TY - JOUR
T1 - A multiplex real-time PCR for identifying and differentiating B. anthracis virulent types
AU - Wielinga, Peter
AU - Hamidjaja, Raditijo A.
AU - Ågren, Joakim
AU - Knutsson, Rickard
AU - Segerman, Bo
AU - Fricker, Martina
AU - Ehling-Schulz, Monika
AU - de Groot, Astrid
AU - Burton, Jane
AU - Brooks, Tim
AU - Janse, Ingmar
AU - van Rotterdam, Bart
PY - 2011
Y1 - 2011
N2 - Bacillus anthracis is closely related to the endospore forming bacteria Bacillus cereus and Bacillus thuringiensis. For accurate detection of the life threatening pathogen B. anthracis, it is essential to distinguish between these three species. Here we present a novel multiplex real-time PCR for simultaneous specific identification of B. anthracis and discrimination of different B. anthracis virulence types. Specific B. anthracis markers were selected by whole genome comparison and different sets of primers and probes with optimal characteristic for multiplex detection of the B. anthracis chromosome, the B. anthracis pXO1 and pXO2 plasmids and an internal control (IC) were designed. The primer sets were evaluated using a panel of B. anthracis strains and exclusivity was tested using genetically closely related B. cereus strains. The robustness of final primer design was evaluated by laboratories in three different countries using five different real-time PCR thermocyclers. Testing of a panel of more than 20 anthrax strains originating from different locations around the globe, including the recent Swedish anthrax outbreak strain, showed that all strains were detected correctly.
AB - Bacillus anthracis is closely related to the endospore forming bacteria Bacillus cereus and Bacillus thuringiensis. For accurate detection of the life threatening pathogen B. anthracis, it is essential to distinguish between these three species. Here we present a novel multiplex real-time PCR for simultaneous specific identification of B. anthracis and discrimination of different B. anthracis virulence types. Specific B. anthracis markers were selected by whole genome comparison and different sets of primers and probes with optimal characteristic for multiplex detection of the B. anthracis chromosome, the B. anthracis pXO1 and pXO2 plasmids and an internal control (IC) were designed. The primer sets were evaluated using a panel of B. anthracis strains and exclusivity was tested using genetically closely related B. cereus strains. The robustness of final primer design was evaluated by laboratories in three different countries using five different real-time PCR thermocyclers. Testing of a panel of more than 20 anthrax strains originating from different locations around the globe, including the recent Swedish anthrax outbreak strain, showed that all strains were detected correctly.
U2 - 10.1016/j.ijfoodmicro.2010.07.039
DO - 10.1016/j.ijfoodmicro.2010.07.039
M3 - Journal article
C2 - 20826037
SN - 0168-1605
VL - 145
SP - 137
EP - 144
JO - International Journal of Food Microbiology
JF - International Journal of Food Microbiology
IS - 1
ER -