Borba-Santos Luana P, Nicoletti Caroline Deckmann, Vila Taissa, Ferreira Patricia Garcia, Araújo-Lima Carlos Fernando, Galvão Bárbara Verena Dias, Felzenszwalb Israel, de Souza Wanderley, de Carvalho da Silva Fernando, Ferreira Vitor Francisco, Futuro Debora Omena, Rozental Sonia
Laboratório de Biologia Celular de Fungos, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, RJ, Rio de Janeiro, Brazil.
Departamento de Tecnologia Farmacêutica, Faculdade de Farmácia, Universidade Federal Fluminense, Niteroi, RJ, Brazil.
Braz J Microbiol. 2022 Jun;53(2):749-758. doi: 10.1007/s42770-022-00725-1. Epub 2022 Mar 8.
Sporotrichosis is a subcutaneous mycosis that affects humans and animals, with few therapeutic options available in the pharmaceutical market. We screened the in vitro antifungal activity of fourteen 1,4-naphthoquinones derivative compounds against Sporothrix brasiliensis and Sporothrix schenckii, the main etiological agents of sporotrichosis in Latin America. The most active compound was selected for further studies exploring its antibiofilm activity, effects on yeast morphophysiology, interaction with itraconazole, and selectivity to fungal cells. Among the fourteen 1,4-naphthoquinones tested, naphthoquinone 5, a silver salt of lawsone, was the most active compound. Naphthoquinone 5 was able to inhibit Sporothrix biofilms and induced ROS accumulation, mitochondrial disturbances, and severe plasmatic membrane damage in fungal cells. Furthermore, naphthoquinone 5 was ten times more selective towards fungal cells than fibroblast, and the combination of itraconazole with naphthoquinone 5 improved the inhibitory activity of the azole. Combined, the data presented here indicate that the silver salt naphthoquinone 5 exerts promising in vitro activity against the two main agents of sporotrichosis with important antibiofilm activity and a good toxicity profile, suggesting it is a promising molecule for the development of a new family of antifungals.
孢子丝菌病是一种影响人类和动物的皮下真菌病,在制药市场上可用的治疗选择很少。我们筛选了十四种1,4-萘醌衍生物化合物对巴西孢子丝菌和申克孢子丝菌的体外抗真菌活性,这两种菌是拉丁美洲孢子丝菌病的主要病原体。选择活性最强的化合物进行进一步研究,探索其抗生物膜活性、对酵母形态生理学的影响、与伊曲康唑的相互作用以及对真菌细胞的选择性。在所测试的十四种1,4-萘醌中,萘醌5(即紫铆素银盐)是活性最强的化合物。萘醌5能够抑制孢子丝菌生物膜,并诱导真菌细胞内活性氧积累、线粒体紊乱和严重的质膜损伤。此外,萘醌5对真菌细胞的选择性比对成纤维细胞高十倍,伊曲康唑与萘醌5联合使用可提高唑类药物的抑制活性。综合来看,本文提供的数据表明,萘醌5银盐对孢子丝菌病的两种主要病原体具有有前景的体外活性,具有重要的抗生物膜活性和良好的毒性特征,表明它是开发新型抗真菌药物家族的一个有前景的分子。