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[Application of the multiplex PCR and PCR-RFLP method in the identification of the Bacillus anthracis].
Med Dosw Mikrobiol 2005; 57(3):277-85MD

Abstract

The aim of this study was to apply the multiplex PCR and PCR-RFLP method for the identification of the B. anthracis strains and to distinguish those bacteria from other members of the Bacillus cereus group. The multiplex PCR method enables to detect the virulence factors, i.e. the toxin and the capsule in B. anthracis strains. To do that, the authors have used 5 primer pairs specific for the fragments of lef, cya, pag genes which are present in the pXO1 plasmid and encode the toxin, the cap gene, which is present in the pXO2 plasmid and encodes the capsule, and the Ba813 chromosomal sequence. Among the four B. anthracis strains examined, three contained two plasmids and the Ba813 chromosomal sequence, while the fourth one contained the pXO1 plasmid only, together and the Ba813 chromosomal sequence. Other bacterial species, belonging to the B. cereus group, were also examined: 6 strains of B. cereus, 4 strains of B. thuringiensis and one strain of B. mycoides. The presence of Ba813 chromosomal sequence has been detected in two B. cereus strains. Neither plasmids nor Ba813 chromosomal sequence have been discovered in other B. cereus, B. thuringiensis and B. mycoides strains. The results of the survey indicate that the Ba813 chromosomal sequence does not occur solely in B. anthracis strains. The PCR-RFLP method with the use of SG-749f and SG-749r primers enabled to demonstrate the presence of DNA sequence (SG-749) in B. anthracis, B. cereus, B. thuringiensis and B. mycoides strains. Restriction analysis with enzyme AluI of the SG-749 sequence, has shown the presence of two DNA fragments at the size of about 90 and 660 bp in all B. anthracis strains. The restriction profile obtained was characteristic for B. anthracis strains and it did not occur in other investigated bacterial species belonging to the B. cereus group. It was not observed even in such B. cereus strains in which the presence of Ba813 sequence was discovered and it enabled to differentiate between B. anthracis strains and other closely related species of the B. cereus group.

Authors+Show Affiliations

Ośrodek Diagnostyki i Zwalczania Zagrozeń Biologicznych Wojskowego Instytutu Higieny i Epidemiologii. uszymajda@obw-wihe.pulawy.plNo affiliation info available

Pub Type(s)

English Abstract
Journal Article

Language

pol

PubMed ID

16494204

Citation

Szymajda, Urszula, and Michał Bartoszcze. "[Application of the Multiplex PCR and PCR-RFLP Method in the Identification of the Bacillus Anthracis]." Medycyna Doswiadczalna I Mikrobiologia, vol. 57, no. 3, 2005, pp. 277-85.
Szymajda U, Bartoszcze M. [Application of the multiplex PCR and PCR-RFLP method in the identification of the Bacillus anthracis]. Med Dosw Mikrobiol. 2005;57(3):277-85.
Szymajda, U., & Bartoszcze, M. (2005). [Application of the multiplex PCR and PCR-RFLP method in the identification of the Bacillus anthracis]. Medycyna Doswiadczalna I Mikrobiologia, 57(3), pp. 277-85.
Szymajda U, Bartoszcze M. [Application of the Multiplex PCR and PCR-RFLP Method in the Identification of the Bacillus Anthracis]. Med Dosw Mikrobiol. 2005;57(3):277-85. PubMed PMID: 16494204.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Application of the multiplex PCR and PCR-RFLP method in the identification of the Bacillus anthracis]. AU - Szymajda,Urszula, AU - Bartoszcze,Michał, PY - 2006/2/24/pubmed PY - 2006/6/29/medline PY - 2006/2/24/entrez SP - 277 EP - 85 JF - Medycyna doswiadczalna i mikrobiologia JO - Med Dosw Mikrobiol VL - 57 IS - 3 N2 - The aim of this study was to apply the multiplex PCR and PCR-RFLP method for the identification of the B. anthracis strains and to distinguish those bacteria from other members of the Bacillus cereus group. The multiplex PCR method enables to detect the virulence factors, i.e. the toxin and the capsule in B. anthracis strains. To do that, the authors have used 5 primer pairs specific for the fragments of lef, cya, pag genes which are present in the pXO1 plasmid and encode the toxin, the cap gene, which is present in the pXO2 plasmid and encodes the capsule, and the Ba813 chromosomal sequence. Among the four B. anthracis strains examined, three contained two plasmids and the Ba813 chromosomal sequence, while the fourth one contained the pXO1 plasmid only, together and the Ba813 chromosomal sequence. Other bacterial species, belonging to the B. cereus group, were also examined: 6 strains of B. cereus, 4 strains of B. thuringiensis and one strain of B. mycoides. The presence of Ba813 chromosomal sequence has been detected in two B. cereus strains. Neither plasmids nor Ba813 chromosomal sequence have been discovered in other B. cereus, B. thuringiensis and B. mycoides strains. The results of the survey indicate that the Ba813 chromosomal sequence does not occur solely in B. anthracis strains. The PCR-RFLP method with the use of SG-749f and SG-749r primers enabled to demonstrate the presence of DNA sequence (SG-749) in B. anthracis, B. cereus, B. thuringiensis and B. mycoides strains. Restriction analysis with enzyme AluI of the SG-749 sequence, has shown the presence of two DNA fragments at the size of about 90 and 660 bp in all B. anthracis strains. The restriction profile obtained was characteristic for B. anthracis strains and it did not occur in other investigated bacterial species belonging to the B. cereus group. It was not observed even in such B. cereus strains in which the presence of Ba813 sequence was discovered and it enabled to differentiate between B. anthracis strains and other closely related species of the B. cereus group. SN - 0025-8601 UR - https://www.unboundmedicine.com/medline/citation/16494204/[Application_of_the_multiplex_PCR_and_PCR_RFLP_method_in_the_identification_of_the_Bacillus_anthracis]_ DB - PRIME DP - Unbound Medicine ER -