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从1999 - 2000年PROTEKT研究中分离出的肺炎链球菌和化脓性链球菌大环内酯类耐药机制的分子特征

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

作者信息

Farrell D J, Morrissey I, Bakker S, Felmingham D

机构信息

GR Micro Ltd, 7-9 William Road, London NW1 3ER, UK.

出版信息

J Antimicrob Chemother. 2002 Sep;50 Suppl S1:39-47. doi: 10.1093/jac/dkf806.

DOI:10.1093/jac/dkf806
PMID:12239227
Abstract

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).

摘要

在本研究中,对从1999 - 2000年PROTEKT研究(一项关于社区获得性下呼吸道感染相关细菌病原体抗菌药敏性的全球纵向研究)中分离出的肺炎链球菌和化脓性链球菌菌株,确定了大环内酯类耐药机制的分布情况。从25个国家收集的1043株大环内酯类耐药肺炎链球菌菌株的全球大环内酯类耐药机制分布结果如下:mef(A)占35.3%,erm(B)占56.2%,mef(A)和erm(B)两者均有的占6.8%,erm(A)亚类erm(TR)占0.2%,检测机制呈阴性的占1.5%。发现大环内酯类耐药机制在不同国家和不同地理区域之间差异很大,mef(A)在北美占主导,erm(B)在欧洲占主导。在未通过分子方法确定耐药机制的情况下,根据大环内酯类最低抑菌浓度(MIC)估算基因型会导致10.2%(106株菌株)的误差。总体而言,对于143株大环内酯类耐药化脓性链球菌菌株,46.1%的检测菌株为mef(A),30.8%为erm(B),23.1%为erm(A)亚类erm(TR),且没有检测的所有基因标记均为阴性的菌株。同样,其分布在不同国家和地理区域之间差异很大。本研究为持续监测这些重要呼吸道病原体中大环内酯类耐药性演变提供了有价值的基线数据。无论大环内酯类耐药机制如何,酮内酯类药物泰利霉素均保持优异的抗肺炎链球菌活性,对mef(A)、erm(B)和mef(A)+erm(B)大环内酯类耐药肺炎链球菌的MIC90分别为0.25、0.5和0.5mg/L。它对通过mef(A)(MIC90 0.5mg/L)或erm(TR)(MIC90 0.03mg/L)对大环内酯类产生耐药性的化脓性链球菌也表现出强效活性。

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