Department of Chemistry and Biochemistry, University of Colorado, 215 UCB, Boulder, CO 80309, USA.
Genome Biol. 2011;12(5):R50. doi: 10.1186/gb-2011-12-5-r50.
BACKGROUND: Understanding the normal temporal variation in the human microbiome is critical to developing treatments for putative microbiome-related afflictions such as obesity, Crohn’s disease, inflammatory bowel disease and malnutrition. Sequencing and computational technologies, however, have been a limiting factor in performing dense time series analysis of the human microbiome. Here, we present the largest human microbiota time series analysis to date, covering two individuals at four body sites over 396 timepoints. RESULTS: We find that despite stable differences between body sites and individuals, there is pronounced variability in an individual’s microbiota across months, weeks and even days. Additionally, only a small fraction of the total taxa found within a single body site appear to be present across all time points, suggesting that no core temporal microbiome exists at high abundance (although some microbes may be present but drop below the detection threshold). Many more taxa appear to be persistent but non-permanent community members. CONCLUSIONS: DNA sequencing and computational advances described here provide the ability to go beyond infrequent snapshots of our human-associated microbial ecology to high-resolution assessments of temporal variations over protracted periods, within and between body habitats and individuals. This capacity will allow us to define normal variation and pathologic states, and assess responses to therapeutic interventions.
背景:了解人类微生物组的正常时间变化对于开发针对肥胖、克罗恩病、炎症性肠病和营养不良等与微生物组相关疾病的治疗方法至关重要。然而,测序和计算技术一直是对人类微生物组进行密集时间序列分析的限制因素。在这里,我们展示了迄今为止最大的人类微生物组时间序列分析,涵盖了两个个体的四个身体部位的 396 个时间点。
结果:我们发现,尽管身体部位和个体之间存在稳定的差异,但个体的微生物组在数月、数周甚至数天内都存在明显的可变性。此外,在单个身体部位中发现的总分类群中只有一小部分似乎存在于所有时间点,这表明不存在高丰度的核心时间微生物组(尽管有些微生物可能存在但低于检测阈值)。更多的分类群似乎是持久但非永久性的群落成员。
结论:这里描述的 DNA 测序和计算进展提供了超越我们人类相关微生物生态学的频繁快照的能力,能够对身体栖息地和个体内部和之间的长时间内的时间变化进行高分辨率评估。这种能力将使我们能够定义正常变异和病理状态,并评估对治疗干预的反应。
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