"

B. Bedenić, S. Sardelić
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引用次数: 5

摘要

碳青霉烯类通常被认为是革兰氏阴性和革兰氏阳性微生物引起的严重感染的最后治疗选择。尽管它们在大多数β-内酰胺酶的水解下是稳定的,但由于碳青霉烯水解酶(碳青霉烯酶)的出现,它们作为最后一种抗生素的使用受到了严重损害。这些酶主要由肠杆菌科和革兰氏阴性非发酵细菌如铜绿假单胞菌和鲍人- nii不动杆菌产生。真正的碳青霉烯酶属于Ambler分子类A、B和D,通常由嵌入在质粒、整合子和转座子等可移动遗传元件中的基因编码,这些基因通常含有多个耐药决定因素,进一步限制了治疗选择。目前,碳青霉烯耐药革兰氏阴性菌在世界范围内的传播所引起的大量医院和社区获得性感染已成为一个重大的公共卫生问题。尽管多粘菌素仍然具有活性,但体外联合方案的益处报告支持这种策略对抗产生碳青霉烯酶的革兰氏阴性杆菌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Carbapenemases
Carbapenems are usually regarded as the last treatment option for serious infections caused by Gram-negative and Gram-positive microorganisms. Although they are stable to hydrolysis by most β-lactamases, their usage as the last resort antbiotics was seriously compromised by the appearance of carbapenem-hydrolyzing enzymes called carbapenemases. These enzymes are produced mostly by Enterobacteriaceae and Gram-negative nonfermentative bacteria such as Pseudomonas aeruginosa and Acinetobacter bauman- nii . True carbapenemases belonging to Ambler molecular classes A, B, and D are often encoded by genes embedded in mobile genetic elements like plasmids, integrons, and transposons, which often harbor multiple resistance determinants limiting further the treatment options. At present, large number of nosocomial and community-acquired infections caused by worldwide spread of carbapenem-resistant Gram-negative bacte ria have become a major public health problem. Although polymyxins remain active, in vitro reports of benefits of combination schemes favor this strategy against carbapene -mase-producing Gram-negative bacilli.
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