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Whole Genome Sequencing of Candida glabrata for Detection of Markers of Antifungal Drug Resistance
Published on: December 28, 2017
Evaluation of outbreak persistence caused by multidrug-resistant and echinocandin-resistant Candida parapsilosis
Farnaz Daneshnia1,2, Daniel J Floyd1, Adam P Ryan3
1Division of Infectious Diseases, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Abstract:
Candida parapsilosis is known to cause severe and persistent outbreaks in clinical settings. Patients infected with multidrug-resistant C. parapsilosis (MDR Cp) isolates were identified in a large Turkish hospital from 2017-2020. We subsequently identified three additional patients infected with MDR Cp isolates in 2022 from the same hospital and two echinocandin-resistant (ECR) isolates from a single patient in another hospital. The increasing number of MDR and ECR isolates contradicts the general principle that the severe fitness cost associated with these phenotypes could prevent their dominance in clinical settings. Here, we employed a multidimensional approach to systematically assess the fitness costs of MDR and ECR C. parapsilosis isolates. Whole-genome sequencing revealed a novel MDR genotype infecting two patients in 2022. Despite severe in vitro defects, the levels and tolerances of the biofilms of our ECR and MDR isolates were generally comparable to those of susceptible wild-type isolates. Surprisingly, the MDR and ECR isolates showed major alterations in their cell wall components, and some of the MDR isolates consistently displayed increased tolerance to the fungicidal activities of primary human neutrophils and were more immunoevasive during exposure to primary human macrophages. Our systemic infection mouse model showed that MDR and ECR C. parapsilosis isolates had comparable fungal burden in most organs relative to susceptible isolates. Overall, we observed a notable increase in the genotypic diversity and frequency of MDR isolates and identified MDR and ECR isolates potentially capable of causing persistent outbreaks in the future.
Insights
Multidrug-resistant and echinocandin-resistant Candida parapsilosis (MDR Cp and ECR Cp) show increased virulence despite predicted fitness costs. These resistant strains exhibit enhanced immune evasion and tolerance, posing a future outbreak risk.
Area of Science:
- Mycology
- Infectious Diseases
- Antimicrobial Resistance
Background:
- Candida parapsilosis causes severe hospital outbreaks, with increasing multidrug-resistant (MDR) and echinocandin-resistant (ECR) isolates observed.
- The dominance of MDR and ECR isolates challenges the assumption of significant fitness costs associated with these resistance phenotypes.
Purpose of the Study:
- To systematically assess the fitness costs and pathogenic potential of MDR and ECR Candida parapsilosis isolates.
- To investigate the genotypic diversity and clinical implications of resistant C. parapsilosis strains.
Main Methods:
- Whole-genome sequencing to identify novel MDR genotypes.
- In vitro assessment of biofilm formation, cell wall components, and tolerance to human immune cells (neutrophils and macrophages).
- In vivo systemic infection mouse model to evaluate fungal burden.
Main Results:
- A novel MDR genotype was identified. Despite in vitro defects, MDR and ECR isolates showed comparable biofilm levels and tolerances.
- Significant alterations in cell wall components were observed in resistant isolates.
- MDR isolates exhibited increased tolerance to neutrophils and enhanced immunoevasiveness against macrophages; in vivo fungal burden was comparable to susceptible isolates.
Conclusions:
- MDR and ECR Candida parapsilosis isolates possess mechanisms for immune evasion and tolerance, potentially explaining their clinical success despite fitness costs.
- Increased genotypic diversity and frequency of MDR isolates suggest a potential for future persistent outbreaks.
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