Iyobe S
Laboratory of Drug-Resistance in Bacteria, Gunma University School of Medicine.
Nihon Rinsho. 1997 May;55(5):1219-24.
Extended-spectrum beta-lactamases (ESBLs) are enzymes which hydrolyze broad-spectrum beta-lactam antibiotics by expanding the substrate spectra into the so-called anti-beta-lactamase beta-lactams such as oxyimino-cephalosporins, cephamycins, oxacephems, carbapenems and monobactams, conferring resistance to many kinds of beta-lactams on pathogenic bacteria. Recently, ESBLs have been demonstrated from various types of beta-lactamases phylogenetically belonging to the molecular class, A, B, C, or D. The genes coding for ESBLs are chromosome- or plasmid-mediated and some of them have developed by point or insertion mutations in the parental genes coding for the narrow-spectrum beta-lactamase. If the genes are plasmid-mediated, the dissemination among various species of pathogenic bacteria would cause hospital-acquired infections by ESBL-producing bacteria.
超广谱β-内酰胺酶(ESBLs)是一类能通过将底物谱扩展到所谓的抗β-内酰胺酶β-内酰胺类药物(如氧亚氨基头孢菌素、头孢霉素、氧头孢烯类、碳青霉烯类和单环β-内酰胺类)来水解广谱β-内酰胺抗生素的酶,从而使病原菌对多种β-内酰胺类药物产生耐药性。最近,已从系统发育上属于分子类别A、B、C或D的各种类型β-内酰胺酶中证实了ESBLs的存在。编码ESBLs的基因是由染色体或质粒介导的,其中一些是通过编码窄谱β-内酰胺酶的亲本基因中的点突变或插入突变而产生的。如果这些基因是由质粒介导的,那么它们在各种病原菌中的传播将导致产ESBLs细菌引起医院获得性感染。