Integrated cross-sectoral surveillance of antimicrobial resistance genotypes and phenotypes across disparate reservoirs.

IF 5.2 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2026-10-20 Epub Date: 2026-09-28 DOI:10.1128/msystems.00741-26
Thomas D Watts, Thanavit Jirapanjawat, Laura Perlaza-Jiménez, Francesco Ricci, Eve Tudor-Matthew, Eleonora Chiri, Sean K Bay, Rhys Grinter, Rachael Lappan, Trevor Lithgow, Laura C Woods, Chris Greening
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引用次数: 0

Abstract

Antimicrobial-resistant (AMR) bacteria and genes are continually exchanged among humans, animals, and environmental reservoirs. Disparate and siloed surveillance methods present a major challenge for tracing and disrupting AMR transmission, with clinical monitoring focusing on detecting specific pathogens or specific genes of interest, and environmental surveys often relying on inferences drawn from indicator organisms. Here, we demonstrate that, following sample-specific pre-processing, common surveillance approaches can be applied consistently to profile AMR abundance, distribution, and phenotypes across diverse reservoirs in both urban and agricultural settings. Across all sample types, three core methods provided complementary insights: (i) quantitative PCR (qPCR) arrays to measure multiple AMR genes, (ii) gene- and genome-centric metagenomics for comprehensive resistome profiling, and (iii) culture-based genomics with susceptibility testing to link genotypes to phenotypes. We applied this approach to profile 1,032 metagenome-assembled genomes, 66 bacterial isolate genomes, and 78 and 6,642 AMR genes/reference sequences via qPCR and metagenomics, respectively. This integrated framework revealed the prevalence and diversity of resistance mechanisms in both putative pathogens and non-pathogenic bacteria with potentially transmissible genes, with wastewater especially enriched in AMR genes. We detected mismatches between genotype and phenotype predictions and a prevalence of intermediate resistance phenotypes, highlighting how many mechanisms of environmental resistance remain poorly understood. Overall, this study demonstrates that unified, field-leading surveillance methods can be used in diverse environmental and animal samples while highlighting that multiple methods are needed to capture the diverse AMR genotypes and phenotypes in these settings to enable comprehensive monitoring and adaptive solutions to restrict transmission.IMPORTANCEAntimicrobial resistance (AMR) is driven by the exchange of resistant bacteria and genes across interconnected human, animal, and environmental reservoirs, yet fragmented surveillance limits our ability to track transmission and intervene effectively. We demonstrate that widely used surveillance methods can be applied cohesively across diverse sample types, including wastewater, soil, water, agricultural environments, and fecal samples, to generate comparable insights into AMR abundance, diversity, and phenotype. By integrating qPCR, metagenomics, and culture-based genomics, we reveal resistance in both pathogenic and non-pathogenic bacteria, reaffirm wastewater as a major AMR reservoir, and uncover frequent mismatches between genetic predictions and observed susceptibility. The prevalence of intermediate resistance further suggests that many environmental resistance mechanisms remain poorly understood. These findings show that no single method captures AMR complexity and highlight the need for unified, multi-method surveillance to support comprehensive monitoring and strategies to control the spread of resistance.

跨部门综合监测抗菌素耐药性基因型和表型在不同的水库。
抗菌素耐药(AMR)细菌和基因在人类、动物和环境宿主之间不断交换。不同和孤立的监测方法对追踪和破坏抗菌素耐药性传播提出了重大挑战,临床监测侧重于检测特定病原体或感兴趣的特定基因,而环境调查往往依赖于从指示生物中得出的推论。在这里,我们证明,在样本特异性预处理之后,常见的监测方法可以一致地应用于城市和农业环境中不同水库的AMR丰度、分布和表型。在所有样品类型中,三种核心方法提供了互补的见解:(i)定量PCR (qPCR)阵列测量多个AMR基因,(ii)以基因和基因组为中心的宏基因组学用于全面的抗性组分析,以及(iii)基于培养的基因组学与敏感性测试,将基因型与表型联系起来。我们应用该方法分别通过qPCR和宏基因组学分析了1032个宏基因组组装的基因组、66个细菌分离基因组以及78和6642个AMR基因/参考序列。这一综合框架揭示了具有潜在传播基因的推定致病菌和非致病菌耐药机制的普遍性和多样性,废水中AMR基因尤其富集。我们检测到基因型和表型预测之间的不匹配以及中间抗性表型的流行,强调了环境抗性的许多机制仍然知之甚少。总体而言,本研究表明,统一的、现场领先的监测方法可以用于不同的环境和动物样本,同时强调需要多种方法来捕获这些环境中的不同AMR基因型和表型,以实现全面监测和自适应解决方案,以限制传播。抗菌素耐药性(AMR)是由耐药细菌和基因在相互关联的人类、动物和环境宿主之间的交换所驱动的,但分散的监测限制了我们追踪传播和有效干预的能力。我们证明,广泛使用的监测方法可以凝聚力地应用于不同的样本类型,包括废水、土壤、水、农业环境和粪便样本,以产生对AMR丰度、多样性和表型的可比性见解。通过整合qPCR、宏基因组学和基于培养的基因组学,我们揭示了致病性和非致病性细菌的耐药性,重申废水是AMR的主要储藏库,并揭示了遗传预测和观察到的易感性之间经常不匹配。中间耐药的流行进一步表明,许多环境耐药机制仍然知之甚少。这些发现表明,没有一种方法能够捕捉到抗生素耐药性的复杂性,并强调需要统一的多方法监测,以支持全面监测和控制耐药性传播的战略。
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
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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