Hamad Tarza, Hellmark Bengt, Nilsdotter-Augustinsson Åsa, Söderquist Bo
Department of Laboratory Medicine, Clinical Microbiology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Department of Infectious Diseases, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.
APMIS. 2015 Dec;123(12):1055-60. doi: 10.1111/apm.12465.
In recent years, coagulase-negative staphylococci such as Staphylococcus epidermidis have gained importance as nosocomial pathogens, especially in immunocompromised patients and prosthetic joint infections (PJIs). These infections are often long lasting and difficult to treat due to the production of bacterial biofilm and the transformation of the bacteria into a stationary growth phase. Rifampicin is able to penetrate the biofilm, but to reduce the risk of development of rifampicin resistance it should be used in combination with an additional antibiotic. In this study we used Etest to investigate the antimicrobial susceptibility of 134 clinical isolates of S. epidermidis obtained from PJIs to six oral antibiotics: doxycycline, rifampicin, linezolid, fusidic acid, clindamycin, and ciprofloxacin. We also performed synergy testing on doxycycline in combination with each of the remaining antibiotics. Ninety-three (69%) of the 134 isolates were susceptible to doxycycline, 94/134 (70%) to rifampicin, 56/134 (42%) to clindamycin, 25/134 (19%) to ciprofloxacin, 81/134 (60%) to fusidic acid, and 100% to linezolid. Thirty-two (80%) of the 40 isolates not fully susceptible to rifampicin were susceptible to doxycycline. Doxycycline in combination with each of the other investigated antibiotics exerted an additive effect on nearly half of the isolates, with the exception of clindamycin, which displayed an even higher percentage of additive effect (69%). To conclude, as the majority of the S. epidermidis isolates were susceptible to doxycycline, this antimicrobial agent may provide a potential alternative for combination therapy together with rifampicin.
近年来,凝固酶阴性葡萄球菌,如表皮葡萄球菌,作为医院感染病原体变得越来越重要,尤其是在免疫功能低下的患者和人工关节感染(PJI)中。由于细菌生物膜的产生以及细菌转变为稳定生长期,这些感染往往持续时间长且难以治疗。利福平能够穿透生物膜,但为了降低利福平耐药性产生的风险,应与另一种抗生素联合使用。在本研究中,我们使用Etest来调查从人工关节感染中分离出的134株表皮葡萄球菌临床分离株对六种口服抗生素的抗菌敏感性:强力霉素、利福平、利奈唑胺、夫西地酸、克林霉素和环丙沙星。我们还对强力霉素与其余每种抗生素联合进行了协同试验。134株分离株中,93株(69%)对强力霉素敏感,94/134(70%)对利福平敏感,56/134(42%)对克林霉素敏感,25/134(19%)对环丙沙星敏感,81/134(60%)对夫西地酸敏感,对利奈唑胺的敏感率为100%。40株对利福平不完全敏感的分离株中,32株(80%)对强力霉素敏感。除克林霉素显示出更高比例的相加作用(69%)外,强力霉素与其他每种研究的抗生素联合对近一半的分离株产生相加作用。总之,由于大多数表皮葡萄球菌分离株对强力霉素敏感,这种抗菌剂可能为与利福平联合治疗提供一种潜在的替代方案。