首页> 美国卫生研究院文献>other >Plasmid-Mediated Sulfamethoxazole Resistance Encoded by the sul2 Gene in the Multidrug-Resistant Shigella flexneri 2a Isolated from Patients with Acute Diarrhea in Dhaka Bangladesh
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Plasmid-Mediated Sulfamethoxazole Resistance Encoded by the sul2 Gene in the Multidrug-Resistant Shigella flexneri 2a Isolated from Patients with Acute Diarrhea in Dhaka Bangladesh

机译:孟加拉国达卡的多药耐药志贺菌志贺菌2a中由sul2基因编码的质粒介导的磺胺甲恶唑抗性

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摘要

In this study, mechanisms of plasmid-mediated sulfamethoxazole resistances in the clinical strains of multi-drug resistant (MDR) Shigella flexneri 2a were elucidated for the first time in Bangladesh. From 2006 to 2011, a total of 200 S. flexneri 2a strains were randomly selected from the stock of the Enteric and Food Microbiology Laboratory of icddr,b. Antimicrobial susceptibility of the strains showed 73%, 98%, 93%, 58%, 98%, 64% and 4% resistance to trimethoprim-sulfamethoxazole, nalidixic acid, ampicillin, erythromycin, tetracycline, ciprofloxacin and ceftriaxone respectively. Plasmid profiling revealed heterogeneous patterns and interestingly, all the trimethoprim-sulfamethoxazole resistant (SXTR) strains yielded a distinct 4.3 MDa plasmid compared to that of the trimethoprim-sulfamethoxazole susceptible (SXTS) strains. Curing of this 4.3 MDa plasmid resulted in the susceptibility to sulfamethoxazole alone suggesting the involvement of this plasmid in the resistance of sulfamethoxazole. Moreover, PCR analysis showed the presence of sul2 gene in SXTR strains which is absent in SXTS strains as well as in the 4.3 MDa plasmid-cured derivatives, confirming the involvement of sul2 in the resistance of sulfamethoxazole. Furthermore, pulsed-field gel electrophoresis (PFGE) analysis revealed that both the SXTR and SXTS strains were clonal. This study will significantly contributes to the knowledge on acquired drug resistance of the mostly prevalent S. flexneri 2a and further warrants continuous monitoring of the prevalence and correlation of this resistance determinants amongst the clinical isolates of Shigella and other enteric pathogens around the world to provide effective clinical management of the disease.
机译:在这项研究中,首次在孟加拉国阐明了耐多药志贺氏菌2a临床菌株中质粒介导的磺胺甲恶唑耐药性的机制。从2006年到2011年,从icddr,b肠和食物微生物实验室的库存中随机选择了200株弗氏志贺氏菌2a菌株。菌株对甲氧苄啶-磺胺甲基异恶唑,萘啶酸,氨苄青霉素,红霉素,四环素,环丙沙星和头孢曲松的耐药性分别为73%,98%,93%,58%,98%,64%和4%。质粒分析显示出不同的模式,有趣的是,与耐甲氧苄啶-磺胺甲基异恶唑(SXT S )相比,所有抗甲氧苄氨嘧啶-磺胺甲恶唑的菌株均产生了独特的4.3 MDa质粒>)毒株。此4.3 MDa质粒的固化导致仅对磺胺甲恶唑的敏感性,表明该质粒参与了对磺胺甲恶唑的抗性。另外,PCR分析显示SXT R 菌株中存在sul2基因,而SXT S 菌株以及4.3 MDa质粒固化的衍生物中均不存在。 sul2对磺胺甲恶唑的抗药性。此外,脉冲场凝胶电泳(PFGE)分析表明,SXT R 和SXT S 菌株均为克隆。这项研究将大大有助于了解最普遍的弗氏链球菌2a的获得性耐药性,并进一步保证在全球志贺氏菌和其他肠道病原体的临床分离株中持续监测这种耐药性决定因素的发生率和相关性,以提供有效的信息。该疾病的临床管理。

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