Engineered Nanoparticles Enhance Photodynamic Inactivation Against the WHO Fungal Priority Pathogens. A Systematic Review DOI
Abdênego Rodrigues da Silva, Bruno L. Raposo,

Gilberto Sarmento Marques de Lima

et al.

BioNanoScience, Journal Year: 2025, Volume and Issue: 15(2)

Published: April 10, 2025

Language: Английский

Antifungal Action of Valencene and Nootkatone Compounds in Association with Fluconazole and Their Mechanism of Action Against Candida spp. and Pichia kudriavzevii Strains DOI
Joara Nályda Pereira Carneiro, Antônia Thassya Lucas dos Santos, Victor Juno Alencar Fonseca

et al.

Current Microbiology, Journal Year: 2025, Volume and Issue: 82(4)

Published: March 5, 2025

Language: Английский

Citations

0

Unveiling antifungal resistance and biocide tolerance in clinical isolates of Candida spp DOI
Jamile de Paiva Macedo,

Aripuanã Sakurada Aranha Watanabe,

Alessandra Barbosa Ferreira Machado

et al.

Future Microbiology, Journal Year: 2025, Volume and Issue: unknown, P. 1 - 12

Published: March 22, 2025

Aims Candidiasis, caused by Candida spp. is an opportunistic infection with significant healthcare risks, worsened trends in antifungal resistance. This study aimed to evaluate the susceptibility profile, investigate resistance mechanisms, assess efflux pump activity, and examine biocide tolerance clinical isolates.

Language: Английский

Citations

0

Antimicrobial Investigation of Phthalimide and N-Phthaloylglycine Esters: Activity, Mechanism of Action, Synergism and Ecotoxicity DOI Creative Commons

Francinara S. Alves,

Abraão Pinheiro de Sousa,

Alexandre Almeida Júnior

et al.

Life, Journal Year: 2025, Volume and Issue: 15(4), P. 518 - 518

Published: March 21, 2025

Motivated by the search for novel antimicrobials against opportunistic resistant pathogens and based on reported antimicrobial activity of phthalimides, two series phthalimide N-phthaloylglycine esters were designed to investigate whether addition butyl aryl groups enhances their properties. Thus, in vitro activity, antifungal mechanism action, effect combined with Chloramphenicol, silico/vitro toxicity, a docking molecular studied. Phthalimide obtained yields 75–98%. ester 3b (R = Me) showed best results Gram-(+) Gram-(−) bacteria, S. aureus P. aeruginosa, respectively, yeast fungi, C. tropicalis albicans, MIC values equal 128 µg·mL−1. Regarding action compound changed from 1024 µg·mL−1 presence ergosterol. Furthermore, synergy Chloramphenicol FICI value 0.5. Finally, four most promising compounds had toxicity evaluated, which moderate non-toxicity Artemia salina larvae. With exception all selected compounds, including Fluconazole, are potentially hepatotoxic, but they predicted not cause skin sensitization, suggesting potential application topical use. Molecular revealed that exhibits superior binding affinity stability 50S ribosomal subunit (−92.69 kcal·mol−1) compared unique π–sulfur interaction CYP51, its as dual-action antibacterial candidate pathogens.

Language: Английский

Citations

0

Synergistic antifungal activity of minocycline as an effective augmenting agent of fluconazole against drug-resistant Candida tropicalis DOI Creative Commons

Yun-Zhu Zhu,

Xiang Li,

Qingyue Zhang

et al.

Microbiology Spectrum, Journal Year: 2025, Volume and Issue: unknown

Published: March 31, 2025

ABSTRACT Invasive candidiasis has emerged as a significant healthcare challenge, with rising incidence rate attributed to the widespread use of organ transplantation, chemotherapy, immunosuppressants, and broad-spectrum antibiotics. The increasing prevalence drug-resistant strains, particularly among Candida tropicalis , necessitated exploration novel therapeutic strategies. Our study investigated synergistic effects minocycline (MIN) combined fluconazole (FLC) against FLC-resistant C. both in vitro vivo . activity MIN FLC was evaluated using checkerboard titration time-kill assays. Galleria mellonella larvae mouse model were employed assess efficacy, histopathological examination fungal burden quantification. Whole-genome RNA sequencing elucidated mechanisms observed. FLC/MIN combination significantly lowered minimum inhibitory concentration (MIC) improved fungicidal activity, evidenced by enhanced survival rates reduced G. models. Histopathological analysis confirmed less tissue damage load therapy. suggested that impact on amino acid metabolism contributes effects. This approach holds promise for treating antifungal efficacy reducing drug resistance risks, warranting further clinical exploration. IMPORTANCE highlights potential therapy combating It shows promising effects, MIC enhancing activity. Further trials are needed validate its infections.

Language: Английский

Citations

0

Engineered Nanoparticles Enhance Photodynamic Inactivation Against the WHO Fungal Priority Pathogens. A Systematic Review DOI
Abdênego Rodrigues da Silva, Bruno L. Raposo,

Gilberto Sarmento Marques de Lima

et al.

BioNanoScience, Journal Year: 2025, Volume and Issue: 15(2)

Published: April 10, 2025

Language: Английский

Citations

0