# Metagenomic Comparison of Bat Colony Resistomes Across Anthropogenic and Pristine Habitats

**Authors:** Julio David Soto-López, Omar Velásquez-González, Manuel A. Barrios-Izás, Moncef Belhassen-García, Juan Luis Muñoz-Bellido, Pedro Fernández-Soto, Antonio Muro

PMC · DOI: 10.3390/antibiotics15010051 · Antibiotics · 2026-01-03

## TL;DR

This study compares bacterial resistance genes in bat colonies from human-impacted and pristine areas, finding more diverse resistance in human-impacted sites.

## Contribution

The study reveals how anthropogenic factors influence the diversity and composition of antimicrobial resistance genes in bat-associated microbiomes.

## Key findings

- Salamanca samples showed higher resistome diversity and included clinically relevant resistance genes.
- Guangdong samples had a more restricted resistome dominated by β-lactamase and MurA homologs.
- Resistome composition differed significantly between the two sites, indicating ecological structuring.

## Abstract

Background/Objectives: The mammalian microbiota constitutes a reservoir of antimicrobial resistance genes (ARGs), which can be shaped by environmental and anthropogenic factors. Although bat-associated bacteria have been reported to harbor diverse ARGs globally, the ecological and evolutionary determinants driving this diversity remain unclear. Methods: To characterize ARG diversity in wildlife exposed to contrasting levels of human influence, we analyzed homologs of resistance mechanisms from the Comprehensive Antibiotic Resistance Database in shotgun metagenomes of bat guano. Samples were collected from a colony exposed to continuous anthropogenic activity in Spain (Salamanca) and from a wild, non-impacted bat community in China (Guangdong). Metagenomic analyses revealed marked differences in taxonomic and resistome composition between sites. Results: Salamanca samples contained numerous hospital-associated genera (e.g., Mycobacterium, Staphylococcus, Corynebacterium), while Guangdong was dominated by Lactococcus, Aeromonas, and Stenotrophomonas. β-lactamases and MurA transferase homologs were the most abundant ARGs in both datasets, yet Salamanca exhibited higher richness and functional diversity (median Shannon index = 1.5; Simpson = 0.8) than Guangdong (Shannon = 1.1; Simpson = 0.66). Salamanca also showed enrichment of clinically relevant ARGs, including qacG, emrR, bacA, and acrB, conferring resistance to antibiotics critical for human medicine. In contrast, Guangdong exhibited a more restricted resistome dominated by β-lactamase and MurA homologs. Beta diversity analysis confirmed significant compositional differences between resistomes (PERMANOVA, R2 = 0.019, F = 1.33, p = 0.001), indicating ecological rather than stochastic structuring. Conclusions: These findings suggest that anthropogenic exposure enhances the diversity and evenness of resistance mechanisms within bat-associated microbiomes, potentially increasing their role as reservoirs of antimicrobial resistance.

## Linked entities

- **Genes:** qacG (quaternary ammonium compound efflux SMR transporter QacG) [NCBI Gene 79052829], emrR (transcriptional repressor of emrAB operon) [NCBI Gene 1254336], bacA (undecaprenyl-diphosphatase) [NCBI Gene 877690], acrB (multidrug efflux system protein) [NCBI Gene 915267]
- **Species:** Mycobacterium (taxon 1763), Staphylococcus (taxon 1279), Corynebacterium (taxon 1716), Lactococcus (taxon 1357), Aeromonas (taxon 642), Stenotrophomonas (taxon 40323)

## Full-text entities

- **Genes:** ABL2 (ABL proto-oncogene 2, non-receptor tyrosine kinase) [NCBI Gene 27] {aka ABLL, ARG}
- **Diseases:** Antibiotic (MESH:D004761)
- **Species:** Lactococcus (lactic streptococci, genus) [taxon 1357], Homo sapiens (human, species) [taxon 9606], Stenotrophomonas (genus) [taxon 40323], Staphylococcus (genus) [taxon 1279], Mycobacterium (genus) [taxon 1763], Aeromonas (genus) [taxon 642], Bacillus sp. AT (species) [taxon 1196779]

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12838372/full.md

## References

135 references — full list in the complete paper: https://tomesphere.com/paper/PMC12838372/full.md

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Source: https://tomesphere.com/paper/PMC12838372