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整合子介导的儿童腹泻性大肠杆菌的抗菌药物耐药性:体外和计算机分析。

Integron mediated antimicrobial resistance in diarrheagenic Escherichia coli in children: in vitro and in silico analysis.

机构信息

Epidemiology and Environmental Biology, Indian Council of Medical Research (ICMR)-ICMR-National Institute of Malaria Research, New Delhi, India.

Department of Microbiology, University College of Medical Sciences & GTB Hospital (University of Delhi), Delhi, India; Research and Scientific Studies Unit, College of Nursing and Allied Health Sciences, Jazan University, Jazan, Saudi Arabia.

出版信息

Microb Pathog. 2021 Jan;150:104680. doi: 10.1016/j.micpath.2020.104680. Epub 2020 Dec 7.

Abstract

The exchange of genes between bacterial chromosome and plasmid(s) and their integration into integrons are mainly responsible for acquisition and dissemination of antibiotic resistance. We investigated the role of integrons and their underlying molecular mechanisms leading to development of adaptability in E. coli and eventual resistance to antimicrobials. Escherichia coli isolates (n = 120); including 40 diarrheagenic isolates, an even number of isolates from cases other than diarrhea, and equal number of isolates from healthy children recovered from fresh stool samples were used for identification of integron genes and gene cassettes. The association of integrons with antibiotic resistance was assayed before phylogenetic analysis. DNA sequence analysis revealed class 1 and 2 integrons in 55.83% and 21.66% isolates, respectively. The integron presence was found significantly associated with the probability of antibiotic resistance in E. coli; the association being highest with class 1 integron. Modelling and molecular docking along with molecular dynamics simulation analyses found ceftriaxone and amoxicillin as potential inhibitors of dihydrofolate reductase (DHFR). The class 1 integrons of these pathogenic isolates can serve as prospective therapeutic targets using specific silencing strategies and combinational antimicrobial therapy. The findings may be useful for the development of a potent and versatile drug for DHFR inhibition.

摘要

细菌染色体与质粒之间的基因交换及其整合到整合子中是导致抗生素耐药性获得和传播的主要原因。我们研究了整合子及其潜在的分子机制在大肠杆菌中的适应性发展和最终对抗微生物药物的耐药性的作用。我们使用了 120 株大肠杆菌分离株(包括 40 株腹泻性分离株、与腹泻无关的病例的偶数分离株和来自健康儿童的新鲜粪便样本的偶数分离株),用于鉴定整合子基因和基因盒。在进行系统发育分析之前,检测了整合子与抗生素耐药性的关联。DNA 序列分析显示,55.83%的分离株存在 1 类整合子,21.66%的分离株存在 2 类整合子。整合子的存在与大肠杆菌中抗生素耐药性的概率显著相关;与 1 类整合子的相关性最高。建模、分子对接和分子动力学模拟分析发现头孢曲松和阿莫西林可能是二氢叶酸还原酶 (DHFR) 的抑制剂。这些致病分离株的 1 类整合子可以作为潜在的治疗靶点,使用特定的沉默策略和联合抗菌治疗。这些发现可能有助于开发一种针对 DHFR 抑制的有效且多功能药物。

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