Development of a PCR Lateral Flow Assay for Rapid Detection of Bacillus anthracis, the Causative Agent of Anthrax
Autor: | Swati Banger, Ajay Kumar Goel, Nagesh K. Tripathi, Vijai Pal |
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Rok vydání: | 2021 |
Předmět: |
0106 biological sciences
Anthrax toxin Bioengineering 01 natural sciences Applied Microbiology and Biotechnology Biochemistry law.invention 03 medical and health sciences chemistry.chemical_compound Plasmid law 010608 biotechnology Molecular Biology Gene 030304 developmental biology Gel electrophoresis 0303 health sciences biology Chemistry biology.organism_classification Molecular biology Bacillus anthracis genomic DNA Recombinant DNA DNA Biotechnology |
Zdroj: | Molecular Biotechnology. 63:702-709 |
ISSN: | 1559-0305 1073-6085 |
DOI: | 10.1007/s12033-021-00335-6 |
Popis: | Bacillus anthracis, the causative agent of anthrax is one of the most potent listed biological warfare agents. The conventional microbiological methods of its detection are labor intensive and time consuming, whereas molecular assays are fast, sensitive and specific. PCR is one of the most reliable diagnostic tools in molecular biology. The combination of PCR with lateral flow strips can reduce the diagnostic/detection time. It gives an alternative to gel electrophoresis and offers easy and clear interpretation of results. In the present study, a PCR Lateral flow (PCR-LF) assay targeting cya gene present on pXO1 plasmid of B. anthracis has been developed. The forward and reverse primers were tagged with 6-carboxyflourescein (6-FAM) and biotin, respectively, at 5′ end. The dual labeled PCR products were detected using lateral flow (LF) strips developed in this study. The PCR-LF assay could detect ≥ 5 pg of genomic DNA and ≥ 500 copies of target DNA harboured in a recombinant plasmid. The assay was able to detect as few as 103 and 10 CFU/mL of B. anthracis Sterne cells spiked in human blood after 6 and 24 h of enrichment, respectively. |
Databáze: | OpenAIRE |
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