Enterotoxigenic profiles and polymerase chain reaction detection of Bacillus cereus group cells and B-cereus strains from foods and food-borne outbreaks
Ym. Hsieh et al., Enterotoxigenic profiles and polymerase chain reaction detection of Bacillus cereus group cells and B-cereus strains from foods and food-borne outbreaks, J APPL MICR, 87(4), 1999, pp. 481-490
Bacillus cereus is one of the important food pathogens. Since B. cereus gro
up cells, such as B. cereus, B. thuringiensis, B. anthracis and B. mycoides
, share many phenotypical properties and a high level of chromosomal sequen
ce similarity, it is interesting to investigate the virulence profiles for
B. cereus group cells, including B. cereus strains isolated from foods and
samples associated with food-poisoning outbreaks. For this investigation, t
he presence of enterotoxin genes, such as those of haemolysin BL, B. cereus
enterotoxin T and enterotoxin FM, were assayed by polymerase chain reactio
n (PCR) methods. Meanwhile, their enterotoxin activities were assayed using
the BCET-RPLA kit, haemolytic patterns on sheep blood agar and their cytot
oxicity to Chinese hamster ovary (CHO) cells. Results showed that there wer
e 12 enterotoxigenic profiles for the 98 B. cereus group strains collected.
In addition, if any of the three types of enterotoxins was present in the
B. cereus group cells, these cells were shown to be cytotoxic to the CHO ce
lls. Similar enterotoxigenic profiles could be found among strains of B. ce
reus, B. mycoides and B. thuringiensis. Thus, all B. cereus group strains m
ay be potentially toxigenic and the detection of these cells in foods is im
portant. We thus designed PCR primers, termed Ph1/Ph2, from the sphingomyel
inase gene of B. cereus cells. These primers were specific for all B. cereu
s group strains and could be used for the detection of B. cereus cells cont
aminated in food samples.