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FEMS Yeast Res ; 19(6)2019 09 01.
Artigo em Inglês | MEDLINE | ID: mdl-31403663

RESUMO

The commensal species Candida parapsilosis is an emerging human pathogen that has the ability to form biofilms. In this study, we explored the impact of the divalent cations cobalt (Co2+), copper (Cu2+), iron (Fe3+), manganese (Mn2+), nickel (Ni2+) and zinc (Zn2+) on biofilm formation of clinical isolates of C. parapsilosis with no, low and high biofilm forming abilities at 30 and 37°C. All strains besides one isolate showed a concentration-dependent enhancement of biofilm formation at 30°C in the presence of Mn2+ with a maximum at 2 mM. The biofilm forming ability of no and low biofilm forming isolates was >2-fold enhanced in the presence of 2 mM Mn2+, while the effect in high biofilm forming isolate was significantly less pronounced. Of note, cells in the biofilms of no and low biofilm forming strains differentiated into yeast and pseudohyphal cells similar in morphology to high biofilm formers. The biofilm transcriptional activator BCR1 has a dual developmental role in the absence and presence of 2 mM Mn2+ as it promoted biofilm formation of no biofilm forming strains, and, surprisingly, suppressed cells of no biofilm forming strains to develop into pseudohyphae and/or hyphae. Thus, environmental conditions can significantly affect the amount of biofilm formation and cell morphology of C. parapsilosis with Mn2+ to overcome developmental blocks to trigger biofilm formation and to partially relieve BCR1 suppressed cell differentiation.


Assuntos
Biofilmes/crescimento & desenvolvimento , Candida parapsilosis/efeitos dos fármacos , Candidíase/microbiologia , Cátions Bivalentes/farmacologia , Proteínas Fúngicas/metabolismo , Manganês/farmacologia , Biofilmes/efeitos dos fármacos , Candida parapsilosis/citologia , Candida parapsilosis/crescimento & desenvolvimento , Diferenciação Celular/efeitos dos fármacos , Proteínas Fúngicas/genética , Humanos , Hifas/citologia , Hifas/efeitos dos fármacos , Hifas/crescimento & desenvolvimento , Deleção de Sequência , Fatores de Transcrição/genética , Fatores de Transcrição/metabolismo
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