Programa de Pós Graduação em Ciências da Saúde, Laboratório de Micologia, Faculdade de Medicina (FAMED), Universidade Federal Do Rio Grande (FURG), Campus Saúde, Visconde de Paranaguá 102, Centro, Rio Grande, RS, 96201-900, Brazil.
Programa de Pós Graduação em Bioquímica Toxicológica, Universidade Federal de Santa Maria (UFSM), Santa Maria, RS, Brazil.
Braz J Microbiol. 2021 Sep;52(3):1271-1274. doi: 10.1007/s42770-021-00506-2. Epub 2021 Apr 28.
We evaluated the in vitro susceptibility of Sporothrix schenckii s.str. and Sporothrix globosa to diphenyl diselenide (PhSe) alone and in association with itraconazole (ITZ). Eight clinical isolates were tested in microdilution and checkerboard assays. (PhSe) alone inhibited all isolates in concentration ≤ 8 µg/mL and was effective in killing one S. schenckii isolate. Inhibitory and fungicidal beneficial effects in its interaction with ITZ were shown against 87.5% (7/8) and 50% (4/8) of the isolates tested, respectively. Our study demonstrates the in vitro antifungal activity of (PhSe) against two pathogenic Sporothrix species, suggesting studies of in vivo applications are warranted.
我们评估了二苯基二硒(PhSe)单独以及与伊曲康唑(ITZ)联合应用时对申克孢子丝菌和球形孢子丝菌的体外敏感性。在微量稀释和棋盘试验中测试了 8 株临床分离株。PhSe 单独在浓度≤8μg/ml 时抑制所有分离株,并能有效杀死一株申克孢子丝菌分离株。其与 ITZ 相互作用表现出抑菌和杀菌的有益效果,分别对 87.5%(7/8)和 50%(4/8)的受试分离株有效。我们的研究表明,PhSe 对两种致病性孢子丝菌具有体外抗真菌活性,提示有必要进行体内应用研究。