来自伊朗的泌尿病原性大肠杆菌分离物中酸黄素耐药性机制
Shayesteh Novin1, Seyedeh Elham Rezatofighi2, Mohammad Roayaei Ardakani3
1Department of Biology, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Annals of clinical microbiology and antimicrobials
|November 5, 2025
概括
泌尿病原性大肠杆菌 (UPEC) 中的酸黄素耐药性是由染色体基因nfsA和nfsB的突变驱动的. 这些耐药的UPEC菌株表现出多种药物耐药性和具有毒性因子,需要进一步的流行病学研究.
科学领域:
- 微生物学 微生物学
- 遗传学 遗传学 是一个
- 抗微生物耐药性 抗微生物耐药性
背景情况:
- 尼托福兰是治疗无并发性尿路感染 (UTI) 的关键抗生素.
- 泌尿病原性大肠杆菌 (UPEC) 的新兴耐药性构成了重大的临床挑战.
- 了解这种耐药性的遗传基础对于有效的治疗策略至关重要.
研究的目的:
- 为了研究耐素抗性UPEC分离物的遗传多样性.
- 描述与UPEC中耐黄因耐药性相关的机制和遗传特征.
主要方法:
- 一项横截面研究分析了235个UPEC分离物以检测耐素的耐药性.
- 聚合酶链反应 (PCR) 用于检测染色体 (nfsA,nfsB,ribE) 和等离子体 (oqxA,oqxB) 基因.
- 基因测序确定了nfsA,nfsB和ribE的变异;表型和基因型特征也被评估.
主要成果:
- 确定了六个 (2.55%) 耐尼托福兰因耐药的UPEC分离体.
- 检测到nfsA和nfsB中的有害突变是可能的耐药性驱动因素;没有发现ribE突变和等离子体基因qxA/oqxB.
- 所有耐药分离物都是多抗药性 (MDR),并携带各种毒性相关基因 (VAG) 和致病性岛屿 (PAI).
结论:
- 染色体nfsA和/或nfsB基因中的有害突变是研究UPEC隔离物中尼托福兰因耐药性的主要驱动因素.
- 在 ribE 和通过 oqxAB 的等离子体介导耐药性的突变似乎起到较小的作用.
- 抗性和毒性因子在这些分离物中同时出现,强调需要更广泛的流行病学评估.
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