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Antibiotics stimulates the development of persistent cells in biofilms of Candida albicans bloodstream isolates.

Fernando Victor Monteiro PortelaAna Raquel Colares de AndradeLívia Maria Galdino PereiraBruno Nascimento da SilvaPaulo Henrique Soares PeixotoBruno Rocha AmandoNicole de Mello FiallosPedro de Freitas Santos Manzi de SouzaReginaldo Gonçalves de Lima-NetoGlaucia Morgana de Melo GuedesDébora de Souza Collares Maia Castelo-BrancoRossana de Aguiar Cordeiro
Published in: Biofouling (2024)
Candida albicans invasive candidiasis is considered a global health problem. In such cases, biofilm formation on implanted devices represents a therapeutic challenge and the presence of metabolically inactive persistent cells (PCs) in these communities increases their tolerance to fungicidal drugs. This study investigated the influence of amoxicillin, AMX; cefepime, CEF; gentamicin, GEN; amikacin, AMK; vancomycin, VAN; and ciprofloxacin, CIP; on the production of PCs in biofilms of C. albicans bloodstream isolates. 48 h-mature biofilms ( n  = 6) grown in RPMI-1640 supplemented with antibiotics were treated with 100 μg ml -1 amphotericin B and then evaluated for PCs. Biofilms grown in the presence of antibiotics produced more PCs, up to 10×, when exposed to AMX and CIP; 5 × to CEF; and 6 × to GEN and VAN. The results indicate that antibiotics can modulate PC production in C. albicans biofilms. This scenario may have clinical repercussions in immunocompromised patients under broad-spectrum antibiotic therapy.
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