Huang David B, de Piano Cyntia, Magnet Sophie
Motif BioSciences, New York, USA.
Rutgers New Jersey Medical School, Trenton, New Jersey, USA.
Access Microbiol. 2019 May 20;1(3):e000027. doi: 10.1099/acmi.0.000027. eCollection 2019.
In this pilot study, the antimicrobial activity of iclaprim, a diaminopyrimidine, tested in combination with other antimicrobials against recent and common Gram-positive and Gram-negative respiratory pathogens, was examined by the checkerboard method. The range of minimal inhibitory concentrations (MICs) for iclaprim against all bacteria tested in the study was 0.03 to >128 µg ml. Iclaprim exhibited synergy with sulfamethoxazole against 11 of the 16 bacterial strains tested, with mean fractional inhibitory concentration index (FICI) values of 0.2-0.5. Synergy with sulfamethoxazole was demonstrated against all Gram-positive bacteria and selected Gram-negative bacteria. Neither synergy nor antagonism was observed for combinations of iclaprim with ampicillin, meropenem, tetracycline, levofloxacin, aztreonam, piperacillin/tazobactam, colistin, cefepime or gentamicin against any of the bacterial strains tested. The significant reduction in the MIC values observed with the combination of iclaprim and sulfamethoxazole demonstrates that this regimen could be effective against common Gram-positive and selected Gram-negative respiratory bacteria.
在这项初步研究中,采用棋盘法检测了二氨基嘧啶类药物依拉普利与其他抗菌药物联合使用时,对近期常见的革兰氏阳性和革兰氏阴性呼吸道病原体的抗菌活性。依拉普利对本研究中所有测试细菌的最低抑菌浓度(MIC)范围为0.03至>128μg/ml。依拉普利与磺胺甲恶唑对16株测试细菌中的11株表现出协同作用,平均分数抑菌浓度指数(FICI)值为0.2 - 0.5。对所有革兰氏阳性菌和部分革兰氏阴性菌均显示出与磺胺甲恶唑的协同作用。依拉普利与氨苄西林、美罗培南、四环素、左氧氟沙星、氨曲南、哌拉西林/他唑巴坦、黏菌素、头孢吡肟或庆大霉素联合使用时,对任何测试菌株均未观察到协同或拮抗作用。依拉普利与磺胺甲恶唑联合使用时观察到的MIC值显著降低表明,该方案可能对常见的革兰氏阳性菌和部分革兰氏阴性呼吸道细菌有效。