Performance characteristics of an automated, high-throughput RT-PCR assay for the detection of on 3-point and nasal swabs.

UNLABELLED

is a multidrug-resistant yeast responsible for invasive infections with high mortality rates, primarily spread through prolonged colonization on biotic and abiotic surfaces and traveling. Effective control necessitates comprehensive screening protocols, as recommended by the Centers for Disease Control and Prevention, which endorses a real-time polymerase chain reaction-based assay for screening. This study evaluates the performance of this assay on the Hologic Panther Fusion System using nasal and 3-point swab specimens (nares/axilla/groin) compared with culture. The assay was assessed for accuracy, sensitivity, specificity, and reproducibility, alongside an evaluation of probe primer reagent (PPR) onboard stability over 30 working days. Analytical sensitivity studies determined limits of detection of 1.95 Log CFU/mL for nasal swabs and 2.18 Log CFU/mL for 3-point swabs, both with >95.0% confidence intervals. The assay demonstrated 100% specificity ( = 25), with no false positives from genetically similar or clinically relevant species, and no significant interference from co-infecting microbes on cycle threshold (CT) values. Both swab types exhibited high intra- and inter-reproducibility, with low coefficients of variation (1.79% and 1.06%, respectively). The assay detected in 100% of 108 spiked-positive samples across both swab types. Clinical analysis showed 100% concordance with culture for 3-point swabs. Additionally, the nasal swab method showed 96.0% overall agreement, with 86.2% sensitivity and 100.0% specificity. The PPR mixes remained stable over 30 working days, with no significant CT value changes. This study confirms the assay's robust sensitivity, specificity, reproducibility, and accuracy for both nasal and 3-point screening swabs.

IMPORTANCE

is a multidrug-resistant yeast responsible for severe infections with high mortality rates. Rapid and accurate detection is critical for preventing the spread of this pathogen in healthcare settings. This study assesses the performance of an automated real-time PCR screening assay for detecting s using nasal and 3-point swabs. The findings demonstrate the assay's high sensitivity, specificity, and reproducibility, making it a valuable tool for infection control. By providing a reliable and efficient screening method, this assay can significantly enhance efforts to control outbreaks, ultimately improving patient outcomes and reducing the spread of this dangerous pathogen.