Literature DB >> 33978150

Positive correlation between Candida auris skin-colonization burden and environmental contamination at a ventilator-capable skilled nursing facility in Chicago.

D Joseph Sexton1, Meghan L Bentz1, Rory M Welsh1, Gordana Derado2, William Furin3, Laura J Rose3, Judith Noble-Wang3, Massimo Pacilli4, Tristan D McPherson4,5, Stephanie Black4, Sarah K Kemble4, Owen Herzegh6, Ausaf Ahmad6, Kaitlin Forsberg1, Brendan Jackson1, Anastasia P Litvintseva1.   

Abstract

BACKGROUND: Candida auris is an emerging multidrug-resistant yeast that contaminates healthcare environments causing healthcare-associated outbreaks. The mechanisms facilitating contamination are not established.
METHODS: C. auris was quantified in residents' bilateral axillary/inguinal composite skin swabs and environmental samples during a point-prevalence survey at a ventilator-capable skilled-nursing facility (vSNF A) with documented high colonization prevalence. Environmental samples were collected from all doorknobs, windowsills and handrails of each bed in 12 rooms. C. auris concentrations were measured using culture and C. auris-specific qPCR. The relationship between C. auris concentrations in residents' swabs and associated environmental samples were evaluated using Kendall's tau-b (τb) correlation coefficient.
RESULTS: C. auris was detected in 70 /100 tested environmental samples and 31/ 57 tested resident skin swabs. The mean C. auris concentration in skin swabs was 1.22 x 10 5 cells/mL by culture and 1.08 x 10 6 cells/mL by qPCR. C. auris was detected on all handrails of beds occupied by colonized residents, as well as 10/24 doorknobs and 9/12 windowsills. A positive correlation was identified between the concentrations of C. auris in skin swabs and associated handrail samples based on culture (τb = 0.54, p = 0.0004) and qPCR (τb = 0.66, p = 3.83e -6). Two uncolonized residents resided in beds contaminated with C. auris.
CONCLUSIONS: Colonized residents can have high C. auris burdens on their skin, which was positively related with contamination of their surrounding healthcare environment. These findings underscore the importance of hand hygiene, transmission-based precautions, and particularly environmental disinfection in preventing spread in healthcare facilities.
© The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America.

Entities:  

Keywords:  zzm321990 Candida auriszzm321990 ; HAI; fungi; infection control; transmission

Year:  2021        PMID: 33978150     DOI: 10.1093/cid/ciab327

Source DB:  PubMed          Journal:  Clin Infect Dis        ISSN: 1058-4838            Impact factor:   9.079


  4 in total

Review 1.  Tools for Detecting a "Superbug": Updates on Candida auris Testing.

Authors:  Shawn R Lockhart; Meghan M Lyman; D Joseph Sexton
Journal:  J Clin Microbiol       Date:  2022-01-05       Impact factor: 11.677

2.  In vivo emergence of high-level resistance during treatment reveals the first identified mechanism of amphotericin B resistance in Candida auris.

Authors:  Jeffrey M Rybak; Katherine S Barker; José F Muñoz; Josie E Parker; Suhail Ahmad; Eiman Mokaddas; Aneesa Abdullah; Rehab S Elhagracy; Steve L Kelly; Christina A Cuomo; P David Rogers
Journal:  Clin Microbiol Infect       Date:  2021-12-13       Impact factor: 13.310

3.  Impact of Erg11 Amino Acid Substitutions Identified in Candida auris Clade III Isolates on Triazole Drug Susceptibility.

Authors:  Benjamin Williamson; Adam Wilk; Kevin D Guerrero; Timothy D Mikulski; Tony N Elias; Indira Sawh; Geselle Cancino-Prado; Dianne Gardam; Christopher H Heath; Nelesh P Govender; David S Perlin; Milena Kordalewska; Kelley R Healey
Journal:  Antimicrob Agents Chemother       Date:  2021-10-11       Impact factor: 5.938

4.  Modeling Candida auris skin colonization: Mice, swine, and humans.

Authors:  Emily F Eix; Jeniel E Nett
Journal:  PLoS Pathog       Date:  2022-09-08       Impact factor: 7.464

  4 in total

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