2018
DOI: 10.1111/jam.14053
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Effects of cytochalasin E onParacoccidioides brasiliensis

Abstract: Paracoccidioides spp. are the etiological agents of paracoccidioidomycosis (PCM). Treatment is prolonged to control the clinical manifestations and prevent relapse. The study on the effects of cytochalasin E in P. brasiliensis is important because it can be used as a prototype for new antifungal drugs and consequently, broadens the treatment options for PCM.

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Cited by 3 publications
(3 citation statements)
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“…Nine compounds were present in the pure culture of C. coccodes growing on MEA plates. They were mainly unspecific components with the exception of bacterial monocerin and cytochalasin E, originally isolated from the Aspergillus species [ 65 ], as a probable effect of cross-contamination. Eleven metabolites were identified in potatoes inoculated with C. coccodes , mostly unrelated to fungal activity, except for several compounds originally isolated from the Fusarium species, such as beauvericin, bikaverin, and deoxygerfelin ( Table 5 ).…”
Section: Resultsmentioning
confidence: 99%
“…Nine compounds were present in the pure culture of C. coccodes growing on MEA plates. They were mainly unspecific components with the exception of bacterial monocerin and cytochalasin E, originally isolated from the Aspergillus species [ 65 ], as a probable effect of cross-contamination. Eleven metabolites were identified in potatoes inoculated with C. coccodes , mostly unrelated to fungal activity, except for several compounds originally isolated from the Fusarium species, such as beauvericin, bikaverin, and deoxygerfelin ( Table 5 ).…”
Section: Resultsmentioning
confidence: 99%
“…(Table S2). The extracts and cytochalasin E isolated from Aspergillus felis presented an MIC of 31.2 µg/mL (3.6 µM) [55]. The extract of the endophytic fungus Fusarium sp.…”
Section: New Anti-paracoccidioides Compounds: Do We Already Have Any Ideal Antifungals?mentioning
confidence: 99%
“…The choice of the drug to be administered depends on various circumstances such as clinical severity, previous history of therapeutic resistance, gastrointestinal drug absorption capacity, association with comorbidities, and treatment adherence. P. brasiliensis is sensitive to most antifungal drugs, including sulfonamides, azoles (ketoconazole, fluconazole, itraconazole, posaconazole, voriconazole), amphotericin B (AB), and terbinafine (Mahajan, 2014;Ambrósio et al, 2014;Orofino-Costa et al, 2017) Sulfamethoxazole-trimethoprim or itraconazole can be used in the mild or moderate localized forms (Borges et al, Research, Society and Development, v. 11, n. 12, e165111234460, 2022 (CC BY 4.0) | ISSN 2525-3409 | DOI: http://dx.doi.org/10.33448/rsd-v11i12.34460 3 2014; Mendes et al, 2018) being amphotericin B reserved for the disseminated and severe forms, as in the central nervous system (CNS) (Hahn & Hamdan, 2000;Alonso et al, 2022).…”
Section: Introductionmentioning
confidence: 99%