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β-内酰胺酶:现状与临床重要性

Beta-lactamases: current situation and clinical importance.

作者信息

Garau J

机构信息

Hospital de Mutua de Terrassa, Barcelona, Spain.

出版信息

Intensive Care Med. 1994 Jul;20 Suppl 3:S5-9. doi: 10.1007/BF01745244.

DOI:10.1007/BF01745244
PMID:7962990
Abstract

Production of beta-lactamases is the most important means of bacterial resistance to beta-lactam antibiotics. The traditional, plasmid-mediated beta-lactamases were initially confined to Enterobacteriaceae but have now spread to other genera and species including Pseudomonas aeruginosa, Haemophilus influenzae, and Neisseria gonorrhoeae. Extended-spectrum plasmid-mediated beta-lactamases have been identified in Enterobacteriaceae, particularly Klebsiella spp. and Escherichia coli. They are capable of hydrolyzing second- and third-generation cephalosporins and older beta-lactams. Chromosomally mediated beta-lactamases may be produced constitutively or induced by the presence of a beta-lactam. Mutation within the bacterial genome may lead to constitutive enzyme hyperproduction. Strains that produce these enzymes are resistant to practically all beta-lactams, with the exception of carbapenems. The wide-spread occurrence of antibiotic resistance dictates that therapies be judiciously chosen with attention to the resistance patterns of the causative organisms.

摘要

产生β-内酰胺酶是细菌对β-内酰胺类抗生素耐药的最重要方式。传统的质粒介导的β-内酰胺酶最初局限于肠杆菌科细菌,但现在已传播到其他属和种,包括铜绿假单胞菌、流感嗜血杆菌和淋病奈瑟菌。在肠杆菌科细菌中已鉴定出超广谱质粒介导的β-内酰胺酶,尤其是克雷伯菌属和大肠埃希菌。它们能够水解第二代和第三代头孢菌素以及较老的β-内酰胺类药物。染色体介导的β-内酰胺酶可以组成性产生,也可由β-内酰胺的存在诱导产生。细菌基因组内的突变可能导致组成性酶的过量产生。产生这些酶的菌株实际上对所有β-内酰胺类药物耐药,但碳青霉烯类除外。抗生素耐药性的广泛出现表明,治疗方法应根据致病微生物的耐药模式谨慎选择。

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本文引用的文献

1
Moxalactam therapy for bacterial infections.莫西拉坦治疗细菌感染。
Arch Intern Med. 1981 Nov;141(12):1607-12.
2
Experience with cefsulodin therapy for lower respiratory tract infections caused by Pseudomonas aeruginosa in adults without cystic fibrosis or granulocytopenia.
Rev Infect Dis. 1984 Sep-Oct;6 Suppl 3:S711-20. doi: 10.1093/clinids/6.supplement_3.s711.
3
Transferable resistance to cefotaxime, cefoxitin, cefamandole and cefuroxime in clinical isolates of Klebsiella pneumoniae and Serratia marcescens.肺炎克雷伯菌和粘质沙雷氏菌临床分离株对头孢噻肟、头孢西丁、头孢孟多和头孢呋辛的可转移性耐药性。
来自菌血症患者的铜绿假单胞菌分离株外膜蛋白谱与对头孢他啶、亚胺培南和环丙沙星耐药性之间的关系
Eur J Clin Microbiol Infect Dis. 1996 Jan;15(1):82-5. doi: 10.1007/BF01586192.
Infection. 1983 Nov-Dec;11(6):315-7. doi: 10.1007/BF01641355.
4
The beta-lactamases of gram-negative bacteria and their possible physiological role.革兰氏阴性菌的β-内酰胺酶及其可能的生理作用。
Adv Microb Physiol. 1973;9:31-88. doi: 10.1016/s0065-2911(08)60376-8.
5
Occurrence of cefotaxime-resistant Enterobacter during therapy of cardiac surgery patients.
Chemioterapia. 1985 Feb;4(1):110-2.
6
Gentamicin vs cefotaxime for therapy of neonatal sepsis. Relationship to drug resistance.
Am J Dis Child. 1985 Nov;139(11):1086-9. doi: 10.1001/archpedi.1985.02140130024022.
7
Moxalactam in nosocomial infections with Serratia marcescens.莫西拉坦治疗粘质沙雷氏菌医院感染
Intensive Care Med. 1985;11(4):179-83. doi: 10.1007/BF00272399.
8
Ceftazidime in the treatment of serious Pseudomonas aeruginosa sepsis.
Scand J Infect Dis. 1986;18(5):425-9. doi: 10.3109/00365548609032359.
9
Emergence of resistance in gram-negative bacteria during therapy with expanded-spectrum cephalosporins.
Eur J Clin Microbiol. 1987 Aug;6(4):456-9. doi: 10.1007/BF02013110.
10
Clinical consequences of development of resistance to third generation cephalosporins.对第三代头孢菌素耐药性产生的临床后果。
Eur J Clin Microbiol. 1987 Aug;6(4):446-50. doi: 10.1007/BF02013108.