A novel sensitive bioassay for detection of Bacillus cereus emetic toxin and related depsipeptide ionophores

MA Andersson*, R Mikkola, J Helin, MC Andersson, M Salkinoja-Salonen

*Corresponding author for this work

Research output: Contribution to journalArticleScientificpeer-review


Of the toxins produced by Bacillus cereus, the emetic toxin is likely the most dangerous but, due to the lack of a suitable assay, the least well known. In this paper, a nem, sensitive, inexpensive, rand rapid bioassay for detection of the emetic toxin of B. cereus is described, The assay is based on the loss of motility of boar spermatozoa upon 24 h of exposure to extracts of emetic B. cereus strains or contaminated food, The paralyzed spermatozoa exhibited swollen mitochondria, but no depletion of cellular ATP or damage to plasma membrane integrity was observed, Analysis of the purified toxin by electrospray tandem mass spectrometry showed that it was a dodecadepsipeptide with a mass fragmentation pattern similar to that described for cereulide. The 50% effective concentration of the purified toxin to boar spermatozoa was 0.5 ng of purified toxin mt of extended boar semen(-1), This amount corresponds to 10(4) to 10(5) CFU of B. cereals cells. No toxicity was detected for 27 other B, cereus strains up to 10(8) CFU ml(-1), The detection limit for food was 3 g of rice containing 10(6) to 10(7) CFU of emetic B. cereus per gram, Effects similar to those provoked by emetic B, cereus toxin were also induced in boar spermatozoa by valinomycin and gramicidin at 2 and 3 ng ml of extended bean, semen(-1), respectively, The symptoms provoked by the toxin in spermatozoa indicated that B, cereus emetic toxin was acting res a membrane channel-forming ionophore, damaging mitochondria and blocking the oxidative phosphorylation required for the mobility of boar spermatozoa.

Original languageEnglish
Pages (from-to)1338-1343
Number of pages6
JournalApplied and Environmental Microbiology
Issue number4
Publication statusPublished - Apr 1998
MoE publication typeA1 Journal article-refereed




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