Shibata K, Adachi Y, Kato E, Nagano R, Fuse A, Hashizume T, Ohtake N, Okamoto O, Nakagawa S
Tsukuba Research Institute, Banyu Pharmaceutical Co., Ltd., Japan.
J Antibiot (Tokyo). 1997 Feb;50(2):135-8. doi: 10.7164/antibiotics.50.135.
The in vitro and in vivo activity of BO-2727, a carbapenem antibiotic, against resistant clinical isolates of Pseudomonas aeruginosa was studied. The geometric mean MICs against three groups of clinical isolates resistant to imipenem, meropenem and both carbapenems were 4.28, 4.08 and 5.44 micrograms/ml, respectively. BO-2727 also inhibited multiply antibiotic resistant isolates and laboratory mutants including a nalB-type mutant, which showed resistance to antibiotics such as imipenem, meropenem, ceftazidime, and/or ciprofloxacin, at less than 1.56 micrograms/ml. Overall, BO-2727 was 4-fold more active than biapenem, meropenem, panipenem and imipenem with an MIC90 of less than 6.25 micrograms/ml. The presence of basic amino acids in minimal medium less affected the antipseudomonal activity to a minimal extent, suggesting that BO-2727 has diverse penetration routes through the outer membrane other than OprD channel, which facilitates the diffusion of basic amino acids and carbapenems. The in vitro activity of BO-2727 reflected well in its therapeutic efficacy in experimental systemic infection in mice. These results suggest a possibility for the development of antipseudomonal carbapenems having activity against imipenem- and/or meropenem-resistant P. aeruginosa as well as a broad spectrum encompassing Gram-positive and -negative bacteria.
研究了碳青霉烯类抗生素BO - 2727对铜绿假单胞菌耐药临床分离株的体外和体内活性。针对耐亚胺培南、美罗培南以及对两种碳青霉烯类抗生素均耐药的三组临床分离株,其几何平均MIC分别为4.28、4.08和5.44微克/毫升。BO - 2727还能抑制多重耐药分离株和实验室突变株,包括nalB型突变株,该突变株对亚胺培南、美罗培南、头孢他啶和/或环丙沙星等抗生素耐药,其MIC小于1.56微克/毫升。总体而言,BO - 2727的活性比比阿培南、美罗培南、帕尼培南和亚胺培南高4倍,MIC90小于6.25微克/毫升。在基本培养基中存在碱性氨基酸对其抗铜绿假单胞菌活性的影响极小,这表明BO - 2727除了通过促进碱性氨基酸和碳青霉烯类扩散的OprD通道外,还有多种穿过外膜的途径。BO - 2727的体外活性在小鼠实验性全身感染的治疗效果中得到了很好的体现。这些结果表明,有可能开发出对耐亚胺培南和/或美罗培南的铜绿假单胞菌有活性且对革兰氏阳性菌和阴性菌具有广谱抗菌活性的抗铜绿假单胞菌碳青霉烯类药物。