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Rapid genotypic detection of Bacillus anthracis and the Bacillus cereus group by multiplex real-time PCR melting curve analysis

Authors
Kim, KijeongSeo, JuwonWheeler, KatherinePark, ChulminKim, DaewhanPark, SeungjoonKim, WonyongChung, Sang-InLeighton, Terrance
Issue Date
Feb-2005
Publisher
WILEY
Keywords
Bacillus anthracis; Bacillus cereus group; multiplex detection; real-time polymerase chain reaction; LightCycler
Citation
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, v.43, no.2, pp 301 - 310
Pages
10
Journal Title
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY
Volume
43
Number
2
Start Page
301
End Page
310
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/24665
DOI
10.1016/j.femsim.2004.10.005
ISSN
0928-8244
1574-695X
Abstract
Bacillus anthracis has four plasmid possible virulence genotypes: pXO1(+)/pXO2(+), pXO1(+)/pXO2(-), pXO1(-)/pXO2(+) or pXO1(-)/pXO2(-). Due to the lack of a specific chromosomal marker for B. anthracis, differentiation of the pXO1(-)/pXO2(-) form of B. anthracis from closely related Bacillus cereus group species is difficult. In this study, we evaluate the ability of sspE, pXO1 and pXO2 primers to discriminate individual B. anthracis and the B. cereus group genotypes using multiplex real-time PCR and melting curve analysis. Optimal conditions for successful multiplex assays have been established. Purified DNAs from 38 bacterial strains including 11 strains of B. anthracis and 18 B. cereus group strains were analyzed. Nine of the B. cereus group near-neighbor strains were shown by multilocus sequence typing to be phylogenetically proximate to the B. anthracis clade. We have demonstrated that the four plasmid genotypes of B. anthracis and B. cereus group near-neighbors were differentially and simultaneously discriminated by this assay. (C) 2004 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
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