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Aryl-alkyl-lysines: Membrane-Active Fungicides That Act against Biofilms of Candida albicans.
Ghosh, Chandradhish; Yadav, Vikas; Younis, Waleed; Mohammad, Haroon; Hegazy, Youssef A; Seleem, Mohamed N; Sanyal, Kaustuv; Haldar, Jayanta.
Afiliação
  • Ghosh C; Chemical Biology and Medicinal Chemistry Laboratory, New Chemistry Unit, Jawaharlal Nehru Centre for Advanced Scientific Research , Jakkur, Bangalore, Karnataka 560064, India.
  • Yadav V; Molecular Mycology Laboratory, Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research , Jakkur, Bangalore, Karnataka 560064, India.
  • Younis W; Department of Comparative Pathobiology, Purdue University , 625 Harrison Street, West Lafayette, Indiana 47907, United States.
  • Mohammad H; Department of Comparative Pathobiology, Purdue University , 625 Harrison Street, West Lafayette, Indiana 47907, United States.
  • Hegazy YA; Department of Comparative Pathobiology, Purdue University , 625 Harrison Street, West Lafayette, Indiana 47907, United States.
  • Seleem MN; Department of Comparative Pathobiology, Purdue University , 625 Harrison Street, West Lafayette, Indiana 47907, United States.
  • Sanyal K; Purdue Institute for Inflammation, Immunology, and Infectious Disease, Purdue University , West Lafayette, Indiana 47907, United States.
  • Haldar J; Molecular Mycology Laboratory, Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research , Jakkur, Bangalore, Karnataka 560064, India.
ACS Infect Dis ; 3(4): 293-301, 2017 04 14.
Article em En | MEDLINE | ID: mdl-28238268
Mortality due to pathogenic fungi has been exacerbated by the rapid development of resistance to frontline antifungal drugs. Fungicidal compounds with novel mechanisms of action are urgently needed. Aryl-alkyl-lysines, which are membrane-active small molecules, were earlier shown to be broad-spectrum antibacterial agents with potency in vitro and in vivo. Herein, we report the antifungal properties of aryl-alkyl-lysines. After identifying the most active compound (NCK-10), we tested its activity against a panel of clinically relevant pathogenic fungi and examined NCK-10's effect against immature and mature biofilms of Candida albicans. NCK-10 was capable of inhibiting the growth of various species of fungi (including Candida spp., Cryptococcus spp., and Aspergillus fumigatus) at concentrations similar to those of antifungal drugs used clinically. It was observed that polarization and permeability of the fungal cell membrane were compromised upon addition of NCK-10, indicating its mechanism is disruption of the fungal cell membrane. In addition to interfering with the growth of planktonic fungi, NCK-10 demonstrated the ability to both inhibit biofilm formation and reduce the metabolic activity of cells in C. albicans biofilm. Additionally, our compound was capable of crossing the blood-brain barrier in an in vitro model, expanding the potential antifungal applications for NCK-10. Overall, aryl-alkyl-lysines were found to be excellent compounds that warrant further investigation as novel antifungal agents.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Candida albicans / Biofilmes / Antifúngicos Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Candida albicans / Biofilmes / Antifúngicos Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article