# The Microbial Trojan Horse and Antimicrobial Resistance: Acanthamoeba as an Environmental Reservoir for Multidrug Resistant Bacteria

**Authors:** Ronnie Mooney, Erin Corbett, Elisa Giammarini, Kiri Rodgers, Carla Donet, Ernest Mui, Arhama T. A. Ansari, Ayush Ransingh, Pradnya S. Vernekar, Harleen K. Walia, Jyoti Sharma, John Connolly, Andrew Hursthouse, Suparna Mukherji, Soumyo Mukherji, Fiona L. Henriquez

PMC · DOI: 10.1111/1462-2920.70193 · Environmental Microbiology · 2025-10-29

## TL;DR

Bacteria living inside Acanthamoeba amoebae show higher antibiotic resistance than those in sediment, possibly due to exposure to toxic elements.

## Contribution

This study provides the first direct evidence linking toxic elements to the antibiotic resistance of bacteria inside Acanthamoeba.

## Key findings

- Acanthamoeba-associated bacteria showed significantly higher multidrug resistance compared to sediment-associated bacteria.
- Resistance in Acanthamoeba-associated bacteria was linked to potentially toxic elements like arsenic, vanadium, and calcium.
- The study supports a model where protists like Acanthamoeba act as selective environments for antibiotic-resistant bacteria.

## Abstract

Antimicrobial resistance (AMR) is shaped by environmental pressures, yet the role of microbial predators such as Acanthamoeba in resistance dynamics remains poorly characterized. In this study, Acanthamoeba‐associated bacterial communities (AAB) exhibited significantly higher multidrug resistance than sediment‐associated bacterial communities (SAB) in a polluted estuarine system. All isolated amoebae belonged to the T4 genotype, suggesting selection for resilient host organisms. AAB displayed elevated multiple antibiotic resistance (MAR) indices and increased resistance to multiple antibiotic classes, particularly aminoglycosides, macrolides, fluoroquinolones and β‐lactams. Correlation analysis revealed that resistance in AAB, but not SAB, was associated with potentially toxic elements (PTEs) known to influence phagocyte survival, including arsenic, vanadium, and calcium. These elements may select for traits that confer metal and antibiotic resistance. The findings support a model where protists act as selective environments for AMR, favoring bacteria that possess enhanced tolerance mechanisms. This work provides the first direct evidence linking PTE exposure to the intracellular resistome of Acanthamoeba‐associated bacteria. It underscores the need for AMR monitoring frameworks that include protist‐bacteria interactions, with implications for One Health and environmental risk assessment strategies. Moreover, this approach is scalable for application in low/middle‐income countries, where AMR burden is greatest and surveillance capacity remains limited.

Bacteria associated with Acanthamoeba exhibit greater antibiotic resistance than those from sediment and, on average, show a higher likelihood of multi‐antibiotic tolerance, reflected in significantly elevated multiple‐antibiotic resistance (MAR) index values. Potentially toxic elements driving resistance also differ depending on the type of survival; Acanthamoeba‐associated or sediment associated.

## Linked entities

- **Chemicals:** arsenic (PubChem CID 5359596), vanadium (PubChem CID 23990), calcium (PubChem CID 5460341)
- **Species:** Acanthamoeba (taxon 5754)

## Full-text entities

- **Chemicals:** arsenic (MESH:D001151), aminoglycosides (MESH:D000617), metal (MESH:D008670), vanadium (MESH:D014639), fluoroquinolones (MESH:D024841), beta-lactams (MESH:D047090), macrolides (MESH:D018942), PTE (-), calcium (MESH:D002118)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Acanthamoeba (genus) [taxon 5754]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12572456/full.md

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12572456/full.md

## References

112 references — full list in the complete paper: https://tomesphere.com/paper/PMC12572456/full.md

---
Source: https://tomesphere.com/paper/PMC12572456