Suppr超能文献

流感嗜血杆菌中的氨苄西林耐药性:耐药机制的鉴定

Ampicillin resistance in Haemophilus influenzae: identification of resistance mechanisms.

作者信息

Reid A J, Simpson I N, Harper P B, Amyes S G

机构信息

Bacteriology Department, Medical School, University of Edinburgh, U.K.

出版信息

J Antimicrob Chemother. 1987 Nov;20(5):645-56. doi: 10.1093/jac/20.5.645.

Abstract

The incidence and mechanisms of ampicillin resistance (MIC greater than 1 mg/l) were investigated in 105 clinical isolates of Haemophilus influenzae collected in Edinburgh during 1983/4. Fifteen (14.3%) ampicillin-resistant strains were identified and these were non-serotypable and comprised six biotypes. Isoelectric focusing and beta-lactamase-inhibition studies demonstrated that production of the TEM-1 beta-lactamase was the principal mechanism of resistance in nine (60%) strains. Radiolabelling revealed that one beta-lactamase-positive strain also had an unusual penicillin-binding protein (PBP) profit. No beta-lactamase activity was detected in the other six (40%) ampicillin-resistant strains. Two beta-lactamase-negative ampicillin-resistant strains had atypical PBP profiles. SDS-PAGE analysis showed that four beta-lactamase-negative ampicillin-resistant strains, including one with altered PBPs, exhibited outer membrane protein profiles which differed from those of sensitive strains of the same biotype. The ampicillin-resistance mechanism of the remaining strain could not be determined. Thus, several resistance mechanisms, either acting individually or in combination, are implicated in ampicillin resistance in H. influenzae.

摘要

1983/4年期间,在爱丁堡收集了105株流感嗜血杆菌临床分离株,对氨苄西林耐药(最低抑菌浓度大于1mg/l)的发生率和机制进行了研究。鉴定出15株(14.3%)氨苄西林耐药菌株,这些菌株不可分型,包括6种生物型。等电聚焦和β-内酰胺酶抑制研究表明,9株(60%)菌株中TEM-1β-内酰胺酶的产生是主要耐药机制。放射性标记显示,1株β-内酰胺酶阳性菌株也有异常的青霉素结合蛋白(PBP)谱。在其他6株(40%)氨苄西林耐药菌株中未检测到β-内酰胺酶活性。2株β-内酰胺酶阴性的氨苄西林耐药菌株具有非典型的PBP谱。SDS-PAGE分析显示,4株β-内酰胺酶阴性的氨苄西林耐药菌株,包括1株PBP改变的菌株,其外膜蛋白谱与相同生物型的敏感菌株不同。其余菌株的氨苄西林耐药机制无法确定。因此,几种耐药机制单独或联合作用与流感嗜血杆菌对氨苄西林耐药有关。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验