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首页> 外文期刊>The Japanese journal of antibiotics >Antimicrobial activities of macrolides against recent clinical isolates, and analysis of resistant mechanisms
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Antimicrobial activities of macrolides against recent clinical isolates, and analysis of resistant mechanisms

机译:大胶质剂对近期临床分离株的抗菌活性,以及抗性机制分析

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摘要

We examined antibacterial activities of 4 kinds of macrolides, erythromycin (EM), clarithromycin (CAM), azithromycin (AZM) and rokitamycin (RKM), against 6 bacterial species of clinical strains isoleted in 2002. Bacterial isolates used were each 50 strains of methicillin-susceptible Staphylococcus aureus (MSSA), Streptococcus pyogenes, Streptococcus agalactiae, Moraxella (Branhamella) catarrhalis, Haemophilus influenzae and 43 strains of Streptococcus pneumoniae. S. agalactiae were derived from gynecological samples, and other species were isolated from respiratory specimens. Antimicrobial activities against S. aureus, S. pyogenes, S. agalactiae, M. catarrhalis and H. influenzae of 14-membered macrolides, such as EM and CAM, were higher than those of 16-membered macrolide, RKM. By contrast, against S. pneumoniae, RKM was more effective than 14-membered macrolides. Six, three and four strains of S. aureus, S. pyogenes and S. agalactiae, respectively, were resistant to macrolides. Thirty-five among 43 pneumococcal isolates were resistant, and 15 of the 35 were highly-resistant, MIC of > 128 micrograms/ml, to any one of EM, CAM or AZM. Isolation frequency of resistant strains to RKM was lower than those to 14- and 15-membered macrolides: only one strain was highly-resistant and 12 were intermediately-resistant. No resistant strain was recognized in M. catarrhalis and H. influenzae. Further, we analyzed the resistant mechanisms, methylation or efflux, of macrolide resistant strains by the double-disk method. Methylation was major mechanism in S. aureus, and in S. pyogenes, all of the resistance was caused by methylation. In S. agalactiae and S. pneumoniae, methylation and efflux shared about half and half.
机译:我们检查了4种大环内酯,红霉素(EM),克拉霉素(凸轮),四胞质霉素(AZM)和瑞康霉素(RKM)的抗菌活性,2002年患有6种细菌临床菌株。使用的细菌分离株每50株甲氧西林-Uscrectible金黄色葡萄球菌(MSSA),链球菌Pyogenes,链球菌嗜碱剂,Moraxella(Branhamella)Catarrhalis,嗜血杆菌嗜血杆菌和43株肺炎链球菌。 S.嗜虾症源自妇科样品,并从呼吸样品中分离其他物种。对针对金黄色葡萄球菌,S. pyogenes,S.Agalactiae,M. catarrhalis和H的抗菌活性的活性活动均为14元大环的甲酰胺,例如EM和凸轮,高于16元大环内酯,RKM。相比之下,针对S.肺炎,RKM比14元大环内酯更有效。分别六,三,三和四株金黄色葡萄球菌,S. pyogenes和S.嗜虾症,对大环内酯抗性。在43个肺炎球菌分离物中的35个抗性,35个中的15个是EM,凸轮或AZM中任一项的高度抗性MIC> 128微克/ mL。将抗性菌株的分离频率低于14-14-14-14-14-14-14-15元大氯:仅一个菌株是高度抗性的,12个是中间抗性的。在M. catarrhalis和H. flofenzae中,不识别耐药菌株。此外,通过双盘法分析了大环内酯抗性菌株的抗性机制,甲基化或流出。甲基化是S.UUREUS中的主要机制,在S. pyogenes中,所有抵抗力都是由甲基化引起的。在S. ArAlactiae和S.肺炎,甲基化和流出分为大约一半和一半。

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