糖尿病创面相关大肠杆菌的研究多重耐药和尼日利亚西南部β -内酰胺酶生产的发生

I. Ibeh, O. Florence, Omorodion Nosa Tery
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引用次数: 0

摘要

β-内酰胺类药物,如青霉素、2型头孢菌素、单巴菌素和碳青霉烯类,是世界上最常用的抗生素之一。在革兰氏阴性病原体中,β-内酰胺酶仍然是导致β-内酰胺耐药的最重要因素3,β-内酰胺酶的日益流行及其惊人的进化似乎与新型β-内酰胺亚类的临床使用直接相关。β-内酰胺酶是一种细菌酶,通过水解使β-内酰胺类抗生素失活,从而产生无效的化合物来自临床分离的至少400种不同类型的β-内酰胺酶已被描述,并建立了一个网站来监测较新型b-内酰胺酶的最新发展最近发表了几篇优秀的综述,描述了产生新型b-内酰胺酶的微生物学、特征、结构、流行病学和治疗选择。本报告的目的并非全面,而是说明产生广谱b-内酰胺酶(ESBL)的细菌是社区中的新兴病原体,临床实验室在其检测和控制方面发挥着关键作用。革兰氏阴性菌的许多属具有自然发生的,染色体介导的β-内酰胺酶。这些酶被认为是从青霉素结合蛋白进化而来的,它们与青霉素结合蛋白显示出一些序列同源性。这种发展可能是由于在环境中发现的产生β-内酰胺的土壤生物施加的选择压力第一个质粒介导的革兰氏阴性β-内酰胺酶TEM-1是在20世纪60年代初发现的TEM-1酶最初是在从希腊一位名叫Temoniera的病人的血液培养中分离出的一株大肠杆菌中发现的,因此被命名为tem .8,9。质粒和转座子介导的TEM-1促进了TEM-1向其他细菌的传播。在首次分离后的几年内,TEM1 β-内酰胺酶在世界范围内传播,现在在肠杆菌科的许多不同物种、铜绿假单胞菌、流感嗜血杆菌和淋病奈瑟菌中都有发现。在肺炎克雷伯菌和大肠杆菌中发现的另一种常见的质粒介导的β-内酰胺酶是SHV-1(硫羟基变量)。SHV-1 β-内酰胺酶在大多数肺炎克雷伯菌分离株中由染色体编码,但在大肠杆菌中通常由质粒介导
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Studies on Escherichia coli associated with diabetic wounds; multi drug resistance and the occurrence of beta lactamase production in south-western Nigeria
The β-Lactam agents such as penicillins,2 cephalosporin’s, monobactams and carbapenems, are among the most frequently prescribed antibiotics worldwide. In Gram-negative pathogens, β-lactamases remain the most important contributing factor to β-lactam resistance,3 and their increasing prevalence as well as their alarming evolution seem to be directly linked to the clinical use of novel sub-classes of β-lactams.4 β-Lactamases are bacterial enzymes that inactivate β-lactam antibiotics by hydrolysis, which result in ineffective compounds.5 At least 400 different types of β-lactamases, originating from clinical isolates, have been described and a website has been created to monitor the latest developments among the newer types of b-lactamases.6 Several excellent reviews have recently been published describing the microbiology, characteristics, and structure, epidemiology and treatment options of organisms producing newer types of b-lactamases. This report does not aim to be comprehensive, but rather to illustrate that extended-spectrum b-lactamase-(ESBL) producing bacteria are emerging pathogens in the community, and that clinical laboratories play a critical role for their detection and control. Many genera of gram-negative bacteria possess a naturally occurring, chromosomally mediated β-lactamase. These enzymes are thought to have evolved from penicillin-binding proteins, with which they show some sequence homology. This development was likely due to the selective pressure exerted by β-lactam-producing soil organisms found in the environment.7 The first plasmid-mediated β-lactamase in gram-negatives, TEM-1, was described in the early 1960s.5 The TEM-1 enzyme was originally found in a single strain of E. coli isolated from a blood culture from a patient named Temoniera in Greece, hence the designation TEM.8,9 Being plasmid and transposon mediated has facilitated the spread of TEM-1 to other species of bacteria. Within a few years after its first isolation, the TEM1 β-lactamase spread worldwide and is now found in many different species of members of the family Enterobacteriaceae, Pseudomonas aeruginosa, Haemophilus influenzae, and Neisseria gonorrhoeae. Another common plasmid-mediated β-lactamase found in Klebsiella pneumoniae and E. coli is SHV-1 (for sulphurhydryl variable). The SHV-1 β-lactamase is chromosomally encoded in the majority of isolates of K. pneumoniae but is usually plasmid mediated in E. coli.10
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