A 30-year-old bombing victim with a fracture-related pandrug-resistant Klebsiella pneumoniae infection after long-term (>700 days) antibiotic therapy is treated with a pre-adapted bacteriophage along with meropenem and colistin, followed by ceftazidime/avibactam. This salvage therapy results in objective clinical, microbiological and radiological improvement of the patient’s wounds and overall condition. In support, the bacteriophage and antibiotic combination is highly effective against the patient’s K. pneumoniae strain in vitro, in 7-day mature biofilms and in suspensions.
The increasing number of cases of fracture-related infection (FRI) due to multidrug-resistant (MDR) bacteria limits treatment options and surgical re-interventions are often necessary1. Among the MDR nosocomial pathogens, Klebsiella pneumoniae is a major concern because of its ability to form biofilms, to avoid the immune system, and to acquire genes coding for rapidly evolving enzymes, such as extended-spectrum β-lactamases (ESBLs) and carbapenemases2. Biofilms are structures elaborated by bacterial communities attached to the surface of implants or avascular tissue fragments. Within biofilms, persister cells form a subpopulation of metabolically dormant cells that play a major role in the capacity of biofilms to survive and recover from antibiotic treatment3. The treatment of FRI caused by MDR bacteria is very challenging, as it increasingly requires long-term administration of high-doses of broad-spectrum antibiotics, often associated with reversible and irreversible adverse events and low success rates. Phage therapy, the use of (bacterio)phages (viruses that infect bacteria) to treat bacterial infections, is emerging as an additional tool in the fight against MDR bacteria4. Usually, phages only infect a subset of strains belonging to a single bacterial species. That is why personalized phage therapy approaches use one or more phages selected from a preprepared bank, based on their lytic activity against the bacterial strains isolated from the patient’s infection. When time and resources permit, the selected phages can be pre-adapted or trained, i.e., phage mutants with increased infectivity and reduced capacity to provoke bacterial resistance are selected in vitro5. The last decade has seen a surge in phage therapy research, including the use of phages to treat orthopedic-device-related infections6.
On March 22, 2016, a 30-year-old woman suffered a polytrauma during the suicide bombing at the Brussels Airport. Upon admission to the intensive care unit of the Erasme Hospital, she presented a cardiac arrest secondary to hemorrhagic shock caused by heavy bleeding from explosion wounds on her left flank and thigh. After an aggressive multidisciplinary intervention, including reanimation, partial amputation of the iliac bone, and external fixation of a broken femur, the patient was stabilized (Fig. 1).
However, on day 4, the patient progressed to a septic shock due to a surgical wound infection of the left thigh, despite antibiotic treatment with amoxicillin/clavulanate upon admission, followed by piperacillin/tazobactam. Bacterial culture of surgical biopsies showed a polymicrobial flora, consisting of Enterococcus faecium, Pseudomonas aeruginosa, Enterobacter cloacae, and K. pneumoniae. This was the starting point of a long-term, high-dose, broad-spectrum poly-antibiotic therapy guided by therapeutic drug monitoring (Fig. 1). To control the infection, a grand dorsal muscle autograft was used to close the major blast wound on the left leg, 14 days after admission. However, the graft immediately necrotized superficially, requiring further debridement. The high-dose and prolonged antibiotic treatment led to adverse events, resulting in the premature stopping of certain antibiotics: febrile neutropenia due to meropenem, aggravation of the patient’s post-traumatic deafness due to amikacin, and renal tubulopathy due to colistin. To complicate matters even further, the patient was diagnosed with invasive mucormycosis attributed to immune dysfunction due to severe critical illness, 25 days after admission. Extensive necrosis was observed and complete gastrectomy and splenectomy were performed7. A 6-week course of high-dose antifungals (Fig. 1) and an experimental treatment with nivolumab, a cell death protein 1 (PD-1) antagonist, and IFNγ were initiated8. After more than 4 months of intensive antibiotic therapy, treatment was suspended and the patient was monitored closely. A skin autograft was applied on the left thigh wound in July 2016. However, shortly after grafting, a sinus tract with purulent discharge appeared in the middle of the skin graft. Pus also discharged from the orifices of the external-fixator pins. FRI facilitated by the remaining small bone fragments, the retained metal shrapnel from the bomb, and the external fixator was suspected. The external fixator was replaced and the wound was debrided 170 days post-injury. Surgical biopsies (from the femur) showed the presence of 2 K. pneumoniae strains (Fig. 1 and Table 1), one of them (Kp040762) exhibiting an extensively drug-resistant (XDR) phenotype; i.e., it was non-susceptible to at least 1 agent in all but 2 antimicrobial categories9. Two other microorganisms were found in the biopsies: multi-susceptible S. aureus and Mycobacterium xenopi. An adapted antibiotic regimen was started on day 175 (Fig. 1).
Long-term antibiotic treatment failed to cure the FRI, translating into delayed wound healing and complete absence of femur consolidation. Confronted with this therapeutic failure, the clinicians decided to turn to phage therapy. The 2 day-170 K. pneumoniae isolates (Kp040741 and Kp040762) were sent to the Eliava Institute in Tbilisi (Georgia) to select and pre-adapt a therapeutic phage. Phage vB_KpnM_M1 (M1) was shown to exhibit the highest activity against the patient’s K. pneumoniae isolates. It was isolated from a sewage water sample in Tbilisi, in 2012. Transmission electron microscopy revealed a myovirus morphology (Fig. 2a). Phage M1 showed a broad host range (~65%) against clinical isolates of different species of the genus Klebsiella (Fig. 2b). A one-step growth experiment revealed that phage M1 has a productive reproduction cycle with a short adsorption period (91% of phage particles adsorbed in 2 min, 99% in 6 min) (Fig. 2c), causing bacterial cell lysis within 8–10 min after a latent period of 35 min, and an average burst size of 43 phage particles per infected cell (Fig. 2d). Maximal phage activity was observed over the pH range of 5.0–10.0 (Fig. 2e) and the phage was thermostable until 50 °C (Fig. 2f).
Fifteen rounds of co-evolution using Appelmans’ method10 significantly reduced the incidence of bacterial phage resistance. Stable lysis (i.e., without the emergence of phage insensitive mutants) of the patient’s K. pneumoniae strains was achieved in broth for at least 6 h, at a concentration of 103 plaque-forming units (PFU)/ml and a multiplicity of infection (MOI) of 0.0001. Whole-genome sequencing showed that this myovirus belongs to the Slopekvirus genus within the Tevenvirinae subfamily, having type species Klebsiella phage KP15 as its closest relative (Fig. 3a)11. A sequence-based comparison between the pre-adapted and the originally selected variants of phage M1 suggests that a missense mutation (Thr281Arg) in the loop region of the hinge connector of the distal tail fiber protein (Fig. 3b and Supplementary Data 1), which may cause alterations in the phage receptor, is at the basis of the observed improved lytic activity against the patient’s day-170 K. pneumoniae isolates. However, conclusive proof of this genotype-phenotype association would require engineering the originally selected phage M1 variant to reintroduce this mutation independently, which we have not been able to achieve to date. No known depolymerase genes were detected in the genome of phage M1. Importantly, its genome does not encode proteins associated with toxicity, lysogeny or antibiotic resistance; the absence of these protein-coding genes being required for a phage to be used in phage therapy in Belgium12.
The ethical committee of Erasme Hospital gave clearance for the use of experimental phage therapy in XDR K. pneumoniae FRI in November 2016 and the patient signed an informed consent. However, due to a lack of consensus among the treating physicians, phage therapy was put on hold. On 21 February 2018 (702 days postinjury), facing a therapeutic dead end, the phage preparation was applied at the end of a surgical intervention, which consisted of radical debridement followed by the transplantation of rifampicin-impregnated autologous bone grafts (IABGs) (Fig. 1). In the absence of robust pharmacological data with regard to the use of phages in FRI and without medical consensus for intravenous administration, phages were applied locally (through a catheter left in place) to obtain the highest concentration of phages at the site of infection. A short course of treatment (6 days) was chosen to minimize possible immunogenicity and the ongoing antibiotic therapy was continued (Fig. 1).
Here, we show that salvage therapy consisting of a preadapted phage along with meropenem and colistin, followed by ceftazidime/avibactam results in clinical, microbiological and radiological improvement of the patient’s wounds and overall condition. We provide evidence that the phage and antibiotic combination is highly effective against the patient’s K. pneumoniae strain in vitro, in suspensions as well as in biofilms.
Results and discussion
Susceptibility testing of a day-702 K. pneumoniae isolate from a biopsy taken during surgery showed a pandrug-resistant (PDR) status (isolate Kp36336 in Table 1); i.e., non-susceptibility to all agents in all antimicrobial categories9. Sequencing analysis showed that all K. pneumoniae isolates belonged to sequence type ST893, which was associated with outbreaks in Iran in the period 2014–201613, and harbored a predicted capsular type K20. Isolates Kp040741 and Kp040762 originated from the same wound sample, but displayed different colony morphologies and antibiotic resistance profiles (Table 1). Analysis of their genomes revealed that both isolates were clonal, but had different plasmid contents, with isolate Kp040741 containing 3 plasmids, compared to the 5 plasmids of isolate Kp040762 (Figs. 4 and 5). One of the plasmids (pSID3), present in all 3 isolates, appeared to be a prophage element similar to bacteriophage SSU5 (Supplementary Data 2), which was previously suggested to be the phylogenetic origin of cryptic plasmid pHCM2 harbored by a Salmonella Typhi strain14. SNP analysis indicated limited within-host adaptation (Supplementary Data 3). All isolates were shown to possess the pOXA48 plasmid, which contains the class D carbapenem-hydrolyzing β-lactamase OXA-4815. Multiple antibiotic resistance genes (ARGs) were observed in the different isolates, often in multiple copies, with PDR isolate Kp36336 containing the most ABR genes (Fig. 5 and Supplementary Data 4). The strain harbored no less than 4 widely distributed ESBL genes (blaSHV-145, blaOXA-1, blaTEM-1, and blaCTX-M-15), 5 aminoglycoside modifying enzyme (AME) genes [aac(6’)-Ib, aph(3”)-Ib, aadA1, aac(3)-IIe, and aph(6)-Id)], quinolone resistance gene qnrB1, and the multidrug resistance oqxA5 and oqxB19 pump genes. Trimethroprim/sulfamethoxazole (dfrA14 and sul2), tetracycline (tetA), fosfomycin (fosA6), and choramphenicol (catA1) resistance genes were also identified. Fortunately, the K. pneumoniae phage that had been pre-adapted to target the 2 day-170 isolates was equally active against the day-702 isolate (Fig. 6). Even though the patient showed signs of improvement within 2 days of starting phage therapy, the longstanding antibiotic therapy was replaced by ceftazidime/avibactam, which had just become available through a compassionate use program, complemented with high-doses of tigecycline and ciprofloxacin (Fig. 1). With a minimal inhibitory concentration (MIC) of 2.0/0.5 μg/ml, the day-702 isolate was found to be susceptible to ceftazidime/avibactam. Ceftazidime/avibactam was administered at the recommended dosage (2 g/0.5 g, q8h), which was predicted to lead to peak plasma concentration of 90.4 μg/ml and 14.6 μg/ml for ceftazidime and avibactam, respectively (according to the FDA-approved labeling information).
Two weeks later, the patient developed grade A acute pancreatitis due to tigecycline. Therefore, the drug was suspended and symptoms resolved. Oral ciprofloxacin was replaced by moxifloxacin (first intravenously, then orally) due to persisting nausea. The adapted antibiotic treatment was administered for a period of 3 months (Fig. 1).
No adverse events associated with the use of phages were observed. Three months after the day-702 surgical intervention and initiation of the combined phage-antibiotic therapy (Fig. 1) the patient’s clinical, biological, microbiological and radiological conditions were assessed and compared to the pre-surgery status (Fig. 7a). The skin graft appeared vascularized and viable, the sinus tract was closed and dry, and pus no longer discharged from the pin sites of the external fixator (Fig. 7b), indicating that the FRI was controlled16. The patient’s general condition had also improved, with a weight gain of 5 kg and a restored muscle function of the left thigh. Biological blood parameters were within normal reference values. A computed tomography (CT) scan of the left femur showed partial consolidation of the fractures (Fig. 7c). The patient’s immune system began to synthesize neutralizing antibodies sometime between days 8 and 18 post phage application (Fig. 7d). It is thus highly unlikely that phage-neutralizing antibodies hampered the course of phage therapy. Of interest, on February 23, 2021, 3 years after phage application, the patient’s serum no longer contained phage-neutralizing antibodies.
In the absence of clinical signs of FRI, it was decided to discontinue antibiotic treatment 3 months post-surgery and 798 days post-injury (Fig. 1). A week later, the external fixator was removed. No biopsies were performed, to not disturb the fragile consolidation, but 3 bone fragments that detached while removing the external fixator were collected for bacterial culture. These cultures, as well as several subsequent wound cultures, showed no growth. There was no sign of persistent or recurrent K. pneumoniae infection after discontinuation of antibiotics (Fig. 1). At the time of writing, 3 years after phage-antibiotic combination treatment, the patient has regained ambulation and mobility, usually with the aid of crutches, and participates in sporting events (e.g., cycling)17, and there are no signs of recurrent K. pneumoniae infection.
The present case report illustrates the complexity of management of FRI caused by MDR bacteria and the urgent need for new antimicrobial agents. Pre-adapted phage-antibiotic combination therapy ultimately led to a positive clinical outcome of a long-standing PDR K. pneumoniae FRI. Concordantly, in vitro data indicates that the phage-antibiotic combination was more effective in reducing bacterial counts for K. pneumoniae in mature biofilms than antibiotics or phage alone (Fig. 8). We observed that ceftazidime/avibactam dose- and time-dependently reduced bacterial counts for K. pneumoniae in mature biofilms, but without complete eradication even at the highest concentration that can be achieved in the systemic circulation (Cmax, 90/22.5 µg/ml). High doses of the phage did not eradicate the bacteria in such mature biofilms either. However, combinations of high doses of pre-adapted phage M1 and moderate concentrations of ceftazidime/avibactam were significantly more effective than the antibiotic alone.
As planktonic bacteria also play a role in infection, we investigated whether a synergistic activity of preadapted phage M1 and administered antibiotics could also be observed in suspension (in vitro). Results revealed that combinations of preadapted phage M1 and ceftazidime/avibactam (Fig. 9a–c) and meropenem (Fig. 9d), but not colistin (Fig. 9e), were considerably more effective against PDR K. pneumoniae isolate Kp36336 than phage M1 or these antibiotics alone. Considering the clinical data and the in vitro phage-antibiotic synergy data, there are solid indications that the combination of phage M1 and the antibiotics meropenem and ceftazidime/avibactam finally led to the clinical resolution of infection in this patient.
The current state of the art with regard to infections with carbapenem-resistant Enterobacteriaceae advocates the use of combination therapies to prevent or delay the emergence of resistance during antimicrobial therapy18. In a mouse model of diabetic foot ulcers infected with methicillin-resistant S. aureus, the combination of lytic phages and linezolid was more effective in controlling the infection than phages or linezolid alone19. Phages were also shown to infect persister cells in biofilms and turn them into metabolically active cells prior to killing them20. Recently, administration of phages was associated with a satisfactory clinical outcome in a case of intractable biofilm-associated prosthetic knee K. pneumoniae infection21. Whether phages and antibiotics should be used sequentially or simultaneously is still an unresolved question. “Trojan horse” strategies could be considered where phages are used first to destroy biofilms and activate quiescent cells that will become more susceptible to the antibiotics introduced in a second phase. In addition, some phages have the ability to revert resistance against antibiotics22. We cannot exclude that in the present case other factors such as the surgical procedure, including the use of rifampicin-IABG, may have contributed to the recovery of the patient. But then again, rifampicin had no in vitro activity against the infecting K. pneumoniae strains, suggesting that the rifampicin-IABG alone did not play a major role in the improvement of the patient’s K. pneumoniae FRI.
Most phage preparations that are currently researched and developed by western companies are defined phage cocktails, which seem to underappreciate a number of phage peculiarities such as target specificity and antagonistic coevolution23. In recent randomized controlled trials, these static phage cocktails showed disappointing results, which contrast with those of an increasing number of case studies using phages as adjunctive therapy24, or preadapted (or even engineered) phages that are more effective against the infecting bacteria25,26. The present case study can open a new way of thinking about phage therapy: the use of individually adjusted phage-antibiotic combinations.
The research protocol (P2016/516) was approved by the ethical committee of the Erasme Hospital, and the participant gave written informed consent, according to CARE guidelines and in compliance with the Declaration of Helsinki principles. Consent to publish clinical information potentially identifying individuals was also obtained.
Antibiotic susceptibilities of K. pneumoniae isolates were ascertained using the VITEK 2 system (bioMéreux). Moxifloxacin and tigecycline susceptibilities were determined using the Kirby-Bauer disk-diffusion method (NeoSensitabs, International Medical Products). Categorization (therapeutic interpretation) of minimum inhibitory concentrations (MICs) or inhibition zone diameters were based on European Committee on Antimicrobial Susceptibility Testing (EUCAST) guidelines.
Genome sequencing and analysis of K. pneumoniae isolates
The genomes of the 2 day-170 isolates (Kp040741 and Kp040762) and of the day-702 K. pneumoniae isolate (Kp36336) were sequenced (day-4 isolate Kp1 was not stored), as previously described27. Total genomic DNA (gDNA) was extracted from the isolates with the DNeasy UltraClean Microbial kit (Qiagen) according to the manufacturer’s instructions. The gDNA was subsequently prepared for Illumina sequencing using the Nextera Flex (Illumina) and sequenced on an Illumina MiniSeq machine using a paired-end approach (2*150 bp). In addition, the gDNA was also prepared for long-read sequencing using the Rapid barcoding kit SQK-RBK004 (Oxford Nanopore Technology) and sequenced on a MinION equipped with a R9.4.1 flowcell (Oxford Nanopore Technology), with Guppy (v3.1.5) as basecaller. The quality of the Illumina sequencing data was assessed using FastQC v0.11.9 and trimmomatic v0.38 for adapter clipping, quality trimming (LEADING:3 TRAILING:3 SLIDINGWINDOW:4:15), and minimum length exclusion (>50 bp). The quality of the Nanopore reads was assessed using Nanoplot v1.28.2, and Porechop v0.2.3 was used for barcode clipping and NanoFilt v2.6.0 for filtering on quality (Q > 8) and length (>500 bp). The genomes were reconstructed using the hybrid assembler Unicycler v0.4.8. Single Nucleotide polymorphism (SNP) calling was done using snippy v4.4.5 against the PGAP annotation of isolate Kp36336. The assemblies were visually inspected using Bandage28 and the plasmid elements were checked using BLASTn against the NCBI plasmid database (accessed in October 2020). Further functional annotation, antibiotics resistance genes, prophage elements, and genomic islands were annotated using respectively eggNOG-mapper v2.0.029, ABRicate v1 (https://github.com/tseemann/abricate, accessed in October 2020), PHASTER30 (https://phaster.ca, accessed in October 2020), and IslandViewer 431. Unless specified otherwise, programs were run using the default parameters. The sequence type and capsule type of the strain were determined using the software mlst to query the pubMLST database32 (https://github.com/tseemann/mlst, accessed in October 2020) and Kaptive v0.7.333, respectively. The genomic datasets were deposited in the NCBI databases. The initial Illumina and Nanopore sets of reads are available in the SRA database via the accession numbers mentioned in Supplementary Data 5.
Phage selection, preadaptation, and propagation
The lytic activity of 12 Klebsiella phage clones from the Eliava IBMV collection against the patient’s day-170 isolates Kp040741 and Kp040762 was determined by spot test and the double agar overlay method34. To enhance the lytic activity of phages on the patient’s isolates, a phage adaptation procedure based on Appelmans’ method10 was applied for 15 rounds, using both day-170 K. pneumoniae isolates. The selected and adapted phage was propagated on isolate Kp040762 using the double agar overlay method.
Relevant parameters of phage adsorption and reproduction cycle, such as adsorption time, latent period (LT), and burst size (BS), were determined for the K. pneumoniae propagation strain 1a, of clinical origin, using the methods described by Adams34. The morphology and size of the phage particles were evaluated using a JEOL 100SX electron microscope (Jeol). Phages were transferred onto carbon-coated copper grids for 30 s, to let the particles settle, and stained with 1% of uranyl acetate for 40 min. The grids were examined at 250,000x magnification. The infectivity and stability of the selected phage in different environments (acidity and temperature) were evaluated on the K. pneumoniae strain 1a. To determine the impact of acidity, phages were incubated at a titer of 2 × 107 PFU/ml in lysogeny broth (LB) with pH ranging from 2.0 to 14.0 at 37 °C for 1 h. The proportion of persistent phage particles showing infectivity towards the host strain was determined by the double agar overlay method34. To determine the impact of temperature, phages were incubated at a titer of 3 × 107 PFU/ml in LB at temperatures ranging from 20 to 75 °C (with 5 °C steps) for 1 h. After incubation, the number of viable phage particles was determined by the double agar overlay method on the host strain34.
Bacterial growth kinetics in the presence of phage M1 and/or antibiotics
Bacterial respiration was measured using the Omnilog system (Biolog, Hayward, CA, USA)25,35. The growth kinetics of K. pneumoniae isolates Kp040741, Kp040762, and Kp36336 were assessed in the presence of phage M1 (at different MOIs), relevant antibiotics (ceftazidime/avibactam, meropenem, and colistin, at different concentrations), and phage-antibiotic combinations. Experiments were done in 96-well plates (Thermo Fisher Scientific, Roskilde, Denmark) in a final volume of 200 µl of LB supplemented with 100-fold diluted tetrazolium dye mix A, according to the manufacturer’s instructions. Bacterial cells were added at a concentration of 104 CFU/well, calculated based on optical density (OD, at 600 nm) measurements (with an OD of 0.5 corresponding to 4 × 108 CFU/ml, on average), which were validated using a classical plate culture method. Antibiotics and the phage M1 were diluted and used according to the concentrations and MOIs indicated in the captions of Figs. 6 and 9). The titer of the phage M1 was also confirmed after each experiment using the classical double agar overlay method34. Plates were incubated at 37 °C for 72 h and reduction (causing a color change) of the tetrazolium dye due to bacterial respiration (during growth) was recorded every 15 min by the Omnilog system. Experiments were performed in triplicate (biological replicates).
Phage genome sequencing and analysis
Phage DNA was extracted from a high-titer stock of the originally selected variant and the pre-adapted variant of phage M1 and subsequently sequenced using in-house MiniSeq Illumina sequencing as described in Makalatia et al.36. Genome assembly was performed using SPAdes (Galaxy v3.12.0 + Galaxy1)37. Next, using MEGA X v10.1.2, the phage genome was aligned to Klebsiella phage vB_KpnM_KP15, which was identified as the closest type species by BLASTn against the NCBI nucleotide database (accessed in March 2021). Finally, the phage genome was annotated using RASTtk (PATRIC v3.6.12)38 and manually curated by BLASTp against the NCBI protein database (accessed in March 2020). The genome was screened for tRNAs using tRNAscan-SE 2.0 and was visualised as a genome map using EasyFig 2.2.239. We used VirulenceFinder v2.040, ABRicate v1 (https://github.com/tseemann/abricate, accessed in October 2020) and manually verified the annotated proteins to screen for lysogeny-related proteins. The genomes of the originally selected variant and the pre-adapted variant of phage M1 used in therapy were analyzed for distinguishing mutations using the variant caller snippy v4.6.0. The mutated protein was modelled using AlphaFold v2.041 (https://doi.org/10.1038/s41586-021-03819-2, accessed in September 2021).
Biofilm assay and exposure to ceftazidime/avibactam, phages and combinations thereof
Frozen stocks of PDR K. pneumoniae strain Kp36336 in 20% (v/v) glycerol (Thermo Fisher Diagnostic BV) were thawn and then spread on plates with trypticase soy agar with 5% (v/v) sheep blood (bioMérieux) and cultured overnight at 37 °C. Subsequently, several colonies were resuspended in tryptic soy broth (Oxoid Ltd) and cultured for 2.5 h at 37 °C under slow rotation (200 rpm). The mid-logarithmic phase bacteria were harvested by centrifugation (1,000 x g for 10 min), washed with phosphate-buffered saline (PBS; pH 7.4), and then diluted (based on the optical density at 600 nm) in brain heart infusion broth (Oxoid Ltd) to a concentration of 1 × 107 CFU/ml. Next, 100 μl of the bacterial suspension were transferred to 96-wells polystyrene wells flat-bottom plates (Greiner Bio-One) which were then sealed with breathable Ryon film sealers (VWR European). The bacteria were cultured for 7 days at 37 °C in a plastic box to maintain a humidified environment and medium controls were included to monitor possible contamination. Thereafter, the wells were washed twice with saline to remove planktonic bacteria and the biofilms were exposed daily for 3 days to fresh preparations of ceftazidime/avibactam (Pfizer, range: 0–90/22.5 μg/ml), phage (range: 7.7 × 107 to 7.7 × 1010 PFU/ml), or combinations thereof. After 1, 2 and 3 days, the biofilms in 96-wells plates were washed with saline and then sonicated (10 min at 40 kHz) in 100 μl of saline for 10 min. Finally, serial dilutions of the bacterial suspensions were plated on Mueller Hinton agar plates (Oxoid Ltd) for CFU enumeration. In order to neutralize residual bacteriolytic activity in the samples from biofilms exposed to phages bacterial suspensions were diluted in saline supplemented with 10 µM ammonium iron (II) sulphate hexahydrate (Sigma-Aldrich) prior to the assessment of the bacterial counts as described above.
At the end of the surgical intervention, 100 ml of the phage preparation (108 PFU/ml) diluted in 1,000 ml of sterile normal saline (0.9% NaCl) were instilled locally in the surgical wound via a catheter. The catheter was left in place to facilitate local applications of 20 ml of undiluted phages, three times per day for 5 days (Fig. 1). This regimen was based on previous experiences at the Eliava Institute in Tbilisi (Georgia).
Phage neutralization by patient sera
The ability of the patient’s serum to neutralize the phages was evaluated according to Adams34 with some modifications. Whole blood samples were collected 0, 1, 2, 5, 8, 18, 161 days, and 3 years post-phage application. Blood was allowed to clot for a minimum of 30 min in a vertical position and then centrifuged at room temperature in a swinging bucket rotor for 10 min at 2,000 x g. Serum samples were stored at −80 °C ± 5 °C. To assess the effect of the sequential serum samples on phage lytic activity, 0.9 ml of the diluted sera (1:100) were mixed with 0.1 ml of the phage at a concentration of 2 × 107 PFU/ml and incubated at 37 °C for 30 min. After incubation, the phages were titered with 2 of the patient’s K. pneumoniae strains (Kp040741 and Kp040762) to determine the remaining number of non-neutralized phages and thus also the proportion of neutralized phages. Each sample was tested in triplicate on each bacterial strain and the mean value and standard deviation were determined for each serum sample.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
The Illumina and Nanopore sequencing datasets of the Klebsiella pneumoniae genomes were deposited in the Sequence Read Archive (SRA) database under accession codes SRR13350373-SRR13350378. The genome of isolate Kp36336 was deposited in the GenBank database under accession codes CP066511-CP066515. The Illumina data of the wild type and the adapted phages can be accessed via the NCBI SRA database under the accession codes SRR15604575 and SRR15694574, respectively. The genome sequence of phage vB_KpnM_M1 was deposited in the GenBank database under accession code MW448170. Source data are provided with this paper. The authors declare that all other data supporting the findings of this study are available within the article and its Supplementary Data files. Source data are provided with this paper.
Govaert, G. A. M. et al. Diagnosing Fracture-Related Infection: Current Concepts and Recommendations. J. Orthop. Trauma 34, 8–17 (2020).
De Oliveira, D. M. P. et al. Antimicrobial Resistance in ESKAPE Pathogens. Clin. Microbiol. Rev. 33, e00181–19 (2020).
Lewis, K. Persister cells, dormancy and infectious disease. Nat. Rev. Microbiol. 5, 48–56 (2007).
Kortright, K. E. et al. Phage Therapy: A Renewed Approach to Combat Antibiotic-Resistant Bacteria. Cell Host Microbe 25, 219–232 (2019).
Friman, V. P. et al. Pre-adapting parasitic phages to a pathogen leads to increased pathogen clearance and lowered resistance evolution with Pseudomonas aeruginosa cystic fibrosis bacterial isolates. J. Evol. Biol. 29, 188–198 (2016).
Onsea, J. et al. Bacteriophage therapy as a treatment strategy for orthopaedic-device-related infections: where do we stand? Eur. Cell Mater. 39, 193–210 (2020).
Cornely, O. A. et al. Global guideline for the diagnosis and management of mucormycosis: an initiative of the European Confederation of Medical Mycology in cooperation with the Mycoses Study Group Education and Research Consortium. Lancet Infect. Dis. 19, e405–e421 (2019).
Grimaldi, D., Pradier, O., Hotchkiss, R. S. & Vincent, J. L. Nivolumab plus interferon-γ in the treatment of intractable mucormycosis. Lancet Infect. Dis. 17, 18 (2017).
Magiorakos, A. P. et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin. Microbiol. Infect. 18, 268–281 (2012).
Burrowes, B. H., Molineux, I. J. & Fralick, J. A. Directed in Vitro Evolution of Therapeutic Bacteriophages: The Appelmans Protocol. Viruses 11, E241 (2019).
Kęsik-Szeloch, A. et al. Characterising the biology of novel lytic bacteriophages infecting multidrug resistant Klebsiella pneumoniae. Virol. J. 10, 100 (2013).
Pirnay, J. P. et al. The Magistral Phage. Viruses 10, 64 (2018).
Solgi, H., Badmasti, F., Giske, C. G., Aghamohammad, S. & Shahcheraghi, F. Molecular epidemiology of NDM-1- and OXA-48-producing Klebsiella pneumoniae in an Iranian hospital: clonal dissemination of ST11 and ST893. J. Antimicrob. Chemother. 73, 1517–1524 (2018).
Minsik, K., Sujin, K., Bookyung, P. & Sangryeol, R. Core lipopolysaccharide-specific phage SSU5 as an Auxiliary Component of a Phage Cocktail for Salmonella biocontrol. Appl. Environ. Microbiol. 80, 1026–1034 (2014).
Skalova, A. et al. Molecular Characterization of OXA-48-Like-Producing Enterobacteriaceae in the Czech Republic and Evidence for Horizontal Transfer of pOXA-48-Like Plasmids. Antimicrob. Agents Chemother. 61, e01889–16 (2017).
Metsemakers, W. J. et al. Fracture-related infection: A consensus on definition from an international expert group. Injury 49, 505–510 (2018).
Northshield K. Dans le souffle de la bombe (Kennes éditions: Loverval, 2021).
Tamma, P. D., Cosgrove, S. E. & Maragakis, L. L. Combination therapy for treatment of infections with gram-negative bacteria. Clin. Microbiol. Rev. 25, 450–470 (2012).
Chhibber, S., Kaur, T. & Kaur, S. Co-therapy using lytic bacteriophage and linezolid: effective treatment in eliminating methicillin resistant Staphylococcus aureus (MRSA) from diabetic foot infections. PLoS ONE 8, e56022 (2013).
Akanda, Z. Z., Taha, M. & Abdelbary, H. Current review-The rise of bacteriophage as a unique therapeutic platform in treating peri-prosthetic joint infections. J. Orthop. Res. 36, 1051–1060 (2018).
Cano, E. J. et al. Phage Therapy for Limb-threatening Prosthetic Knee Klebsiella pneumoniae Infection: Case Report and In Vitro Characterization of Anti-biofilm Activity. Clin. Infect. Dis. 73, e144–e151 (2021).
Chan, B. K. et al. Phage treatment of an aortic graft infected with Pseudomonas aeruginosa. Evol. Med. Public Health 2018, 60–66 (2018).
Pirnay, J. P. & Kutter, E. Bacteriophages: it’s a medicine, Jim, but not as we know it. Lancet Infect. Dis. 21, 309–311 (2021).
Petrovic Fabijan, A. et al. Safety of bacteriophage therapy in severe Staphylococcus aureus infection. Nat. Microbiol. 5, 465–472 (2020).
Schooley, R. T. et al. Development and Use of Personalized Bacteriophage-Based Therapeutic Cocktails To Treat a Patient with a Disseminated Resistant Acinetobacter baumannii Infection. Antimicrob. Agents Chemother. 61, e00954–17 (2017).
Dedrick, R. M. et al. Engineered bacteriophages for treatment of a patient with a disseminated drug-resistant Mycobacterium abscessus. Nat. Med. 25, 730–733 (2019).
Lood, C. et al. Genomics of an endemic cystic fibrosis Burkholderia multivorans strain reveals low within-patient evolution but high between-patient diversity. PLoS Pathog. 17, e1009418 (2021).
Wick, R. R. et al. Bandage: interactive visualization of de novo genome assemblies. Bioinformatics 31, 3350–3352 (2015).
Huerta-Cepas, J. et al. Fast Genome-Wide Functional Annotation through Orthology Assignment by eggNOG-Mapper. Mol. Biol. Evol. 34, 2115–2122 (2017).
Arndt, D. et al. PHASTER: a better, faster version of the PHAST phage search tool. Nucleic Acids Res. 44, W16–W21 (2016).
Bertelli, C. et al. IslandViewer 4: expanded prediction of genomic islands for larger-scale datasets. Nucleic Acids Res. 45, W30–W35 (2017).
Jolley, K. A. & Maiden, M. C. J. BIGSdb: Scalable analysis of bacterial genome variation at the population level. BMC Bioinforma. 11, 595 (2010).
Wick, R. R. et al. Kaptive Web: User-Friendly Capsule and Lipopolysaccharide Serotype Prediction for Klebsiella Genomes. J. Clin. Microbiol., 56, e00197–18 (2018).
Adams, M. H. Bacteriophages (Interscience Publishers: NewYork, 1959).
Duplessis, C. A. & Biswas, B. A Review of Topical Phage Therapy for Chronically Infected Wounds and Preparations for a Randomized Adaptive Clinical Trial Evaluating Topical Phage Therapy in Chronically Infected Diabetic Foot Ulcers. Antibiotics (Basel) 9, 377 (2020).
Makalatia, K. et al. Characterization of Salmonella Isolates from Various Geographical Regions of the Caucasus and Their Susceptibility to Bacteriophages. Viruses 12, 1418 (2020).
Afgan, E. et al. The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2018 update. Nucleic Acids Res. 46, W537–W544 (2018).
Wattam, A. R. et al. Improvements to PATRIC, the all-bacterial Bioinformatics Database and Analysis Resource Center. Nucleic Acids Res. 45, D535–D542 (2016).
Sullivan, M. J. et al. Easyfig: a genome comparison visualizer. Bioinformatics 27, 1009–1010 (2011).
Malberg Tetzschner, A. M. et al. In Silico Genotyping of Escherichia coli Isolates for Extraintestinal Virulence Genes by Use of Whole-Genome Sequencing Data. J. Clin. Microbiol. 58, e01269–20 (2020).
Jumper, J. et al. Highly accurate protein structure prediction with AlphaFold. Nature 596, 583–589 (2021).
We thank A. Vanderkelen for helping facilitate the application of phages. We thank S. Djebara for sample collection. We thank J. Onsea for her critical reading of the manuscript.
The authors declare no competing interests.
Peer review information
Nature Communications thanks Andrzej Gorski, Gina Suh and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Eskenazi, A., Lood, C., Wubbolts, J. et al. Combination of pre-adapted bacteriophage therapy and antibiotics for treatment of fracture-related infection due to pandrug-resistant Klebsiella pneumoniae. Nat Commun 13, 302 (2022). https://doi.org/10.1038/s41467-021-27656-z
Journal of Biomedical Science (2022)
Reactions Weekly (2022)