首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Interplay of cell wall barrier and beta-lactamase activity determines high resistance to beta-lactam antibiotics in Mycobacterium chelonae.
【2h】

Interplay of cell wall barrier and beta-lactamase activity determines high resistance to beta-lactam antibiotics in Mycobacterium chelonae.

机译:细胞壁屏障和β-内酰胺酶活性之间的相互作用决定了在分枝杆菌中对β-内酰胺抗生素的高抗性。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

We calculated the target access index, which reflects the probability that a drug will reach its target at an effective concentration, and the predictive MICs of cephaloridine, cephalothin, and cefazolin for Mycobacterium chelonae from the drug concentrations inhibiting the binding of benzylpenicillin to penicillin-binding proteins, the permeability coefficients, and the beta-lactamase properties. Despite a low level of beta-lactamase activity and because of a very effective permeability barrier, the target access indices were very low, e.g., 100 times lower than for penicillinase-producing Escherichia coli. The predicted MICs were within one to three twofold dilutions of the experimentally determined values (which ranged between 512 and greater than or equal to 2,048 micrograms/ml). These results demonstrate that the interplay of the cell wall barrier and beta-lactamase activity determines high resistance of M. chelonae to beta-lactam antibiotics.
机译:我们计算了目标访问指数,该指数反映了药物将在有效浓度下达到目标的可能性,以及通过抑制苄青霉素与青霉素结合的药物浓度预测的头孢分枝杆菌的头孢啶,头孢菌素和头孢唑啉的MIC蛋白质,渗透系数和β-内酰胺酶特性。尽管β-内酰胺酶活性水平低并且由于非常有效的渗透性屏障,但是靶标进入指数非常低,例如,比产生青霉素酶的大肠杆菌低100倍。预测的MIC在实验确定的值的1-3倍稀释范围内(范围在512和大于或等于2,048微克/ ml之间)。这些结果表明,细胞壁屏障和β-内酰胺酶活性的相互作用决定了M. chelonae对β-内酰胺抗生素的高抗性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号