Literature DB >> 15788318

Pseudomonas aeruginosa biofilm formation and slime excretion on antibiotic-loaded bone cement.

Daniëlle Neut1, Johannes G E Hendriks, Jim R van Horn, Henny C van der Mei, Henk J Busscher.   

Abstract

BACKGROUND: Infection is an infrequent but serious complication of prosthetic joint surgery. These infections will usually not clear until the implant is removed and re-implantation has a high failure rate, especially when Pseudomonas aeruginosa is involved.
MATERIAL AND METHODS: We examined Pseudomonas aeruginosa biofilm formation on plain and gentamicin-loaded bone cement with confocal scanning laser microscopy (CSLM). Two different stains were applied in order to visualize and quantify the distribution of bacterial cells and extracellular polymeric substances (slime) from the bone cement surface to the top of the biofilm. Staining with LIVE/DEAD viability stain differentiated between live and dead bacteria within the biofilm, and slime production was evaluated after staining with Calcofluor white.
RESULTS: CSLM showed that the biofilm was a nonuniform structure of variable thickness, with differences in local bacterial cell and slime densities. Incorporation of gentamicin in bone cement resulted in a 44% reduction in bacterial viability, while the slime density increased significantly. In addition, conventional plate counting showed the development of small-colony variants on gentamicin-loaded bone cement with a decreased sensitivity for gentamicin (MIC: 8 m/L), as compared with normal-sized colonies taken from plain and gentamicin-loaded bone cement (MIC: 3 m/L). The enhanced slime production on antibiotic-loaded bone cement, together with the formation of small-colony variants, resulted in decreased susceptibility to antibiotics--probably concomitant with the onset of persistent and relapsing infections.
INTERPRETATION: In the clinical situation, our findings help to explain the frequent re-implantation failure of joint replacements infected with P. aeruginosa when the procedure has been performed using antibiotic-loaded bone cement.

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Year:  2005        PMID: 15788318     DOI: 10.1080/00016470510030427

Source DB:  PubMed          Journal:  Acta Orthop        ISSN: 1745-3674            Impact factor:   3.717


  24 in total

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3.  Reinfected revised TKA resolves with an aggressive protocol and antibiotic infusion.

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4.  Remission after treatment of osteoarticular infections due to Pseudomonas aeruginosa versus Staphylococcus aureus: a case-controlled study.

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5.  Spacer prostheses in two-stage revision of infected knee arthroplasty.

Authors:  E Jämsen; P Sheng; P Halonen; M U K Lehto; T Moilanen; J Pajamäki; T Puolakka; Y T Konttinen
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6.  Methicillin-resistant Staphylococcus aureus in TKA treated with revision and direct intra-articular antibiotic infusion.

Authors:  Leo A Whiteside; Michael Peppers; Tariq A Nayfeh; Marcel E Roy
Journal:  Clin Orthop Relat Res       Date:  2011-01       Impact factor: 4.176

7.  Effects of growth in the presence of subinhibitory concentrations of dicloxacillin on Staphylococcus epidermidis and Staphylococcus haemolyticus biofilms.

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8.  Direct observation and analysis of bacterial growth on an antimicrobial surface.

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9.  Modelling the bacterial communities associated with cystic fibrosis lung infections.

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Journal:  Eur J Clin Microbiol Infect Dis       Date:  2010-01-23       Impact factor: 3.267

Review 10.  Outcome of prosthesis exchange for infected knee arthroplasty: the effect of treatment approach.

Authors:  Esa Jämsen; Ioannis Stogiannidis; Antti Malmivaara; Jorma Pajamäki; Timo Puolakka; Yrjö T Konttinen
Journal:  Acta Orthop       Date:  2009-02       Impact factor: 3.717

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