An Unusual 'Gift' from Humans: Third-Generation Cephalosporin-Resistant Enterobacterales in migratory birds along the East Asian-Australasian Flyway

IF 9.7 1区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Environment International Pub Date : 2025-03-01 Epub Date: 2025-02-12 DOI:10.1016/j.envint.2025.109320
Zile Cheng , Yiwen Chen , Min Li , Chao Lv , Nan Zhou , Weiye Chen , JieWen Huang , QingTian Li , Zijing Gao , Xuesong Feng , Li Shi , YuFeng Yao , Xiaokui Guo , Yongzhang Zhu
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Abstract

Migratory birds play a pivotal role in the global dissemination of antimicrobial resistance genes (ARGs), with shorebirds relying on coastal wetlands during their long-distance migrations, environments often contaminated and conducive to ARG transmission. However, systematic investigations into antimicrobial resistance (AMR) in shorebirds remain scarce. During spring and autumn of 2023, we collected 893 throat and cloacal swabs from 480 shorebirds, representing 28 species, at Chongming Dongtan, a critical stopover along the East Asian-Australasian Flyway. Our analysis identified six strains, including four extra-intestinal pathogenic E. coli (ExPEC) and two K. pneumoniae, that exhibited resistance to third-generation cephalosporins, with three ExPEC strains exhibiting significant virulence in Galleria mellonella infection assays. We identified two conjugative plasmids: E042113F_p1, carrying the blaCMY-2 gene in E. coli, and M50_p2, carrying the blaKPC-2 gene in a hypervirulent K. pneumoniae with a virulence plasmid harboring the aerobactin system. Bioinformatic and experimental analyses confirmed that these plasmids could transfer without any fitness cost, remaining stable for at least 30 passages. Surprisingly, genomic tracing revealed that among the plasmids similar to E042113F_p1 (blaCMY-2), the earliest was identified in a Chinese swallow in 2015, with subsequent detections in wild birds from Mongolia (2017), Russia (2018), and Australia (2019). Notably, these E04-CMY-like/M50-KPC-like plasmids predominantly originated from human sources, underscoring the pivotal role of human activity in the cross-species transmission of AMR. This human-mediated transmission of resistance elements into wildlife posed a substantial risk for amplifying and disseminating AMR through long-range migratory bird movements, highlighting the urgent need for international collaboration under a One Health framework. Integrated surveillance, environmental management, and stringent antibiotic stewardship are critical to mitigating the risks posed by migratory birds in amplifying and spreading AMR across ecosystems.

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来自人类的不寻常的“礼物”:东亚-澳大拉西亚迁徙路线上的候鸟中的第三代头孢菌素抗性肠杆菌含有广泛的抗性质粒
候鸟在抗微生物药物耐药性基因(ARGs)的全球传播中起着关键作用,而滨鸟在其长途迁徙中依赖于沿海湿地,这些环境往往受到污染,有利于ARG的传播。然而,对滨鸟抗菌素耐药性(AMR)的系统调查仍然很少。本文于2023年春秋两季在崇明东滩(东亚-澳大拉西亚迁徙路线的重要中途站)采集了28种480只滨鸟的喉咙和泄殖腔拭子893份。我们的分析确定了6株菌株,包括4株肠外致病性大肠杆菌(ExPEC)和2株肺炎克雷伯菌,它们对第三代头孢菌素具有耐药性,其中3株ExPEC菌株在mellonella Galleria感染试验中表现出显著的毒力。我们发现了两个结合质粒:E042113F_p1,在大肠杆菌中携带blaCMY-2基因,M50_p2,在高毒力肺炎克雷伯菌中携带blaKPC-2基因,其毒力质粒含有有氧肌动蛋白系统。生物信息学和实验分析证实,这些质粒可以在没有任何适应度成本的情况下转移,至少在30次传代中保持稳定。令人惊讶的是,基因组追踪显示,在与E042113F_p1 (blaCMY-2)相似的质粒中,最早于2015年在一只中国燕子中被发现,随后在蒙古(2017年)、俄罗斯(2018年)和澳大利亚(2019年)的野生鸟类中也被发现。值得注意的是,这些e04 - cmy样质粒/ m50 - kpc样质粒主要来源于人类,这强调了人类活动在AMR跨物种传播中的关键作用。这种由人介导的耐药性元素向野生动物的传播,对通过远距离候鸟运动放大和传播抗微生物药物耐药性构成了重大风险,突出表明迫切需要在“同一个健康”框架下开展国际合作。综合监测、环境管理和严格的抗生素管理对于减轻候鸟在生态系统中放大和传播抗菌素耐药性所带来的风险至关重要。
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来源期刊
Environment International
Environment International 环境科学-环境科学
CiteScore
21.90
自引率
3.40%
发文量
734
审稿时长
2.8 months
期刊介绍: Environmental Health publishes manuscripts focusing on critical aspects of environmental and occupational medicine, including studies in toxicology and epidemiology, to illuminate the human health implications of exposure to environmental hazards. The journal adopts an open-access model and practices open peer review. It caters to scientists and practitioners across all environmental science domains, directly or indirectly impacting human health and well-being. With a commitment to enhancing the prevention of environmentally-related health risks, Environmental Health serves as a public health journal for the community and scientists engaged in matters of public health significance concerning the environment.
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