首页> 外文期刊>Infection, Genetics and Evolution: Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases >Genetic analysis of carbapenemase-producing Gram-negative bacteria isolated from a university teaching hospital in Egypt
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Genetic analysis of carbapenemase-producing Gram-negative bacteria isolated from a university teaching hospital in Egypt

机译:埃及大学教学医院中分离出碳碱酶的革兰阴性细菌的遗传分析

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A total of 65 non-replicate Gram-negative bacterial strains were recovered from clinical specimens between April and September 2014 at a University Hospital in Egypt. This collection was screened by PCR for carbapenemase-encoding genes, 16S rRNA methylases, and colistin resistance genes (mcr-1-mcr-8). Twenty-two strains (22/65, 33.8%) were positive for carbapenemase-encoding genes [13 NDM-1-producers (four Escherichia coli, two Klebsiella pneumoniae, and seven Providencia stuartii), two E. coli co-carrying NDM-5 and OXA-181, and seven Pseudomonas aeruginosa (three VIM-2, four VIM-24) strains]. The 16S rRNA methylase RmtC was detected in 12 NDM-1-producers for the first time in Egypt; no mcr genes were detected. A self-transmissible A/C plasmid was found to carry bla(NDM-1) in all NDM-1-producing strains. NDM-5 and OXA-181 were located on an untypeable and IncX3 plasmid, respectively. Additionally, Enterobacterial repetitive intergenic consensus (ERIC)-PCR revealed five clonally related P. stuartii isolates collected over a 1.5-month period. Thirteen carbapenemase-producing strains were isolated from burn patients who are at a high risk of developing infections and require special medical care. To our knowledge, this is the first report of NDM-1-producing-P. stuartii strains in an African burn unit, NDM-1- and RmtC-positive non-lactose fermenting E. coli globally, VIM-24-producing P. aeruginosa in Africa, and 16S RMTase rmtC-NDM-1-producers in Egypt. This work highlights the detection of different carbapenemase-producing bacterial strains within an Egyptian teaching hospital compromising the effectiveness of carbapenems and urgently asking the Egyptian medical authorities for implementation of antimicrobial surveillance plans and infection control policies to early detect and to effectively halt the rapid spread of these superbugs.
机译:从4月和2014年9月在埃及的大学医院之间从临床标本中回收了总共65个非重复革兰氏阴性细菌菌株。该集合由PCR筛选用于碳结构酶 - 编码基因,16S rRNA甲基酶和菌根抗性基因(MCR-1-MCR-8)。二十二种菌株(22/65,33.8%)对碳癌酶 - 编码基因呈阳性[13个Ndm-1-生产者(四个大肠杆​​菌,两个克雷布拉肺炎和七个普罗维西西亚斯图拉蒂),两种大肠杆菌共同携带NDM- 5和Oxa-181,七种假单胞菌铜绿假单胞菌(三个Vim-2,四个Vim-24)菌株]]。在埃及首次在12个Ndm-1-生产商中检测到16S rRNA甲基酶RMTC;没有检测到MCR基因。发现自变传式A / C质粒在所有NDM-1产生菌株中携带BLA(NDM-1)。 NDM-5和Oxa-181分别位于可分别的和Incx3质粒上。此外,肠杆菌重复性癌症(ERIC)-PCR揭示了五个月内收集的五个克隆相关的P.斯图里西分离物。从发育感染的风险高的烧伤患者中分离出13例碳丙二酸酶产生的菌株,需要特殊医疗。据我们所知,这是NDM-1生产的第一个报告。在非洲燃烧单元,NDM-1和RMTC阳性非乳糖发酵大肠杆菌的斯图尔蒂菌株,非洲的Vim-24生产P.铜绿假单胞菌和埃及的16S RMTase RMTC-NDM-1-生产商。这项工作突出了埃及教学医院内产生不同碳结构酶的细菌菌株的检测,损害了肉豆蔻的有效性,并迫切地向埃及医学当局实施了抗微生物监测计划和感染控制政策,并有效地停止了快速蔓延这些超级素。

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