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A54145一种新型脂肽抗生素复合物:微生物学评价

A54145 a new lipopeptide antibiotic complex: microbiological evaluation.

作者信息

Counter F T, Allen N E, Fukuda D S, Hobbs J N, Ott J, Ensminger P W, Mynderse J S, Preston D A, Wu C Y

机构信息

Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana 46285.

出版信息

J Antibiot (Tokyo). 1990 Jun;43(6):616-22. doi: 10.7164/antibiotics.43.616.

Abstract

A54145 complex is made up of eight factors; A, A1, B, B1, C, D, E, and F which were active in vitro (MIC 0.25 approximately greater than 32 micrograms/ml) against Gram-positive aerobic organisms. The complex, factor B and B1 were found to be active against two strains of Clostridium perfringens. A calcium dependence study on some of the factors showed that their in vitro antibacterial activity was greatly enhanced by the presence of calcium (50 mg/liter) in the media. Resistance build-up was seen when Staphylococcus sp. and Streptococcus sp. were passed seven times in the presence of sublethal concentrations of A54145 antibiotics. This resistance disappeared immediately when the resistant organisms were passed in the absence of the antibiotics. Factor A was very effective against Staphylococcus aureus and Streptococcus pyogenes infections in mice (sc ED50s of 3.3 approximately 2.4 mg/kg x 2, respectively). Factor B was more active against S. pyogenes in vivo (sc ED50, 0.9 mg/kg x 2). Acute mouse toxicities were determined with these antibiotics. Semisynthetic derivatives were evaluated.

摘要

A54145复合物由八个因子组成,即A、A1、B、B1、C、D、E和F,它们在体外对革兰氏阳性需氧菌具有活性(最低抑菌浓度约为0.25至大于32微克/毫升)。该复合物、因子B和B1对两株产气荚膜梭菌具有活性。对其中一些因子的钙依赖性研究表明,培养基中钙(50毫克/升)的存在大大增强了它们的体外抗菌活性。当葡萄球菌属和链球菌属在亚致死浓度的A54145抗生素存在下传代七次时,出现了耐药性增强。当耐药菌在无抗生素的情况下传代时,这种耐药性立即消失。因子A对小鼠的金黄色葡萄球菌和化脓性链球菌感染非常有效(皮下半数有效剂量分别约为3.3和2.4毫克/千克×2)。因子B在体内对化脓性链球菌更具活性(皮下半数有效剂量,0.9毫克/千克×2)。测定了这些抗生素的小鼠急性毒性。对半合成衍生物进行了评估。

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