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J Mycol Med ; 34(1): 101460, 2024 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-38266397

RESUMO

This study evaluated the repositioning of the ketolide antibacterial telithromycin (TLT) against the oomycete Pythium insidiosum and verified the combination of TLT and the antimicrobials azithromycin (AZM) and amorolfine hydrochloride (AMR), which have known anti-P. insidiosum activity. Susceptibility tests of P. insidiosum isolates (n = 20) against the drugs were carried out according to CLSI protocol M38-A2, and their combinations were evaluated using the checkerboard microdilution method. The minimum inhibitory concentrations were 0.5-4 µg/mL for TLT, 2-32 µg/mL for AZM, and 16-64 µg/mL for AMR. For the TLT+AZM combination, 52.75 % of interactions were indifferent, 43.44 % were antagonistic, and 9.70 % were synergistic. As for interactions of the TLT+AMR combination, 60.43 % were indifferent, 39.12 % were antagonistic, and 10.44 % synergistic interactions. This study is the first to evaluate the repositioning of the antibacterial TLT against mammalian pathogenic oomycetes, and our results show that its isolated action is superior to its combinations with either AZM or AMR. Therefore, we recommend including TLT in future research to evaluate therapeutic approaches in different clinical forms of human and animal pythiosis.


Assuntos
Cetolídeos , Morfolinas , Pitiose , Pythium , Animais , Humanos , Antifúngicos/farmacologia , Azitromicina/farmacologia , Azitromicina/uso terapêutico , Cetolídeos/farmacologia , Cetolídeos/uso terapêutico , Antibacterianos/farmacologia , Pitiose/tratamento farmacológico , Pitiose/microbiologia , Mamíferos
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