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Mathematical Modeling of Regulation of Type III Secretion System in Salmonella enterica Serovar Typhimurium by SirA

机译:SirA调控肠炎沙门氏菌鼠伤寒沙门氏菌III型分泌系统的数学模型

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Salmonella enterica serovar Typhimurium invades the intestinal epithelial cells using type three secretion system (TTSS) encoded on Salmonella pathogenicity island-1 (SPI-1). The key regulator of this secretion system is HiIA, which is in turn regulated by HiID, HiIC and RtsA. It is also known that SirA/BarA system, a two-component regulatory system plays a crucial role in regulating HiIA.There are two different mechanisms that have been proposed earlier for regulation of HilD-HiIC-RtsA-HiIA network by SirA. One considers SirA to be acting through HiIA and HiIC, whereas the other considers SirA to be acting through HiID. In this paper, we have built mathematical models corresponding to both these scenarios and carried out simulations under different gene knock-out conditions. Additionally, since the two proposed mechanisms based on the experimental data are equally likely,we also considered a mechanism which is a combination of the two proposed mechanisms. The simulations were carried out to check the levels of HilA, the factor regulating the virulence, as well as the levels of the intermediate components in the network,namely HiIC and RtsA. The simulation results were used to check the consistency of various models and also to suggest the most probable mechanism of hilA regulation.The results of our study show that while most of the mathematical models are able to predict the virulence data, the models considering SirA to regulate through HilA and HiIC fail to predict the levels of intermediate components, HiIC and RtsA.Nevertheless, one of the models considering regulation of virulence by SirA via HilD was able to predict results comparable to the experimental data. In addition, combination of this model (regulation by SirA via HiID) with the model considering regulation by SirA through HilA and HiIC, also predicted results consistent with experimental observations. Our conclusions were further validated by testing the stability of the results against changes in parameter values, thus confirming the relative robustness of the proposed modeling system.
机译:肠沙门氏菌血清型鼠伤寒沙门氏菌利用在沙门氏菌致病岛-1(SPI-1)上编码的三型分泌系统(TTSS)侵入肠道上皮细胞。该分泌系统的关键调节剂是HiIA,它又由HiID,HiIC和RtsA调节。众所周知,SirA / BarA系统是一种由两部分组成的调节系统,它在调节HiIA中起着至关重要的作用。SirA对HilD-HiIC-RtsA-HiIA网络进行调节的机制早有两种。一个认为SirA通过HiIA和HiIC行动,而另一个认为SirA通过HiID行动。在本文中,我们建立了与这两种情况相对应的数学模型,并在不同的基因敲除条件下进行了模拟。另外,由于基于实验数据的两种提议的机制是同等可能的,因此我们还考虑了将两种提议的机制结合在一起的机制。进行了仿真以检查HilA的水平,调节毒力的因素以及网络中中间成分(即HiIC和RtsA)的水平。仿真结果用于检验各种模型的一致性,并提出最可能的hilA调控机制。我们的研究结果表明,尽管大多数数学模型都能够预测毒力数据,但考虑到SirA通过HilA和HiIC进行的调控不能预测中间成分HiIC和RtsA的水平。尽管如此,考虑通过Siril通过HilD调控毒力的模型之一仍能够预测与实验数据相当的结果。此外,该模型(由SirA通过HiID进行的调节)与考虑由SirA通过HilA和HiIC进行调节的模型的组合,也可预测与实验观察结果一致的结果。通过针对参数值的变化测试结果的稳定性,进一步验证了我们的结论,从而确认了所提出建模系统的相对鲁棒性。

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