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. 1999 Apr;65(4):1483–1490. doi: 10.1128/aem.65.4.1483-1490.1999

TABLE 7.

Comparison of gyrB PCR and 16S rDNA hybridization probe techniques in the differentiation of B. cereus and B. thuringiensis

Bacterial strain or serotype Hybridization signal positive for:
Amplification of gyrB PCR fragment that is specific to:
B. cereusa B. thurin-giensisb B. cereusc B. thurin-giensisd B. an-thracise
B. cereus
 JCM 2152T + +
 H5 +
 H6 +
 H7 +
 H16 + +
 H17 +
 Nagoya 126f + +
 Nagoya 127f + +
B. thuringiensis
 berliner (IAM 12077T) + +
 kurstaki (HD-1) + +
 galleriae + +
 aizawai + +
 israelensis + +
B. anthracis Pasteur #2H +
B. mycoides ATCC 6462T +
a

B. cereus-specific 16S rDNA-based probe (39). 

b

B. thuringiensis-specific 16S rDNA-based probe (39). 

c

BC1-BC2r primer set was used. 

d

BT1-BT2r primer set was used. 

e

BA1-BA2r primer set was used. Ba primer set was also used (35). 

f

Food isolate obtained from Nagoya Public Health Research Institute.