Department of Environmental Science and Policy, George Mason University, Fairfax, VA 22030, USA.
Chem Biodivers. 2010 May;7(5):1065-75. doi: 10.1002/cbdv.200900322.
Recent advances in molecular techniques have now made it possible to interrogate the human microbiome in depth to better understand the interactions with the host organism and its role in diseases. We now report the utility of Length Heterogeneity Polymerase Chain Reaction (LH-PCR) to survey samples and a proprietary Multitagged Pyrosequencing (MTPS) methodology to interrogate the gut microbiome in healthy and disease states. We present an overview of our studies demonstrating the application of these molecular-biology techniques to an example disease state such as Inflammatory Bowel Disease (IBD). The findings show that there is a core mucosal bacterial microbiome (i.e., a mucosal biofilm) that is distinct from the luminal microbiome in health, and that the mucosal microbiome appears to be dysbiotic in IBD. We propose that the mucosal microbiome forms a synergistic and stable interaction with the host immune system, while the lumen microbiome varies based on diet or other environmental factors. We define this composite ecosystem of the human microbiome and human host as the Human Metabiome.
近年来,分子技术的进步使得深入研究人类微生物组成为可能,从而更好地了解微生物组与宿主生物体的相互作用及其在疾病中的作用。我们现在报告使用长度异质性聚合酶链反应 (LH-PCR) 来检测样本,以及使用专有的多标签焦磷酸测序 (MTPS) 方法来检测健康和疾病状态下的肠道微生物组。我们介绍了我们的研究概述,这些研究展示了这些分子生物学技术在炎症性肠病 (IBD) 等示例疾病状态中的应用。研究结果表明,在健康状态下,存在一个核心的黏膜细菌微生物组(即黏膜生物膜),与腔微生物组不同,而在 IBD 中,黏膜微生物组似乎存在失调。我们提出,黏膜微生物组与宿主免疫系统形成协同和稳定的相互作用,而腔微生物组则根据饮食或其他环境因素而变化。我们将人类微生物组和人类宿主的这种复合生态系统定义为人类代谢组。