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In vivo Activity of Copper(II), Manganese(II), and Silver(I) 1,10-Phenanthroline Chelates Against Candida haemulonii Using the Galleria mellonella Model.
- Source :
-
Frontiers in microbiology [Front Microbiol] 2020 Mar 24; Vol. 11, pp. 470. Date of Electronic Publication: 2020 Mar 24 (Print Publication: 2020). - Publication Year :
- 2020
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Abstract
- Candida haemulonii is an emerging opportunistic pathogen resistant to most antifungal drugs currently used in clinical arena. Metal complexes containing 1,10-phenanthroline (phen) chelating ligands have well-established anti- Candida activity against different medically relevant species. This study utilized larvae of Galleria mellonella , a widely used model of in vivo infection, to examine C. haemulonii infection characteristics in response to different copper(II), manganese(II), and silver(I) chelates containing phen, which had demonstrated potent anti- C. haemulonii activity in a previous study. The results showed that C. haemulonii virulence was influenced by inoculum size and incubation temperature, and the host G. mellonella immune response was triggered in an inoculum-dependent manner reflected by the number of circulating immune cells (hemocytes) and observance of larval melanization process. All test chelates were non-toxic to the host in concentrations up to 10 μg/larva. The complexes also affected the G. mellonella immune system, affecting the hemocyte number and the expression of genes encoding antifungal and immune-related peptides (e.g., inducible metalloproteinase inhibitor protein , transferrin , galiomycin , and gallerimycin ). Except for [Ag <subscript>2</subscript> (3,6,9-tdda)(phen) <subscript>4</subscript> ].EtOH (3,6,9-tddaH <subscript>2</subscript> = 3,6,9-trioxoundecanedioic acid), all chelates were capable of affecting the fungal burden of infected larvae and the virulence of C. haemulonii in a dose-dependent manner. This work shows that copper(II), manganese(II), and silver(I) chelates containing phen with anti- C. haemulonii activity are capable of (i) inhibiting fungal proliferation during in vivo infection, (ii) priming an immune response in the G. mellonella host and (iii) affecting C. haemulonii virulence.<br /> (Copyright © 2020 Gandra, McCarron, Viganor, Fernandes, Kavanagh, McCann, Branquinha, Santos, Howe and Devereux.)
Details
- Language :
- English
- ISSN :
- 1664-302X
- Volume :
- 11
- Database :
- MEDLINE
- Journal :
- Frontiers in microbiology
- Publication Type :
- Academic Journal
- Accession number :
- 32265890
- Full Text :
- https://doi.org/10.3389/fmicb.2020.00470