在孟加拉国达卡的一家三级保健医院,多重耐药肠杆菌分离株中出现了磷霉素耐药性

Q4 Medicine
Nazmun Nahar Munny, SM Shamsuzzaman, Tamzeed Hossain
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引用次数: 0

摘要

背景:多重耐药肠杆菌的出现是一种令人担忧的耐药病原菌,严重威胁着人类健康。常用抗生素的耐药率不断上升,限制了人们的选择,因此迫切需要对磷霉素等老药的抗菌活性进行评估。目的:了解临床分离的肠杆菌对磷霉素的耐药频率,并检测其耐药基因及耐药模式。方法:本横断面研究于2018年7月至2019年6月在孟加拉国一家三级医院微生物科进行。采用标准微生物学方法从350份样品中分离出肠杆菌。采用纸片扩散法进行药敏试验。采用琼脂稀释法测定磷霉素的药敏和最低抑菌浓度。采用特异性引物聚合酶链反应(PCR)检测耐磷肠杆菌中磷霉素耐药基因fosA、fosA3、fosA4、fosA5、fosB、fosB2、fosC、fosC2和fox。通过毛细管法对fosA和fosA₅进行测序,并且fosA₅的核苷酸序列已存入GenBank。结果:28株肠杆菌中,琼脂稀释法检出耐磷霉素肠杆菌7株(25%)。7株磷霉素耐药菌株中,4株(57.14%)从尿液中分离得到。圆盘扩散法检出15株肠杆菌(53.57%)多重耐药。所有耐磷菌素菌株均为耐多药。磷霉素的MIC在256µg/ml-≥4096µg/ml之间显著升高。PCR结果显示,100%的磷霉素耐药菌株对fosA呈阳性,71.43%和28.57%的菌株对fosA₅和fosB₂呈阳性。fosA₅基因测序建立了fosA家族磷霉素抗性谷胱甘肽转移酶基因。结论:本研究结果显示,在孟加拉国,无论磷霉素的使用情况如何,耐多药肠杆菌中磷霉素耐药的比例都很高。孟加拉国出现的FosA家族磷霉素耐药谷胱甘肽转移酶基因。孟加拉国医疗援助理事会2022年公报;48 (3): 203 - 210
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Emergence of fosfomycin resistance among isolates of multidrug-resistant Enterobacter species at a tertiary care hospital in Dhaka, Bangladesh
Background: The emergence of multidrug-resistant Enterobacter species as a worrying resistant pathogen seriously threatened human health. The rising rate of resistance to commonly used antibiotics limit the choice hence it is urgent to evaluate the antimicrobial activity of older drug like Fosfomycin. Objective: The study aimed to seek the frequency of fosfomycin resistance in the clinical isolates of Enterobacter species and to detect the fosfomycin resistance gene along with antibiotic resistance pattern. Methods: This cross-sectional study was conducted in the Department of Microbiology of a tertiary care hospital in Bangladesh from July 2018 to June 2019. Enterobacter spp. was isolated from a total of 350 samples by a standard microbiological method. Antibiotic susceptibility was performed by the disk diffusion technique. Antibiotic susceptibility and minimum inhibitory concentration (MIC) of fosfomycin were determined by the agar dilution method. Fosfomycin resistance gene fosA, fosA3, fosA4, fosA5, fosB, fosB2, fosC, fosC2 and fosX among fosfomycin‑resistant Enterobacter spp detected by polymerase chain reaction (PCR) using specific primer. Sequencing of fosA and fosA₅ was performed by capillary method, and the nucleotide sequence of fosA₅ has been deposited to GenBank. Results: Out of 28 Enterobacter spp. 7 (25%) fosfomycin resistant Enterobacter spp. were detected by agar dilution method. Out of 7 fosfomycin-resistant strains, 4 (57.14%) were isolated from urine samples. Fifteen (53.57%) isolates of Enterobacter spp. were multidrug-resistant detected by disc diffusion technique. All of the fosfomycin-resistant isolates were MDR. A significant rise in the MIC was found between 256µg/ml- ≥4096 µg/ml to fosfomycin. PCR revealed that 100% of fosfomycin resistant isolates are positive for fosA, 71.43% and 28.57% were positive for fosA₅ and fosB₂ respectively. Sequencing of fosA₅ gene established the FosA family fosfomycin resistance glutathione transferase gene. Conclusion: The results of this study showed a high proportion of fosfomycin resistance among multidrug-resistant Enterobacter spp. irrespective of fosfomycin usage in Bangladesh. FosA family fosfomycin resistance glutathione transferase gene emerging in Bangladesh. Bangladesh Medical Res Counc Bull 2022; 48(3): 203-210
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CiteScore
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48
期刊介绍: The official publication of the Bangladesh Medical Research Council.
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