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In Vitro Activity of CEM-101 against Streptococcus pneumoniae and Streptococcus pyogenes with Defined Macrolide Resistance Mechanisms ▿

机译:CEM-101对肺炎链球菌和化脓性链球菌的体外活性及其明确的大环内酯类耐药机制

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摘要

CEM-101 had MIC ranges of 0.002 to 0.016 μg/ml against macrolide-susceptible pneumococci and 0.004 to 1 μg/ml against macrolide-resistant phenotypes. Only 3 strains with erm(B), with or without mef(A), had CEM-101 MICs of 1 μg/ml, and 218/221 strains had CEM-101 MICs of ≤0.5 μg/ml. CEM-101 MICs were as much as 4-fold lower than telithromycin MICs against all strains. For Streptococcus pyogenes, CEM-101 MICs ranged from 0.008 to 0.03 μg/ml against macrolide-susceptible strains and from 0.015 to 1 μg/ml against macrolide-resistant strains. Against erm(B) strains, erythromycin, azithromycin, and clarithromycin MICs were 32 to >64 μg/ml, while 17/19 strains had telithromycin MICs of 4 to 16 μg/ml; CEM-101 MICs were 0.015 to 1 μg/ml. By comparison, erm(A) and mef(A) strains had CEM-101 MICs of 0.015 to 0.5 μg/ml, clindamycin and telithromycin MICs of ≤1 μg/ml, and erythromycin, azithromycin, and clarithromycin MICs of 0.5 to >64 μg/ml. Pneumococcal multistep resistance studies showed that although CEM-101 yielded clones with higher MICs for all eight strains tested, seven of eight strains had clones with CEM-101 MICs that rose from 0.004 to 0.03 μg/ml (parental strains) to 0.06 to 0.5 μg/ml (resistant clones); for only one erm(B) mef(A) strain with a parental MIC of 1 μg/ml was there a resistant clone with a MIC of 32 μg/ml, with no detectable mutations in the L4, L22, or 23S rRNA sequence. Among two of five S. pyogenes strains tested, CEM-101 MICs rose from 0.03 to 0.25 μg/ml, and only for the one strain with erm(B) did CEM-101 MICs rise from 1 to 8 μg/ml, with no changes occurring in any macrolide resistance determinant. CEM-101 had low MICs as well as low potential for the selection of resistant mutants, independent of bacterial species or resistance phenotypes in pneumococci and S. pyogenes.
机译:CEM-101对大环内酯敏感的肺炎球菌的MIC范围为0.002至0.016μg/ ml,对大环内酯类耐药的表型的MIC范围为0.004至1μg/ ml。只有3个带有erm(B)的菌株(有或没有mef(A))的CEM-101 MIC均为1μg/ ml,而218/221菌株的CEM-101 MIC≤0.5μg/ ml。对于所有菌株,CEM-101 MIC都比telithromycin MIC低4倍之多。对于化脓链球菌,CEM-101 MICs对大环内酯类易感菌株的范围从0.008至0.03μg/ ml,对大环内酯类耐药菌株的范围从0.015至1μg/ ml。针对erm(B)菌株,红霉素,阿奇霉素和克拉霉素的MIC为32至> 64μg/ ml,而17/19菌株的泰利霉素的MIC为4至16μg/ ml; CEM-101 MIC为0.015至1μg/ ml。相比之下,erm(A)和mef(A)菌株的CEM-101 MIC值为0.015至0.5μg/ ml,克林霉素和telithromycin MIC≤1μg/ ml,红霉素,阿奇霉素和克拉霉素的MIC为0.5至> 64微克/毫升肺炎球菌多步抗药性研究表明,尽管对于所有测试的八种菌株,CEM-101产生的MIC均较高,但八种菌株中有七株的CEM-101 MIC的克隆率从0.004至0.03μg/ ml(亲本菌株)上升至0.06至0.5μg / ml(抗性克隆);仅对于一个具有MIC为1μg/ ml的erm(B)mef(A)菌株,存在一个MIC为32μg/ ml的抗性克隆,在L4,L22或23S rRNA序列中没有可检测到的突变。在测试的5个化脓性链球菌菌株中,有2个菌株的CEM-101 MIC从0.03上升至0.25μg/ ml,只有一种具有erm(B)的菌株的CEM-101 MIC从1上升至8μg/ ml,没有任何大环内酯类耐药性决定因素都会发生变化。 CEM-101具有较低的MIC,而且在选择抗性突变体方面也具有较低的潜力,而与肺炎球菌和化脓性链球菌中的细菌种类或抗性表型无关。

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