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Carbapenem and colistin resistance in Enterobacteriaceae: worldwide spread and future perspectives

机译:Carbapenem和Colistin抗性在肠杆菌薄膜:全球蔓延和未来的观点

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Carbapenems and colistin antibiotics are the major weapons against multidrug-resistant (MDR) and extensively drug-resistant Gram-negative bacteria. Escherichia coli, Klebsiella pneumoniae, Enterobacter cloacea, Klebsiella oxytoca, Proteus mirabilis, Citrobac-ter freundii, Citrobacter koseri, Serratia spp., Morganella morganii and Salmonella spp. have been reported as carbapenemase-producing Enterobacteriaceae members. Carbapenem resistance mostly occurs by means of some enzymes such as classes A, B and D carbapenemases. New Delhi metallo-p-lactamases, K. pneumoniae carbapenemase, imipenemase metallo-p-lactamase, Verona integron-encoded metallo-p-lactamase and OXA-48-like subtypes have been reported worldwide with some epidemiological differences. Plasmid-mediated transmission has facilitated their spread. In addition, colistin resistance by means of either chromosomal mutation in one of the three genes involved in the biosynthesis of LipA, LpxA, LpxC and LpxD cell wall components or via extrachromosomal elements (plasmid-mediated mcr genes) has recently reported in some species worldwide. MDR and extensively drug-resistant strains have become nonsusceptible to last-line antibiotics, thus consideration of effective ways such as the implementation of appropriate infection control strategies, separation of patients infected with MDR strains from others, public education, containment of antibiotic consumption in livestock industry, accurate antibiotic susceptibility testing and prescription and the proper implementation of antibiotic surveillance in hospitals are necessary. In addition, the use of last-line antibiotics in livestock and food animals must be restricted or banned. Copyright ? 2018 Wolters Kluwer Health, Inc. All rights reserved.
机译:Carbapenems和Colistin抗生素是针对多药(MDR)和广泛的耐药革兰阴性细菌的主要武器。大肠杆菌,克雷布拉肺炎,肠杆菌核酸,Klebsiella oxytoca,Proteus mirabilis,Citrobac-ter Freundii,酸菌Koseri,Serratia spp。,Morganella morganii和沙门氏菌SPP。已据报道为生产肠杆菌酶的肠杆菌酵母会员。 Carbapenem抗性主要通过一些酶如类A,B和D碳结构酶。新德里金属-P-乳酰胺酶,K.肺炎酸碱酶,亚胺糖酶金属-P-乳酰胺酶,Verona整合编码的金属酰胺酶和Oxa-48样亚型,具有一些流行病学差异。质粒介导的传输促进了它们的涂抹。此外,在全世界的某些物种中最近报道了借助于脂肪酸的生物合成中的三种基因中的三种基因中的三种基因中的三种基因中的三种基因中的一种染色体突变。 MDR和广泛的耐药菌株已成为最后一线抗生素的毒性,因此考虑了有效的方式,如实施适当的感染控制策略,分离来自其他人,公众教育,畜牧业抗生素消费的患者。工业,准确的抗生素易感性测试和处方以及医院抗生素监视的正确实施是必要的。此外,必须限制或禁止使用牲畜和食物动物中的最后一线抗生素。版权? 2018 Wolters Kluwer Health,Inc。保留所有权利。

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