The University of Southampton
University of Southampton Institutional Repository

Reduction in Pseudomonas aeruginosa and Staphylococcus aureus biofilms from implant materials in a diffusion dominated environment: Diffusion mediated biofilm eradication

Reduction in Pseudomonas aeruginosa and Staphylococcus aureus biofilms from implant materials in a diffusion dominated environment: Diffusion mediated biofilm eradication
Reduction in Pseudomonas aeruginosa and Staphylococcus aureus biofilms from implant materials in a diffusion dominated environment: Diffusion mediated biofilm eradication
Antibiotic-loaded calcium sulfate beads (CS-B) are used to treat biofilm related periprosthetic joint infections (PJI). A previous study has shown that such beads are effective in reducing lawns biofilms grown on agar plates; however, the ability of CS-B to eradicate biofilms grown on solid orthopaedic material surfaces has not been investigated. We grew biofilms of bioluminescent strains of Pseudomonas aeruginosa Xen41 and a USA300 MRSA Staphylococcus aureus SAP231 on an ultra-high molecular weight polyethylene (PE), hydroxyapatite (HA), and 316L stainless steel (SS) coupons for three days under static growth conditions, with daily nutrient exchange. The coupons were rinsed with sterile phosphate buffered saline (PBS) to remove planktonic bacteria and placed in a petri dish, surrounded by four either antibiotic vancomycin and tobramycin loaded (CS-BV+T) or unloaded beads (CS-BU). A thin layer of agar was overlaid to simulate a periprosthetic infection where an implant abuts soft tissue, then incubated for 72 hours. The amount of biofilm was measured by bioluminescence imaging (BLI) for activity and viable cell count (CFUs). Coupons exposed to CS-BV+T showed a significant reduction in the amount of biofilm within 24 hours, regardless of the bacterial strain or material type. Whereas, coupons exposed to control CS-BU had no effect on bacteria over 72 hours. Statement of Clinical Significance: Antibiotic-loaded calcium sulfate beads (CS-B) were effective in significantly reducing mature biofilms of P. aeruginosa and S. aureus from orthopaedic relevant surfaces in our novel in vitro periprosthetic-soft tissue model.
Biofilm, antibiotic-loaded calcium sulfate beads, Pseudomonas, Staphylococcus, implant
0736-0266
Moley, James P.
f5180f28-bc99-4862-b0c1-f6d78a2c6e34
McGrath, Mary S.
c3a26261-fef4-472d-b9de-943a3ead23e0
Granger, Jeffrey F.
cac1970b-bff4-4842-a1e3-62cc55d87bd7
Stoodley, Paul
08614665-92a9-4466-806e-20c6daeb483f
Dusane, Devendra H.
9a47c5eb-5587-4f1d-bfd4-8548681be2bc
Moley, James P.
f5180f28-bc99-4862-b0c1-f6d78a2c6e34
McGrath, Mary S.
c3a26261-fef4-472d-b9de-943a3ead23e0
Granger, Jeffrey F.
cac1970b-bff4-4842-a1e3-62cc55d87bd7
Stoodley, Paul
08614665-92a9-4466-806e-20c6daeb483f
Dusane, Devendra H.
9a47c5eb-5587-4f1d-bfd4-8548681be2bc

Moley, James P., McGrath, Mary S., Granger, Jeffrey F., Stoodley, Paul and Dusane, Devendra H. (2018) Reduction in Pseudomonas aeruginosa and Staphylococcus aureus biofilms from implant materials in a diffusion dominated environment: Diffusion mediated biofilm eradication. Journal of Orthopaedic Research. (doi:10.1002/jor.24074).

Record type: Article

Abstract

Antibiotic-loaded calcium sulfate beads (CS-B) are used to treat biofilm related periprosthetic joint infections (PJI). A previous study has shown that such beads are effective in reducing lawns biofilms grown on agar plates; however, the ability of CS-B to eradicate biofilms grown on solid orthopaedic material surfaces has not been investigated. We grew biofilms of bioluminescent strains of Pseudomonas aeruginosa Xen41 and a USA300 MRSA Staphylococcus aureus SAP231 on an ultra-high molecular weight polyethylene (PE), hydroxyapatite (HA), and 316L stainless steel (SS) coupons for three days under static growth conditions, with daily nutrient exchange. The coupons were rinsed with sterile phosphate buffered saline (PBS) to remove planktonic bacteria and placed in a petri dish, surrounded by four either antibiotic vancomycin and tobramycin loaded (CS-BV+T) or unloaded beads (CS-BU). A thin layer of agar was overlaid to simulate a periprosthetic infection where an implant abuts soft tissue, then incubated for 72 hours. The amount of biofilm was measured by bioluminescence imaging (BLI) for activity and viable cell count (CFUs). Coupons exposed to CS-BV+T showed a significant reduction in the amount of biofilm within 24 hours, regardless of the bacterial strain or material type. Whereas, coupons exposed to control CS-BU had no effect on bacteria over 72 hours. Statement of Clinical Significance: Antibiotic-loaded calcium sulfate beads (CS-B) were effective in significantly reducing mature biofilms of P. aeruginosa and S. aureus from orthopaedic relevant surfaces in our novel in vitro periprosthetic-soft tissue model.

Text
Moley et al_2018_JoR_clean - Accepted Manuscript
Download (45kB)
Text
OnlineFirst VoR (Stoodley version for REF) - Version of Record
Restricted to Repository staff only
Request a copy

More information

Accepted/In Press date: 11 June 2018
e-pub ahead of print date: 20 June 2018
Published date: 13 July 2018
Keywords: Biofilm, antibiotic-loaded calcium sulfate beads, Pseudomonas, Staphylococcus, implant

Identifiers

Local EPrints ID: 421508
URI: http://eprints.soton.ac.uk/id/eprint/421508
ISSN: 0736-0266
PURE UUID: ff772387-0531-400d-a550-c3c1083e7033
ORCID for Paul Stoodley: ORCID iD orcid.org/0000-0001-6069-273X

Catalogue record

Date deposited: 14 Jun 2018 16:30
Last modified: 16 Mar 2024 06:45

Export record

Altmetrics

Contributors

Author: James P. Moley
Author: Mary S. McGrath
Author: Jeffrey F. Granger
Author: Paul Stoodley ORCID iD
Author: Devendra H. Dusane

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×