新型系统发育结构与尿路致病性大肠杆菌(UPEC)耐药性、生物膜形成和溶血活性的可能关系

Batoul Rahimifard, V. Soheili, G. Hashemitabar, M. Askari Badouei
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引用次数: 0

摘要

背景:由于引起尿路感染(uti)的微生物中多药耐药(MDR)的增加,我们需要定期调查这些病原体的抗微生物耐药性(AMR)。目的:本横断面研究的主要目的是使用最新的系统分型方法来评估尿路致病性大肠杆菌(UPEC)生物膜产生、溶血素产生和抗生素耐药性之间可能的相关性。材料与方法:对138株UPEC分离株进行生物膜形成、溶血素产生和对5类抗生素(包括喹诺酮类、β-内酰胺类、四环素类和磺胺类)的敏感性评估。系统发育结构是使用原始和最近更新的协议确定的。结果:138株UPEC分离株系统发育类群B2居多(34.7%),F次之(13.7%)。94株(68%)具有溶血活性,但溶血与抗生素耐药性无关,而溶血活性与生物膜形成相关。34.7%的菌株产中强生物膜。73%具有溶血活性,多数属于B2系群(37.5%)。在本研究中,与旧方法相比,检测到系统群F的增加率,这表明该系统型在UTI中可能很重要。此外,检测新的系统群G提供了更精确的数据,这只能通过新方法获得。结论:本研究结果表明,采用新的互补方法对流行病学研究中UPEC的不同方面进行评价,可获得更精确的种型结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Possible Relationship of Novel Phylogenetic Structure With Antimicrobial Resistance, Biofilm Formation, and Hemolytic Activity in Uropathogenic Escherichia coli (UPEC)
Background: Due to the increase of multidrug resistance (MDR) in organisms that cause urinary tract infections (UTIs), we need to investigate anti-microbial resistance (AMR) in these pathogens on a regular basis. Objectives: The main purpose of this cross-sectional study was the use of updated phylotyping method to evaluate the possible correlations between biofilm production, hemolysin production, and antibiotic resistance among uropathogenic Escherichia coli (UPEC). Materials and Methods: A total of 138 UPEC isolates were evaluated for biofilm formation, hemolysin production, and antimicrobial susceptibility to five classes of antibiotics, including quinolones, β-lactams, tetracyclines, and sulfonamides. The phylogenetic structure was determined using the original and recently updated protocols. Results: Our results demonstrated that of 138 UPEC isolates, the majority belonged to phylogenetic group B2 (34.7%), followed by F (13.7%). Ninety-four (68%) isolates showed hemolytic activity but hemolysis had no correlation with antibiotic resistance while a correlation was observed between the hemolytic activity and biofilm formation. Moderate to strong biofilm production was observed in 34.7% of the isolates. Additionally, 73% of them showed hemolytic activity and most of them belonged to B2 phylogroup (37.5%). In this study, increasing rates of phylogroup F were detected compared to the old method that indicates the possible importance of this phylotype in UTI. Additionally, detecting the novel phylogroup G provides more precise data which can only be obtained by the new method. Conclusion: The findings of the present study showed that more precise phylotyping results can be obtained when evaluating different aspects of UPEC in epidemiological studies using the new complementary method.
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