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An Azole-Resistant Candida parapsilosis Outbreak: Clonal Persistence in the Intensive Care Unit of a Brazilian
Danilo Yamamoto Thomaz1, João Nobrega de Almeida1,2, Glaucia Moreira Espindola Lima3
1Laboratory of Medical Mycology-LIM-53, Clinical Dermatology Division, Hospital das Clínicas FMUSP and Instituto de Medicina Tropical de São Paulo, Universidade de São Paulo, São Paulo, Brazil.
Abstract:
The incidence of candidemia by the Candida parapsilosis complex has increased considerably in recent decades, frequently related to use of indwelling intravascular catheters. The ability of this pathogen to colonize healthcare workers (HCW)' hands, and to form biofilm on medical devices has been associated with the occurrence of nosocomial outbreaks and high mortality rates. Fluconazole has been the leading antifungal drug for the treatment of invasive candidiasis in developing countries. However, azole-resistant C. parapsilosis isolates are emerging worldwide, including in Brazil. Few studies have correlated outbreak infections due to C. parapsilosis with virulence factors, such as biofilm production. We thus conducted a microbiological investigation of C. parapsilosis complex isolates from a Brazilian teaching hospital. Additionally, we identified a previously unrecognized outbreak caused by a persistent azole-resistant C. parapsilosis (sensu stricto) clone in the intensive care unit (ICU), correlating it with the main clinical data from the patients with invasive candidiasis. The molecular identification of the isolates was carried out by PCR-RFLP assay; antifungal susceptibility and biofilm formation were also evaluated. The genotyping of all C. parapsilosis (sensu stricto) was performed by microsatellite analysis and the presence of ERG11 mutations was assessed in the azole non-susceptible isolates. Fourteen C. parapsilosis (sensu stricto) isolates were recovered from patients with invasive candidiasis, eight being fluconazole and voriconazole-resistant, and two intermediate only to fluconazole (FLC). All non-susceptible isolates showed a similar pattern of biofilm formation with low biomass and metabolic activity. The A395T mutation in ERG11 was detected exclusively among the azole-resistant isolates. According to the microsatellite analysis, all azole non-susceptible isolates from the adult ICU were clustered together indicating the occurrence of an outbreak. Regarding clinical data, all patients infected by the clonal non-susceptible isolates and none of the patients infected by the susceptible isolates had been previously exposed to corticosteroids (p = 0.001), while the remaining characteristics showed no statistical significance. The current study revealed the persistence of an azole non-susceptible C. parapsilosis clone with low capacity to form biofilm over two years in the adult ICU. These results reinforce the need of epidemiological surveillance and monitoring antifungal susceptibility of C. parapsilosis isolates in hospital wards.
Insights
An azole-resistant Candida parapsilosis clone caused a persistent outbreak in an intensive care unit (ICU). This clone showed low biofilm formation and was linked to corticosteroid use in patients with invasive candidiasis.
Area of Science:
- Medical Mycology
- Infectious Diseases
- Molecular Epidemiology
Background:
- The incidence of candidemia caused by the Candida parapsilosis complex has risen, often linked to indwelling catheters and healthcare worker transmission.
- Candida parapsilosis exhibits biofilm formation on medical devices and azole resistance, contributing to nosocomial outbreaks and high mortality.
- Azole resistance in C. parapsilosis is a growing global concern, particularly in developing countries where fluconazole is a primary treatment.
Purpose of the Study:
- To investigate Candida parapsilosis complex isolates from a Brazilian teaching hospital.
- To identify and characterize an unrecognized outbreak of azole-resistant C. parapsilosis (sensu stricto) in an intensive care unit (ICU).
- To correlate the outbreak with clinical data and virulence factors like biofilm production.
Main Methods:
- Molecular identification using PCR-RFLP.
- Antifungal susceptibility testing and biofilm formation assays.
- Genotyping by microsatellite analysis and assessment of ERG11 mutations in resistant isolates.
Main Results:
- Fourteen C. parapsilosis (sensu stricto) isolates were recovered; eight were resistant to fluconazole and voriconazole.
- Azole-resistant isolates exhibited low biofilm biomass and metabolic activity.
- Microsatellite analysis confirmed an outbreak of azole-non-susceptible C. parapsilosis in the adult ICU, linked to corticosteroid exposure (p = 0.001).
Conclusions:
- A persistent azole-non-susceptible C. parapsilosis clone with low biofilm-forming capacity was identified in an ICU over two years.
- The study highlights the need for continuous epidemiological surveillance and antifungal susceptibility monitoring of C. parapsilosis in hospital settings.
- The findings underscore the emergence of drug-resistant fungal pathogens and the importance of understanding their virulence and transmission dynamics.
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