Microbial Ecology Group, Department of Biosciences, WZW, Technische Universität München, 85354 Freising, Germany.
Food Microbiol. 2011 Apr;28(2):284-90. doi: 10.1016/j.fm.2010.07.001. Epub 2010 Jul 13.
In light of the increasing number of serious food borne outbreaks caused by emetic Bacillus cereus, a better understanding of the cereulide synthetase (ces) gene expression and toxin synthesis is required. Here, the relative expression levels of three ces genes (cesP, cesA and cesB) were investigated using quantitative real-time reverse transcription PCR in relation to growth, degree of sporulation and toxin production of the emetic reference strain B. cereus F4810/72 and the weakly emetic strain IH41385. The strict co-transcription of all three genes confirmed the operon structure of the ces gene cluster responsible for cereulide formation. ces transcription turned out to be highly temporal and tightly regulated; ces mRNA was only detectable during mid to late exponential growth in both strains. The low toxigenic potential of the weakly emetic strain IH41385 correlated well with its respective ces transcripts, showing reduced activity at a transcriptional level. Two non-sporulating mutants (F4810/72Δspo0A and F4810/72INsigH) demonstrated that cereulide synthesis is part of the Spo0A regulon but independent of later sporulation processes. Besides strain specific intrinsic factors, ces transcription was found to be significantly influenced by the cellular growth state as well as by extrinsic abiotic factors, like salt. An increase of sodium chloride in the media resulted in lower ces transcription and coincided with lower cereulide toxin levels. Interestingly, at 25 gl(-1) NaCl, toxin levels were already reduced without strongly affecting the growth of B. cereus, indicating an inhibitory effect of NaCl on cereulide biosynthesis independent of growth. This illustrates that ces gene expression and toxicity cannot be predicted solely from growth rates or cell numbers, but is influenced by complex interactions of various intrinsic as well as extrinsic factors, which remain to be clarified in detail.
鉴于由产吐毒素蜡样芽胞杆菌引起的严重食源性暴发事件日益增多,我们需要更好地了解呕吐毒素合成酶(ces)基因的表达和毒素合成。在此,我们采用实时定量反转录 PCR 法,检测了产吐毒素参考菌株 B. cereus F4810/72 和弱产吐毒素菌株 IH41385 的生长、孢子形成程度和毒素产生与三个 ces 基因(cesP、cesA 和 cesB)相对表达水平之间的关系。所有三个基因的严格共转录证实了负责呕吐毒素形成的 ces 基因簇的操纵子结构。ces 转录具有高度的时间和严格的调控性;在两个菌株的对数中期至晚期生长过程中,ces mRNA 才可以检测到。弱产吐毒素菌株 IH41385 的低产毒潜能与其相应的 ces 转录物密切相关,在转录水平上表现出活性降低。两个不产孢子的突变体(F4810/72Δspo0A 和 F4810/72INsigH)表明,呕吐毒素合成是 Spo0A 调控子的一部分,但独立于后期的孢子形成过程。除了菌株特异性的内在因素外,ces 转录还受到细胞生长状态以及外在非生物因素(如盐)的显著影响。培养基中氯化钠浓度的增加导致 ces 转录水平降低,同时呕吐毒素水平也降低。有趣的是,在 25 gl(-1) NaCl 时,毒素水平已经降低,而不会强烈影响蜡样芽胞杆菌的生长,这表明氯化钠对呕吐毒素生物合成具有抑制作用,这种抑制作用独立于生长。这表明,ces 基因表达和毒性不能仅根据生长速率或细胞数量来预测,而是受到各种内在和外在因素的复杂相互作用的影响,这些因素仍需详细阐明。