First experience of implementing Candida auris real-time PCR for surveillance in the UK: detection of multiple introductions with two international clades and improved patient outcomes
Autor: | S K, Taori, J, Rhodes, K, Khonyongwa, A, Szendroi, M, Smith, A M, Borman, J, Kumarage, C S, Brown, G, Moore, N, Desai |
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Přispěvatelé: | Wellcome Trust |
Rok vydání: | 2022 |
Předmět: |
Microbiology (medical)
Antifungal Agents Epidemiology Candidiasis 1103 Clinical Sciences General Medicine Candida auris Real-Time Polymerase Chain Reaction United Kingdom 1117 Public Health and Health Services Infectious Diseases Multi-drug-resistant candida Risk reduction Humans Emerging fungi Phylogeny Candida |
Zdroj: | Journal of Hospital Infection. 127:111-120 |
ISSN: | 0195-6701 |
DOI: | 10.1016/j.jhin.2022.06.009 |
Popis: | Background: Candida auris has been associated with rapid transmission and high mortality. A novel PCR based surveillance programme was initiated at a London teaching hospital from January 2018. The results of this implementation until March 2019 are presented along with the clinical, transmission and phylogenetic characteristics encountered in that setting. Methods: A real time-PCR assay for C auris was developed, validated, and implemented for direct use on skin swabs and urine. Environmental swabs were also tested by PCR as an emergency outbreak control measure. Clinical risk factors and outcomes of patients were determined. Environmental dispersal was assessed using 24 h settle plate cultures around 9 colonised patients followed by air sampling around one colonised patient during high and low turbulence activities. Sequencing was performed using Illumina HiSeq and maximum likelihood phylogenies were constructed using rapid bootstrap analysis. Results 21 C. auris colonised patients were identified. Median turnaround time of colonisation detection reduced from 141 h (5.8 d) to approximately 24 h enabling rapid infection control precautions. Settle plates detected 70 to 600 CFU/m2 around colonised patients over 24 h and air sampling suggested dispersal during turbulent activities. C. auris DNA was detected from 35.7% environmental swabs. Despite being in a high-risk setting, no patients developed invasive infection. Sequencing analysis of isolates from this centre identified two introductions of the South Asian (Clade I) and one of the South African (Clade III) strain. Conclusion: The PCR offers a rapid, scalable method of screening and supports clinical risk reduction in settings likely to encounter multiple introductions. |
Databáze: | OpenAIRE |
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