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Identification and characterization of Bacillus anthracis by multiplex PCR analysis of sequences on plasmids pXO1 and pXO2 and chromosomal DNA
Authors:Vincent Ramisse  Guy Patra  Henri Garrigue  Jean-Luc Guesdon  Michèle Mock
Institution:Laboratoire de Microbiologie Appliquée, Centre d'Etudes du Bouchet, B.P. no. 3, 91710 Vert-Le-Petit, France; Service Biotechnologies, Centre d'Etudes du Bouchet, B.P. no. 3, 91710 Vert-Le-Petit, France; Laboratoire de Prédéveloppement des Sondes, Institut Pasteur, 75724 Paris Cedex 15, France; Laboratoire de Génétique Moléculaire des Toxines, CNRS URA 1858, Institut Pasteur, 75724 Paris Cedex 15, France
Abstract:Abstract Bacillus anthracis can be identified on the basis of the detection of virulence factor genes located on two plasmids, pXO1 and pXO2. Thus isolates lacking both pXO1 and pXO2 are indistinguishable from closely related B. cereus group bacteria. We developed a multiplex PCR assay for characterization of B. anthracis isolates, and simultaneous confirmation of the species identity independent of plasmid content. The assay amplifies lef, cya, pag (pXO1) and cap (pXO2) genes, and a B. anthracis specific chromosomal marker, giving an easy-to-read profile. This system unambiguously identified virulent (pXO1+/2+) and avirulent (pXO1+/2?, pXO1?/2+ and pXO1?/2?) strains of B. anthracis and distinguished 'anthrax-like' strains from other B. cereus group bacteria.
Keywords:Bacillaceae              Bacillus anthracis                        Bacillus cereus                        Bacillus anthracis genetics  Anthrax epidemiology  Bacterial identification  Diagnosis  Polymerase chain reaction
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