Detection of toxins in patients with gastroenteritis has increasingly been accomplished through the use of enteric multiplex syndromic panels. Comparisons of the performance of these panels to both direct-from-stool (DFS) and culture-enriched stools followed by polymerase chain reaction (PCR) methods in pediatric populations are limited. Here, we compare the performance of the Luminex xTAG Gastrointestinal Pathogen Panel (GPP) to our DFS in-house real-time PCR (DFS RT-PCR) assay for the detection of toxin gene, , using 2641 stool specimens collected from children enrolled in the Alberta Provincial Pediatric EnTeric Infection Team (APPETITE) study in Alberta, Canada. We used culture enrichment followed by in-house RT-PCR to resolve discordant results between the two assays. We found excellent agreement ( = 0.89) between the GPP and our DFS RT-PCR assay: the positive percent agreement between the two assays was 97%, and the negative percent agreement was 99%. GPP, a multi-analyte platform can easily be implemented into a routine diagnostic laboratory for detecting enteric pathogens including .

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9693576PMC
http://dx.doi.org/10.3390/microorganisms10112214DOI Listing

Publication Analysis

Top Keywords

luminex xtag
8
xtag gastrointestinal
8
gastrointestinal pathogen
8
pathogen panel
8
real-time pcr
8
detection toxin
8
gpp dfs
8
dfs rt-pcr
8
rt-pcr assay
8
percent agreement
8

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!