Description:
CDC researchers have developed a bead-based nucleic acid assay for serotyping members of the
Salmonella genus; this assay will identify serotypes for approximately 95% of all human-obtained
Salmonella isolates in the United States.
Presently, production and quality control for the more than 250 antisera required to cover the >2,500 known serotypes using current methods is difficult, expensive and laborious. Many clinical
Salmonella isolates can require three to five days to determine serotype, delaying conclusive serotype identification and postponing alerts to public health monitoring programs. To that end, this new assay provides improved diagnostic identification and discrimination as well as reducing reagent consumption and technician labor. The assay has been developed and optimized in parallel with traditional serotyping methods on a panel of 368 isolates that represents all subspecies/serogroup combinations in the current Kauffmann-White
Salmonella classification scheme, and the assay has been shown to be more specific than traditional molecular assay formats. This diagnostic assay will improve the rate and accuracy of
Salmonella detection serotyping within human, animal, food and environmental samples.