Identification of Bacillus anthracis by rpoB sequence analysis and multiplex PCR.

Abstract:

:Comparative sequence analysis was performed upon Bacillus anthracis and its closest relatives, B. cereus and B. thuringiensis. Portions of rpoB DNA from 10 strains of B. anthracis, 16 of B. cereus, 10 of B. thuringiensis, 1 of B. mycoides, and 1 of B. megaterium were amplified and sequenced. The determined rpoB sequences (318 bp) of the 10 B. anthracis strains, including five Korean isolates, were identical to those of Ames, Florida, Kruger B, and Western NA strains. Strains of the "B. cereus group" were separated into two subgroups, in which the B. anthracis strains formed a separate clade in the phylogenetic tree. However, B. cereus and B. thuringiensis could not be differentiated. Sequence analysis confirmed the five Korean isolates as B. anthracis. Based on the rpoB sequences determined in the present study, multiplex PCR generating either B. anthracis-specific amplicons (359 and 208 bp) or cap DNA (291 bp) in a virulence plasmid could be used for the rapid differential detection and identification of virulent B. anthracis.

journal_name

J Clin Microbiol

authors

Ko KS,Kim JM,Kim JW,Jung BY,Kim W,Kim IJ,Kook YH

doi

10.1128/jcm.41.7.2908-2914.2003

subject

Has Abstract

pub_date

2003-07-01 00:00:00

pages

2908-14

issue

7

eissn

0095-1137

issn

1098-660X

journal_volume

41

pub_type

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