Occurrence of blaOXA-116 Carbapenemase in Escherichia coli ST2519 of Clinical Origin: A Report from Northeast India.

IF 2.3 4区 医学 Q3 INFECTIOUS DISEASES
Microbial drug resistance Pub Date : 2024-10-01 Epub Date: 2024-08-30 DOI:10.1089/mdr.2024.0022
Bhaskar Jyoti Das, K Melson Singha, Jayalaxmi Wangkheimayum, Debadatta Dhar Chanda, Amitabha Bhattacharjee
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引用次数: 0

Abstract

Carbapenem-resistant Escherichia coli pose a significant threat to global public health due to the dearth of available treatment options, resulting in infections with high mortality and morbidity. The study aimed to investigate the mechanism of carbapenem resistance in a carbapenem non-susceptible E. coli isolate recovered from an urinary tract infection patient admitted to a tertiary referral hospital, through whole-genome sequencing using Illumina NovaSeq 6000 platform. Carbapenemase production followed by antibiotic susceptibility testing were performed following Clinical Laboratory Standard Institute guidelines. Polymerase chain reaction targeting carbapenemase genes was performed followed by an investigation of horizontal transferability. The Center for Genomic Epidemiology database was used to analyze the sequenced data. ST2519 E. coli BJD_EC1808 with a genome size of 5.8 Mb harbored Col440I plasmid and a chromosomally located blaOXA-116 gene with an IS18 element upstream, along with multiple antibiotic resistance genes conferring clinical resistance toward beta-lactams, aminoglycosides, amphenicols, sulfonamides, tetracyclines, trimethoprim, rifampin, macrolide, and streptogramin antibiotics and antiseptics. E. coli ST2519 harboring blaOXA-116 associated with a mobile genetic element exhibiting carbapenem resistance is a public health threat due to its limiting effect on the therapeutic usage of carbapenem and their dissemination into carbapenem non-susceptible phenotypes will contribute to carbapenem resistance burden and, therefore, warrants urgent monitoring and clinical intervention.

临床来源大肠埃希菌 ST2519 中出现 blaOXA-116 碳青霉烯酶:来自印度东北部的报告。
由于缺乏可用的治疗方案,耐碳青霉烯类大肠杆菌对全球公共卫生构成了重大威胁,导致感染的死亡率和发病率居高不下。本研究旨在通过使用 Illumina NovaSeq 6000 平台进行全基因组测序,研究从一家三级转诊医院收治的尿路感染患者中分离出的对碳青霉烯类无敏感性的大肠埃希菌对碳青霉烯类耐药的机制。碳青霉烯酶的产生和抗生素敏感性检测均按照临床实验室标准协会的指南进行。针对碳青霉烯酶基因进行聚合酶链式反应,然后对横向转移性进行调查。基因组流行病学中心数据库用于分析测序数据。ST2519 大肠杆菌 BJD_EC1808 的基因组大小为 5.8 Mb,含有 Col440I 质粒和位于染色体上的 blaOXA-116 基因,其上游含有 IS18 元件,同时还含有多种抗生素耐药基因,可产生对 beta-内酰胺类、氨基糖苷类、氨苄青霉素类、磺胺类、四环素类、三甲氧苄青霉素类、利福平类、大环内酯类、链霉素类抗生素和抗菌素的临床耐药性。携带 blaOXA-116 的大肠杆菌 ST2519 与表现出碳青霉烯类耐药性的移动遗传因子相关联,由于其对碳青霉烯类药物治疗使用的限制作用而对公共卫生构成威胁,它们传播到碳青霉烯类药物非敏感表型中将加重碳青霉烯类药物耐药性负担,因此需要进行紧急监测和临床干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbial drug resistance
Microbial drug resistance 医学-传染病学
CiteScore
6.00
自引率
3.80%
发文量
118
审稿时长
6-12 weeks
期刊介绍: Microbial Drug Resistance (MDR) is an international, peer-reviewed journal that covers the global spread and threat of multi-drug resistant clones of major pathogens that are widely documented in hospitals and the scientific community. The Journal addresses the serious challenges of trying to decipher the molecular mechanisms of drug resistance. MDR provides a multidisciplinary forum for peer-reviewed original publications as well as topical reviews and special reports. MDR coverage includes: Molecular biology of resistance mechanisms Virulence genes and disease Molecular epidemiology Drug design Infection control.
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