AmpC酶是临床上重要的β-内酰胺酶,编码在许多肠杆菌科和其他生物体的染色体或质粒上,它们介导对大多数青霉素类药物和β-内酰胺酶抑制剂/β-的英语翻译

AmpC酶是临床上重要的β-内酰胺酶,编码在许多肠杆菌科和其他生物体的

AmpC酶是临床上重要的β-内酰胺酶,编码在许多肠杆菌科和其他生物体的染色体或质粒上,它们介导对大多数青霉素类药物和β-内酰胺酶抑制剂/β-内酰胺类药物的联合耐药。在许多细菌中,AmpC酶是可诱导的,并可通过突变高水平表达。同时,染色体和质粒基因编码的AmpC酶也在进化,过度表达使其对包括头孢噻肟、头孢他啶和头孢曲松在内的广谱头孢菌素类药物产生耐药性,甚至在某些生物体中,通过减少内流(外膜孔蛋白丢失)或增强外排(外排泵激活)的突变,可对碳青霉烯类抗生素产生耐药。在世界大部分地区,虽然 AmpC酶引起的耐药性比产超广谱β-内酰胺酶(ESBL)少,但其更难检测,而且范围更广。故对AmpC展开更深层次的研究对于指导临床检测以及后续用药有着重要的意义。
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AmpC enzyme is a clinically important β-lactamase, encoded on the chromosomes or plasmids of many Enterobacteriaceae and other organisms. They mediate the effects of most penicillin drugs and β-lactamase inhibitors/β-lactamases. Joint resistance to amide drugs. In many bacteria, the AmpC enzyme is inducible and can be expressed at high levels through mutations. At the same time, the AmpC enzymes encoded by chromosomes and plasmid genes are also evolving. Overexpression makes them resistant to broad-spectrum cephalosporins including cefotaxime, ceftazidime and ceftriaxone, even in certain organisms. In, mutations that reduce influx (loss of outer membrane porins) or enhance efflux (activation of efflux pump) can develop resistance to carbapenem antibiotics. In most parts of the world, although the AmpC enzyme causes less resistance than the extended-spectrum β-lactamase (ESBL), it is more difficult to detect and has a wider range. Therefore, a deeper research on AmpC is of great significance for guiding clinical testing and follow-up medication.
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AmpC enzyme is clinically important β- Lactamases, encoded on the chromosomes or plasmids of many Enterobacteriaceae and other organisms, mediate resistance to most penicillins and β- Lactamase inhibitor/ β- Combined resistance of lactam drugs. In many bacteria, AmpC enzyme is inducible and can be expressed at high levels by mutation. At the same time, the AmpC enzyme encoded by chromosome and plasmid genes is also evolving. Overexpression makes it resistant to a wide range of cephalosporins, including cefotaxime, ceftazidime and ceftriaxone. Even in some organisms, it is mutated by reducing influx (loss of outer membrane porin) or enhancing efflux (activation of efflux pump), It can be resistant to carbapenem antibiotics. In most parts of the world, although AmpC enzyme induced drug resistance is more broad-spectrum than production β- Lactamase (ESBL) is less, but it is more difficult to detect and has a wider range. Therefore, further research on AmpC is of great significance for guiding clinical detection and follow-up medication.
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AmpC enzyme is an important β -lactamase in clinic, which is encoded on chromosomes or plasmids of many enterobacteriaceae and other organisms. They mediate the combined resistance to most penicillin drugs and β -lactamase inhibitors/β-lactam drugs. In many bacteria, AmpC enzyme is inducible and can be expressed at a high level by mutation. At the same time, the AmpC enzyme encoded by chromosome and plasmid genes is also evolving. Over-expression makes it resistant to broad-spectrum cephalosporins including cefotaxime, ceftazidime and ceftriaxone, and even in some organisms, it can be resistant to carbapenem antibiotics by reducing the mutation of influx (loss of outer membrane pore protein) or enhancing efflux (activation of efflux pump). In most parts of the world, although AmpC enzyme causes less drug resistance than extended-spectrum β -lactamase (ESBL), it is more difficult to detect and has a wider range. Therefore, it is of great significance to conduct a deeper study on AmpC to guide clinical detection and follow-up medication.
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