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Mathematical modelling reveals properties of TcdC required for it to be a negative regulator of toxin production in Clostridium difficile

机译:数学建模揭示了TcdC成为艰难梭菌毒素产生负调节剂所需的特性

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摘要

The role of the protein TcdC in pathogenicity of the bacterium Clostridium difficile is currently unclear: conflicting reports suggest it is either a negative regulator of toxin production or, on the other hand, has no effect on virulence at all. We exploit a theoretical approach by taking what is known about the network of proteins surrounding toxin production by C. difficile and translating this into a mathematical model. From there it is possible to investigate a range of possible interactions (using numerical and asymptotic analyses), identifying properties of TcdC which would make it a realistic candidate as a toxin inhibitor. Our findings imply that if TcdC is really an inhibitor of toxin production then TcdC production should be at least as fast as that of the protein TcdR and TcdC should remain in the cells throughout growth. These are experimentally-testable hypotheses and are equally applicable to alternative candidates for toxin production inhibition.
机译:TcdC蛋白在艰难梭菌致病性中的作用目前尚不清楚:相互矛盾的报道表明,它要么是毒素产生的负调节剂,要么对毒力完全没有影响。通过采用关于艰难梭菌产生毒素的蛋白质周围网络的已知知识并将其转换为数学模型,我们采用了一种理论方法。从那里可以研究一系列可能的相互作用(使用数值和渐进分析),确定TcdC的特性,使其成为实际的毒素抑制剂。我们的发现暗示,如果TcdC确实是毒素产生的抑制剂,那么TcdC的产生应至少与TcdR蛋白的产生一样快,并且TcdC在整个生长过程中应保留在细胞中。这些是实验可检验的假设,同样适用于毒素产生抑制的替代候选物。

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