Argonne National Laboratory, Lemont, IL, USA.
FEMS Microbiol Lett. 2012 Jul;332(2):91-8. doi: 10.1111/j.1574-6968.2012.02588.x. Epub 2012 May 28.
Microbial communities exhibit exquisitely complex structure. Many aspects of this complexity, from the number of species to the total number of interactions, are currently very difficult to examine directly. However, extraordinary efforts are being made to make these systems accessible to scientific investigation. While recent advances in high-throughput sequencing technologies have improved accessibility to the taxonomic and functional diversity of complex communities, monitoring the dynamics of these systems over time and space - using appropriate experimental design - is still expensive. Fortunately, modeling can be used as a lens to focus low-resolution observations of community dynamics to enable mathematical abstractions of functional and taxonomic dynamics across space and time. Here, we review the approaches for modeling bacterial diversity at both the very large and the very small scales at which microbial systems interact with their environments. We show that modeling can help to connect biogeochemical processes to specific microbial metabolic pathways.
微生物群落表现出极其复杂的结构。目前,从物种数量到总相互作用数量等许多方面的复杂性都非常难以直接研究。然而,人们正在做出巨大努力,以使这些系统能够接受科学研究。尽管高通量测序技术的最新进展提高了对复杂群落的分类和功能多样性的可访问性,但使用适当的实验设计来监测这些系统随时间和空间的动态仍然很昂贵。幸运的是,建模可以用作一种透镜,将对群落动态的低分辨率观察聚焦起来,从而能够对功能和分类动态进行跨空间和时间的数学抽象。在这里,我们回顾了在微生物系统与其环境相互作用的非常大和非常小的尺度上对细菌多样性进行建模的方法。我们表明,建模可以帮助将生物地球化学过程与特定的微生物代谢途径联系起来。