Novel Antifungal Activity for the Lectin Scytovirin: Inhibition of Cryptococcus neoformans and Cryptococcus gattii

被引:13
|
作者
Jones, Tyler H. [1 ]
McClelland, Erin E. [2 ]
McFeeters, Hana [1 ]
McFeeters, Robert L. [1 ]
机构
[1] Univ Alabama, Dept Chem, Huntsville, AL 35899 USA
[2] Middle Tennessee State Univ, Dept Biol, Murfreesboro, TN 37130 USA
关键词
Scytovirin; Cryptococcus neoformans; Cryptococcus gattii; novel antifungal; lectin; cryptococcosis; FUNGAL CELL-WALL; IN-VITRO; SEROTYPE; PROTEIN; POLYSACCHARIDE; VIRULENCE; CAPSULE; POTENT; IDENTIFICATION; MENINGITIS;
D O I
10.3389/fmicb.2017.00755
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Pathogenic cryptococci are encapsulated yeast that can cause severe meningoencephalitis. Existing therapeutic options are dated and there is a growing need for new alternative antifungal agents for these fungi. Here we report novel inhibition of pathogenic cryptococci by the antimicrobial lectin Scytovirin. Inhibition was most potent against Cryptococcus neoformans var neoformans and C. gattii, with MFC values of 500 nM. Scytovirin binding was localized to the cell wall and shown to affect capsule size and release. No effect was observed on melanization or with cells grown in the presence the cell wall stressor Congo red. Synergy with existing antifungals was indicated, most strongly for amphotericin B. Overall, Scytovirin serves as a much needed new avenue for anticryptococcal development.
引用
收藏
页数:9
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