Synergistic Effects of Pulsed Lavage and Antimicrobial Therapy Against Staphylococcus aureus Biofilms in an in-vitro Model
Background: Prosthetic joint infections (PJI) are difficult to treat complications of joint arthroplasty. Debridement with implant retention is a common treatment strategy and frequently involves the use of pulsed lavage (PL). However, PL effects on biofilms and antibiotic activity have been scarcel...
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Published in | Frontiers in medicine Vol. 7; p. 527 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Frontiers Media S.A
17.09.2020
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Abstract | Background:
Prosthetic joint infections (PJI) are difficult to treat complications of joint arthroplasty. Debridement with implant retention is a common treatment strategy and frequently involves the use of pulsed lavage (PL). However, PL effects on biofilms and antibiotic activity have been scarcely studied
in-vitro
. We report the effects of PL, vancomycin or flucloxacillin used independently or in combination against
Staphylococcus aureus
biofilms.
Methods:
Biofilms of 3 methicillin-susceptible (MSSA) and of 3 methicillin-resistant (MRSA)
S. aureus
were grown on Ti6Al4V coupons in TGN (TSB + 1%glucose + 2%NaCl). After 24 h, PL was applied to half of the samples (50 mL saline from 5 cm). Samples were either reincubated for 24 h in TGN or TGN + flucloxacillin or vancomycin. Analyses included CFUs counts, biomass assays or fluorescence microscopy.
Results:
PL transiently reduced bacterial counts by 3–4 Log
10
CFU/coupon, but bacterial regrowth to baseline levels was seen after 24 h. At 20 mg/L, flucloxacillin reduced both the CFU counts (3 Log
10
CFU/coupon) and biomass (−70%) in one MSSA only, while vancomycin had no effects against MRSA. PL combined with a 24 h reincubation with vancomycin or flucloxacillin at 20 mg/L was synergistic (−5 to 6.5 Log
10
CFU/coupon; 81–100% biomass reduction). Fluorescence microscopy confirmed that PL removed most of the biofilm and that subsequent antibiotic treatment partially killed bacteria.
Conclusions:
While PL only transiently reduces the bacterial load and antibiotics at clinically relevant concentrations show no or limited activity on biofilms, their combination is synergistic against MRSA and MSSA biofilms. These results highlight the need for thorough PL before antibiotic administration in PJI. |
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AbstractList | Background:
Prosthetic joint infections (PJI) are difficult to treat complications of joint arthroplasty. Debridement with implant retention is a common treatment strategy and frequently involves the use of pulsed lavage (PL). However, PL effects on biofilms and antibiotic activity have been scarcely studied
in-vitro
. We report the effects of PL, vancomycin or flucloxacillin used independently or in combination against
Staphylococcus aureus
biofilms.
Methods:
Biofilms of 3 methicillin-susceptible (MSSA) and of 3 methicillin-resistant (MRSA)
S. aureus
were grown on Ti6Al4V coupons in TGN (TSB + 1%glucose + 2%NaCl). After 24 h, PL was applied to half of the samples (50 mL saline from 5 cm). Samples were either reincubated for 24 h in TGN or TGN + flucloxacillin or vancomycin. Analyses included CFUs counts, biomass assays or fluorescence microscopy.
Results:
PL transiently reduced bacterial counts by 3–4 Log
10
CFU/coupon, but bacterial regrowth to baseline levels was seen after 24 h. At 20 mg/L, flucloxacillin reduced both the CFU counts (3 Log
10
CFU/coupon) and biomass (−70%) in one MSSA only, while vancomycin had no effects against MRSA. PL combined with a 24 h reincubation with vancomycin or flucloxacillin at 20 mg/L was synergistic (−5 to 6.5 Log
10
CFU/coupon; 81–100% biomass reduction). Fluorescence microscopy confirmed that PL removed most of the biofilm and that subsequent antibiotic treatment partially killed bacteria.
Conclusions:
While PL only transiently reduces the bacterial load and antibiotics at clinically relevant concentrations show no or limited activity on biofilms, their combination is synergistic against MRSA and MSSA biofilms. These results highlight the need for thorough PL before antibiotic administration in PJI. Background: Prosthetic joint infections (PJI) are difficult to treat complications of joint arthroplasty. Debridement with implant retention is a common treatment strategy and frequently involves the use of pulsed lavage (PL). However, PL effects on biofilms and antibiotic activity have been scarcely studied in-vitro. We report the effects of PL, vancomycin or flucloxacillin used independently or in combination against Staphylococcus aureus biofilms.Methods: Biofilms of 3 methicillin-susceptible (MSSA) and of 3 methicillin-resistant (MRSA) S. aureus were grown on Ti6Al4V coupons in TGN (TSB + 1%glucose + 2%NaCl). After 24 h, PL was applied to half of the samples (50 mL saline from 5 cm). Samples were either reincubated for 24 h in TGN or TGN + flucloxacillin or vancomycin. Analyses included CFUs counts, biomass assays or fluorescence microscopy.Results: PL transiently reduced bacterial counts by 3–4 Log10 CFU/coupon, but bacterial regrowth to baseline levels was seen after 24 h. At 20 mg/L, flucloxacillin reduced both the CFU counts (3 Log10 CFU/coupon) and biomass (−70%) in one MSSA only, while vancomycin had no effects against MRSA. PL combined with a 24 h reincubation with vancomycin or flucloxacillin at 20 mg/L was synergistic (−5 to 6.5 Log10 CFU/coupon; 81–100% biomass reduction). Fluorescence microscopy confirmed that PL removed most of the biofilm and that subsequent antibiotic treatment partially killed bacteria.Conclusions: While PL only transiently reduces the bacterial load and antibiotics at clinically relevant concentrations show no or limited activity on biofilms, their combination is synergistic against MRSA and MSSA biofilms. These results highlight the need for thorough PL before antibiotic administration in PJI. |
Author | Cornu, Olivier Ruiz-Sorribas, Albert Sakoulas, George Van Bambeke, Françoise Rodriguez-Villalobos, Hector Poilvache, Hervé |
AuthorAffiliation | 5 Clinical Microbiology Department, Cliniques Universitaires Saint-Luc , Brussels , Belgium 2 Laboratoire de Pharmacologie Cellulaire et Moléculaire, Louvain Drug Research Institute, Université Catholique de Louvain , Brussels , Belgium 1 Laboratoire de Neuro-Musculo-Squelettique, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain , Brussels , Belgium 4 School of Medicine, University of California, San Diego , San Diego, CA , United States 3 Orthopaedic Surgery Department, Cliniques Universitaires Saint-Luc , Brussels , Belgium |
AuthorAffiliation_xml | – name: 2 Laboratoire de Pharmacologie Cellulaire et Moléculaire, Louvain Drug Research Institute, Université Catholique de Louvain , Brussels , Belgium – name: 1 Laboratoire de Neuro-Musculo-Squelettique, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain , Brussels , Belgium – name: 3 Orthopaedic Surgery Department, Cliniques Universitaires Saint-Luc , Brussels , Belgium – name: 5 Clinical Microbiology Department, Cliniques Universitaires Saint-Luc , Brussels , Belgium – name: 4 School of Medicine, University of California, San Diego , San Diego, CA , United States |
Author_xml | – sequence: 1 givenname: Hervé surname: Poilvache fullname: Poilvache, Hervé – sequence: 2 givenname: Albert surname: Ruiz-Sorribas fullname: Ruiz-Sorribas, Albert – sequence: 3 givenname: George surname: Sakoulas fullname: Sakoulas, George – sequence: 4 givenname: Hector surname: Rodriguez-Villalobos fullname: Rodriguez-Villalobos, Hector – sequence: 5 givenname: Olivier surname: Cornu fullname: Cornu, Olivier – sequence: 6 givenname: Françoise surname: Van Bambeke fullname: Van Bambeke, Françoise |
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CitedBy_id | crossref_primary_10_1155_2021_1562605 crossref_primary_10_1016_j_bas_2022_100919 crossref_primary_10_1016_j_arth_2024_06_024 crossref_primary_10_1111_os_13948 crossref_primary_10_3390_ijms221910243 crossref_primary_10_1080_08927014_2021_1919301 crossref_primary_10_1128_AAC_01699_20 |
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Copyright | Copyright © 2020 Poilvache, Ruiz-Sorribas, Sakoulas, Rodriguez-Villalobos, Cornu and Van Bambeke. 2020 Poilvache, Ruiz-Sorribas, Sakoulas, Rodriguez-Villalobos, Cornu and Van Bambeke |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Sebastien Lustig, Université de Lyon, France ORCID: Albert Ruiz-Sorribas orcid.org/0000-0002-4497-1138 Reviewed by: Bingbing Xiao, Peking University First Hospital, China; Jérôme Josse, Université Claude Bernard Lyon 1, France This article was submitted to Infectious Diseases - Surveillance, Prevention and Treatment, a section of the journal Frontiers in Medicine |
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Snippet | Background:
Prosthetic joint infections (PJI) are difficult to treat complications of joint arthroplasty. Debridement with implant retention is a common... Background: Prosthetic joint infections (PJI) are difficult to treat complications of joint arthroplasty. Debridement with implant retention is a common... |
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StartPage | 527 |
SubjectTerms | biofilm flucloxacillin Medicine MRSA MSSA pulsed lavage vancomycin |
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Title | Synergistic Effects of Pulsed Lavage and Antimicrobial Therapy Against Staphylococcus aureus Biofilms in an in-vitro Model |
URI | https://search.proquest.com/docview/2449994883 https://pubmed.ncbi.nlm.nih.gov/PMC7527469 https://doaj.org/article/33600d1ea34249358fce2dada269cd65 |
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