# Fullerene Gallium Phosphonate Shows Antimycobacterial Effect Against Mycobacterium avium

**Authors:** Sonyeol Yoon, Kayvan Sasaninia, Iffat Hasnin Era, Sanya Dhama, Aishvaryaa Shree Mohan, Ami Patel, Lannhi Nguyen, Arshavir Karapetyan, Cristian Sy, Nickolas Yedgarian, Nezam Newman, Xiaoning Bi, Michel Baudry, Peter R. Yang, Vishwanath Venketaraman

PMC · DOI: 10.3390/ijms26209998 · International Journal of Molecular Sciences · 2025-10-14

## TL;DR

A new compound called Fullerene Gallium Phosphonate (FGP) shows promise in fighting Mycobacterium avium infections by reducing bacterial load and inflammation.

## Contribution

The study introduces FGP as a novel compound with dual antimycobacterial and antioxidant effects against Mycobacterium avium.

## Key findings

- FGP reduced M. avium colony-forming units by nearly 3-fold compared to a 2-fold decrease with FDSP.
- FGP significantly decreased bacterial load in infected macrophages at 1 and 10 µg/mL.
- FGP lowered oxidative stress and inflammatory markers like IL-6 and TNF-α.

## Abstract

Mycobacterium avium complex (MAC) infections present significant therapeutic challenges due to their inherent antibiotic resistance, demanding innovative treatment approaches. This study investigated the antimicrobial and antioxidant potential of a novel compound, Fullerene Gallium Phosphonate (FGP), and compared its effects against a previously tested similar compound, Fullerene Disodium Phosphonate (FDSP). Results of experiments using MAC cultures and infected THP-1 macrophages treated with varying FGP and FDSP concentrations (1, 10, 100 µg/mL) revealed that FGP demonstrated greater efficacy than FDSP in reducing M. avium colony-forming units (CFU), achieving a nearly 3-fold reduction by day 8, compared to a 2-fold decrease with FDSP. In infected macrophages, FGP significantly decreased bacterial load at 1 and 10 µg/mL (p < 0.01). FGP also lowered oxidative stress, reflected by a significant reduction in malondialdehyde (MDA) levels on day 4 (p < 0.05) and decreased IL-6 (2-fold) and TNF-α levels (3-fold) by day 8, indicating both antimicrobial and anti-inflammatory effects. However, FGP paradoxically increased MAC burden at its highest concentration and showed no significant difference in efficacy of different concentrations. These findings suggest that FGP may serve as a promising candidate for antimycobacterial therapy with dual antibacterial and antioxidant effects. Further research is crucial to fully elucidate its mechanism of action and find the optimal therapeutic window.

## Linked entities

- **Chemicals:** malondialdehyde (PubChem CID 10964), IL-6 (PubChem CID 165368475)
- **Diseases:** Mycobacterium avium complex (MONDO:0005866)
- **Species:** Mycobacterium avium (taxon 1764)

## Full-text entities

- **Diseases:** inflammatory (MESH:D007249), Mycobacterium avium complex (MAC) infections (MESH:D015270)
- **Chemicals:** MDA (MESH:D008315), FDSP (-)
- **Species:** Mycobacterium avium (species) [taxon 1764]
- **Cell lines:** THP-1 — Homo sapiens (Human), Childhood acute monocytic leukemia, Cancer cell line (CVCL_0006)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12563641/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12563641/full.md

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Source: https://tomesphere.com/paper/PMC12563641