Genomic Characterization and Antimicrobial Resistance of ESBL-Producing, Escherichia coli Isolates in Suzhou, China.

IF 2.9 3区 医学 Q2 INFECTIOUS DISEASES
Infection and Drug Resistance Pub Date : 2025-02-20 eCollection Date: 2025-01-01 DOI:10.2147/IDR.S488794
Cailin Wang, Hong Zhang, Rongfen Zhao, Clement Kin-Ming Tsui, Shuwen Deng
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引用次数: 0

Abstract

Background: The prevalence of third-generation cephalosporin-resistant and extended-spectrum beta-lactamases (ESBL) producing Escherichia coli poses a significant global public health concern due to their resistance to multiple antibiotics; however, their prevalence and epidemiological patterns in China are not very well investigated.

Objective: This study aimed to investigate the molecular epidemiology, and antimicrobial susceptibility of ESBL-producing E. coli among clinical isolates in China.

Methods: Phenotypic ESBL-producing E. coli isolates were collected from in-patients at a non-tertiary hospital in Suzhou from 2018.06.01 -2019.11.30. All isolates were identified and analyzed by conventional microbiological methods, and antimicrobial susceptibility testing was determined. Genes associated with resistance to β-lactamases, fluoroquinolone, aminoglycosides, sulfonamides, sequence types (STs), and genetic relationship were characterized through whole-genome sequencing (WGS) data.

Results: Eighty-six isolates were collected and sequenced, and genomic analysis identified twenty-five different sequence types (STs). The most prevalent STs were ST131 (n=22, 25.6%), ST1193 (n=16, 18.6%), ST38 (n=9, 10.5%) and ST167 (n=6, 7.0%). blaCTX-M genotypes were the most dominant, comprising a variety of subtypes (eg, blaCTX-M-14, blaCTX-M-15, blaCTX-M-27, blaCTX-M-55) and blaTEM-type among ESBL-producing E. coli in our study. All cases of co-carriage of β-lactamase genes showed a strong link to amoxicillin/sulbactam resistance, while the co-carriage of blaCTX-M-15/TEM-1B or blaCTX-M-15/OXA-1 were strongly linked to resistance against cefepime, ceftazidime, and aztreonam. In addition, genes associated with resistance to fluoroquinolone, aminoglycosides, and sulfonamides were also detected.

Conclusion: Our findings highlighted the prevalence of globally circulating ESBL-producing E. coli clones, such as ST131 and ST1193, in Suzhou, China. These clones and sublineages are also resistant to quinolones. No predominant blaCTX-M subtypes were detected, while the coexistence of different ESBL types was strongly linked to resistance to amoxicillin/sulbactam, cefepime, ceftazidime, and aztreonam, suggesting the widespread circulation of diverse blaCTX-M genes within the Suzhou community. In clinical cases of ESBL resistance, carbapenem therapy is recommended as most (>90%) isolates were susceptible.

中国苏州产ESBL大肠埃希菌分离物的基因组特征和耐药性。
背景:产生第三代头孢菌素耐药和广谱β -内酰胺酶(ESBL)的大肠杆菌的流行,由于其对多种抗生素的耐药性,引起了重大的全球公共卫生关注;然而,其在中国的流行程度和流行病学模式尚未得到很好的调查。目的:了解中国产esbl大肠杆菌的分子流行病学及药敏情况。方法:2018.06.01 -2019.11.30从苏州某非三级医院住院患者中采集产esbl的大肠杆菌分离株。所有分离株均采用常规微生物学方法进行鉴定和分析,并进行药敏试验。通过全基因组测序(WGS)数据表征了与β-内酰胺酶、氟喹诺酮、氨基糖苷、磺胺类药物、序列类型(STs)和遗传关系相关的基因。结果:对86株分离株进行测序,鉴定出25种不同的序列类型(st)。最常见的STs是ST131 (n=22, 25.6%)、ST1193 (n=16, 18.6%)、ST38 (n=9, 10.5%)和ST167 (n=6, 7.0%)。blaCTX-M基因型在我们研究的产esbl大肠杆菌中以blaCTX-M基因型最占优势,包括多种亚型(如blaCTX-M-14、blaCTX-M-15、blaCTX-M-27、blaCTX-M-55)和blem型。共携带β-内酰胺酶基因的病例均与阿莫西林/舒巴坦耐药密切相关,而共携带blaCTX-M-15/TEM-1B或blaCTX-M-15/OXA-1的病例与头孢吡肟、头孢他啶和氨曲南耐药密切相关。此外,还检测到与氟喹诺酮类、氨基糖苷类和磺胺类药物耐药相关的基因。结论:我们的研究结果强调了在中国苏州全球流行的产esbl的大肠杆菌克隆,如ST131和ST1193。这些克隆和亚系也对喹诺酮类药物耐药。未检测到blaCTX-M的优势亚型,而不同ESBL类型的共存与对阿莫西林/舒巴坦、头孢吡肟、头孢他啶和氨曲南的耐药密切相关,表明多种blaCTX-M基因在苏州社区广泛流传。在ESBL耐药的临床病例中,推荐碳青霉烯类药物治疗,因为大多数(约90%)分离株对ESBL敏感。
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
Infection and Drug Resistance
Infection and Drug Resistance Medicine-Pharmacology (medical)
CiteScore
5.60
自引率
7.70%
发文量
826
审稿时长
16 weeks
期刊介绍: About Journal Editors Peer Reviewers Articles Article Publishing Charges Aims and Scope Call For Papers ISSN: 1178-6973 Editor-in-Chief: Professor Suresh Antony An international, peer-reviewed, open access journal that focuses on the optimal treatment of infection (bacterial, fungal and viral) and the development and institution of preventative strategies to minimize the development and spread of resistance.
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