Genomic analysis of Candida auris transmission within an urban region

<i>Candida auris</i> emerged in Chicago, IL, USA, in 2016 and has since become endemic. We used whole-genome sequencing (WGS) of 494 isolates, epidemiologic metadata and patient transfer data to describe the transmission of <i>C. auris</i> among Chicago healthcare facilities between 2016 and 2021. In total, 99% of isolates formed a single clade IV phylogenetic lineage, suggesting a single introduction. The remaining isolates were clade III. Isolates were grouped into genomic clusters based on phylogenetic clustering and relatedness. Isolates from 14 facilities were included in 77 genomic clusters with evidence of inter- and intra-facility transmission; 62% of isolates included in genomic clusters clustered with another from the same facility. Patient transfer data corroborated transmission among facilities in large genomic clusters, and patient transfers between facilities correlated with more similar genomes. In total, 30% of individuals who had serial samples collected over time had isolates collected during different facility stays. Most of these individuals carried closely related isolates over time, although 25% carried isolates whose genomes diverged. Integrating WGS data and patient metadata to describe inter- and intra-facility clusters revealed regional transmission patterns within and between healthcare facilities that could be used to guide targeted interventions to prevent transmission. Given that patient transfer data were concordant with WGS analysis, they may serve as a predictive tool for risk of inter-facility transmission.

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Publication Details

Journal
Microbial Genomics
Published
2025-09-10
DOI
https://doi.org/10.1099/mgen.0.001478
Citations
1
Primary Topic
Antifungal resistance and susceptibility
Type
article
Field-Weighted Citation Impact
1.40
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article

Genomic analysis of Candida auris transmission within an urban region

Hannah J. Barbian, Ann Valley, Hira Adil, Stefan J. Green et al.
1 citations
Microbial Genomics
Antifungal resistance and susceptibility
1.40
article

Genomic analysis of Candida auris transmission within an urban region

Hannah J. Barbian, Ann Valley, Hira Adil, Stefan J. Green, Kelly Walblay, Mary K. Hayden, Erin Newcomer, Christy Zelinski, Stephanie R. Black, Alyse Kittner, Do Young ‍Kim
article en
1 citations

Abstract

<i>Candida auris</i> emerged in Chicago, IL, USA, in 2016 and has since become endemic. We used whole-genome sequencing (WGS) of 494 isolates, epidemiologic metadata and patient transfer data to describe the transmission of <i>C. auris</i> among Chicago healthcare facilities between 2016 and 2021. In total, 99% of isolates formed a single clade IV phylogenetic lineage, suggesting a single introduction. The remaining isolates were clade III. Isolates were grouped into genomic clusters based on phylogenetic clustering and relatedness. Isolates from 14 facilities were included in 77 genomic clusters with evidence of inter- and intra-facility transmission; 62% of isolates included in genomic clusters clustered with another from the same facility. Patient transfer data corroborated transmission among facilities in large genomic clusters, and patient transfers between facilities correlated with more similar genomes. In total, 30% of individuals who had serial samples collected over time had isolates collected during different facility stays. Most of these individuals carried closely related isolates over time, although 25% carried isolates whose genomes diverged. Integrating WGS data and patient metadata to describe inter- and intra-facility clusters revealed regional transmission patterns within and between healthcare facilities that could be used to guide targeted interventions to prevent transmission. Given that patient transfer data were concordant with WGS analysis, they may serve as a predictive tool for risk of inter-facility transmission.

Microbial GenomicsVol. 11(9)
Rush University Medical Center (US), Chicago Department of Public Health (US)
Openalex Percentile: Top 16%
Antifungal resistance and susceptibility
1.40
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