# Antimicrobial resistance in diverse urban microbiomes: uncovering patterns and predictive markers

**Authors:** Rodolfo Brizola Toscan, Wojciech Lesiński, Piotr Stomma, Balakrishnan Subramanian, Paweł P. Łabaj, Witold R. Rudnicki

PMC · DOI: 10.3389/fgene.2025.1460508 · Frontiers in Genetics · 2025-01-29

## TL;DR

This study explores how antimicrobial resistance spreads in urban areas by analyzing microbiomes from six U.S. cities.

## Contribution

The study introduces a novel approach combining metagenomic data and machine learning to identify predictive markers of antimicrobial resistance.

## Key findings

- AMR++ and Bowtie showed superior performance in detecting diverse AMR markers.
- Mobile genetic elements play a critical role in AMR dissemination across cities.
- New York City exhibited the highest resistome diversity among the studied cities.

## Abstract

Antimicrobial resistance (AMR) is a growing global health concern, driven by urbanization and anthropogenic activities. This study investigated AMR distribution and dynamics across microbiomes from six U.S. cities, focusing on resistomes, viromes, and mobile genetic elements (MGEs). Using metagenomic data from the CAMDA 2023 challenge, we applied tools such as AMR++, Bowtie, AMRFinderPlus, and RGI for resistome profiling, along with clustering, normalization, and machine learning techniques to identify predictive markers. AMR++ and Bowtie outperformed other tools in detecting diverse AMR markers, with binary normalization improving classification accuracy. MGEs were found to play a critical role in AMR dissemination, with 394 genes shared across all cities. Removal of MGE-associated AMR genes altered resistome profiles and reduced model performance. The findings reveal a heterogeneous AMR landscape in urban microbiomes, particularly in New York City, which showed the highest resistome diversity. These results underscore the importance of MGEs in AMR profiling and provide valuable insights for designing targeted strategies to address AMR in urban settings.

## Full-text entities

- **Genes:** CUL9 (cullin 9) [NCBI Gene 23113] {aka H7AP1, PARC}, ABL2 (ABL proto-oncogene 2, non-receptor tyrosine kinase) [NCBI Gene 27] {aka ABLL, ARG}
- **Diseases:** MGEs (MESH:D014086), AMR (MESH:D060467), antibiotic (MESH:D004761), infections (MESH:D007239)
- **Chemicals:** metal (MESH:D008670), quinolones (MESH:D015363), Beta-lactam (MESH:D047090)
- **Species:** Homo sapiens (human, species) [taxon 9606], Enterobacter hormaechei (CDC Enteric Group 75, species) [taxon 158836], Escherichia coli (E. coli, species) [taxon 562], Klebsiella pneumoniae (species) [taxon 573]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11813901/full.md

## References

69 references — full list in the complete paper: https://tomesphere.com/paper/PMC11813901/full.md

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Source: https://tomesphere.com/paper/PMC11813901