae outer membrane, thus decreasing polymyxin affinity (35). These two-component regulatory systems have also been shown to play an important clinical role in K. pneumoniae polymyxin heteroresistance, making them an enticing target for suppression (36).
Previous dynamic in vitro experiments (HFIM and one-compartment model) examining regimens against KPC-Kp have not described pharmacodynamic activity past 72 h (13, 37,–40). Therefore, it is remarkable that in the present study, the triple combination that included a polymyxin B burst, meropenem, and rifampin was bactericidal until at least 78 h for KPC-Kp 9A and 30 h for KPC-Kp 27A despite combatting a starting inoculum that was 10 to 1,000× higher than those previously investigated. The use of KPC-Kp at an inoculum of ~108 CFU/ml was employed to simulate the potentially high bacterial densities in deep-seated infections. In the context of infections with a lower bacterial burden, such as urinary tract infections and bacteremia, our results may underestimate the activity of the individual antibiotics (41). Our study should be examined in concert with the other studies that have explored combinations against KPC-Kp at lower inocula.
Polymyxin nephrotoxicity is the most clinically significant dose-limiting adverse event (42). Administration of a large one-time polymyxin B dose holds significant promise to circumvent cumulative drug exposure concerns which have been predictive of polymyxin-induced nephrotoxicity (43, 44). Remarkably, the triple combination incorporating the polymyxin B burst regimen displayed enhanced bacterial killing compared to the more traditional loading-dose-based combination, despite a cumulative polymyxin B exposure (AUC0–240) of <20% over 10 days. Furthermore, during exposure to polymyxin B burst-based combinations with rifampin, the K. pneumoniae isolates remained polymyxin B susceptible and there were fewer polymyxin B-resistant subpopulations present despite regrowth.
There are a number of important things to consider while interpreting the data contained in the present manuscript. One limitation of the time-kill experiments is that static fCmax concentrations were used, which may in part explain the greater killing that was observed compared to the HFIM. Polymyxin B, meropenem, and rifampin were simulated in the HFIM to approximate human pharmacokinetics in critically ill patients. However, there is likely significant interpatient variability that exists for the pharmacokinetics of these drugs in the clinical setting, which may influence the translation of these findings. Lastly, the polymyxin B burst, meropenem, and rifampin triple combination was tested only against 2 KPC-Kp isolates in the HFIM and its activity should be further validated in other clinically relevant strains.
In conclusion, the promising combination of polymyxin B, meropenem, and rifampin appears to provide a viable option to consider in the treatment of KPC-Kp, including against isolates with higher carbapenem MICs. Importantly, in combination with polymyxin B, rifampin seems to enable temporary suppression of polymyxin B resistance while acting to directly kill the K. pneumoniae strain, suggesting a multifactorial mode of attack. Further investigations in vitro and using animal models are warranted before translation to the clinic.
Research reported in this publication was supported by the National Institute of Allergy and Infectious Diseases of the National Institutes of Health under award number R01AI111990. M.J.S. is the recipient of a career development award through the National Institute of Allergy and Infectious Diseases of the National Institutes of Health under award number K23AI114994. The content is solely our responsibility and does not necessarily represent the official views of the National Institutes of Health.