Temperature exerts control of Bacillus cereus emetic toxin production on post-transcriptional levels

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Abstract

In recent years, the emetic toxin cereulide, produced by Bacillus cereus, has gained high relevance in food production and food safety. Cereulide is synthesized non-ribosomal by the multi-enzyme complex Ces-NRPS, which is encoded on a megaplasmid that shares its backbone with the Bacillus anthracis pX01 toxin plasmid. Due to its resistance against heat, proteolysis and extreme pH conditions, the formation of this highly potent depsipeptide toxin is of serious concern in food processing procedures including slow cooling procedures and/or storage of intermediate products at ambient temperatures. So far, systematic data on the effect of extrinsic factors on cereulide synthesis has been lacking. Thus, we investigated the influence of temperature, a central extrinsic parameter in food processing, on the regulation of cereulide synthesis on transcriptional, translational and post-translational levels over the growth temperature range of emetic B. cereus. Bacteria were grown in 3°C interval steps from 12 to 46°C and cereulide synthesis was followed from ces gene transcription to cereulide toxin production. This systematic study revealed that temperature is a cardinal parameter, which primarily impacts cereulide synthesis on post-transcriptional levels, thereby altering the composition of cereulide isoforms. Our work also highlights that the risk of cereulide production could not be predicted from growth parameters or sole cell numbers. Furthermore, for the first time we could show that the formation of the recently identified cereulide isoforms is highly temperature dependent, which may have great importance in terms of food safety and predictive microbiology. Notably the production of isocereulide A, which is about 10-fold more cytotoxic than cereulide, was specifically supported at low temperatures.

Figures

  • FIGURE 1 | Growth of emetic Bacillus cereus strains in dependence of temperature. Strains were grown in LB broth, 120 rpm, at different temperatures in a range from 12 to 46 ◦C, using 3◦C intervals. Time (in hours) to reach optical densities (OD600) of 1 and 10, at which samples have been taken in parallel for transcriptional, translational and post-translational analyses, is depicted. At 46◦C, OD600 of 10 was not reached, and samples for transcriptional, translational and post-translational analyses were taken after 12 h when strains reached a maximal OD600 between 5 and 7. The inset show growth curves from all four strains recorded at 24◦C, which served as reference temperature. Since all strains showed maximal cesB transcription and translation around an OD600 of 10, this OD was chosen for transcriptional, translational and cereulide toxin analysis at all tested temperatures. In addition, samples were taken at OD600 of 1 to be used as internal calibrator for transcriptional analysis (Figure 2A). Arrows indicate the OD600 sampling points at all tested temperatures. Data represent means and error bars indicating standard deviations of at least two independent growth experiments.
  • FIGURE 2 | Cereulide synthetase expression in dependence of temperature. Cultures were grown to an OD600 of 10 in LB broth, 120 rpm, at different temperatures in a range from 12 to 46 ◦C, using 3◦C intervals. Samples were taken for cesB gene transcription (A) and CesB translation analysis (B). Transcription was analyzed by qRT-PCR according to Dommel et al. (2011) and translation was analyzed by immunoblotting using a novel CesB-specific monoclonal antibody (Lücking et al., 2015). For relative expression analyses of cesB at OD600 of 10, the cesB transcript level at an OD600 of 1 was used as the calibrator (RE = 1.0) for each strain at all tested temperatures. Relative translation of the CesB protein at different temperatures was determined by calculation CesB blot signal intensity of each sample relative to CesB showing highest blot signal intensity (RE = 100%). Data represent means and error bars indicate standard deviations of at least two independent growth experiments. ∗N.D., not determined.
  • FIGURE 3 | Cereulide toxin and isocereulide production in dependence of temperature. Cultures were grown to an OD600 of 10 in LB broth, 120 rpm, at different temperatures in a range from 12 to 46 ◦C, using 3◦C intervals. Cereulide and isocereulide extraction was carried out with acetonitrile (99%) and quantitation was performed by ESI-HPLC MS/MS analysis. Cereulide (A) and isocereulide (B) levels are depicted as µg cereulide per g bacterial wet weight as well as relative amount of cereulide isoforms, referred to the amount of cereulide values, are shown (C). Data represent means and error bars indicating standard deviations of at least two independent growth experiments.

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Kranzler, M., Stollewerk, K., Rouzeau-Szynalski, K., Blayo, L., Sulyok, M., & Ehling-Schulz, M. (2016). Temperature exerts control of Bacillus cereus emetic toxin production on post-transcriptional levels. Frontiers in Microbiology, 7(OCT). https://doi.org/10.3389/fmicb.2016.01640

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