Department of Biomedical Engineering, University of Virginia, MR-5 2041a, Box 800759, Health System, Charlottesville, VA 22908 USA.
Department of Biomedical Engineering, University of Virginia, MR-5 2041a, Box 800759, Health System, Charlottesville, VA 22908 USA; Department of Medicine, Division of Infectious Diseases & International Health, University of Virginia, Charlottesville, VA, USA; Department of Biochemistry & Molecular Genetics, University of Virginia, Charlottesville, VA, USA.
Curr Opin Microbiol. 2022 Feb;65:108-115. doi: 10.1016/j.mib.2021.11.002. Epub 2021 Nov 25.
The progress of infection by Clostridioides difficile is strongly influenced by metabolic cues it encounters as it colonizes the gastrointestinal tract. Both colonization and regulation of virulence have a multi-factorial interaction between host, microbiome, and gene expression cascades. While these connections with metabolism have been understood for some time, many mechanisms of control have remained difficult to directly assay due to high metabolic variability among C. difficile isolates and difficult genetic systems. Computational systems offer a means to interrogate structure of complex or noisy datasets and generate useful, tractable hypotheses to be tested in the laboratory. Recently, in silico techniques have provided powerful insights into metabolic elements of C. difficile infection ranging from virulence regulation to interactions with the gut microbiota. In this review, we introduce and provide context to the methods of computational modeling that have been applied to C. difficile metabolism and virulence thus far. The techniques discussed here have laid the foundation for future multi-scale efforts aimed at understanding the complex interplay of metabolic activity between pathogen, host, and surrounding microbial community in the regulation of C. difficile pathogenesis.
艰难梭菌的感染进展受到其在胃肠道定植时遇到的代谢线索的强烈影响。定植和毒力调节都与宿主、微生物组和基因表达级联之间存在多因素相互作用。尽管人们已经了解了这些与代谢的联系,但由于艰难梭菌分离株之间存在高度的代谢变异性和困难的遗传系统,许多控制机制仍然难以直接检测。计算系统提供了一种方法,可以对复杂或嘈杂的数据集进行结构分析,并生成有用的、可处理的假设,以便在实验室中进行测试。最近,计算技术为艰难梭菌感染的代谢元素提供了有力的见解,从毒力调节到与肠道微生物群的相互作用。在这篇综述中,我们介绍并提供了迄今为止应用于艰难梭菌代谢和毒力的计算建模方法的背景。这里讨论的技术为未来的多尺度努力奠定了基础,旨在理解病原体、宿主和周围微生物群落之间代谢活动的复杂相互作用,以调节艰难梭菌的发病机制。