Implant-related infection is difficult to treat without extended antibiotic courses. However, the long-term use of antibiotics has led to the development of multidrug- and methicillin-resistant Staphylococcus aureus. Thus, alternatives to conventional antibiotic therapy are needed. Recently, mesenchymal stem cells have been shown to have antimicrobial properties. This study aimed to evaluate the antimicrobial activity and therapeutic effect of local treatment with antibiotic-loaded adipose-derived stem cells (ADSCs) plus an antibiotic in a rat implant-associated infection model. Liquid chromatography/tandem mass spectrometry revealed that ADSCs cultured in the presence of ciprofloxacin for 24 h showed time-dependent antibiotic loading. Next, we studied the therapeutic effects of ADSCs and ciprofloxacin alone or in combination in an implant-related infection rat model. The therapeutic effects of ADSCs plus antibiotics, antibiotics, and ADSCs were compared with no treatment as a control. Rats treated with ADSCs plus ciprofloxacin had the lowest modified osteomyelitis scores, abscess formation, and bacterial burden on the implant among all groups (P < 0.05). Thus, local treatment with ADSCs plus an antibiotic has an antimicrobial effect in implant-related infection and decrease abscess formation. Thus, our findings indicate that local administration of ADSCs with antibiotics represents a novel treatment strategy for implant-associated osteomyelitis.
Periprosthetic infections are a tremendous burden to patients and healthcare institutions worldwide1. With the increase in arthroplasty procedures and the ongoing development of drug-resistant microorganisms, the incidence of such infections has been increasing1. To address this challenge, novel treatments are necessary1.
Staphylococcus aureus (S. aureus) is one of the primary pathogens responsible for implant-associated osteomyelitis2. The ability of S. aureus to establish chronic, implant-associated infections and our inability to cure them are directly associated with its capacity to form biofilms, creating an environment where the bacteria can grow and persist while being protected from the patient’s immune response and antibiotics3. At present, systemic administration of antibiotics is the standard therapy for implant-associated infections. However, the long-term use of antibiotics has led to the development of multidrug-resistant and methicillin-resistant S. aureus4. Strategies for local antibiotic delivery to increase the antimicrobial concentration at the site of infection while keeping systemic levels low to avoid potential side effects have been investigated for several decades5. However, there still is an unmet need for alternatives to conventional antibiotic therapy for the management of chronic infections4.
Recently, mesenchymal stem cells (MSCs) have been shown to have antimicrobial properties6,7,8,9,10. MSCs reportedly participate in the innate immune response through the secretion of antimicrobial peptides7. Bone marrow-derived stem cells (BMSCs) can be loaded with antibiotics and other drugs, and MSCs including adipose-derived stem cells (ADSCs) co-administered with antibiotic therapy may be a novel effective, antimicrobial approach to the treatment of chronic, drug-resistant infections5,11,12. Among the various types of MSCs, ADSCs have numerous unique advantages. They are abundant in subcutaneous adipose tissues and can be easily harvested using a syringe or by minimally invasive lipoaspiration13. In addition, they contribute to the complex wound-repair processes, comprising inflammation, granulation, and remodelling14,15. While ADSCs are known to exert antibacterial activity, their activity in implant-related osteomyelitis has not been previously investigated. We hypothesized that ADSCs loaded with an antibiotic can exert an antimicrobial therapeutic effect in implant-related osteomyelitis. Therefore, we studied the effects of local treatment with ADSCs and ADSCs plus an antibiotic in a rat model of implant-associated osteomyelitis to evaluate their effectiveness in implant-related infection.
Effect of the antibiotic on ADSCs
Ciprofloxacin (CPFX) dose-dependently suppressed the proliferation of ADSCs, with half-maximum inhibitory concentration (IC50) values of 99.5 mg/L at 24 h and of 103.6 mg/L at 7 days (Fig. 1A, B). Based on the findings, we established 100 mg/L as an optimal CPFX dose for priming ADSCs. Alizarin red and alkaline phosphatase (ALP) staining showed that ADSCs and antibiotic-loaded ADSCs were well differentiated at 2 weeks after osteogenic induction (Fig. 1C). Moreover, mRNA levels of ALP and osteocalcin were examined to determine the osteogenic capacity. Quantitative reverse-transcription (RT-q)PCR showed that antibiotic-loaded ADSCs had similar ALP mRNA levels, but reduced osteocalcin mRNA levels when compared to ADSCs (Fig. 1D, E). The mRNA level of rat cathelicidin-related antimicrobial peptide (rCRAMP) was also examined to assess the antimicrobial peptide secretion ability. rCRAMP was expressed to similar levels in both antibiotic-loaded ADSCs and ADSCs (Fig. 1F).
Quantification of CPFX in and released from ADSCs
Both ADSCs and BMSCs showed a time-dependent loading of CPFX during 24 h of culture in the presence of CPFX (Fig. 2A). The concentration of CPFX in ADSCs was significantly higher than that in BMSCs (Fig. 2A). At 10 min and 1 h, CPFX concentrations significantly differed between ADSCs than BMSCs, whereas at 12 h and 24 h, no significant differences were detected (Fig. 2A). CPFX adsorption to the plate was hardly observed (Fig. 2A). In the release phase, CPFX was detected at 72 h in conditioned media (CM) of both ADSCs and BMSCs (Fig. 2B). The concentrations of CPFX in CM of ADSCs and BMSCs showed no significant differences at 24 h, 48 h, and 72 h after CPFX release (Fig. 2C). The antimicrobial activity of antibiotic-loaded ADSCs and CM of these cells was evaluated using the broth dilution method (Fig. 2D, E). The minimum inhibitory concentration (MIC) values for S. aureus were determined using a 1:2 serial dilution of a standard preparation of CPFX. Complete growth inhibition of S. aureus was observed at 0.125 mg/L of CPFX (Fig. 2F, row A). Antibiotic-loaded ADSCs induced visible growth inhibition at a dilution of 1:8 (Fig. 2F, row B), and the CM of the antibiotic-loaded ADSCs induced growth inhibition at a dilution of 1:2 (Fig. 2F, row C). Growth inhibition was not detected in ADSCs and CM of these cells (Fig. 2F, rows D and E). These results showed that ADSCs could load enough CPFX to exert antimicrobial activity against S. aureus.
In-vivo analysis of implant-related infection in rats
For S. aureus exposure, we coated the screw with 5 × 107 colony-forming units (CFU), which induced infection in 100% of non-treated rats by day 7 day after surgery. Intra-rater reliability of the modified osteomyelitis score was assessed, and the intra-class coefficient was 0.902 (95% confidence interval, 0.850–0.947). The no-treatment group showed obvious swelling at the surgical site, whereas rats in the antibiotic-loaded ADSCs plus CPFX (ADSCs-ant) and ADSCs groups showed very limited swelling (Fig. 3A). Rats in the no-treatment group clearly showed abscess formation. Rats in the ADSCs-ant group showed very limited abscess formation, whereas those in the antibiotic and ADSCs groups showed moderate abscess formation (Fig. 3B). The no-treatment group had the highest modified osteomyelitis score, whereas the ADSCs-ant group had the lowest score among all groups (Kruskal–Wallis test followed by Dunn’s post-hoc test, P < 0.05; Fig. 3C). The antibiotic and ADSCs groups showed no significant differences when compared to the no-treatment group. Micro-computed tomography (μCT) analysis showed obvious osteolysis around the screw hole in the no-treatment, antibiotic, and ADSCs groups, especially around the distal screw hole (Fig. 4A). The healthy bone ratio of the proximal screws was significantly higher in the ADSCs-ant and antibiotic groups, and osteolysis around screw holes was significantly reduced in these groups when compared to the no-treatment and ADSCs groups (Fig. 4B, C). There were no significant differences in osteolysis of the distal screw holes among the groups (Fig. 4D).
Histological assessment of abscess formation
Histological analysis provided apparent evidence of advanced spongy alteration, partial disappearance of cortical substance, and abscess formation (Fig. 5A–C). The abscessed area in the total area was evaluated in all groups (Fig. 5D). The abscessed area was significantly reduced in the ADSCs-ant group when compared with the no-treatment group (ordinary one-way ANOVA followed by Sidak’s post-hoc test, P < 0.05, Fig. 5E), whereas the antibiotic and ADSCs groups did not show reduced abscess formation. Rats in the ADSCs-ant group showed no abscess formation in the proximal screw hole. Rats in the no-treatment, antibiotic, and ADSCs groups showed abscess formation around the screw hole and the plate. Rats in the no-treatment and antibiotic groups showed necrotic cancellous bone in the central area, whereas animals in the ADSCs-ant and ADSCs groups had viable cancellous bone in this area. All groups showed abscess formation in the distal screw hole, although ADSCs-ant-treated rats had smaller abscessed areas than others (Supplementary Fig. S1).
Effects of ADSCs-ant on implant and soft-tissue bacterial burden
Bacterial infection was detected in all rats in the no-treatment group. Treatment with ADSCs-ant significantly suppressed the bacterial burden on the proximal screw compared to that in no treatment (Kruskal–Wallis test followed by Dunn’s post-hoc test, P < 0.001, Fig. 6). ADSCs-ant, antibiotic, and ADSCs significantly reduced the bacterial burden on the distal screw compared to no treatment (one-way ANOVA followed by Sidak’s post-hoc test, P < 0.05, P < 0.001, P < 0.05, respectively). Only the antibiotic group showed significantly decreased bacterial burden on the plate when compared to the no-treatment group (Kruskal–Wallis test followed by Dunn’s post-hoc test, P < 0.05). ADSCs-ant induced a significant decrease in bacterial burden in the soft tissue as compared to that in no treatment (Kruskal–Wallis test followed by Dunn’s post-hoc test, P < 0.05). ADSCs-ant, antibiotic, and ADSCs significantly reduced total bacterial burden compared to that in no treatment (Brown-Forsythe and Welch ANOVA followed by Dunnett’s T3 post-hoc test, P < 0.0001, P < 0.05, and P < 0.05, respectively).
Our in vitro results demonstrated that ADSCs could be primed with CPFX by a simple method, and the concentration of CPFX in the ADSCs increased with exposure time. The in vivo studies demonstrated that ADSCs combined with CPFX improved osteomyelitis scores and decreased osteolysis and bacterial loads in rats with implant-related infection as compared to that in no treatment in a rat model of implant-related infection. Furthermore, only the ADSCs-ant group showed a significant decrease in abscess formation among all groups. ADSCs alone lowered bacterial loads compared to no treatment, but the effect was not larger than that of antibiotic alone. These results demonstrated that ADSCs have an antimicrobial effect and effectively decrease the bacterial burden on the implant, and the effect was enhanced when the ADSCs were combined with an antibiotic.
Owing to their differentiation plasticity, immunomodulatory properties, angiogenic modulation, and paracrine support16,17,18,19 , MSCs have been investigated in a wide spectrum of diseases, as evidenced by the approximately 500 trials registered in the ClinicalTrials.gov database of the National Institutes of Health (https://www.clinicaltrials.gov/, queried in December 2016)20. However, the use of local injection of ADSCs loaded and combined with an antibiotic to treat implant-related osteomyelitis had not been reported to date. Multiple, complementary mechanisms of action (both direct and indirect) likely account for the ability of MSCs to help control infections, although it is not fully understood whether the main weapon is the cell itself or its secretome7,9. They might act indirectly through their role in the host immune response against pathogens, especially in the dynamic coordination of pro- and anti-inflammatory elements of the immune system21,22,23 or by increasing the activity of phagocytes24,25,26. They might act directly through the secretion of antimicrobial peptides and proteins27,28,29,30 and the expression of molecules, such as indoleamine 2,3-dioxygenase31 and interleukin-1732. Our in vitro experiments showed that both ADSCs and ADSCs-ant expressed the gene encoding the antimicrobial peptide cathelicidin at similar levels. This implied that the combination with an antibiotic did not suppress the expression of antimicrobial peptides.
Antimicrobial peptides are evolutionarily conserved small effector molecules (10–150 amino acids) found in organisms ranging from prokaryotes to humans33. Antimicrobial peptide-mediated cell killing occurs by disrupting membrane integrity, by inhibiting protein, DNA, or RNA synthesis, and by interacting with certain intracellular targets34. Importantly, antimicrobial peptides can be active against certain pathogens that are resistant to conventional antibiotics, such as multidrug-resistant bacteria20. Previous studies in mice reported that cathelicidin is one of the factors produced by systemic MSCs that significantly contributes to Staphylococcus killing9. Thus, ADSCs seem to express antimicrobial peptides. This is likely, at least in part, responsible for the reduction in bacterial burden on the implant.
The capacity of MSCs to interact with the innate and adaptive immune responses to inhibit T-cell proliferation and upregulate regulatory T cells35,36 makes this cell population a strong candidate for cell therapy in graft-versus-host disease or vascularized composite allotransplantation. MSCs have been shown to exert immunomodulatory effects through cell contact and paracrine effects37,38. This protective role of MSCs in the host reportedly is dual: on one hand, they can create an immunosuppressive environment, thus avoiding exacerbation of pathological symptoms, helping to heal tissue damage, and allowing the establishment of an immune-tolerant environment; on the other hand, however, excessive immune suppression as well as the sensitivity of MSCs to microbial infection can lead to the opposite effect, hampering the host’s ability to fight the infection and, instead, encouraging the spread of microbial effectors9. Therefore, the immunomodulatory capacity of locally administered MSCs in infectious diseases is not fully understood. A previous study reported negative effects of MSCs on orthopaedic implant-associated bone infection39, which is in contrast to studies reporting a beneficial effect of intravenously administered MSCs on the development of sepsis through a reduction in systemic inflammation and increased bacterial killing and phagocytosis39. The authors reasoned that, although immune suppression may be beneficial in systemic infection with whole-body inflammation, local and chronic infections such as osteomyelitis may be promoted by a local immunosuppressive environment39. Although their infection model—consisting of a bone defect contaminated with S. aureus and administration of bone marrow-derived MSCs—was different from ours, our study revealed no negative effect of ADSCs on implant-related infection, and, in contrast, showed a positive effect of ADSCs-ant. Therefore, we conclude from the combined findings that locally injected MSCs may have an immunosuppressive capacity, but do not always promote an immunosuppressive environment, and ADSCs combined with an antibiotic are an effective option for local treatment.
Systemic ADSC-assisted antibiotics therapy offered an additional benefit by reducing acute urogenital organ damage in a rat model40, and ADSC therapy improved ischemia reperfusion injury not only by suppressing the inflammatory and immune responses, but also by enhancing paracrine effects40,41. A previous in-vitro study showed that BMSCs can uptake antibiotics12. Our results suggest that ADSCs can also uptake antibiotics, with the antibiotic concentration increasing over time. Whether CPFX was internalized in the cells or attached to the cell surface was not clarified in this study. However, a previous in-vitro study using confocal microscopy showed that the anti-cancer drug paclitaxel was internalized in MSCs via Golgi-derived vesicles42. Based on this finding, we considered that CPFX might be internalized in the ADSCs and subsequently released from the cells at the infection site. In situ drug injection probably has lower efficacy than drug-loaded MSCs because of rapid dilution of the drug. MSCs have the ability to migrate into inflammatory sites4,43. In vivo, MSCs have been observed to accumulate in the spleen as well as in wound areas following intravenous administration4. Therefore, ADSCs loaded and combined with antibiotics may improve the delivery of antibiotics to the infected area. While our results showed that ADSCs-ant had the strongest therapeutic effect in rats with implant-related infection, the additive or synergistic interaction between ADSCs and antibiotics was not elucidated in this study. Further studies are needed to determine whether there is synergistic interaction between ADSCs and CPFX, and what the optimum antibiotic, dose, and regimen are.
Systemic antibiotics alone cannot completely remove biofilms, and thus, surgical debridement is generally necessary for the treatment of implant-related infection. However, surgical debridement and revision implant have not always been successful. Achieving a high local antibiotic concentration around an infected implant is of major clinical importance, because bacteria protected by the biofilm require antibiotic concentrations that are orders of magnitude greater than the MIC required for killing the bacteria44,45,46, and an intravenous antibiotic injection is not suitable to this end47. Therefore, recently, direct local antibiotic injection has been highlighted as an option because it achieves high local antibiotic concentrations47,48. Furthermore, a recent study has shown that MSCs secrete cysteine proteases that destabilize methicillin-resistant S. aureus biofilms, thereby increasing the efficacy of antibiotics that were previously tolerated by biofilms49. Therefore, by using ADSCs or ADSCs-ant, the effect of local antibiotic treatment could be enhanced. However, systemic treatment is also useful as it is easier to be carried out as compared to the ease of performing a local treatment. Therefore, we are currently researching the effect of systemic ADSC treatment for implant-related infection.
The relevance of our findings to human subjects remains to be studied. In future, it will be necessary to confirm the effect of ADSCs on implant-related infection in larger animal models before clinical studies in humans can be conducted. For clinical application, the source of ADSCs is important. In our study, ADSCs were collected from allogenic rats. Autologous ADSC applications have some potential limitations. It is difficult to obtain sufficient quantities of healthy autologous ADSCs with high activity from patients with the targeted diseases50. Allogeneic MSCs have been previously safely administered to humans for a number of conditions, and their use as a treatment for chronic infections would not pose a unique risk50. One limitation of using ADSCs as a delivery vehicle for antibiotics is that their ability to do so is dependent on cell viability and integration at the injection site. By using DiI staining of ADSCs, a previous study showed that numerous ADSCs were distributed throughout granulation tissue up to 21 days post-transplantation13. We did not study cell viability and distribution after injection, which requires further study. Furthermore, in this in vivo study, the effect of antibiotic-loaded ADSCs alone was not assessed, but only loaded ADSCs combined with antibiotic were assessed. Therefore, the combinatorial effect of CPFX and ADSCs was shown, but the individual effect of ADSCs loaded with CPFX was not considered in this study protocol, since CPFX leaked out into the media before the cells could be administered. In the in vitro study, the concentration of CPFX in cells was higher than the MIC for S. aureus, but was substantially lower than the concentration of CPFX in the antibiotic group (100 mg/L). Therefore, we expected not only antibiotic delivery in cells, but also a synergistic or additive effect of the administered antibiotic and loaded ADSCs.
In summary, ADSCs can uptake antibiotics without suppression of antimicrobial peptide gene expression. Injected ADSCs exerted an antimicrobial effect, and local administration of ADSCs with CPFX suppressed chronic S. aureus infection in implant-related osteomyelitis. These findings suggest that local ADSC therapy combined with an antibiotic represents a novel treatment strategy for patients with implant-associated osteomyelitis. The results of this study highlight the potential use of this combined regimen in patients with implant-related osteomyelitis who responded poorly to conventional medical treatment.
ADSC and BMSCs for in vitro experiments were isolated from 20 9-week-old female Wistar rats (Japan SLC Co., Shizuoka, Japan). ADSCs were prepared as previously reported13, with modification. BMSCs were isolated from the same rats, as previously reported51, with modifications in the protocol. Further details can be found in the Supplementary information.
Assay of sensitivity of ADSCs to CPFX
The anti-proliferative and cytotoxic effects of CPFX (Wako) on rat ADSCs were determined by a 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium (MTT) assay (Sigma-Aldrich, St. Louis, MO, USA) as previously reported12, with modification. CPFX is a fluoroquinolone and is considered a drug of choice for the treatment of osteomyelitis because it penetrates into poorly vascularized sites of infection12. Cells were seeded in 96-multiwell plates at 10,000 cells/well in 100 μL of Dulbecco’s modified Eagle medium (DMEM) per well. In the anti-proliferative assay, cells were incubated for 24 h or 7 days with various concentrations of CPFX (1.95–250 mg/L, with 1:2 dilutions from one concentration to the following one). At the end of incubation, cell proliferation or viability was evaluated by MTT assay.
CPFX loading of ADSCs and BMSCs
ADSCs and BMSCs (1 × 105 cells/mL) were plated in 100-mm dishes containing DMEM including fetal bovine serum (FBS) and CPFX (100 mg/L) for 10 min, 1 h, 12 h, or 24 h, as previously described12. At the end of the incubation, the cells were washed three times with phosphate-buffered saline (PBS). After loading with CPFX, the cell medium was changed to DMEM without CPFX. The concentration of CPFX released from ADSCs and BMSCs after the medium exchange was measured in 1 mL of medium obtained at 24, 48, or 72 h. The medium was exchanged each time after sample collection.
Assay of the ability of ADSCs and ADSCs-ant to differentiate into osteoblasts
Antibiotic-loaded ADSCs and ADSCs were analysed for their capacity for osteogenic differentiation using ALP staining and alizarin red histochemistry. To induce differentiation, cells were cultured in osteogenic medium composed of α-MEM (Wako Pure Chemical Industries) containing 10% FBS, 0.1 mM dexamethasone, 50 mM ascorbate-2-phosphate, 10 mM β-glycerophosphate, and 1% penicillin-streptomycin52. Alkaline phosphatase (ALP) histochemistry was performed at 2 weeks after osteogenic induction culture. For ALP staining, cells were rinsed with PBS three times and fixed in 4% paraformaldehyde phosphate buffer (Wako) at room temperature for 5 min. They were then washed with deionized water. The fixed cells were incubated with 1-Step NBT/BCIP plus Suppressor Solution (Thermo Fisher Scientific) at 37 °C for 30 min, washed with deionized water, and observed both with the naked eye and under a light microscope (Biorevo BZ-9000; Keyence, Osaka, Japan). For alizarin red staining, cells were rinsed with PBS three times, fixed in 4% paraformaldehyde phosphate buffer, and stained using an Osteogenesis Assay Kit (ECM815; Millipore) per the manufacturer’s instructions.
The mRNA expression of rat osteocalcin, rat ALP, and rat CRAMP was evaluated by qPCR. Briefly, RNA was extracted from the cells, and cDNA was generated using RNA to cDNA EcoDry Premix (Oligo dT) (Takara Bio, Kusatsu, Japan). qPCRs were run using THUNDERBIRD SYBR qPCR Mix (Toyobo, Tokyo, Japan) and the following primer sets: 5′-GACTGCATTCTGCCTCTCTG-3′ and 5′-ATTCACCACCTTACTGCCCT-3′ for osteocalcin, 5′-AACAACCTGACTGACCCTTC-3′ and 5′-TCCACTAGCAAGAAGAAGCC-3′ for ALP, 5′-GGTTCCGAGTGAAGGAGACTG-3′ and 5′-TACCAGGCGCATCACAACTG-3′ for rCRAMP, and 5′- ATCACCATCTTCCAGGAGCG-3′ and 5′-CCTTCTCCATGGTGGTGAAG-3′ for rat glyceraldehyde-3-phosphate dehydrogenase (Gapdh)53,54. Target mRNA levels were normalized to that of Gapdh.
Liquid chromatography-tandem mass spectrometry (LC–MS/MS) for the measurement of the concentration of CPFX in ADSCs and BMSCs, and CM
The concentrations of CPFX in ADSCs and CM, and in BMSCs and CM as a control, were quantified using LC–MS/MS, as previously reported12. CPFX concentrations in cells were determined at 10 min, 1 h, 12 h, and 24 h after treatment with CPFX (100 mg/L) as described above, and those in CM at 24, 48, and 72 h after medium exchange. Furthermore, CPFX concentrations in cells after release were analysed at 24, 48, and 72 h. To assess potential adsorption of CPFX to the plate, we measured the concentration of CPFX in DMEM without cells after the changing the medium following a 24-h incubation with DMEM containing 100 mg/L CPFX, without cells. Detailed methods are described in the Supplementary information.
Assay of the antimicrobial activity of cells and CM of ADSCs-ant
The concentration of CPFX in antibiotic-loaded ADSCs was assessed using the broth microdilution method in cation-adjusted Mueller–Hinton broth55. Antibiotic-loaded ADSCs and the CM of the antibiotic-loaded ADSCs were tested for their activity on S. aureus strain ATCC29213 (American Type Culture Collection, Manassas, VA, USA). Further details of the method can be found in the Supplementary information.
The protocol for establishing the implant-related infection model is shown in Fig. 7. Thirty-six 9-week-old female Wistar rats were purchased from Japan SLC Co. (Shizuoka, Japan). Twelve rats were used to obtain ADSCs and the remaining 24 rats were randomly assigned to four treatment groups. Prior to surgery, the rats were sedated and anesthetized with medetomidine (0.5 mg/kg) (Zenoaq, Fukushima, Japan), midazolam (2.5 mg/kg) (Astellas Pharma, Tokyo, Japan), and butorphanol tartrate (2.5 mg/kg) (Meiji Seika Pharma, Tokyo, Japan) injected intraperitoneally. Animals were allowed full activity in their cages and were medicated with meloxicam (0.2 mg/kg) on post-operative day two. Their drinking and feeding behaviours were monitored regularly. The left femur was exposed by a direct lateral approach, and a 3-hole stainless plate was fixed to the femur with two stainless screws inserted into the outermost screw holes of the plate (straight miniplate, DePuy Synthes, Raynham, MA, USA). To establish infection, the distal screw was incubated in an overnight culture of S. aureus strain ATCC29213 and air-dried for 20 min prior to insertion using a previously reported method56. The wound was then closed with nylon sutures. Seven days after the primary surgery, the rats were sedated and anesthetized again, and the surgical scar was reopened and irrigated with 10 mL of PBS. Rats were clarified for 4 groups: rats in the no-treatment group (n = 6) were injected using an 18-gauge needle locally into the surgical site with DMEM (2 mL), rats in the ADSCs-ant group (n = 6) with ADSCs-ant (1 × 105 ADSCs/mL pre-loaded with CPFX in DMEM containing CPFX 50 mg/L, 2 mL), and rats in the in antibiotic group (n = 6) with CPFX alone (2 mL of DMEM containing 100 mg/L CPFX), and rats in the ADSCs group (n = 6) with ADSCs alone (2 mL of DMEM containing 1 × 105 ADSCs/mL). In the ADSCs-ant group, ADSCs loaded with CPFX were washed, harvested by trypsinization with 0.05% trypsin, and resuspended in DMEM containing 100 mg/L CPFX for preservation until use so that the final CPFX concentration was 50 mg/L. The ADSCs, ADSCs-ant, and DMEM with CPFX were produced in the laboratory at the Department of Orthopaedic Surgery, Kanazawa University Graduate School of Medical Sciences, and then transferred to the laboratory at the Institute for Gene Research, Kanazawa University immediately. The rats were euthanized on day 7 post injection (14 days after infection) after evaluating the general impression and soft tissue swelling. After euthanization, abscess formation was evaluated to reopen the surgical scar.
Ex vivo analyses
Rats were euthanized on day 14 post primary surgery (day 7 post injection), and the implants and femurs were harvested in a sterile manner for ex-vivo analyses. Osteomyelitis was scored by two examiners (Y.J. and Y.Y.) according to a modified score reported previously39,57,58 (Supplementary Table 1).
Modified osteomyelitis scores
Modified osteomyelitis scoring by two examiners was based on (1) general impression, (2) soft tissue swelling, (3) abscess formation, (4) proximal screw loosening, and (5) distal screw loosening. In case of disagreements between the two examiners, the lowest score was taken. Parameters 1–3 ranged from 0 (good or absent), 1 (mild), 2 (moderate) to 3 (bad or severe). Parameters 4 and 5 were judged based on micro-CT images, which was as follows: We calculated the degree of osteolysis as a healthy bone ratio (cortical bone area/total bone area). A mean ratio of > 0.7 was scored as 0, 0.6–0.7 was scored as 1, < 0.6 was scored as 2, and fracture was scored as 3. The maximum score to be achieved was 15 [5 parameters, 3 points maximum score (see Supplementary Table 1)].
At post-surgery day 14 (day 7 post revision), the plated femurs were disarticulated, the implant and soft tissue were removed carefully, and the samples were subjected to μCT scanning at 10.5-micron resolution (LaTheta LCT-200; Hitachi-Aloka, Tokyo, Japan). To quantify osteolysis in the screw holes, μCT images in digital imaging and communications in medicine (DICOM) format were obtained for volumetric osteolysis analysis using the DICOM viewer software Synapse Vincent (Version 5; Fujifilm, Tokyo, Japan, https://www.fujifilm.com/jp/ja/healthcare/healthcare-it/it-3d/vincent#). The femoral bone was automatically traced as the region of interest, and the Hounsfield Unit (HU) value was calculated59. The osteolytic volume of the screw hole was determined by calculating the total screw hole volume of the 5 slices and comparing the cortical bone (voxels ≥ 230 Hu) within the total screw hole volume56. We calculated the degree of osteolysis as the healthy bone ratio (cortical bone area/total bone area).
The femoral bone was fixed in 10% neutralized formalin solution and dehydrated using an ethanol gradient (70%, 80%, 90%, and 100%). The fixed specimens were decalcified in 10% formic sodium citrate solution, embedded in paraffin, and sectioned in the coronal plane at 0.2-μm thickness. The sections were stained with haematoxylin and eosin, and the slides were observed under an optical microscope (Biorevo BZ-9000; Keyence, Osaka, Japan). The abscessed area in the total area was evaluated in three regions, including at the distal screw hall, the proximal screw hall, and the region between the two screw halls. The assessment was confirmed by a pathologist (N.T.).
The bacterial burden on the implants was determined by CFU assay following sonication, as previously described60. Briefly, the implants were placed into 1 ml PBS in 1.5 ml microtubes. The solution was subjected to rapid vortex mixing for 15 s and then sonicated for 5 min (Bransonic Branson 5,210, Kanagawa, Japan) at a frequency of 40 Hz to disrupt the formed biofilm. Finally, rapid vortex mixing of the solution was performed again for 1 min. This method of disrupting the biofilm was performed in accordance with the method reported by Braem et al.61, with slight modification. CFU assays were performed on the explanted proximal (sterile) screws, distal (contaminated) screws, and plates and soft tissues around the implant obtained on day 14 after surgery.
Data are reported as the median ± interquartile range. The Shapiro–Wilk test was used to check normal distribution, and the Bartlett’s test was used to evaluate equality of variances. Means of two groups were compared using unpaired Student’s t-tests. Multiple groups were compared using one of the following: ordinary one-way ANOVA followed by Sidak’s post-hoc test (for normally distributed data with equal variances), Brown-Forsythe and Welch ANOVA followed by Dunnett’s T3 post-hoc test (for normally distributed data without equal variances), or Kruskal–Wallis test followed by Dunn’s post-hoc test (for non-normally distributed data). P < 0.05 was considered significant. All analyses were conducted using Prism8 software (Version 188.8.131.522; GraphPad Software, San Diego, CA, https://www.graphpad.com/scientific-software/prism/).
The investigational protocol was approved by the Kanazawa University Advanced Science Research Centre (Approval Number: AP-173878), and all animals were treated in accordance with Kanazawa University Animal Experimentation Regulations.
All the data used to draw the conclusions of this paper are available in the data presented in the figures and/or table. The raw/processed data required to reproduce these findings are available from the corresponding author upon request.
Kapadia, B. H. et al. Periprosthetic joint infection. Lancet 387, 386–394 (2016).
Nishitani, K. et al. Quantifying the natural history of biofilm formation in vivo during the establishment of chronic implant-associated Staphylococcus aureus osteomyelitis in mice to identify critical pathogen and host factors. J. Orthop. Res. 33, 1311–1319 (2015).
Brady, R. A., Leid, J. G., Calhoun, J. H., Costertron, J. W. & Shirtliff, M. E. Osteomyelitis and the role of biofilms in chronic infection. FEMS Immunol. Med. Microbiol. 52, 13–22 (2008).
Johnson, V. et al. Activated mesenchymal stem cells interact with antibiotics and host innate immune responses to control chronic bacterial infections. Sci. Rep. 7, 1–18 (2017).
Harris, M. A., Beenken, K. E., Smeltzer, M. E., Haggard, W. O. & Jennings, J. A. Phosphatidylcholine coatings deliver local antimicrobials and reduce infection in a murine model: a preliminary study. Clin. Orthop. Relat. Res. 475, 1847–1853 (2017).
Mezey, E. & Nemeth, K. Mesenchymal stem cells and infectious diseases: smarter than drugs. Immunol. Lett. 168, 208–214 (2015).
Krasnodembskaya, A. et al. Antibacterial effect of human mesenchymal stem cells is mediated in part from secretion of the antimicrobial peptide LL-37. Stem Cells 28, 2229–2238 (2012).
Yuan, Y. et al. Marrow mesenchymal stromal cells reduce methicillin-resistant Staphylococcus aureus infection in rat models. Cytotherapy 16, 56–63 (2014).
Marrazzo, P., Crupi, A. N., Alviano, F., Tedori, L. & Bonsi, L. Exploring the roles of MSCs in infections: focus on bacterial diseases. J. Mol. Med. 97, 437–450 (2019).
Criman, E. T. et al. Bone marrow-derived mesenchymal stem cells enhance bacterial clearance and preserve bioprosthetic integrity in a model of mesh infection. Plast. Reconstr. Surg. Glob. Open 4, e751 (2016).
Bonomi, A. et al. Adipose tissue-derived stromal cells primed in vitro with paclitaxel acquire anti-tumor activity. Int. J. Immunopathol. Pharmacol. 26, 33–41 (2013).
Sisto, F. et al. Human mesenchymal stromal cells can uptake and release ciprofloxacin, acquiring in vitro anti-bacterial activity. Cytotherapy 16, 181–190 (2014).
Hamada, T. et al. Autologous adipose-derived stem cell transplantation enhances healing of wound with exposed bone in a rat model. PLoS ONE 14, e0214106 (2019).
Martin, P. M. et al. Enhancing repair of full-thickness excisional wounds in a murine model: impact of tissue-engineered biological dressings featuring human differentiated adipocytes. Acta Biomater. 22, 39–49 (2015).
Broughton, B. 2nd., Janis, J. E. & Attinger, C. E. The basic science of wound healing. Plast. Reconstr. Surg. 117, 12S-34S (2006).
Le Blanc, K. et al. Mesenchymal stem cells for treatment of steroid-resistant, severe, acute graft-versus-host disease: a phase II study. Lancet 371, 1579–1586 (2008).
Chamberlain, G., Fox, J., Ashton, B. & Middleton, J. Concise review: mesenchymal stem cells: their phenotype, differentiation capacity, immunological features, and potential for homing. Stem Cells 25, 2739–2749 (2007).
Liang, X., Ding, Y., Zhang, Y., Tse, H. F. & Lian, Q. Paracrine mechanisms of mesenchymal stem cell-based therapy: current status and perspectives. Cell Transplant. 23, 1045–1059 (2014).
Pacini, S. & Petrini, I. Are MSCs angiogenic cells? New insights on human nestin-positive bone marrow-derived multipotent cells. Front. Cell Dev. Biol. 2, 20 (2014).
Alcayaga-Miranda, F., Cuenca, J. & Khoury, M. Antimicrobial activity of mesenchymal stem cells: current status and new perspectives of antimicrobial peptide-based therapies. Front. Immunol. 8, 1–15 (2017).
Maqbool, M., Vidyadaran, S., George, E. & Ramasamy, R. Human mesenchymal stem cells protect neutrophils from serum-deprived cell death. Cell Biol. Int. 35, 1247–1251 (2011).
Cassatella, M. A. et al. Toll-like receptor-3-activated human mesenchymal stromal cells significantly prolong the survival and function of neutrophils. Stem Cells 29, 1001–1011 (2011).
Raffaghello, L. et al. Human mesenchymal stem cells inhibit neutrophil apoptosis: a model for neutrophil preservation in the bone marrow niche. Stem Cells 26, 151–162 (2008).
Krasnodembskaya, A. et al. Human mesenchymal stem cells reduce mortality and bacteremia in gram-negative sepsis in mice in part by enhancing the phagocytic activity of blood monocytes. Am. J. Physiol. Lung Cell Mol. Physiol. 302, L1003–L1013 (2012).
Lee, J. W. et al. Therapeutic effects of human mesenchymal stem cells in ex vivo human lungs injured with live bacteria. Am. J. Respir. Crit. Care Med. 187, 751–760 (2013).
Mei, S. H. J. et al. Mesenchymal stem cells reduce inflammation while enhancing bacterial clearance and improving survival in sepsis. Am. J. Respir. Crit. Care Med. 182, 1047–1057 (2010).
Alcayaga-Miranda, F. et al. Combination therapy of menstrual derived mesenchymal stem cells and antibiotics ameliorates survival in sepsis. Stem Cell Res. Ther. 6, 199 (2015).
Sutton, M. T. et al. Antimicrobial properties of mesenchymal stem cells: therapeutic potential for cystic fibrosis infection, and treatment. Stem Cells Int. 2016, 5303048 (2016).
Sung, D. K. et al. Antibacterial effect of mesenchymal stem cells against Escherichia coli is mediated by secretion of beta-defensin-2 via toll-like receptor 4 signalling. Cell. Microbiol. 18, 424–436 (2016).
Krasnodembskaya, A. et al. Antibacterial effect of human mesenchymal stem cells is mediated in part from secretion of the antimicrobial peptide LL-37. Stem Cells 28, 2229–2238 (2010).
Meisel, R. et al. Human but not murine multipotent mesenchymal stromal cells exhibit broad-spectrum antimicrobial effector function mediated by indoleamine 2,3-dioxygenase. Leukemia 25, 648–654 (2011).
Yang, R. et al. A subset of IL-17(+) mesenchymal stem cells possesses anti-Candida albicans effect. Cell Res. 23, 107–121 (2013).
Zhang, L.-J. & Gallo, R. L. Antimicrobial peptides. Curr. Biol. 26, R14–R19 (2016).
Brogden, K. A. Antimicrobial peptides: pore formers or metabolic inhibitors in bacteria?. Nat. Rev. Microbiol. 3, 238–250 (2005).
Najar, M. et al. Mesenchymal stromal cells and immunomodulation: a gathering of regulatory immune cells. Cytotherapy 18, 160–171 (2016).
Selmani, Z. et al. Human leukocyte antigen-G5 secretion by human mesenchymal stem cells is required to suppress T lymphocyte and natural killer function and to induce CD4+CD25highFOXP3+ regulatory T cells. Stem Cells 26, 212–222 (2008).
Fontaine, M. J., Shih, H., Schafer, R. & Pittenger, M. F. Unraveling the mesenchymal stromal cells’ paracrine immunomodulatory effects. Transfus. Med. Rev. 30, 37–43 (2016).
Uccelli, A., Moretta, L. & Pistoia, V. Mesenchymal stem cells in health and disease. Nat. Rev. Immunol. 8, 726–736 (2008).
Seebach, E. et al. Mesenchymal stromal cell implantation for stimulation of long bone healing aggravates Staphylococcus aureus induced osteomyelitis. Acta Biomater. 21, 165–177 (2015).
Sung, P.-H. et al. Combined therapy with adipose-derived mesenchymal stem cells and ciprofloxacin against acute urogenital organ damage in rat sepsis syndrome induced by intrapelvic injection of cecal bacteria. Stem Cells Transl. Med. 5, 782–792 (2016).
Sun, C.-K. et al. Mixed serum-deprived and normal adipose-derived mesenchymal stem cells against acute lung ischemia-reperfusion injury in rats. Am. J. Transl. Res. 7, 209–231 (2015).
Pessina, A. et al. Mesenchymal stromal cells primed with paclitaxel provide a new approach for cancer therapy. PLoS ONE 6, 8–12 (2011).
Moodley, Y. et al. Anti-inflammatory effects of adult stem cells in sustained lung injury: a comparative study. PLoS ONE 8, e69299 (2013).
Cha, J.-O., Park, Y.-K., Lee, Y. S. & Chung, G. T. In vitro biofilm formation and bactericidal activities of methicillin-resistant Staphylococcus aureus clones prevalent in Korea. Diagn. Microbiol. Infect. Dis. 70, 112–118 (2011).
Dosler, S. & Karaaslan, E. Inhibition and destruction of Pseudomonas aeruginosa biofilms by antibiotics and antimicrobial peptides. Peptides 62, 32–37 (2014).
Dosler, S. & Mataraci, E. In vitro pharmacokinetics of antimicrobial cationic peptides alone and in combination with antibiotics against methicillin resistant Staphylococcus aureus biofilms. Peptides 49, 53–58 (2013).
Roy, M. E., Peppers, M. P., Whiteside, L. A. & Lazear, R. M. Vancomycin concentration in synovial fluid: direct injection into the knee vs. intravenous infusion. J. Arthroplasty 29, 564–568 (2014).
Whiteside, L. A. & Roy, M. E. One-stage revision with catheter infusion of intraarticular antibiotics successfully treats infected THA. Clin. Orthop. Relat. Res. 475, 419–429 (2017).
Marx, C., Gardner, S., Harman, R. M. & Van de Walle, G. R. The mesenchymal stromal cell secretome impairs methicillin-resistant Staphylococcus aureus biofilms via cysteine protease activity in the equine model. Stem Cells Transl. Med. https://doi.org/10.1002/sctm.19-0333 (2020).
Zhang, J. et al. The challenges and promises of allogeneic mesenchymal stem cells for use as a cell-based therapy. Stem Cell Res. Ther. 6, 234 (2015).
Song, K., Huang, M., Shi, Q., Du, T. & Cao, Y. Cultivation and identification of rat bone marrow-derived mesenchymal stem cells. Mol. Med. Rep. 10, 755–760 (2014).
Fang, X. et al. A novel method to apply osteogenic potential of adipose derived stem cells in orthopaedic surgery. PLoS ONE 9, e88874 (2014).
Liu, S. Y. et al. Exercise affects biological characteristics of mesenchymal stromal cells derived from bone marrow and adipose tissue. Int. Orthop. 41, 1199–1209 (2017).
Yang, Y. H. et al. The cationic host defense peptide rCRAMP promotes gastric ulcer healing in rats. J. Pharmacol. Exp. Ther. 318, 547–554 (2006).
Nagayama, A. et al. Final report from the Committee on Antimicrobial Susceptibility Testing, Japanese Society of Chemotherapy, on the agar dilution method (2007). J. Infect. Chemother. 14, 383–392 (2008).
Yokogawa, N. et al. Immunotherapy synergizes with debridement and antibiotic therapy in a murine 1-stage exchange model of MRSA implant-associated osteomyelitis. J. Orthop. Res. 36, 1590–1598 (2018).
Lucke, M. et al. A new model of implant-related osteomyelitis in rats. J. Biomed. Mater. Res. B Appl. Biomater. 67, 593–602 (2003).
Güzel, Y. et al. The efficacy of boric acid used to treat experimental osteomyelitis caused by methicillin-resistant Staphylococcus aureus: an in vivo study. Biol. Trace Elem. Res. 173, 384–389 (2016).
Hounsfield, G. N. Computed medical imaging. Science 210, 22–28 (1980).
Inoue, D. et al. Inhibition of biofilm formation on iodine-supported titanium implants. Int. Orthop. 41, 1093–1099 (2017).
Braem, A. et al. Staphylococcal biofilm growth on smooth and porous titanium coatings for biomedical applications. J. Biomed. Mater. Res. A 102, 215–224 (2014).
This work was supported by JSPS KAKENHI Grant Number 20K18057, a grant of Japan Orthopaedics and Traumatology Foundation (Grant No. 413) and Shibuya Science Culture and Sports Foundation.
The authors declare no competing interests.
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Yoshitani, J., Kabata, T., Arakawa, H. et al. Combinational therapy with antibiotics and antibiotic-loaded adipose-derived stem cells reduce abscess formation in implant-related infection in rats. Sci Rep 10, 11182 (2020). https://doi.org/10.1038/s41598-020-68184-y
Stem Cell Reviews and Reports (2021)