Abstract Background Candida auris is a drug-resistant fungus that poses a growing risk in healthcare environments, particularly among intensive care unit (ICU) patients. While other Candida species routinely colonize the gut, it is unknown if the gastrointestinal (GI) tract is a niche for C. auris. We aimed to determine the presence of C. auris in the gut of ICU patients and evaluate whether these isolates exhibit phenotypic traits that support intestinal colonization.Figure 1.Abbreviations: DCA, deoxycholic acid; ICU, intensive care unit; MALDI-ToF, matrix-assisted laser desorption/ionization-time of flight; WGS, whole genome sequencing.Figure 2.C. auris gut colonization and clinical detection in intensive care unit (ICU) patients. Methods We assessed C. auris gut colonization in ICU patients by collecting stool samples and demographic/clinical information from enrolled patients from 01/2021-06/2024 (Figure 1). Stool samples were cultured on Candida selective media, isolates were identified using MALDI-ToF and their genomes were sequenced. To evaluate bile acid resistance, representative stool isolates of C. auris and C. albicans were exposed to increasing concentrations of the secondary bile acid deoxycholic acid (DCA), and growth was measured over time. Antifungal minimum inhibitory concentrations (MICs) were determined by broth microdilution.Figure 3.Phylogenetic tree of C. auris isolates (Clade III), collected in triplicate from each patient on different days from stool and clinical cultures.Figure 4.Growth of C. auris vs. C. albicans gut colonizing isolates in deoxycholic acid (DCA). Results Of 150 ICU patients enrolled, the mean age was 60.8 ± 15.6 years, 83 (56%) were male, and 24% were Hispanic/Latino. Mean Charlson Comorbidity Index was 4.9 ± 3.0; 34 patients (23%) were solid organ transplant recipients, and 54 (36%) were in shock on ICU admission. C. auris was detected in stool cultures of three patients (2%), of which two had colonization at other body sites (Figure 2). Genomic analysis showed that these isolates were highly clonal and belonged to Clade III (Figure 3). All C. auris isolates were resistant to fluconazole and susceptible to micafungin. When exposed to DCA, C. auris stool isolates exhibited significantly less growth inhibition compared to C. albicans stool isolates. At high (0.3%) DCA concentrations, the mean inhibition rates were 17% for C. auris stool isolates and 66% for C. albicans stool isolates (Figure 4). Conclusion These findings provide evidence of C. auris GI colonization in ICU patients. Moreover, the demonstrated resistance of C. auris stool isolates to DCA highlights its potential adaptive mechanisms for survival in the gut. These findings indicate that the GI tract may be a persistent reservoir for C. auris with implications for transmission and infection control. Disclosures All Authors: No reported disclosures
Pinto et al. (Thu,) studied this question.
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