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Molecular analytical evaluation of macrolide- and ketolide-resistant Streptococcus pneumoniae--mechanism of action of telithromycin and resistance to it

机译:大氯化物和酮铁酯抗性链球菌的分子分析评价肺炎素肺炎料和汽力霉素作用机制及其抗性

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PROTEKT (Prospective Resistant Organism Tracking and Epidemiology for the Ketolide Telithromycin) is a worldwide epidemiologic survey for investigating drug susceptibility against major bacterial pathogens in respiratory tract infections, and that is also designed to identify the action mechanism of telithromycin (TEL), a ketolide antibacterial agent, on the resistant Streptococcus pneumoniae and the resistance mechanism for TEL on the TEL-resistant S. pneumoniae strain, in addition to determine macrolide/ketolide resistant S. pneumoniae activities of TEL using molecular analysis. TEL exerted the antibacterial action on the macrolide-resistant S. pneumoniae regardless maintaining the macrolide-resistant mechanism and exhibited the potent antibacterial activity against all of ermB gene-positive strains, mefA gene-positive strains and ribosome variants. This result was considered to reflect the fact that TEL did not induce resistance to ermB and had extremely low ability to select resistant strain by mutation. These actions of TEL were considered to be derived from its novel chemical structure and might be characteristics of ketolides not possessed by macrolides. In the survey of PROTEKT in 1999 to 2002, among 13,864 strains of S. pneumoniae isolated worldwide, ketolide-resistant strain (TEL MIC > or = 4 microg/ml) was observed in 10 strains (0.07%). MIC of these 10 strains was 4 or 8 microg/mL and all of these strains were ermB-positive strains. Based on this fact, potential involvement of adenine demethylase (ermB gene product) was considered in the background of development of ketolide-resistant S. pneumoniae.
机译:Protekt(前瞻性生物跟踪和酮型Telitroomycin的流行病学)是全球流行病学调查,用于调查呼吸道感染中的主要细菌病原体的药物易感性,并且还旨在鉴定Telitroomycin(Tel),酮类抗菌的作用机制代理商,对抗肺炎链球菌抗肺炎链球菌和抗性S.肺炎肺炎菌株的抗性机制,除了测定Macrolide /酮醇抗性S.Spneumoniae使用分子分析的活动。 Tel施加了抗性S.肺炎的抗菌作用,无论维持大茂的抗性机制,并表现出对所有ERMB基因阳性菌株,MEFA基因阳性菌株和核糖体变体的有效抗菌活性。该结果被认为反映了Tel没有诱导对ERMB抗性的事实,并且具有极低的能力通过突变选择抗性菌株。考虑到的这些作用被认为是从其新的化学结构中衍生的,并且可能是长醇未被具有睾烷的特征。在1999年至2002年的Protekt调查中,在全球隔离的13,864株S.肺炎菌株中,在10个菌株(0.07%)中观察到致氯化物抗性菌株(Tel MIC>或= 4微粒/ mL)。这10个菌株的MIC为4或8微孔/ ml,所有这些菌株都是ERMB阳性菌株。基于这一事实,在酮丙胺抗性S.肺炎的发展背景下考虑了腺嘌呤脱甲基酶(ERMB基因产物)的潜在参与。

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