首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Molecular characterization of macrolide resistance mechanisms among Streptococcus pneumoniae and Streptococcus pyogenes isolated from the PROTEKT 1999-2000 study.
【24h】

Molecular characterization of macrolide resistance mechanisms among Streptococcus pneumoniae and Streptococcus pyogenes isolated from the PROTEKT 1999-2000 study.

机译:从PROTEKT 1999-2000研究中分离出的肺炎链球菌和化脓性链球菌之间的大环内酯类耐药机制的分子表征。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

In this study, the distribution of macrolide resistance mechanisms was determined for isolates of Streptococcus pneumoniae and Streptococcus pyogenes obtained from the PROTEKT 1999-2000 study (a global, longitudinal study of the antibacterial susceptibility of bacterial pathogens associated with community-acquired lower respiratory tract infections). The global macrolide resistance mechanism distribution results for 1043 macrolide-resistant S. pneumoniae isolates collected from 25 countries were as follows: 35.3% mef(A), 56.2% erm(B), 6.8% both mef(A) and erm(B), 0.2% erm(A) subclass erm(TR) and 1.5% negative for mechanisms tested. Mechanisms of macrolide resistance were found to vary widely between countries and different geographical regions with mef(A) predominating in North America and erm(B) in Europe. Approximation of genotype from macrolide MIC without molecular determination of the mechanism of resistance resulted in an error of 10.2% (106 isolates). Overall, for 143 macrolide-resistant S. pyogenes isolates, 46.1% of the isolates tested were mef(A), 30.8% were erm(B), 23.1% were erm(A) subclass erm(TR) and no isolates were negative for all the genetic markers tested. Again, the distribution varied widely between countries and geographical regions. This study provides valuable baseline data for the continued monitoring of the evolution of macrolide resistance development in these important respiratory tract pathogens. The ketolide telithromycin retained excellent anti-pneumococcal activity irrespective of macrolide resistance mechanism, having a MIC(90) of 0.25, 0.5 and 0.5 mg/L against mef(A), erm(B) and mef(A)+erm(B) macrolide-resistant S. pneumoniae, respectively. It also exhibited potent activity against S. pyogenes that had become resistant to macrolides via either mef(A), (MIC(90 )0.5 mg/L) or erm(TR), (MIC(90) 0.03 mg/L).
机译:在这项研究中,确定了从PROTEKT 1999-2000研究获得的肺炎链球菌和化脓性链球菌分离株的大环内酯类耐药机制分布(一项全球细菌感染病原体与社区获得性下呼吸道感染相关的细菌敏感性的纵向研究。 )。从25个国家/地区收集到的1043株耐大环内酯酶肺炎链球菌的全球大环内酯耐药机制分布结果如下:mef(A)和erm(B)分别为35.3%mef(A),56.2%erm(B),6.8% ,对于所测试的机制,erm(A)子类为erm(TR)为0.2%,负值为1.5%。人们发现,大环内酯类药物的抗药性机制在国家和不同地区之间差异很大,其中北美以mef(A)为主,欧洲以erm(B)为主。从大环内酯MIC进行基因型近似,而没有分子确定抗药性机制,则导致10.2%的误差(106个分离株)。总体而言,对于143个耐大环内酯化脓性链球菌,分离株的46.1%为mef(A),erm(B)为30.8%,erm(A)erm(TR)亚类为23.1%,没有分离株对所有测试的遗传标记。同样,国家和地理区域之间的分布差异很大。这项研究为继续监测这些重要的呼吸道病原体中大环内酯耐药性的发展提供了有价值的基线数据。不论大环内酯耐药机制如何,酮利特铁霉素都具有优异的抗肺炎球菌活性,对mef(A),erm(B)和mef(A)+ erm(B)的MIC(90)为0.25、0.5和0.5 mg / L耐大环内酯的肺炎链球菌。它也表现出针对化脓性链球菌的有效活性,该化脓性链球菌通过mef(A)(MIC(90)0.5mg / L)或erm(TR)(MIC(90)0.03 mg / L)变得对大环内酯类耐药。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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