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Review
. 2022 Oct 24:3:1010782.
doi: 10.3389/ffunb.2022.1010782. eCollection 2022.

Fluconazole-resistant Candida parapsilosis: A new emerging threat in the fungi arena

Affiliations
Review

Fluconazole-resistant Candida parapsilosis: A new emerging threat in the fungi arena

Pilar Escribano et al. Front Fungal Biol. .

Abstract

Candida parapsilosis is a leading cause of invasive candidiasis in southern Europe, Latin America and Asia. C. parapsilosis has been mostly considered susceptible to triazoles, but fluconazole resistance is on the rise in some countries. The main mechanism related to fluconazole resistance is the presence of ERG11p substitutions, dominated by the Y132F amino acid substitution. Isolates harbouring this substitution mimic C. auris given that they may cause hospital outbreaks, become endemic, and emerge simultaneously in distant areas around the world. At the moment, Spain is experiencing a brusque emergence of fluconazole resistance in C. parapsilosis; isolates harbouring the Y132F substitution were detected for the first time in 2019. A recent study on Candida spp isolates from blood cultures collected in 16 hospitals located in the Madrid metropolitan area (2019 to 2021) reported that fluconazole resistance in C. parapsilosis reached as high as 13.6%. Resistance rates rose significantly during those three years: 3.8% in 2019, 5.7% in 2020, and 29.1% in 2021; resistant isolates harboured either the dominant Y132F substitution (a single clone found in four hospitals) or G458S (another clone found in a fifth hospital). The COVID-19 pandemic may have increased the number of candidaemia cases. The reason for such an increase might be a consequence of uncontrolled intra-hospital patient-to-patient transmission in some hospitals, as an increase not only in C. parapsilosis candidaemia episodes but also in the spread of clonal fluconazole-resistant isolates might have occurred in other hospitals during the pandemic period. Patients affected with fluconazole-resistant C. parapsilosis harbouring the Y132F substitution presented a mortality rate ranging from 9% to 78%, were mainly admitted to intensive care wards but did not have differential risk factors compared to those infected by susceptible isolates. With scarce exceptions, few patients (≤20%) infected with fluconazole-resistant isolates had previously received fluconazole, thus supporting the fact that, although fluconazole might have been a key factor to promote resistance, the main driver promoting the spread of fluconazole-resistant isolates was patient-to-patient transmission.

Keywords: Candida parapsilosis; ERG11; G458S; K128N; K143R; Y132F; fluconazole; resistance.

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Conflict of interest statement

JG has received funds for participating in educational activities organized on behalf of Pfizer, Gilead, and MSD; he has also received research funds from FIS, Gilead, Scynexis, F2G, and Cidara outside the submitted work. The remaining author declares that the research was conducted in the absence of any commercial or financial relationships that could be constructed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Map indicating the countries in which fluconazole-resistant C. parapsilosis isolates harbouring the Y132F ERG11p substitution were reported (depicted in red) alongside the year of detection of the first isolate.

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