In vitro activity of gentamicin as an adjunct to penicillin against biofilm group B Streptococcus

Objectives: Group B Streptococcus (GBS) increasingly causes invasive disease in non-pregnant adults, particularly in elderly persons and those with underlying diseases. Combination therapy with penicillin plus gentamicin has been suggested for periprosthetic joint infection. The postulated synergism of this combination is based on experiments with planktonic bacteria. We aimed to assess the efficacy of this combination against sessile bacteria. Methods: Four different GBS strains were used. We compared results of MICs with those of minimal biofilm eradication concentrations (MBECs), applied chequerboard assays to the MBEC device and calculated the fractional inhibitory concentration index. Synergism was evaluated with time–kill assays against bacteria adherent to cement beads, using penicillin (0.048, 0.2 and 3 mg/L), gentamicin (4 and 12.5 mg/L) and a combination thereof. Results were evaluated via colony counting after sonication of beads and scanning electron microscopy. Results: MBEC/MIC ratios were 2000–4000 for penicillin and 1–4 for gentamicin. In chequerboard assays, synergism was observed in all four isolates. In time–kill assays, penicillin and 12.5 mg/L gentamicin showed synergism in two isolates. In the other two isolates 12.5 mg/L gentamicin alone was as efficient as the combination therapy. Conclusions: These in vitro investigations show activity of 12.5 mg/L gentamicin, alone or as an adjunct to penicillin, against four strains of biofilm GBS. This concentration cannot be achieved in bone with systemic administration, but can be reached if administered locally. The combination of systemic penicillin plus local gentamicin indicates a potential application in orthopaedic-device-associated GBS infections. Studies with a larger number of strains are required to confirm our results.

[1]  S. Mauerer,et al.  Chromosomally and Extrachromosomally Mediated High-Level Gentamicin Resistance in Streptococcus agalactiae , 2016, Antimicrobial Agents and Chemotherapy.

[2]  A. Holmberg,et al.  Antibiotic regimens with rifampicin for treatment of Enterococcus faecium in biofilms. , 2014, International journal of antimicrobial agents.

[3]  K. Boggian,et al.  Group B streptococcus in prosthetic hip and knee joint-associated infections. , 2011, The Journal of hospital infection.

[4]  D. Livermore Kucers' The use of antibiotics , 2011 .

[5]  Christer Ekdahl,et al.  Swedish guidelines for diagnosis and treatment of infective endocarditis , 2007, Scandinavian journal of infectious diseases.

[6]  P. Tulkens,et al.  Combined effect of pH and concentration on the activities of gentamicin and oxacillin against Staphylococcus aureus in pharmacodynamic models of extracellular and intracellular infections. , 2006, The Journal of antimicrobial chemotherapy.

[7]  John Heritage,et al.  Measurement of ampicillin, vancomycin, linezolid and gentamicin activity against enterococcal biofilms. , 2006, The Journal of antimicrobial chemotherapy.

[8]  Carmen Buchrieser,et al.  Genome sequence of Streptococcus agalactiae, a pathogen causing invasive neonatal disease , 2002, Molecular microbiology.

[9]  H. Ceri,et al.  Biofilm bacteria: formation and comparative susceptibility to antibiotics. , 2002, Canadian journal of veterinary research = Revue canadienne de recherche veterinaire.

[10]  T. Vail,et al.  Pharmacokinetics of a Degradable Drug Delivery System in Bone , 1998, Clinical orthopaedics and related research.

[11]  C H Nightingale,et al.  Experience with a once-daily aminoglycoside program administered to 2,184 adult patients , 1995, Antimicrobial agents and chemotherapy.

[12]  R. Facklam,et al.  Synergism, killing kinetics, and antimicrobial susceptibility of group A and B streptococci , 1981, Antimicrobial Agents and Chemotherapy.

[13]  T. Peel,et al.  Prosthetic Joint Infections , 2018, Springer International Publishing.

[14]  L. Olaison,et al.  Infective endocarditis caused by group B Streptococcus: the role of aminoglycoside-combination. , 2012, The Journal of infection.

[15]  U. Holzgrabe,et al.  Penetration of antibacterials into bone: pharmacokinetic, pharmacodynamic and bioanalytical considerations. , 2009, Clinical pharmacokinetics.