Abstract
Rapid and accurate differentiation of Salmonella spp. causing enteric fever from nontyphoidal Salmonella is essential for clinical management of cases, laboratory risk management, and implementation of public health measures. Current methods used for confirmation of identification, including biochemistry and serotyping as well as whole-genome sequencing analyses, take several days. Here we report the development and evaluation of a real-time PCR assay that can be performed directly on crude DNA extracts from bacterial colonies for the rapid identification of typhoidal and nontyphoidal Salmonella.
Original language | English |
---|---|
Article number | e00167-19 |
Journal | Journal of Clinical Microbiology |
Volume | 57 |
Issue number | 8 |
DOIs | |
Publication status | Published - 2019 |
Bibliographical note
Funding Information:We thank Sarah Alexandra and Julie Russell from the National Collection of Type Cultures for providing positive-control strains. We also thank Lailanie Aqunino from GBRU for support in undertaking PCR. We have no conflict of interest to declare. This study was funded by PHE.
Publisher Copyright:
© Crown copyright 2019.
Keywords
- Nontyphoidal salmonellae
- Real-time PCR
- Salmonella
- Typhoidal salmonellae
- Whole-genome sequencing