Carneiro Joara Nályda Pereira, Dos Santos Antonia Thassya Lucas, Fonseca Victor Juno Alencar, de Freitas Maria Audilene, Dos Santos Silva Francildo, de Souza Larissa Alves Lopes, Araújo Nadine Monteiro Salgueiro, de Oliveira Bezerra de Sousa Daniele, Silva Rafael Guimarães Gomes, da Silva Neto João Xavier, de Menezes Irwin Rose Alencar, Coutinho Henrique Douglas Melo, Morais-Braga Maria Flaviana Bezerra
Cariri Applied Mycology Laboratory, Regional University of Cariri, Crato, Ceara, Brazil.
Plant Toxin Laboratory, Federal University of Ceara, Fortaleza, Ceara, Brazil.
Curr Microbiol. 2025 Mar 5;82(4):168. doi: 10.1007/s00284-025-04133-0.
Candidemia is a public health challenge as it causes thousands of annual deaths and combating it has become difficult due to the development of resistance in Candida spp. Compounds derived from natural products may counter this resistance. Therefore, we evaluate the intrinsic and combined antifungal activity of valencene and nootkatone compounds and their possible mechanism of action against Candida spp. Using the microdilution method, the antifungal effect of sesquiterpenes and their combination with fluconazole was determined. The results comprised the yeast growth curve and its 50% Inhibitory Concentration (IC). They showed that the compounds alone inhibited microbial growth at a concentration of 1024 µg/mL for valencene being able to kill the fungus Pichia kudriavzevii (Candida krusei), for nootkatone the inhibition occurred at 512 µg/mL and was able to kill the species P. kudriavzevii and Candida tropicalis. Combined with the antifungal, the inhibition occurred at low concentrations (2 and 4 µg/mL) against all strains except P. kudriavzevii, which the combination with nootkatone inhibited at 512 µg/mL. The IC revealed inhibition of the strains at higher concentrations in the compounds and fluconazole alone compared to the combination concentrations. In addition, both compounds acted through the production of reactive oxygen species, helping the antifungal against C. albicans and P. kudriavzevii, contributing minimally to compromising membrane viability. Thus, the compounds show promise for combined activity with fluconazole.
念珠菌血症是一项公共卫生挑战,因为它每年导致数千人死亡,并且由于念珠菌属产生耐药性,对抗念珠菌血症变得困难。天然产物衍生的化合物可能会对抗这种耐药性。因此,我们评估了瓦伦烯和诺卡酮化合物的内在和联合抗真菌活性及其对念珠菌属可能的作用机制。采用微量稀释法,测定了倍半萜及其与氟康唑联合使用的抗真菌效果。结果包括酵母生长曲线及其50%抑制浓度(IC)。结果表明,单独使用这些化合物时,瓦伦烯在浓度为1024µg/mL时可抑制微生物生长,能够杀死季也蒙毕赤酵母(克鲁斯念珠菌),诺卡酮在512µg/mL时出现抑制作用,能够杀死季也蒙毕赤酵母和热带念珠菌。与抗真菌药物联合使用时,除季也蒙毕赤酵母外,对所有菌株在低浓度(2和4µg/mL)时均有抑制作用,与诺卡酮联合使用时对季也蒙毕赤酵母在512µg/mL时具有抑制作用。IC显示,与联合浓度相比,单独使用化合物和氟康唑时,在较高浓度下对菌株有抑制作用。此外,这两种化合物都通过产生活性氧发挥作用,有助于抗白色念珠菌和季也蒙毕赤酵母,对损害膜活力的作用最小。因此,这些化合物显示出与氟康唑联合使用的前景。