1
Results All isolates were found to have mecA, but not nuc, consistent with MRSE. The MIC 50, MIC 90 and the percentage of non-susceptible isolates for each of the tested antibiotics are presented in the table. Co-resistance was found in all but one isolate, and 83 % of the isolates were resistant to multiple antibiotic classes. Resistance to erythromycin was found in 74 % of the isolates of which 64 % had a constitutive MLS B resistance, 25 % an inducible MLS B resistance and 11 % had an efflux mechanism. In vitro antimicrobial susceptibilities of Methicillin-resistant Staphylococcus epidermidis P. Christoffer Lindemann 1,2 , Rune Skjåstad 1,2 , Heidi E. Haraldsen 2 , Olav Lutro 3 , Harald G. Wiker 1,2 , Haima Mylvaganam 1 1. Department of Microbiology, Haukeland University Hospital, Bergen, Norway 2. Department of Clinical Science, Faculty of Medicine and Dentistry, University of Bergen, Bergen, Norway 3. Department of Medicine, Haukeland University Hospital, Bergen, Norway Conclusions The high prevalence of resistance to gentamicin, fluoroquinolones, trimethoprim-sulfamethoxazole, erythromycin and clindamycin indicate that these antibiotics are unsuitable for empirical treatment. Screening for mecA and nuc directly from patient samples and finding only mecA would indicate considerable co- resistance. Relevant antibiotics to use alone or in combination seem to be vancomycin, linezolid, tigecycline and rifampicin. However, their effect on biofilm associated MRSE infections remains to be studied. [email protected] Antibiotic MIC range MIC 50 MIC 90 % Non-S Vancomycin 1 - 2 2 2 0 Teicoplanin 0.125 - 4 1 2 0 Gentamicin 0.064 - >256 16 128 74 Trim-sulfa 0.032 - >32 2 64 43 Erythromycin 0.064 - >256 >256 >256 74 Clindamycin 0.032 - >256 0.125 >256 47 Ciprofloxacin 0.125 - >32 >32 >32 85 Levofloxacin 0.064 - >32 8 16 82 Moxifloxacin 0.032 - 4 2 2 74 Ofloxacin 0.125 - >32 >32 >32 85 Linezolid 0.125 - 1 0.25 0.5 0 Tigecycline 0.016 - 0.5 0.125 0.25 0 Rifampicin 0.002 – 0.016 0.008 0.008 0 MIC: Minimal inhibitory concentration. All MIC values are in mg/L. S: Susceptible. The clinical breakpoint (S) refers to EUCAST clinical breakpoint table version 2.0 2012-01-01. Trim-sulfa: Trimethoprim-sulfamethoxazole Objective Staphylococcus epidermidis frequently causes infections in immunocompromised patients and patients with catheters or implants. Most isolates are methicillin resistant, thus resistant to most β-lactam antibiotics. These infections are often treated with vancomycin, but treatment failure can occur due to biofilm formation, often necessitating the removal of catheters or implants. This study tests the in vitro activity of a wider spectrum of antibiotics for treatment of methicillin-resistant S. epidermidis (MRSE) Materials & Methods 72 MRSE isolates regarded as clinically relevant and isolated at the Dept. of Microbiology, Haukeland University Hospital, Norway, during 2011 were included; 52 from blood cultures 20 from sites such as cerebrospinal fluid, burns and foreign body related infections. The isolates were identified as S. epidermidis by Vitek®2 and as MRSE based on non-susceptibility to oxacillin. All isolates were subjected to mecA/nuc PCR. Minimal inhibitory concentrations for 13 relevant antibiotics were obtained using MIC Test Strips (Liofilchem) and their sensitivities determined using EUCAST clinical breakpoints. Acknowledgements Liofilchem is acknowledged for their kind donation of MIC Test Strips for this project. Technicians Bente Skjellstad, Eirik Nybakken and Kathe Skråmestø at the Department of Microbiology, Haukeland University Hospital are acknowledged for their assistance with mecA/nuc PCR and isolate-handling 0 5 10 15 20 25 30 35 40 Moxifloxacin 0 2 4 6 8 10 12 14 Gentamicin 0 2 4 6 8 10 12 14 16 18 20 Trimethoprim-sulfamethaoxazole 0 5 10 15 20 25 30 35 40 Clindamycin 0 5 10 15 20 25 30 35 40 45 Linezolid 0 5 10 15 20 25 30 35 Tigecyclin 0 5 10 15 20 25 30 35 40 Rifampicin 0 5 10 15 20 25 30 35 40 45 Vancomycin 0 5 10 15 20 25 30 35 40 45 50 Erythromycin 0 10 20 30 40 50 60 Ciprofloxacin Figures shows distribution of MICs for selected antibiotics. Y-axis; “Number of isolates”. X-axis; “MIC valus (mg/L)” Clinical breakpoint: R > Clinical breakpoint: S Epidemiological cut-off: Wild type

In vitro antimicrobial susceptibilities of Methicillin-resistant … · 2018-01-26 · • Relevant antibiotics to use alone or in combination seem to be vancomycin, linezolid, tigecycline

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Page 1: In vitro antimicrobial susceptibilities of Methicillin-resistant … · 2018-01-26 · • Relevant antibiotics to use alone or in combination seem to be vancomycin, linezolid, tigecycline

Results All isolates were found to have mecA, but not nuc, consistent with MRSE.

The MIC50, MIC90 and the percentage of non-susceptible isolates for each of the tested antibiotics are presented in the table.

Co-resistance was found in all but one isolate, and 83 % of the isolates were resistant to multiple antibiotic classes.

Resistance to erythromycin was found in 74 % of the isolates of which 64 % had a constitutive MLSB resistance, 25 % an inducible MLSB resistance and 11 % had an efflux mechanism.

In vitro antimicrobial susceptibilities of Methicillin-resistant Staphylococcus epidermidis

P. Christoffer Lindemann1,2, Rune Skjåstad1,2, Heidi E. Haraldsen2, Olav Lutro3, Harald G. Wiker1,2, Haima Mylvaganam1 1.  Department of Microbiology, Haukeland University Hospital, Bergen, Norway 2.  Department of Clinical Science, Faculty of Medicine and Dentistry, University of Bergen, Bergen, Norway 3.  Department of Medicine, Haukeland University Hospital, Bergen, Norway

Conclusions •  The high prevalence of resistance to gentamicin,

fluoroquinolones, trimethoprim-sulfamethoxazole, erythromycin and clindamycin indicate that these antibiotics are unsuitable for empirical treatment.

•  Screening for mecA and nuc directly from patient samples and finding only mecA would indicate considerable co-resistance.

•  Relevant antibiotics to use alone or in combination seem to be vancomycin, linezolid, tigecycline and rifampicin. However, their effect on biofilm associated MRSE infections remains to be studied.

[email protected]

Antibiotic! MIC range MIC50 MIC90 % Non-S Vancomycin 1 - 2 2 2 0

Teicoplanin 0.125 - 4 1 2 0

Gentamicin 0.064 - >256 16 128 74

Trim-sulfa 0.032 - >32 2 64 43

Erythromycin 0.064 - >256 >256 >256 74

Clindamycin 0.032 - >256 0.125 >256 47

Ciprofloxacin 0.125 - >32 >32 >32 85

Levofloxacin 0.064 - >32 8 16 82

Moxifloxacin 0.032 - 4 2 2 74

Ofloxacin 0.125 - >32 >32 >32 85

Linezolid 0.125 - 1 0.25 0.5 0

Tigecycline 0.016 - 0.5 0.125 0.25 0

Rifampicin 0.002 – 0.016 0.008 0.008 0

MIC: Minimal inhibitory concentration. All MIC values are in mg/L. S: Susceptible. The clinical breakpoint (S≤) refers to EUCAST clinical breakpoint table version 2.0 2012-01-01. Trim-sulfa: Trimethoprim-sulfamethoxazole

Objective Staphylococcus epidermidis frequently causes infections in immunocompromised patients and patients with catheters or implants. Most isolates are methicillin resistant, thus resistant to most β-lactam antibiotics. These infections are often treated with vancomycin, but treatment failure can occur due to biofilm formation, often necessitating the removal of catheters or implants. This study tests the in vitro activity of a wider spectrum of antibiotics for treatment of methicillin-resistant S. epidermidis (MRSE)

Materials & Methods •  72 MRSE isolates regarded as clinically relevant and isolated

at the Dept. of Microbiology, Haukeland University Hospital, Norway, during 2011 were included; v  52 from blood cultures v  20 from sites such as cerebrospinal fluid, burns and foreign

body related infections.

•  The isolates were identified as S. epidermidis by Vitek®2 and as MRSE based on non-susceptibility to oxacillin. All isolates were subjected to mecA/nuc PCR.

•  Minimal inhibitory concentrations for 13 relevant antibiotics were obtained using MIC Test Strips (Liofilchem) and their sensitivities determined using EUCAST clinical breakpoints.

Acknowledgements Liofilchem is acknowledged for their kind donation of MIC Test Strips for this project.

Technicians Bente Skjellstad, Eirik Nybakken and Kathe Skråmestø at the Department of Microbiology, Haukeland University Hospital are acknowledged for their assistance with mecA/nuc PCR and isolate-handling

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Figures shows distribution of MICs for selected antibiotics. Y-axis; “Number of isolates”. X-axis; “MIC valus (mg/L)”

Clinical breakpoint: R > Clinical breakpoint: S ≤ Epidemiological cut-off: Wild type ≤