从秘鲁狗体内分离的大肠埃希菌的抗菌药耐药性及相关风险因素:重点关注广谱β-内酰胺酶和可乐定

Margot Ventura, Rosario Oporto-Llerena, Kathya Espinoza, Fernando Guibert, A. Quispe, Nidia Vilar, María López, B. Rojo-Bezares, Y. Sáenz, J. Ruiz, María J Pons
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引用次数: 0

摘要

背景和目的:伴侣动物缺乏成熟的抗菌药耐药性(AMR)监测,尤其是在中低收入国家。本研究旨在分析利马(秘鲁)两家兽医中心从狗身上分离出的大肠埃希菌的抗药性及其风险因素:材料与方法:90 只狗参与了研究。抗菌药敏感性通过磁盘扩散法确定,而可乐定敏感性则采用微量稀释法确定。通过聚合酶链式反应确定了扩展谱β-内酰胺酶(ESBL)和大肠菌素耐药性的相关机制。通过 XbaI 脉冲场凝胶电泳评估了耐药大肠杆菌的克隆关系:结果:分离出 35 株大肠杆菌。对氨苄西林(57.1%)、萘啶酸(54.3%)、四环素(48.6%)和阿奇霉素(25.7%)的耐药性较高。头孢菌素耐药率≥20%,可乐定耐药率为 14.3%。有 12 个(34.2%)分离株产生了 ESBL;其中发现了 6 个 blaCTX-M-55(50.0%)、2 个(16.6%)blaCTX-M-15 和 2 个(16.6%)类 blaCTX-M-8 基因。这 5 个耐秋水仙素的分离株在克隆上没有关联,其中 4 个分离株的 mgrB 基因(V8A)出现氨基酸密码子置换或 mgrB 启动子(a12g、g98t 和 c89t)发生突变。此外,狗的年龄小于 6 岁(p = 0.027)和生食(p = 0.054)与对更多抗生素家族产生耐药性有关:尽管纳入的样本数量较少,但研究发现,所研究的狗是耐多药大肠杆菌的携带者,包括最后的抗菌药,由于狗与人类的密切接触,这代表了一个公共卫生问题。这一问题表明,有必要进行更大规模的研究,以制定策略防止耐药微生物在小动物诊所和家庭环境中传播。关键词:抗生素耐药性、可乐定、狗、广谱β-内酰胺酶、秘鲁、风险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antimicrobial resistance and associated risk factors in Escherichia coli isolated from Peruvian dogs: A focus on extended-spectrum β-lactamases and colistin
Background and Aim: Established antimicrobial resistance (AMR) surveillance in companion animals is lacking, particularly in low-middle-income countries. The aim of this study was to analyze AMR and its risk factors in Escherichia coli isolated from dogs at two veterinary centers in Lima (Peru). Materials and Methods: Ninety dogs were included in the study. Antimicrobial susceptibility was established by disk diffusion, whereas microdilution was used to determine colistin susceptibility. Mechanisms related to extended-spectrum β-lactamases (ESBL) and colistin resistance were determined by polymerase chain reaction. Clonal relationships of colistin-resistant isolates were assessed by XbaI-pulsed-field gel electrophoresis. Results: Thirty-five E. coli strains were isolated. High levels of resistance to ampicillin (57.1%), nalidixic acid (54.3%), tetracycline (48.6%), and azithromycin (25.7%) were detected. Cephalosporin resistance levels were ≥20% and those for colistin were 14.3%. Twelve (34.2%) isolates were ESBL producers; of these, six blaCTX-M-55 (50.0%), 2 (16.6%) blaCTX-M-15, and 2 (16.6%) blaCTX-M-8-like genes were found. The five colistin-resistant isolates were clonally unrelated, with four of them presenting amino acid codon substitutions in the mgrB gene (V8A) or mutations in the mgrB promoter (a12g, g98t, and c89t). Furthermore, dog age, <6 years (p = 0.027) and raw diet (p = 0.054) were associated with resistance to a greater number of antibiotic families. Conclusion: Despite small number of samples included, the study found that dogs studied were carriers of multidrug-resistant E. coli, including last-resort antimicrobials, representing a public health problem due to close contact between dogs and humans. This issue suggests the need for larger studies addressed to design strategies to prevent the spread of resistant micro-organisms in small animal clinics and domestic settings. Keywords: antibiotic resistance, colistin, dogs, extended-spectrum β-lactamases, Peru, risk factor.
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