4.8 Article

Integrated genomic, epidemiologic investigation of Candida auris skin colonization in a skilled nursing facility

Journal

NATURE MEDICINE
Volume 27, Issue 8, Pages 1401-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41591-021-01383-w

Keywords

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Funding

  1. CDC [75D30118C02900]
  2. NIH National Institute of Arthritis and Musculoskeletal and Skin Diseases
  3. National Human Genome Research Institute

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Longitudinal skin sampling in a skilled nursing facility revealed persistent niches of Candida auris, highlighting the importance of universal strategies to reduce its transmission. High concentrations of CHG were associated with suppressing C. auris growth without perturbing commensal microbes, providing insights into skin fungal community alterations as modifiable risk factors for C. auris acquisition and persistence. Failure to detect the extensive, disparate niches of C. auris colonization may reduce the effectiveness of infection-prevention measures, emphasizing the need for broader approaches.
Longitudinal skin site sampling of residents in a skilled nursing facility sheds light on persistent niches of the emerging fungal pathogen Candida auris. Candida auris is a fungal pathogen of high concern due to its ability to cause healthcare-associated infections and outbreaks, its resistance to antimicrobials and disinfectants and its persistence on human skin and in the inanimate environment. To inform surveillance and future mitigation strategies, we defined the extent of skin colonization and explored the microbiome associated with C. auris colonization. We collected swab specimens and clinical data at three times points between January and April 2019 from 57 residents (up to ten body sites each) of a ventilator-capable skilled nursing facility with endemic C. auris and routine chlorhexidine gluconate (CHG) bathing. Integrating microbial-genomic and epidemiologic data revealed occult C. auris colonization of multiple body sites not targeted commonly for screening. High concentrations of CHG were associated with suppression of C. auris growth but not with deleterious perturbation of commensal microbes. Modeling human mycobiome dynamics provided insight into underlying alterations to the skin fungal community as a possible modifiable risk factor for acquisition and persistence of C. auris. Failure to detect the extensive, disparate niches of C. auris colonization may reduce the effectiveness of infection-prevention measures that target colonized residents, highlighting the importance of universal strategies to reduce C. auris transmission.

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