首页> 美国卫生研究院文献>Acta Pharmaceutica Sinica. B >In vitro and in vivo activity of d-serine in combination with β-lactam antibiotics against methicillin-resistant Staphylococcus aureus
【2h】

In vitro and in vivo activity of d-serine in combination with β-lactam antibiotics against methicillin-resistant Staphylococcus aureus

机译:d-丝氨酸联合β-内酰胺类抗生素对耐甲氧西林金黄色葡萄球菌的体外和体内活性

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。

摘要

As d-amino acids play important roles in the physiological metabolism of bacteria, combination of d-amino acids with antibiotics may provide synergistic antibacterial activity. The aim of the study was to evaluate in vitro and in vivo activity of d-serine alone and in combination with β-lactams against methicillin-resistant Staphylococcus aureus (MRSA) strains, and to explore the possible sensitization mechanisms. The activity of d-serine, β-lactams alone and in combinations was evaluated both in vitro by standard MICs, time–kill curves and checkerboard assays, and in vivo by murine systemic infection model as well as neutropenic thigh infection model. An in vitro synergistic effect was demonstrated with the combination of d-serine and β-lactams against MRSA standard and clinical strains. Importantly, the combinations enhanced the therapeutic efficacy in the animal models as compared to β-lactam alone groups. Initial mechanism study suggested possible revision of d-alanine-d-alanine residue to d-alanine-d-serine in peptidoglycan by adding of d-alanine in the medium, which may cause decreased affinity to PBPs during transpeptidation. In conclusion, d-serine had synergistic activity in combination with β-lactams against MRSA strains both in vitro and in vivo. Considering the relatively good safety of d-serine alone or in combination with β-lactams, d-serine is worth following up as new anti-MRSA infection strategies.
机译:由于d-氨基酸在细菌的生理代谢中起着重要的作用,因此d-氨基酸与抗生素的结合可提供协同的抗菌活性。该研究的目的是评估单独的d-丝氨酸以及与β-内酰胺类药物联合使用对耐甲氧西林的金黄色葡萄球菌(MRSA)菌株的体外和体内活性,并探讨可能的致敏机制。 d-丝氨酸,β-内酰胺类单独或组合的活性在体外通过标准MIC,时间杀伤曲线和棋盘分析进行了评估,在体内通过鼠类全身感染模型以及中性粒细胞减少性大腿感染模型进行了评估。 d-丝氨酸和β-内酰胺类药物联合使用对MRSA标准品和临床菌株具有体外协同作用。重要的是,与单独使用β-内酰胺的组相比,该组合增强了在动物模型中的治疗功效。初步的机理研究表明,通过在培养基中添加d-丙氨酸,可以将肽聚糖中的d-丙氨酸-d-丙氨酸残基修改为d-丙氨酸-d-丝氨酸,这可能会导致在转肽过程中对PBP的亲和力降低。总之,在体外和体内,d-丝氨酸与β-内酰胺联用对MRSA菌株均具有协同活性。考虑到单独或与β-内酰胺组合使用d-丝氨酸的相对较好的安全性,值得将d-丝氨酸作为新的抗MRSA感染策略进行随访。

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