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一种新型染色体TEM衍生物与外膜蛋白的改变共同介导大肠杆菌对头孢他啶的选择性耐药。

A novel chromosomal TEM derivative and alterations in outer membrane proteins together mediate selective ceftazidime resistance in Escherichia coli.

作者信息

Weber D A, Sanders C C, Bakken J S, Quinn J P

机构信息

Department of Medical Microbiology, Creighton University School of Medicine, Omaha, Nebraska 68178.

出版信息

J Infect Dis. 1990 Aug;162(2):460-5. doi: 10.1093/infdis/162.2.460.

Abstract

A clinical Escherichia coli isolate (MG32) resistant to ceftazidime but susceptible to other third-generation cephalosporins was previously examined and found to harbor TEM-1 and exhibit alterations in outer membrane proteins. Reexamination of this isolate revealed the additional presence of a novel TEM-1 derivative, now designated TEM-12. Evaluation of ceftazidime and cefotaxime minimum inhibitory concentrations for isogenic derivatives demonstrated a major role for TEM-12 in the decreased susceptibility observed. This was selectively enhanced for ceftazidime resistance by the altered porins of E. coli MG32. TEM-12 appeared identical to TEM-101, an in vitro TEM derivative, in both isoelectric point (pI 5.25) and substrate profile. Hybridization and cloning of the TEM-12 determinant revealed that, unlike other TEM derivatives, TEM-12 is chromosomally encoded, not plasmid-encoded.

摘要

先前对一株临床分离的大肠杆菌(MG32)进行了检测,该菌株对头孢他啶耐药,但对其他第三代头孢菌素敏感,结果发现其携带TEM-1并在外膜蛋白上存在改变。对该分离株的重新检测发现了一种新型TEM-1衍生物的额外存在,现命名为TEM-12。对同基因衍生物的头孢他啶和头孢噻肟最低抑菌浓度的评估表明,TEM-12在观察到的敏感性降低中起主要作用。大肠杆菌MG32改变的孔蛋白选择性地增强了对头孢他啶的耐药性。TEM-12在等电点(pI 5.25)和底物谱方面与体外TEM衍生物TEM-101相同。TEM-12决定簇的杂交和克隆显示,与其他TEM衍生物不同,TEM-12是染色体编码的,而非质粒编码。

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