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Small Bacillus cereus ATCC 14579 subpopulations are responsible for cytotoxin K production.

机译:小蜡样芽孢杆菌ATCC 14579亚群负责细胞毒素K的产生。

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摘要

Aims. Bacillus cereus diarrhoeal food poisoning can be caused by several potential enterotoxins, including the nonhaemolytic enterotoxin (Nhe), haemolysin BL (Hbl) and cytotoxin K (CytK). To get more insights into the CytK expression, a fluorescent reporter strain was created for CytK expression. Methods. Bacillus cereus ATCC 14579 was used as the reporter strain that contained the cyan fluorescent protein (CFPopt) gene under control of the cytK promoter. Transcription of enterotoxin genes nheB, hblC and cytK was assessed by messenger RNA analysis (RT-qPCR), and their full expression was assessed by immunological protein detection in the case of Nhe and Hbl and fluorescence microscopy in the case of CytK, using the reporter gene CFPopt. Results. Transcription of enterotoxins Nhe, Hbl and CytK showed similar kinetics with a peak during the late exponential growth phase. Toxin expression of the reporter strain was unaltered in comparison with the wild type. However, fluorescence, and thus CytK expression, only occurred in a small (1-2%) portion of the cell population. Conclusions. These results suggest that a small subpopulation of B. cereus ATCC 14579 is responsible for CytK production in a homogeneous monoculture. Significance and Impact of the Study. Future research is warranted to determine whether genetically homogeneous B. cereus populations utilize differential gene expression for other toxins and virulence genes than CytK and whether this also applies to other B. cereus strains. If so, differential expression of toxin genes could be used by these bacteria to increase the fitness and survival chances of their population by diversification and specialization into different subpopulations
机译:目的蜡状芽孢杆菌腹泻食物中毒可能由几种潜在的肠毒素引起,包括非溶血性肠毒素(Nhe),溶血素BL(Hbl)和细胞毒素K(CytK)。为了获得有关CytK表达的更多见解,创建了一个荧光报告基因菌株用于CytK表达。方法。蜡状芽孢杆菌ATCC 14579用作报告株,其在cytK启动子的控制下包含青色荧光蛋白(CFPopt)基因。通过信使RNA分析(RT-qPCR)评估肠毒素基因nheB,hblC和cytK的转录,在Nhe和Hbl情况下通过免疫蛋白检测评估其完整表达,在CytK情况下通过荧光镜检使用报告基因基因CFPopt。结果。肠毒素Nhe,Hbl和CytK的转录显示出相似的动力学,并在指数生长后期处于峰值。与野生型相比,报告菌株的毒素表达未改变。但是,荧光和CytK表达仅发生在细胞群的一小部分(1-2%)中。结论。这些结果表明蜡状芽孢杆菌ATCC 14579的一个小亚群负责同质单培养中CytK的产生。研究的意义和影响。有必要进行进一步的研究以确定遗传上均质的蜡状芽孢杆菌种群是否利用不同于CytK的其他毒素和毒力基因的差异基因表达,以及这是否也适用于其他蜡状芽孢杆菌菌株。如果是这样,这些细菌可以利用毒素基因的差异表达,通过多样化和专门化成不同的亚群来增加其种群的适应性和存活机会。

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