A RSI-PCR assay was developed for the detection of a Bacillus anthracis-specific nonsense mutation in the plcR gene. The assay specificity was tested using 170 Bacillus spp. strains including 47 strains of B. anthracis. The plcR RSI-PCR distinguished Bacillus cereus group strains closely related to B. anthracis from the anthrax agent. The assay was found to be a robust, simple and cost effective tool for B. anthracis identification. In contrast to previously developed real time PCR-based methods, the RSI-PCR needs basic molecular biology equipment only, and thus may be easily introduced in developing countries, where anthrax is endemic. © 2007 Federation of European Microbiological Societies.
CITATION STYLE
Gierczyński, R., Zasada, A. A., Raddadi, N., Merabishvili, M., Daffonchio, D., Rastawicki, W., & Jagielski, M. (2007). Specific Bacillus anthracis identification by a plcR-targeted restriction site insertion-PCR (RSI-PCR) assay. FEMS Microbiology Letters, 272(1), 55–59. https://doi.org/10.1111/j.1574-6968.2007.00741.x
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