Mook-Kanamori Barry B, Rouse Mark S, Kang Cheol-In, van de Beek Diederik, Steckelberg James M, Patel Robin
Division of Infectious Disease, Department of Internal Medicine, College of Medicine, Mayo Clinic, Rochester, MN, USA.
BMC Infect Dis. 2009 Apr 30;9:50. doi: 10.1186/1471-2334-9-50.
Daptomycin, a lipopeptide antibiotic, could be an alternative to vancomycin for treatment of pneumococcal meningitis. We determined the activity of daptomycin versus vancomycin, with dexamethasone as an adjuvant, in a murine model of pneumococcal meningitis.
Ninety-six 25-30 gram mice were inoculated intracisternally with serotype 3 Streptococcus pneumoniae modified by the integration of a luminescent lux operon. All mice were treated with either dexamethasone 1 mg/kg intraperitoneally every 6 hours alone or in combination with either vancomycin or daptomycin, also administered intraperitoneally. Serum antimicrobial concentrations were selected to approximate those achieved in humans. Following treatment, bioluminescence and cerebrospinal fluid (CSF) bacterial concentrations were determined. Caspase-3 staining was used to assess apoptosis on brain histopathology.
Sixteen hours post intracisternal inoculation, bacterial titers in CSF were 6.8 log10 cfu/ml. Amongst the animals given no antibiotic, vancomycin 50 mg/kg at 16 and 20 hours or daptomycin 25 mg/kg at 16 hours, CSF titers were 7.6, 3.4, and 3.9 log10 cfu/ml, respectively, at 24 hours post infection (p-value, < 0.001 for both vancomycin or daptomycin versus no antibiotic); there was no significant difference in bactericidal activity between the vancomycin and daptomycin groups (p-value, 0.18). CSF bioluminescence correlated with bacterial titer (Pearson regression coefficient, 0.75). The amount of apoptosis of brain parenchymal cells was equivalent among treatment groups.
Daptomycin or vancomycin, when given in combination with dexamethasone, is active in the treatment of experimental pneumococcal meningitis.
达托霉素是一种脂肽类抗生素,可作为万古霉素治疗肺炎球菌性脑膜炎的替代药物。我们在肺炎球菌性脑膜炎小鼠模型中确定了达托霉素与万古霉素联合地塞米松作为佐剂的活性。
将96只体重25 - 30克的小鼠经脑池内接种整合了发光lux操纵子的3型肺炎链球菌。所有小鼠单独接受每6小时1毫克/千克地塞米松腹腔注射,或与万古霉素或达托霉素联合腹腔注射,腹腔注射的血清抗菌浓度选择接近人类达到的浓度。治疗后,测定生物发光和脑脊液(CSF)细菌浓度。使用半胱天冬酶 - 3染色评估脑组织病理学上的细胞凋亡。
脑池内接种后16小时,脑脊液中的细菌滴度为6.8 log10 cfu/ml。在未给予抗生素的动物、16和20小时给予50毫克/千克万古霉素的动物或16小时给予25毫克/千克达托霉素的动物中,感染后24小时脑脊液滴度分别为7.6、3.4和3.9 log10 cfu/ml(万古霉素或达托霉素与未用抗生素相比,p值均<0.001);万古霉素组和达托霉素组之间的杀菌活性无显著差异(p值,0.18)。脑脊液生物发光与细菌滴度相关(Pearson回归系数,0.75)。各治疗组脑实质细胞的凋亡量相当。
达托霉素或万古霉素与地塞米松联合使用时,对实验性肺炎球菌性脑膜炎有治疗活性。