Virulence factors, antifungal susceptibility and molecular mechanisms of azole resistance among Candida parapsilosis complex isolates recovered from clinical specimens

• Published in: Journal of biomedical science Vol. 24; no. 1; p. 67
• Main Authors: Neji, Sourour, Hadrich, Ines, Trabelsi, Houaida, Abbes, Salma, Cheikhrouhou, Fatma, Sellami, Hayet, Makni, Fattouma, Ayadi, Ali
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 04-09-2017; BioMed Central; BMC
• Subjects: Agar; Amphotericin B; Antifungal agents; Antifungal Agents - pharmacology; Azoles; Azoles - pharmacology; Biofilm production; Biofilms; Candida; Candida parapsilosis - drug effects; Candida parapsilosis - genetics; Candida parapsilosis Complex; Caspofungin; Clinical isolates; Complementarity-determining region 1; Drug resistance; Drug Resistance, Fungal - genetics; Efflux; Enzymatic activity; Fluconazole; Flucytosine; Fungicides; Gelatinase; Gene sequencing; Haemolysin; Health aspects; Heterocyclic compounds; Heterogeneity; Humans; Itraconazole; MDR1 protein; Microbial drug resistance; Microbial Sensitivity Tests; Molecular modelling; Nosocomial infections; Observations; Phospholipase; Phospholipases; Polymerase chain reaction; Proteases; Ribosomal DNA; Statistical analysis; Studies; Tunisia; Virulence; Virulence (Microbiology); Virulence factors; Virulence Factors - genetics; Voriconazole; Yeast; Candida parapsilosis Complex; Biofilm production; Haemolysin; Proteases; Virulence factors; Mechanisms of resistance; Antifungal susceptibility; Phospholipases
• ISSN: 1423-0127; 1021-7770; 1423-0127
• DOI: 10.1186/s12929-017-0376-2

The aim of this study was to determine the biofilm formation, the extracellular enzymatic activities of 182 clinical isolates of the Candida parapsilosis complex.
Molecular identification of the C. parapsilosis species complex was performed using PCR RFLP of SADH gene and PCR sequencing of ITS region. The susceptibility of ours isolates to antifungal agents and molecular mechanisms underlying azole resistance were evaluated.
63.5% of C. parapsilosis were phospholipase positive with moderate activity for the majority of strains. None of the C. metapsilosis or C. orthopsilosis isolates was able to produce phospholipase. Higher caseinase activities were detected in C. parapsilosis (Pz = 0.5 ± 0.18) and C. orthopsilosis (Pz = 0.49 ± 0.07) than in C. metapsilosis isolates (Pz = 0.72 ± 0.1). 96.5% of C. parapsilosis strains and all isolates of C. metapsilosis and C. orthopsilosis produced gelatinase. All the strains possessed the ability to show haemolysis on blood agar. C. metapsilosis exhibited the low haemolysin production with statistical significant differences compared to C. parapsilosis and C. orthopsilosis. The biofilm forming ability of C. parapsilosis was highly strain dependent with important heterogeneity, which was less evident with both C. orthopsilosis and C. metapsilosis. Some C. parapsilosis isolates met the criterion for susceptible dose dependent to fluconazole (10.91%), itraconazole (16.36%) and voriconazole (7.27%). Moreover, 5.45% and 1.82% of C. parapsilosis isolates were respectively resistant to fluconazole and voriconazole. All strains of C. metapsilosis and C. orthopsilosis were susceptible to azoles; and isolates of all three species exhibited 100% of susceptibility to caspofungin, amphotericin B and 5-flucytosine.
A combination of molecular mechanisms, including the overexpression of ERG11, and genes encoding efflux pumps (CDR1, MDR1, and MRR1) were involved in azole resistance in C. parapsilosis.