Therapy of intracellular Staphylococcus aureus by tigecyclin
© Kreis et al.; licensee BioMed Central Ltd. 2013
Received: 18 January 2013
Accepted: 3 June 2013
Published: 5 June 2013
In the fields of traumatology and orthopaedics staphylococci are the most frequently isolated pathogens. Staphylococcus aureus and Staphylococcus epidermidis are known to be the major causative agents of osteomyelitis. The increasing number of multiresistant Staphylococcus aureus and resistant coagulase-negative staphylococci as a trigger of complicated osteomyelitis and implant-associated infections is a major problem. Antibiotic therapy fails in 20% of cases. Therefore the development of novel antibiotics becomes necessary.
This study analyses tigecyclin, the first antibiotic of the glycylines, as a potential therapy for osteomyelitis caused by multiresistant Staphylococcus aureus. Therefore its intracellular activity and the potential use in polymethylmetacrylate-bone cement are examined. The intracellular activity of tigecyclin is determined by a human osteoblast infection model. The investigation of the biomechanical characteristics is conducted concerning the ISO 5833-guidelines.
Tigecyclin shows in vitro an intracellular activity that ranges between the antimicrobial activity of gentamicin and rifampicin. A significant negative effect on the biomechanical characteristics with an impaired stability is detected after adding tigecyclin to polymethylmetacrylate-bone cement with a percentage of 1.225% per weight.
This study shows that tigecyclin might be a potent alternative for the systemic therapy of osteomyelitis and implant-associated infections whereas the local application has to be reconsidered individually.
KeywordsOsteomyelitis Implant associated infection Staphylococcus aureus Tigecyclin Biomechanical stability
Osteomyelitis is an inflammatory process caused by infective microorganism . With a percentage of 80% S. aureus (Staphylococcus aureus) is the most common pathogen of osteomyelitis [1, 3]. Implant-associated infections are also often caused by S. epidermidis (Staphylococcus epidermidis) [3, 4] and occur with a rate from 3-33% . The therapy of osteomyelitis still represents a major challenge . A single antibiotic agent is the standard therapy for osteomyelitis in its early stages . In order to cure the chronic stages of this bone infection a combined therapy has to be chosen, which consists of a combination of two antibiotic substances and the surgical approach, which implies the surgical debridement, the implant removal or the two-step replacement [1, 3, 6, 7]. The combination of rifampicin plus another antibiotic agent shows efficient therapeutic results for the implant-associated infection caused by S. aureus. However, antibiotic therapy fails in 20% of cases. This might be explained by the ability of S. aureus to invade human osteoblast cells [1–3] and to survive intracellularly [1, 2]. Thereby, S. aureus can change its phenotype into SCVs (small colony variants), which is a bacterial subpopulation that is well adapted for long-term intracellular persistence [3, 8]. In general SCVs have a reduced metabolism and have an increased resistance against antibiotics, especially against aminoglycosides [3, 8, 9]. Furthermore, S. aureus and S. epidermidis can adhere to foreign material surfaces and form biofilm [1, 3, 7, 10, 11]. The bacterial biofilm is a matrix out of polysaccharides and proteins  and acts as a diffusion barrier that inhibits the diagnosis and eradication of bacteria . PMMA (polymethylmetacrylate)-bone cement loaded with antibiotic substances is an established treatment for infected endoprotheses for over 40years with good long-term results [6, 12]. Antibiotic-loaded bone cement works as a local antibiotic-carrier with the function of a drug-delivery-system to achieve high antibiotic levels locally [12–14] and to decrease the infection rate . PMMA-bone cement is most commonly loaded with aminoglycosides , especially with gentamicin as a good prophylaxis as well as a treatment for implant-associated infections . It was shown that PMMA-bone cement loaded with gentamicin inhibits 80% of S. aureus-biofilm synthesis . Despite these options the treatment of osteomyelitis remains a challenging problem . MRSA- and VRSA- infections are increasing as well as the number of antibiotic-resistant S. aureus and S. epidermidis[3, 12]. Because of increasing resistance against gentamicin [12, 18] and vancomycin  new  or combined  antibiotics have to be added to bone cement. Furthermore 41% of clinical isolated S. aureus are resistant against gentamicin . S. aureus also has the ability to grow on bone cement loaded with gentamicin . S. epidermidis is able to adhere to bone cement in vivo  and in vitro and to synthesize biofilm on bone cement loaded with gentamicin . Multiresistant pathogens are a major therapeutic problem . Therefore new antibiotics are essential to minimize pathogens and to optimize the therapy of osteomyelitis . In this context tigecyclin has been developed , which is the first antibiotic of the glycylines with efficacy against many important pathogens, multiresistant strains, mixed infections and problematic pathogens [23, 24]. In clinical daily routine tigecyclin shows good therapeutic efficacy against intraabdominal infection, skin- and soft-tissue infections [23, 24]. Tigecyclin shows activity against infection caused by MRSA  and against biofilm associated pathogens . Furthermore tigecyclin is absorbed by bone tissue after intravenous application . Till 2007 only few tigecyclin-resistant S. aureus-strains were known , there are even some rifampicin-resistant S. epidermidis-strains that were sensitive against tigecyclin . This study investigates tigecyclin as a potential therapy for osteomyelitis caused by multiresistant S. aureus. Its intracellular activity is determined in comparison to gentamicin and rifampicin by a human osteoblast infection model . The potential use in PMMA-bone cement is conducted concerning the ISO 5833-guidelines compared to gentamicin (International Organization for Standardization: Implants for surgery - Acrylic resin cements. 2002).
Human osteoblast infection model
Antimicrobial resistant profiles of the S. aureus strains used in this study
S. aureusCowan I ATCC 12598
S. aureusSubspezies Rosenbach ATCC 49230
The investigation of the cure time [min] of PMMA-bone cement loaded with tigecyclin versus customary bone cement loaded with gentamicin is performed concerning the ISO 5833-standards. The antibiotics are added with a weight proportion of 1.225%. After 1min the compound of PMMA-bone cement and antibiotic is touched with a dry and clean glove every 15seconds. To determine the compressive strength [MPa] PMMA-bone cement cylinders with a length of 12 mm (± 0,1 mm) and a diameter of 6mm (± 0,1 mm) are produced by the ISO 5833-guidlines with the antibiotics tigecyclin and gentamicin each with a weight proportion of 1.225%. The cylinders are placed into the uniaxial testing machine (Zwick/Roell), which operates a constant compression with a speed of 22 mm/min until the material shows breakage. The compressive strength [MPa] for each test cylinder is then calculated using the following formula: compressive strength [MPa] = (force [N])/(πr2), in which the force applied until breakage is divided by the cross-sectional area of the cylinder. The bending strength [MPa] and the bending modulus [MPa] of PMMA-bone cement loaded with tigecyclin or gentamicin (1.225% per weight) are examined conducting ISO 5833-standards with created cement bars with the measure of 75 mm (± 0.1 mm) length, 10 mm (± 0.1 mm) width and 3.3 mm (± 0.1 mm) depth. The test bars are placed into the uniaxial testing machine (Zwick/Roell) and a four-point bending test is accomplished. Operating the crosshead with a speed of 5 mm/min ± 1 mm/min the deflection under the specimen and the applied force are recorded until breakage. The bending strength [MPa] and the bending modulus [MPa] are calculated afterwards taking the defined measurements, the deflection under certain loads and the force at breaking point into account with the formulas: bending strength [MPa] = 3Fa/bh2, bending modulus [MPa] = (∆Fa/4fbh3) × (3l2-4a2).
Statistical analysis was performed with the Mann-Whithey-U-test for the results of the infection model. The results of the biomechanical testings besides the bending modulus were statically analysed by the unpaired t-test. Statistical analysis for the bending modulus was performed by the unpaired t-test with Welch correction. A value of * p ≤ 0.05 was consideres siginificant in all cases.
Human osteoblast infection model
The in vitro model of an osteomyelitis displays that the effectiveness of the novel antibiotic tigecyclin has to be ranked between gentamicin and rifampicin after incubation of 20 h and 40 h. The effectivness of rifampicin compared to gentamicin can be confirmed by in vitro and in vivo studies done in 2006 and 2009, in which a reduction of intracellular bacteria after treatment with rifampicin could be shown . In 2008 and 2009 the synergistical effect of tigecyclin to rifampicin and gentamicin against S.aureus could be displayed in vivo and in vitro as a potential combined therapy against multiresistant bacteria [30, 35]. The synergistical effect of tigecyclin to gentamicin was confirmed in our study, whereas the additive effect of tigecyclin to rifampicin could not be shown. It is known that gentamicin has good activity in the extracellular space, whereas an additive effect to the effectiveness of tigecyclin cannot be assigned by our study. However, it remains uncertain if our results can be transferred to in vivo conditions as S. aureus quickly developes resistances . It would be significant to search out if this has validity for tigecyclin as well. A combination of tigecyclin and rifampicin might be recommendable to prevent resistances. Yin et al. show a complete bacterial eradication after a combined treatment with tigecyclin s.c. and rifampicin p.o. in an in vivo MRSA-osteomyelitis-model . Furthermore, it has to be examined if higher doses of tigecyclin would on the one hand reduce the intracellular bacteria completly and on the other hand would induce the SCV-synthesis, which displays a handicap for antibiotic therapy. 1995 Henry and Galloway showed that PMMA-bone cement loaded with antibiotics is an effective therapy for bone or soft tissue infections as it is possible to reach high antibiotic levels locally without their unwanted side effects . Since 2003 gentamicin is added to PMMA-bone cement as the standard antibiotic substance with a broad antibacterial effectiveness, a low influence on biomechanical properties of bone cement and a good release out of bone cement . Despite the study results it is doubtfull if tigecyclin is a potential alternative to gentamicin for the local use in bone cement. Here the biomechanical investigation of tigecyclin shows a reduction of the stability of Palacos ®-bone cement compared to Palacos ®-bone cement loaded with gentamicin. It is known that bone cement loaded with gentamicin or rifampicin shows a good local effectiveness with reduction of implant-associated bacteria and reduction of biofilm synthesis [19, 21, 37]. Similar results are not yet exciting for tigecyclin , which would be important to consider tigecyclin as an alternative to gentamicin in clinical daily routine. With the help of different models the good release of gentamicin out of bone cement could be displayed [12, 38], but it is still uncertain if a constant release of gentamicin induces the synthesis of resistances or not . Bone cement loaded with rifampicin reveals a bimodal elution kinetic with a fast, high concentrated initial release follwed by a slow, low concentrated release . Comparable studies concerning the release of tigecyclin out of bone cement are missing. In actual studies there are only few resistances against tigecyclin listed and it is known as an effective therapy against MRSA-infections and biofilm associated bacteria [25, 26, 28, 39]. Furthermore tigecyclin reduces the expression of some important virulence factors of S. aureus. 91% of multiresistant S. epidermidis are sensitive against tigecyclin . Redvold et al. demonstrate the good bone absorption of tigecyclin after intravenous application . On the other hand there is less clinical data exciting concerning this novel antibiotic substance associated with safety questions . In addition Rose and Poppens demonstrate that tigecyclin does not reduce biofilm-associated S. aureus.
In conclusion there is inconsistent result concerning tigecyclin. Tigecyclin shows effective intracellular activity against S. aureus with negative influence on the biomechanical stability of Palacos ®-bone cement. In total tigecyclin seems to be a possible therapy option or alternative in the systemic treatment of osteomyelitis because of its good intracellular effectiveness. The local application of tigecyclin has to be evaluated individually because of less biomechanical stability of bone cement.
We acknowledge support by Deutsche Forschungsgemeinschaft and Open Access Publication Fund of University of Muenster.
Funding did not influence study outcome.
- Lew DP, Waldvogel FA: Osteomyelitis. Lancet. 2004, 364: 369-379. 10.1016/S0140-6736(04)16727-5.View ArticlePubMedGoogle Scholar
- Ellington JK, Harris M, Hudson MC, et al: Intracellular Staphylococcus Aureus and antibiotic resistance: implications for treatment of staphylococcal osteomyelitis. J Orthop Res. 2006, 24: 87-93. 10.1002/jor.20003.View ArticlePubMedGoogle Scholar
- Ciampolini J, Harding KG: Pathophysiology of chronic bacterial osteomyelitis. why do antibiotics fail so often?. Postgrad Med J. 2000, 76: 479-483. 10.1136/pmj.76.898.479.View ArticlePubMedPubMed CentralGoogle Scholar
- Hellmark B, Unemo M, Nilsdotter-Augustinsson A, Söderquist B, et al: Antibiotic susceptibility among staphylococcus epidermidis isolated from prosthetic joint infections with special focus on rifampicin and variability of the rpoB gene. Clin Microbiol Infect. 2009, 15: 238-244. 10.1111/j.1469-0691.2008.02663.x.View ArticlePubMedGoogle Scholar
- Seligson D, Klemm K: Adult posttraumatic osteomyelitis of the tibial diaphysis of the tibial shaft. Clin Orthop Relat Res. 1999, 360: 30-36.View ArticlePubMedGoogle Scholar
- Buchholz HW, Elson RA, Engelbrecht E, et al: Management of deep infection of total hip replacement. J Bone Joint Surg Br. 1981, 63-B (3): 342-353.PubMedGoogle Scholar
- Trampuz A, Zimmerli W: Prosthetic joint infections: update in diagnosis and treatment. Swiss Med Wkly. 2005, 135 (17–18): 243-252.PubMedGoogle Scholar
- Proctor RA, von Eiff C, Kahl BC, et al: Small colony variants: a pathogenic form of bacteria that facilitates persistent and recurrent infections. Nat Rev Microbiol. 2006, 4: 295-305. 10.1038/nrmicro1384.View ArticlePubMedGoogle Scholar
- von Eiff C, Peters G, Becker K: The small colony variant (SCV) concept – the role of staphylococcal SCVs in persistent infections. Injury. 2006, 37: 526-533.View ArticleGoogle Scholar
- Stewart PS, Costerton JW: Antibiotic resistance of bacteria in biofilms. Lancet. 2001, 358 (9276): 135-138. 10.1016/S0140-6736(01)05321-1.View ArticlePubMedGoogle Scholar
- Tang H, Xu Y: Bacterial biofilms and chronic osteomyelitis. Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2010, 24 (1): 108-111.PubMedGoogle Scholar
- Breusch SJ, Kühn KD: Knochenzemente auf basis von polymethylmethacrylat. Orthopade. 2003, 32: 41-50. 10.1007/s00132-002-0411-0.View ArticlePubMedGoogle Scholar
- Henry SL, Galloway KP: Local antibacterial therapy for the management of orthopaedic infections. Pharmacokinet considerations. Clin Pharmacokinet. 1995, 29 (1): 36-45. 10.2165/00003088-199529010-00005.View ArticlePubMedGoogle Scholar
- Raschke MJ, Schmidmaier G: Biological coating of implants in trauma and orthopedic surgery. Unfallchirurg. 2004, 107 (8): 653-663.PubMedGoogle Scholar
- Reichert P, Rutowski R, Gosk J: Application of gentamycini impregnated polymethylmethacrylate (PMMA) (Septopal) in treatment of infected nonunion. Own exp. Polim Med. 2007, 37 (4): 65-72.Google Scholar
- Anguita-Alonso P, Hanssen AD, Osmon DR, et al: High rate of aminoglycoside resistance among staphylococci causing prosthetic joint infection. Clin Orthop Relat Res. 2005, 439: 43-47. 10.1097/01.blo.0000182394.39601.9d.View ArticlePubMedGoogle Scholar
- Neut D, Kluin OS, Crielaard BJ, et al: A biodegradable antibiotic delivery system based on poly- (trimethylene carbonate) for the treatment of osteomyelitis. Acta Orthop. 2009, 80 (5): 514-519. 10.3109/17453670903350040.View ArticlePubMedPubMed CentralGoogle Scholar
- Anguita-Alonso P, Rouse MS, Piper KE, et al: Comparative study of antimicobial release kinetics from polymethylmethacrylate. Clin Orthop Relat Res. 2006, 445: 239-244.PubMedGoogle Scholar
- van de Belt H, Neut D, Schenk W, et al: Staphylococcus aureus biofilm formation on different gentamicin-loaded polymethylmethacrylate bone cements. Biomaterials. 2001, 22 (12): 1607-1611. 10.1016/S0142-9612(00)00313-6.View ArticlePubMedGoogle Scholar
- Chang CC, Merritt K: Infection at the site of implanted materials with and without preadhered bacteria. J Orthop Res. 1994, 12 (4): 526-531. 10.1002/jor.1100120409.View ArticlePubMedGoogle Scholar
- Chang CC, Merritt K: Microbial adherence on poly(methyl methacrylate) (PMMA) surfaces. J Biomed Mater Res. 1992, 26 (2): 197-207. 10.1002/jbm.820260206.View ArticlePubMedGoogle Scholar
- Barton E, MacGowan A: Future treatment options for gram-positive infections - looking ahead. Clin Micobiol. Infect. 2009, 6: 17-25.View ArticleGoogle Scholar
- Rose WE, Rybak MJ: Tigecycline: first of a new class of antimicrobial agents. Pharmacotherapy. 2006, 26 (8): 1099-1110. 10.1592/phco.26.8.1099.View ArticlePubMedGoogle Scholar
- Hawkey P, Finch R: Tigecycline: in-vitro performance as a predictor of clinical efficacy. Clin Microbio Infect. 2007, 13: 354-362. 10.1111/j.1469-0691.2006.01621.x.View ArticleGoogle Scholar
- Verkade EJ, Verhulst CJ, Huijsdens XW, Kluytmans JA: In vitro activity of tigecycline against methicillin-resistant Staphylococcus aureus, including livestock-associated strains. Eur J Clin Microbiol Infect Dis. 2010, 29 (5): 503-507. 10.1007/s10096-010-0886-2.View ArticlePubMedPubMed CentralGoogle Scholar
- Aslam S: Effect of antibacterials on biofilms. J of Infect Control. 2008, 36: S175 e9-S175 e11.Google Scholar
- Rodvold KA, Gotfried MH, Cwik M, et al: Serum, tissue and body fluid concentrations of tigecycline after a single 100mg dose. J Antimicrob Chemother. 2006, 58 (6): 1221-1229. 10.1093/jac/dkl403.View ArticlePubMedGoogle Scholar
- Anstead GM, Quinones-Nazario G, Lewis JS: Treatment of infections caused by resistant Staphylococcus aureus. Methods Mol Biol. 2007, 391: 227-258. 10.1007/978-1-59745-468-1_17.View ArticlePubMedGoogle Scholar
- Haslinger-Loeffler B, Kahl BC: Multiple virulence factors are required for Staphylococcus aureus-induced apoptosis in endothelial cells. cellular microbiology. Grundmeier Met al. 2005, 7 (8): 1087-1097.Google Scholar
- Duez JM, Adochitei A, Péchinot A, et al: In vitro combinations of five intravenous antibiotics with dalfopristin-quinupristin against Staphylococcus aureus in a 3-dimensional model. J Chemother. 2008, 20 (6): 684-689.View ArticlePubMedGoogle Scholar
- Demczar DJ, Nafziger AN, Beritino JS: Pharmacokinetics of gentamicin at traditional versus high doses: implications for once-daily aminoglycoside dosing. Antimicrob Agents Chemother. 1997, 5: 115-119.Google Scholar
- EUCAST: Technical note on tigecycline. Clin Microbiol Infect. 2006, 12: 1147-1149.View ArticleGoogle Scholar
- Roth B: Penetration of parenterally administered rifampicin into bone tissue. Chemotherapy. 1984, 30 (6): 358-365. 10.1159/000238294.View ArticlePubMedGoogle Scholar
- Sandberg A, Hessler JHR, Skov RL, et al: Intracellular activity of antibiotics against Staphylococcus aureus in a mouse peritonitis model. Antimicrob Agents Chemother. 2009, 53 (5): 1874-1883. 10.1128/AAC.01605-07.View ArticlePubMedPubMed CentralGoogle Scholar
- Entenza JM, Moreillon P: Tigecycline in combination with other antimicrobials: a review of in vitro, animal and case report studies. Int J Antimicrob Agents. 2009, 34 (8): 1-9.Google Scholar
- Yin LY, Lazzarini L, Li F, et al: Comparative evaluation of tigecycline and vancomycin, with and without rifampicin, in the treatment of methicillin-resistant Staphylococcus aureus experimental osteomyelitis in a rabbit model. J Antimicrob Chemother. 2005, 55: 995-1002. 10.1093/jac/dki109.View ArticlePubMedGoogle Scholar
- Trampuz A, Zimmerli W: Antimicrobial agents in orthopaedic surgery: prophylaxis and treatment. Drugs. 2006, 66 (8): 1089-1105. 10.2165/00003495-200666080-00005.View ArticlePubMedGoogle Scholar
- Seldes RM, Winiarsky R, Jordan LC, et al: Liqiud gentamicin in bone cement: a laboratory study of a potentially more cost-effective cement spacer. L Bone Joint Surg. 2005, 87: 268-272. 10.2106/JBJS.C.00728.View ArticleGoogle Scholar
- Kandemir O, Oztuna V, Colak M, et al: Comparison of the efficacy of tigecycline and teicoplanin in an experimental methicillin-resistant Staphylococcus aureus osteomyelitis model. J Chemother. 2008, 20 (1): 53-57.View ArticlePubMedGoogle Scholar
- Smith K, Gould KA, Ramage G, et al: Influence of tigecycline an expression of virulence factors in biofilm-associated cells of methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother. 2010, 380-387.Google Scholar
- Grossi PA: Early appropiate therapy of Gram-positive bloodstream infections: the conservative use of new drugs. Int J of Antimicrob Agents. 2009, 34S: S31-S34.View ArticleGoogle Scholar
- Rose WE, Poppens PT: Impact of biofilm on the in vitro activity of vancomycin alone and in combination with tigecycline and rifampicin against Staphylococcus aureus. J Antimicrob Chemother. 2009, 63: 485-488. 10.1093/jac/dkn513.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/13/267/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.