Gallium: a decisive "Trojan Horse" against microorganisms
- PMID: 39269546
- DOI: 10.1007/s10482-024-02015-2
Gallium: a decisive "Trojan Horse" against microorganisms
Abstract
Controlling multidrug-resistant microorganisms (MRM) has a long history with the extensive and inappropriate use of antibiotics. At the cost of these drugs being scarce, new possibilities have to be explored to inhibit the growth of microorganisms. Thus, metallic compounds have shown to be promising as a viable alternative to contain pathogens resistant to conventional antimicrobials. Gallium (Ga3+) can be highlighted, which is an antimicrobial agent capable of disrupting the essential activities of microorganisms, such as metabolism, cellular respiration and DNA synthesis. It was observed that this occurs due to the similar properties between Ga3+ and iron (Fe3+), which is a fundamental ion for the correct functioning of bacterial activities. The mimetic effect performed by Ga3+ prevents iron transporters from distinguishing both ions and results in the substitution of Fe3+ for Ga3+ and in adverse metabolic disturbances in rapidly growing cells. This review focuses on analyzing the development of research involving Ga3+, elucidating the intracellular incorporation of the "Trojan Horse", summarizing the mechanism of interaction between gallium and iron and comparing the most recent and broad-spectrum studies using gallium-based compounds with antimicrobial scope.
Keywords: Gallium; Microorganisms; Mimetic effect; “Trojan Horse”.
© 2024. The Author(s), under exclusive licence to Springer Nature Switzerland AG.
Similar articles
-
Comparative proteomics unveils the bacteriostatic mechanisms of Ga(III) on the regulation of metabolic pathways in Pseudomonas aeruginosa.J Proteomics. 2023 Oct 30;289:105011. doi: 10.1016/j.jprot.2023.105011. Epub 2023 Sep 28. J Proteomics. 2023. PMID: 37776994
-
Promises and failures of gallium as an antibacterial agent.Future Microbiol. 2014;9(3):379-97. doi: 10.2217/fmb.14.3. Future Microbiol. 2014. PMID: 24762310 Review.
-
In Silico Analysis of the Ga3+/Fe3+ Competition for Binding the Iron-Scavenging Siderophores of P. aeruginosa-Implementation of Three Gallium-Based Complexes in the "Trojan Horse" Antibacterial Strategy.Biomolecules. 2024 Apr 16;14(4):487. doi: 10.3390/biom14040487. Biomolecules. 2024. PMID: 38672503 Free PMC article.
-
The transition metal gallium disrupts Pseudomonas aeruginosa iron metabolism and has antimicrobial and antibiofilm activity.J Clin Invest. 2007 Apr;117(4):877-88. doi: 10.1172/JCI30783. Epub 2007 Mar 15. J Clin Invest. 2007. PMID: 17364024 Free PMC article.
-
Gallium-based anti-infectives: targeting microbial iron-uptake mechanisms.Curr Opin Pharmacol. 2013 Oct;13(5):707-16. doi: 10.1016/j.coph.2013.07.001. Epub 2013 Jul 19. Curr Opin Pharmacol. 2013. PMID: 23876838 Review.
References
-
- Abdalla MY, Switzer BL, Goss CH, Aitken ML, Singh PK, Britigan BE (2015) Gallium compounds exhibit potential as new therapeutic agents against Mycobacterium abscessus. Antimicrob Agents Chemother 59:4826–4834. https://doi.org/10.1128/AAC.00331-15 - DOI - PubMed - PMC
-
- Andrews SC, Robinson AK, Rodríguez-Quiñones F (2003) Bacterial iron homeostasis. FEMS Microbiol Rev 27:215–237. https://doi.org/10.1016/S0168-6445(03)00055-X - DOI - PubMed
-
- Antunes LCS, Imcaoarivetperi F, Minandri F, Visca P (2012) In Vitro and in vivo antimicrobial activities of Gallium Nitrate against Multidrug-Resistant Acinetobacter baumannii. Antimicrob Agents Chemother 56:5961–5970. https://doi.org/10.1128/AAC.01519-12 - DOI - PubMed - PMC
-
- Arivett BA, Fiester SE, Ohneck EJ, Penwell WF, Kaufman CM, Relich RF et al (2015) Antimicrobial activity of gallium protoporphyrin IX against Acinetobacter baumannii strains displaying different antibiotic resistance phenotypes. Antimicrob Agents Chemother 59:7657–7665. https://doi.org/10.1128/AAC.01472-15 - DOI - PubMed - PMC
-
- Assis ASJ, Pegoraro GM, Duarte ICS (2022) Evolution of gallium applications in medicine and microbiology: a timeline. Biometals 35:675–688. https://doi.org/10.1007/s10534-022-00406-4 - DOI - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical