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Applied and Environmental Microbiology, May 2007, p. 2891-2896, Vol. 73, No. 9
0099-2240/07/$08.00+0     doi:10.1128/AEM.02234-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

SYBR Green Real-Time PCR Method To Detect Clostridium botulinum Type A{triangledown}

Lucia Fenicia,1 Fabrizio Anniballi,1 Dario De Medici,2* Elisabetta Delibato,2 and Paolo Aureli1

National Reference Centre for Botulism,1 Unit of Microbiological Food-Borne Hazards, National Centre for Food Quality and Risk Assessment, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy2

Received 22 September 2006/ Accepted 26 February 2007

Botulinum toxins (BoNTs) are classically produced by Clostridium botulinum but rarely also from neurotoxigenic strains of Clostridium baratii and Clostridium butyricum. BoNT type A (BoNT/A), BoNT/B, BoNT/E, and very rarely BoNT/F are mainly responsible for human botulism. Standard microbiological methods take into consideration only the detection of C. botulinum. The presumptive identification of the toxigenic strains together with the typing of BoNT has to be performed by mouse bioassay. The development of PCR-based methods for the detection and typing of BoNT-producing clostridia would be an ideal alternative to the mouse bioassay. The objective of this study was to develop a rapid and robust real-time PCR method for detecting C. botulinum type A. Four different techniques for the extraction and purification of DNA from cultured samples were initially compared. Of the techniques used, Chelex 100, DNeasy tissue kit, InstaGene matrix DNA, and boiling, the boiling technique was significantly less efficient than the other three. These did not give statistically different results, and Chelex 100 was chosen because it was less expensive than the others. In order to eliminate any false-negative results, an internal amplification control was synthesized and included in the amplification mixture according to ISO 22174. The specificity of the method was tested against 75 strains of C. botulinum type A, 4 strains of C. botulinum type Ab, and 101 nontarget strains. The detection limit of the reaction was less than 6 x 101 copies of C. botulinum type A DNA. The robustness of the method was confirmed using naturally contaminated stool specimens to evaluate the tolerance of inhibitor substances. SYBR green real-time PCR showed very high specificity for the detection of C. botulinum types A and Ab (inclusivity and exclusivity, 100%).

* Corresponding author. Mailing address: Centre for Food Quality and Risk Assessment, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy. Phone: 39 06 4990 2477. Fax: 39 06 4990 2045. E-mail: dario.demedici{at}iss.it

{triangledown} Published ahead of print on 16 March 2007.

Applied and Environmental Microbiology, May 2007, p. 2891-2896, Vol. 73, No. 9
0099-2240/07/$08.00+0     doi:10.1128/AEM.02234-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.



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  • Artin, I., Bjorkman, P., Cronqvist, J., Radstrom, P., Holst, E. (2007). First Case of Type E Wound Botulism Diagnosed Using Real-Time PCR. J. Clin. Microbiol. 45: 3589-3594 [Abstract] [Full Text]  


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