» Articles » PMID: 26151486

Histone Deacetylases: Targets for Antifungal Drug Development

Overview
Journal Virulence
Specialty Microbiology
Date 2015 Jul 8
PMID 26151486
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

The interaction of pathogens and its hosts causes a drastic change in the transcriptional landscape in both cells. Among the several mechanisms of gene regulation, transcriptional initiation is probably the main point. In such scenario, the access of transcriptional machinery to promoter is highly regulated by post-translational modification of histones, such as acetylation, phosphorylation and others. Inhibition of histone deacetylases is able to reduce fungal pathogens fitness during infection and, therefore, is currently being considered for the development of new antifungal therapy strategies.

Citing Articles

Sirtulin-Ypk1 regulation axis governs the TOR signaling pathway and fungal pathogenicity in .

Chai Z, Li Y, Zhang J, Ding C, Tong X, Zhang Z Microbiol Spectr. 2024; :e0003824.

PMID: 38912819 PMC: 11302014. DOI: 10.1128/spectrum.00038-24.


Histone deacetylase inhibitor attenuates experimental fungal keratitis in mice.

Li X, Yuan M, Yin R, Liu X, Zhang Y, Sun S Sci Rep. 2019; 9(1):9859.

PMID: 31285488 PMC: 6614500. DOI: 10.1038/s41598-019-46361-y.


Fungal acetylome comparative analysis identifies an essential role of acetylation in human fungal pathogen virulence.

Li Y, Li H, Sui M, Li M, Wang J, Meng Y Commun Biol. 2019; 2:154.

PMID: 31069264 PMC: 6494858. DOI: 10.1038/s42003-019-0419-1.


Selective BET bromodomain inhibition as an antifungal therapeutic strategy.

Mietton F, Ferri E, Champleboux M, Zala N, Maubon D, Zhou Y Nat Commun. 2017; 8:15482.

PMID: 28516956 PMC: 5454392. DOI: 10.1038/ncomms15482.

References
1.
Pfaller M, Messer S, Georgopapadakou N, Martell L, Besterman J, Diekema D . Activity of MGCD290, a Hos2 histone deacetylase inhibitor, in combination with azole antifungals against opportunistic fungal pathogens. J Clin Microbiol. 2009; 47(12):3797-804. PMC: 2786684. DOI: 10.1128/JCM.00618-09. View

2.
Gast C, Basso Jr L, Bruzual I, Wong B . Azole resistance in Cryptococcus gattii from the Pacific Northwest: Investigation of the role of ERG11. Antimicrob Agents Chemother. 2013; 57(11):5478-85. PMC: 3811322. DOI: 10.1128/AAC.02287-12. View

3.
Nguyen L, Lopes L, Cordero R, Nosanchuk J . Sodium butyrate inhibits pathogenic yeast growth and enhances the functions of macrophages. J Antimicrob Chemother. 2011; 66(11):2573-80. DOI: 10.1093/jac/dkr358. View

4.
Simonetti G, Passariello C, Rotili D, Mai A, Garaci E, Palamara A . Histone deacetylase inhibitors may reduce pathogenicity and virulence in Candida albicans. FEMS Yeast Res. 2007; 7(8):1371-80. DOI: 10.1111/j.1567-1364.2007.00276.x. View

5.
Li X, Cai Q, Mei H, Zhou X, Shen Y, Li D . The Rpd3/Hda1 family of histone deacetylases regulates azole resistance in Candida albicans. J Antimicrob Chemother. 2015; 70(7):1993-2003. DOI: 10.1093/jac/dkv070. View