Oral and parenteral treatment with a third-generation cephalosporin promotes the proliferation of diverse ESBL-producing Escherichia coli in the chicken intestinal tract.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
mSphere Pub Date : 2025-06-27 DOI:10.1128/msphere.00227-25
Lázaro López, Melany Jumbo, Pamela Mosquera, Gustavo Donoso, Jay Graham, Gabriel Trueba
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引用次数: 0

Abstract

The global rise of antimicrobial resistance is a major public health threat, with Escherichia coli facilitating the spread of extended-spectrum beta-lactamase (ESBL) genes like blaCTX-M, which confer resistance to third-generation cephalosporins (3GCs). This study examines the impact of 3GC treatment on resistant E. coli clones and horizontal gene transfer (HGT) of ESBL genes in broiler chickens in Quito, Ecuador. Fifteen-day-old Ross broilers were divided into three groups: oral ceftriaxone (100 mg/kg), parenteral ceftriaxone (100 mg/kg intramuscular), and control (no treatment). The study included three phases: baseline, antimicrobial administration (5 days), and recovery (15 days). Fecal cultures on McConkey agar, with and without ceftriaxone (2 µg/mL), measured the ratio of 3GC-resistant lactose fermenters. Regardless of the administration route, ceftriaxone significantly increased resistant coliforms (>80%). Five E. coli colonies per animal and time point were analyzed using single-gene typing, with clonal candidates subjected to whole-genome sequencing. Clonal analysis revealed high genetic diversity, averaging three distinct clones per animal. A unique lineage (H34) emerged exclusively during treatment, and new clones appeared post-treatment. The blaCTX-M-55 variant was the most abundant ESBL gene, persisting despite fluctuations in other blaCTX-M variants. Comparative plasmid analysis suggested blaCTX-M-55 HGT, as plasmids were identified in two genetically distinct E. coli isolates from the same host. Most plasmids belonged to IncFII, with IncX1 and IncN also present. These findings highlight how 3GC treatments rapidly impact ESBL-producing E. coli diversity in the intestine.IMPORTANCEThe global rise of antimicrobial resistance (AMR) poses a critical public health challenge, with Escherichia coli playing a central role in the spread of extended-spectrum beta-lactamase (ESBL) genes like blaCTX-M, which confer resistance to third-generation cephalosporins (3GCs). This study highlights the significant impact of 3GC treatment on the frequency and diversity of 3GC-resistant E. coli clones and horizontal gene transfer of ESBL genes in the intestinal microbiota of broiler chickens. Understanding how antimicrobial treatments drive resistance dynamics in animal populations is crucial for developing strategies to mitigate AMR in both human and veterinary settings.

口服和肠外治疗的第三代头孢菌素促进多种产esbl大肠杆菌在鸡肠道的增殖。
全球抗菌素耐药性的上升是一个主要的公共卫生威胁,大肠杆菌促进了blaCTX-M等广谱β -内酰胺酶(ESBL)基因的传播,这些基因赋予对第三代头孢菌素(3gc)的耐药性。本研究考察了3GC处理对厄瓜多尔基多肉鸡耐药大肠杆菌克隆和ESBL基因水平基因转移(HGT)的影响。将15日龄罗斯肉鸡分为3组:头孢曲松口服组(100 mg/kg)、头孢曲松肌内注射组(100 mg/kg)和对照组(不处理)。该研究包括三个阶段:基线、抗菌药物给药(5天)和恢复(15天)。在McConkey琼脂上进行粪便培养,添加和不添加头孢曲松(2µg/mL),测量3gc抗性乳糖发酵剂的比例。无论何种给药途径,头孢曲松均显著增加耐药大肠菌群(bbb80 %)。使用单基因分型分析每只动物和时间点的5个大肠杆菌菌落,对候选克隆进行全基因组测序。克隆分析显示出较高的遗传多样性,平均每只动物有3个不同的克隆。一个独特的谱系(H34)在处理期间完全出现,并且在处理后出现新的无性系。blaCTX-M-55变体是最丰富的ESBL基因,尽管其他blaCTX-M变体存在波动。质粒比较分析提示为blaCTX-M-55 HGT,因为质粒在来自同一宿主的两个遗传上不同的大肠杆菌分离株中被鉴定出来。大多数质粒属于IncFII, IncX1和IncN也存在。这些发现强调了3GC处理如何快速影响肠道中产生esbl的大肠杆菌多样性。全球抗菌素耐药性(AMR)的上升对公共卫生构成了重大挑战,大肠杆菌在广谱β -内酰胺酶(ESBL)基因(如blaCTX-M)的传播中起着核心作用,该基因赋予对第三代头孢菌素(3gc)的耐药性。本研究强调了3GC处理对肉鸡肠道菌群中耐3GC大肠杆菌克隆频率和多样性以及ESBL基因水平转移的显著影响。了解抗菌素治疗如何推动动物种群的耐药动态,对于制定减轻人类和兽医环境中抗生素耐药性的战略至关重要。
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
mSphere
mSphere Immunology and Microbiology-Microbiology
CiteScore
8.50
自引率
2.10%
发文量
192
审稿时长
11 weeks
期刊介绍: mSphere™ is a multi-disciplinary open-access journal that will focus on rapid publication of fundamental contributions to our understanding of microbiology. Its scope will reflect the immense range of fields within the microbial sciences, creating new opportunities for researchers to share findings that are transforming our understanding of human health and disease, ecosystems, neuroscience, agriculture, energy production, climate change, evolution, biogeochemical cycling, and food and drug production. Submissions will be encouraged of all high-quality work that makes fundamental contributions to our understanding of microbiology. mSphere™ will provide streamlined decisions, while carrying on ASM''s tradition for rigorous peer review.
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