Prevention and Killing Efficacy of Carbapenem ResistantEnterobacteriaceae(CRE) and Vancomycin ResistantEnterococci(VRE) Biofilms by Antibiotic-Loaded Calcium Sulfate Beads

被引:2
作者
Stoodley, Paul [1 ,2 ,3 ,4 ]
Brooks, Jacob [1 ]
Peters, Casey W. [1 ]
Jiang, Nan [1 ]
Delury, Craig P. [5 ]
Laycock, Phillip A. [5 ]
Aiken, Sean S. [5 ]
Dusane, Devendra H. [1 ,6 ]
机构
[1] Ohio State Univ, Dept Microbial Infect & Immun, Columbus, OH 43210 USA
[2] Univ Southampton, Fac Engn, Natl Ctr Adv Tribol, Southampton SO17 1BJ, Hants, England
[3] Univ Southampton, Inst Life Sci, Southampton SO17 1BJ, Hants, England
[4] Ohio State Univ, Dept Orthopaed, Columbus, OH 43210 USA
[5] Biocomposites Ltd, Keele Sci Pk, Keele ST5 5NL, Staffs, England
[6] Nationwide Childrens Hosp, Ctr Clin & Translat Res, Res Inst, 700 Childrens Dr, Columbus, OH 43205 USA
关键词
antibiotic-loaded calcium sulfate beads; biofilm; carbapenem resistantEnterobacteriaceae; vancomycin resistantEnterococci; PROSTHETIC JOINT INFECTIONS; RESISTANT STAPHYLOCOCCUS-AUREUS; CRYSTALLIC SEMIHYDRATE FORM; IN-VITRO ELUTION; RISK-FACTORS; MANAGEMENT; COMBINATION; THERAPY; COLONIZATION; ARTHROPLASTY;
D O I
10.3390/ma13153258
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Carbapenem-resistantEnterobacteriaceae(CRE) and vancomycin-resistantEnterococci(VRE) have emerged as multidrug-resistant (MDR) pathogens associated with periprosthetic joint infections (PJI). In this study, we evaluated the efficacy of antibiotic-loaded calcium sulfate beads (ALCSB) in inhibiting bacterial growth, encouraging biofilm formation and killing preformed biofilms of CRE and VRE. Three strains ofKlebsiella pneumoniae(KP) and a strain ofEnterococcus faecalis(EF) were used. ALCSB of 4.8-mm diameter were loaded with vancomycin (V) and gentamicin (G), V and rifampicin (R), V and tobramycin (T) or R and meropenem (M), and placed onto tryptic soy agar (TSA), spread with one of the test strains and incubated for 24 h at 37 degrees C. Beads were transferred daily onto fresh TSA spread plates and the zone of inhibition (ZOI) was recorded until no inhibition was observed. ALCSB containing R + M or R + V produced the most extensive ZOI up to 5 weeks. Biofilm prevention efficacy was investigated by challenging ALCSB daily with 5 x 10(5)CFU/mL bacterial cells and analyzing for biofilm formation at challenges 1, 2 and 3. In the biofilm killing experiments, ALCSB were added to pre-grown 3-day biofilms of KP and EF strains, which were then analyzed at days 1 and 3 post-exposure. The CFU counts and confocal images of the attached cells showed that ALCSB treatment reduced colonization and biofilm formation significantly (5-7 logs) with combinations of R + M or R + V, compared to unloaded beads. This study provides evidence that the local release of antibiotics from ALCSB may be useful in treating the biofilms of multidrug-resistant strains of CRE and VRE.
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页数:17
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