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TITLE In Vitro and In Vivo Leishmanicidal Activity of Beauvericin
AUTHOR Virlânio A. de Oliveira Filho, Juliana R. Gubiani, Vitória D. Borgonovi, Felipe Hilário, Marcelo R. de Amorim*, Karen Minori, Vitor K. S. Bertolini, Antonio G. Ferreira, Andressa R. Biz, Marcos A. Soares, Helder L. Teles, Fernanda R. Gadelha, Roberto G. S. Berlinck*, Danilo C. Miguel*
YEAR 2024
JOURNAL Journal of Natural Products
ABSTRACT

Leishmaniasis is a worldwide disease caused by more than 20 species of Leishmania parasites. Leishmania amazonensis and L. braziliensis are among the main causative agents of cutaneous leishmaniasis, presenting a broad spectrum of clinical forms. As these pathologies lead to unsatisfactory treatment outcomes, the discovery of alternative chemotherapeutic options is urgently required. In this investigation, a leishmanicidal bioassay-guided fractionation of the growth media extract produced by Aspergillus terreus P63 led to the isolation of the cyclic depsipeptide beauvericin (1). The viability of L. amazonensisL. braziliensis and mammalian cells (macrophages and L929 fibroblasts) was assessed in 1 incubated cultures. Leishmania promastigotes were sensitive to 1, with EC50 values ranging from 0.7 to 1.3 μM. Microscopy analysis indicated that Leishmania spp. parasites showed morphological abnormalities in a dose-dependent manner in the presence of 1L. amazonensis intracellular amastigotes were more sensitive to 1 than promastigotes (EC50 = 0.8 ± 0.1 μM), with a good selectivity index (22–30). 1 reduced the infectivity index at very low concentrations, maintaining the integrity of the primary murine host cell for up to the highest concentration tested for 1In vivo assays of 1 conducted using BALB/c mice infected with stationary-phase promastigotes of L. amazonensis in the tail base presented a significant reduction in the lesion parasite load. A second round of in vivo assays was performed to assess the efficacy of the topical use of 1. The results demonstrated a significant decrease in the total ulcerated area of mice treated with 1 when compared with untreated animals. Our results present promising in vitro and in vivo leishmanicidal effects of beauvericin, emphasizing that systemic inoculation of 1 led to a decrease in the parasite load at the lesion site, whereas topical administration of 1 delayed the progression of leishmaniasis ulcers, a cure criterion established for cutaneous leishmaniasis management.

FULL ARTICLE https://pubs.acs.org/doi/full/10.1021/acs.jnatprod.4c01098
INSTRUMENT P-2000
KEYWORDS Assays, Infectious diseases, Lesions, Parasites, Rodent models
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