Combined effect of pH and concentration on the activities of gentamicin and oxacillin against Staphylococcus aureus in pharmacodynamic models of extracellular and intracellular infections

被引:75
作者
Baudoux, Pierre [1 ]
Bles, Nathalie [1 ]
Lemaire, Sandrine [1 ]
Mingeot-Leclercq, Marie-Paule [1 ]
Tulkens, Paul M. [1 ]
Van Bambeke, Francoise [1 ]
机构
[1] Catholic Univ Louvain, Unite Pharmacol Cellulaire & Mol, B-1200 Brussels, Belgium
关键词
acid pH; beta-lactams; aminoglycosides; pharmacodynamics; antibiotic accumulation;
D O I
10.1093/jac/dkl489
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Staphylococcus aureus survives in acid media, including phagolysosomes. Conflicting in vitrolin vivo data exist on its susceptibility to antibiotics in such environments. Methods: Oxacillin and gentamicin activities against methicillin-susceptible S. aureus ATCC 25923 were compared extracellularly (broth; different pH) and assessed intracellularly (THP-1 macrophages), using a pharmacological approach (antibiotic concentrations: 0.01-1000 x MIC). Antibiotic cellular contents were determined by microbiological assay. Results: MICs and MBCs increased 72-fold for gentamicin, and decreased 8-fold for oxacillin between pH 7.4 and 5.0. Plots of log(10) colony-forming unit changes at 24 h versus log(10) of antibiotic concentration followed sigmoidal shapes, allowing calculation of EC50 (relative potency) and apparent E-max (relative efficacy) in all conditions. In broth, the EC50 Of gentamicin rose 316-fold and that of oxacillin decreased 15-fold with unchanged apparent E-max [-5 log (limit of detection)] between pH 7.4 and 5. Intracellularly, EC(50)s were similar to those observed extracellularly at pH 7.4, but E, x values were much lower (-1 log) for both antibiotics. Calculations based on the assumed pH in phagolysosomes (5.4) and on local accumulation of antibiotics (gentamicin, 23-fold; oxacillin, 0.05-fold) suggest that the contrasting effects of acid pH on relative potencies of gentamicin and oxacillin could be almost exactly compensated for by differences in accumulation. Conclusions: The weak activity of gentamicin and oxacillin towards intraphagocytic S. aureus compared with extracellular forms is not related to an overall decrease of their relative potencies but to impaired efficacy, suggesting the need for new approaches to improve the eradication of intracellular S. aureus.
引用
收藏
页码:246 / 253
页数:8
相关论文
共 38 条
[1]   Persistent wound infection after herniotomy associated with small-colony variants of Staphylococcus aureus [J].
Abele-Horn, M ;
Schupfner, B ;
Emmerling, P ;
Waldner, H ;
Göring, H .
INFECTION, 2000, 28 (01) :53-54
[2]   PENICILLIN-BINDING SITE ON THE ESCHERICHIA-COLI CELL-ENVELOPE [J].
AMARAL, L ;
LEE, Y ;
SCHWARZ, U ;
LORIAN, V .
JOURNAL OF BACTERIOLOGY, 1986, 167 (02) :492-495
[3]  
[Anonymous], 2005, PRINCIPLES PRACTICE
[4]   Pharmacodynamic evaluation of the intracellular activities of antibiotics against Staphylococcus aureus in a model of THP-1 macrophages [J].
Barcia-Macay, M ;
Seral, C ;
Mingeot-Leclercq, MP ;
Tulkens, PM ;
Van Bambeke, F .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (03) :841-851
[5]   Global gene expression in Staphylococcus aureus biofilms [J].
Beenken, KE ;
Dunman, PM ;
McAleese, F ;
Macapagal, D ;
Murphy, E ;
Projan, SJ ;
Blevins, JS ;
Smeltzer, MS .
JOURNAL OF BACTERIOLOGY, 2004, 186 (14) :4665-4684
[6]   In vivo and in vitro demonstration that Staphylococcus aureus is an intracellular pathogen in the presence or absence of fibronectin-binding proteins [J].
Brouillette, E ;
Grondin, G ;
Shkreta, L ;
Lacasse, P ;
Talbot, BG .
MICROBIAL PATHOGENESIS, 2003, 35 (04) :159-168
[7]   Intracellular pharmacodynamics of antibiotics [J].
Carryn, S ;
Chanteux, H ;
Seral, C ;
Mingeot-Leclercq, MP ;
Van Bambeke, F ;
Tulkens, PM .
INFECTIOUS DISEASE CLINICS OF NORTH AMERICA, 2003, 17 (03) :615-+
[8]   Evidence of an intracellular reservoir in the nasal mucosa of patients with recurrent Staphylococcus aureus rhinosinusitis [J].
Clement, S ;
Vaudaux, P ;
Francois, P ;
Schrenzel, J ;
Huggler, E ;
Kampf, S ;
Chaponnier, C ;
Lew, D ;
Lacroix, JS .
JOURNAL OF INFECTIOUS DISEASES, 2005, 192 (06) :1023-1028
[9]   Surviving the acid test: Responses of gram-positive bacteria to low pH [J].
Cotter, PD ;
Hill, C .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2003, 67 (03) :429-+
[10]   Management of bone and joint infections due to Staphylococcus aureus [J].
Davis, JS .
INTERNAL MEDICINE JOURNAL, 2005, 35 :S79-S96