Specific Bacillus anthracis identification by a plcR-targeted restriction site insertion-PCR (RSI-PCR) assay

14Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.

Abstract

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.

Author supplied keywords

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free