Plasmid-mediated antimicrobial resistance across One Health sectors: transmission dynamics and surveillance needs.

IF 4 2区 生物学 Q2 MICROBIOLOGY
mSphere Pub Date : 2026-08-26 Epub Date: 2026-07-17 DOI:10.1128/msphere.00192-26
Nuha Fairusya, Rongxuan Wang, Ryo Honda
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引用次数: 0

Abstract

Antimicrobial resistance (AMR) is increasingly recognized as a One Health challenge driven by the continuous exchange of resistant bacteria and resistance determinants across human, animal, and environmental sectors. While genomic surveillance has substantially improved detection of antimicrobial resistance genes (ARGs), most monitoring frameworks remain gene- or isolate-centric, limiting insight into the mechanisms that govern resistance transmission and persistence. Recent evidence indicates that plasmids, self-replicating mobile genetic elements (MGEs) capable of horizontal transfer across bacterial species, play an important role in disseminating clinically relevant resistance determinants across sectors. In this mini-review, we synthesize genomic and ecological evidence demonstrating that a limited number of plasmid incompatibility (Inc) groups recur across human, animal, and environmental reservoirs, often independent of bacterial host lineages. We highlight how plasmid transmission dynamics are shaped by host-independent mobility, ecological generalism, co-selection with accessory traits, and persistence in engineered and natural environments. We further examine why current AMR surveillance approaches, including ARG-centric metagenomics and isolate-based monitoring, systematically overlook these plasmid-mediated processes. Furthermore, we propose that plasmid-resolved analysis represents a critical and currently underutilized complementary layer for One Health AMR surveillance. Integrating plasmid classification and genomic reconstruction into wastewater-based epidemiology and cross-sector monitoring frameworks can improve attribution of transmission pathways, enhance early detection of high-risk resistance, and provide a mechanistic foundation for risk-informed intervention strategies.

同一卫生部门质粒介导的抗菌素耐药性:传播动态和监测需求。
由于人类、动物和环境部门中耐药细菌和耐药决定因素的不断交换,抗菌素耐药性(AMR)日益被认为是“同一个健康”的挑战。虽然基因组监测大大改善了抗微生物药物耐药性基因(ARGs)的检测,但大多数监测框架仍然以基因或分离物为中心,限制了对控制耐药性传播和持续的机制的了解。最近的证据表明,质粒,能够在细菌物种之间水平转移的自我复制的移动遗传元件(MGEs),在跨部门传播临床相关的耐药决定因素方面发挥着重要作用。在这篇综述中,我们综合了基因组和生态学证据,证明有限数量的质粒不相容(Inc)群体在人类、动物和环境中反复出现,通常独立于细菌宿主谱系。我们强调了质粒传播动力学是如何由宿主独立的移动性、生态普遍性、与附属性状的共同选择以及在工程和自然环境中的持久性所塑造的。我们进一步研究了为什么目前的抗菌素耐药性监测方法,包括以arg为中心的宏基因组学和基于分离的监测,系统地忽略了这些质粒介导的过程。此外,我们建议质粒解析分析是One Health抗菌素耐药性监测的一个关键且目前未充分利用的补充层。将质粒分类和基因组重建整合到基于废水的流行病学和跨部门监测框架中,可以改善传播途径的归因,加强高风险耐药性的早期发现,并为风险知情的干预策略提供机制基础。
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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