| Literature DB >> 30801778 |
Ausaf Ahmad1, Jonathan E Spencer1, Shawn R Lockhart2, Sabrina Singleton2, David J Petway1, Dennis A Bagarozzi1, Owen T Herzegh1.
Abstract
Candida auris is an emerging multidrug-resistant yeast associated with invasive infection in healthcare settings. Recently, C auris cases in the United States have been detected in 11 states with the majority of cases in New York, New Jersey and Illinois. Rapid and accurate identification of C auris is critical for patient care and the implementation of public health measures to control the spread of infection. Our aim was to develop and validate a rapid DNA extraction method using the Roche MagNA Pure 96 instrument and a TaqMan real-time PCR assay for reliable, high-throughput identification of C auris. We evaluated 247 patient dermal swab samples previously analysed by culture/MALDI-TOF. The diagnostic sensitivity and specificity were 93.6% and 97.2%, respectively. The assay was highly reproducible with a detection limit of 1 C auris CFU/10 μL. A receiver operating characteristic curve analysis of the real-time PCR data showed an area of 0.982 under the curve, with a CT cut-off value of ≤37.0. The turnaround time from DNA extraction to real-time PCR results was approximately 200 samples/day. In conclusion, we successfully validated a rapid and high-throughput method for accurate and reproducible identification of C auris with a significantly reduced turnaround time compared to culture/MALDI-TOF based methods. Published 2019. This article is a U.S. Government work and is in the public domain in the USA.Entities:
Keywords: zzm321990Candida auriszzm321990; TaqMan real-time PCR; high-throughput rapid DNA extraction
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Year: 2019 PMID: 30801778 DOI: 10.1111/myc.12907
Source DB: PubMed Journal: Mycoses ISSN: 0933-7407 Impact factor: 4.377