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本文引用的文献

1
Evaluation of 16S rDNA-based community profiling for human microbiome research.基于 16S rDNA 的群落谱分析在人类微生物组研究中的评价。
PLoS One. 2012;7(6):e39315. doi: 10.1371/journal.pone.0039315. Epub 2012 Jun 13.
2
A metagenomic approach to characterization of the vaginal microbiome signature in pregnancy.一种基于宏基因组学的方法,用于描述妊娠期间阴道微生物组特征。
PLoS One. 2012;7(6):e36466. doi: 10.1371/journal.pone.0036466. Epub 2012 Jun 13.
3
A framework for human microbiome research.人类微生物组研究框架。
Nature. 2012 Jun 13;486(7402):215-21. doi: 10.1038/nature11209.
4
Structure, function and diversity of the healthy human microbiome.健康人体微生物组的结构、功能与多样性。
Nature. 2012 Jun 13;486(7402):207-14. doi: 10.1038/nature11234.
5
Microbiota-targeted therapies: an ecological perspective.靶向微生物组的治疗方法:一种生态视角。
Sci Transl Med. 2012 Jun 6;4(137):137rv5. doi: 10.1126/scitranslmed.3004183.
6
Fecal transplant against relapsing Clostridium difficile-associated diarrhea in 32 patients.32例复发性艰难梭菌相关性腹泻患者的粪便移植治疗
Scand J Gastroenterol. 2012 May;47(5):548-52. doi: 10.3109/00365521.2012.672587. Epub 2012 Apr 2.
7
Reducing the effects of PCR amplification and sequencing artifacts on 16S rRNA-based studies.减少 PCR 扩增和测序伪影对基于 16S rRNA 的研究的影响。
PLoS One. 2011;6(12):e27310. doi: 10.1371/journal.pone.0027310. Epub 2011 Dec 14.
8
Enterotypes of the human gut microbiome.人类肠道微生物组的肠型。
Nature. 2011 May 12;473(7346):174-80. doi: 10.1038/nature09944. Epub 2011 Apr 20.
9
Adapting functional genomic tools to metagenomic analyses: investigating the role of gut bacteria in relation to obesity.将功能基因组工具应用于宏基因组分析:研究肠道细菌在肥胖相关问题中的作用。
Brief Funct Genomics. 2010 Dec;9(5-6):355-61. doi: 10.1093/bfgp/elq011. Epub 2010 May 6.
10
Strain-resolved community genomic analysis of gut microbial colonization in a premature infant.对早产儿肠道微生物定植的应变分辨群落基因组分析。
Proc Natl Acad Sci U S A. 2011 Jan 18;108(3):1128-33. doi: 10.1073/pnas.1010992108. Epub 2010 Dec 29.

人类微生物组计划全面采样人类微生物组的策略,以及为什么这很重要。

The Human Microbiome Project strategy for comprehensive sampling of the human microbiome and why it matters.

机构信息

Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

FASEB J. 2013 Mar;27(3):1012-22. doi: 10.1096/fj.12-220806. Epub 2012 Nov 19.

DOI:10.1096/fj.12-220806
PMID:23165986
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3574278/
Abstract

The Human Microbiome Project used rigorous good clinical practice standards to complete comprehensive body site sampling in healthy 18- to 40-yr-old adults, creating an unparalleled reference set of microbiome specimens. To ensure that specimens represented minimally perturbed microbiomes, we first screened potential participants using exclusion criteria based on health history, including the presence of systemic diseases (e.g., hypertension, cancer, or immunodeficiency or autoimmune disorders), use of potential immunomodulators, and recent use of antibiotics or probiotics. Subsequent physical examinations excluded individuals based on body mass index (BMI), cutaneous lesions, and oral health. We screened 554 individuals to enroll 300 (149 men and 151 women, mean age 26 yr, mean BMI 24 kg/m, 20.0% racial minority, and 10.7% Hispanic). We obtained specimens from the oral cavity, nares, skin, gastrointestinal tract, and vagina (15 specimens from men and 18 from women). The study evaluated longitudinal changes in an individual's microbiome by sampling 279 participants twice (mean 212 d after the first sampling; range 30-359 d) and 100 individuals 3 times (mean 72 d after the second sampling; range 30-224 d). This sampling strategy yielded 11,174 primary specimens, from which 12,479 DNA samples were submitted to 4 centers for metagenomic sequencing. Our clinical design and well-defined reference cohort has laid a foundation for microbiome research.

摘要

人类微生物组计划采用严格的良好临床实践标准,对 18 至 40 岁的健康成年人进行全面的身体部位采样,创建了无与伦比的微生物组样本参考集。为确保样本代表最小干扰的微生物组,我们首先根据健康史,包括是否存在全身性疾病(如高血压、癌症、免疫缺陷或自身免疫性疾病)、使用潜在的免疫调节剂以及最近是否使用抗生素或益生菌,使用排除标准筛选潜在参与者。随后的体格检查根据身体质量指数(BMI)、皮肤损伤和口腔健康排除个体。我们筛选了 554 个人,以招募 300 个人(149 名男性和 151 名女性,平均年龄 26 岁,平均 BMI 为 24kg/m,20.0%为少数族裔,10.7%为西班牙裔)。我们从口腔、鼻腔、皮肤、胃肠道和阴道获得样本(男性 15 份,女性 18 份)。该研究通过对 279 名参与者进行两次采样(第一次采样后平均 212 天;范围 30-359 天)和 100 名参与者进行三次采样(第二次采样后平均 72 天;范围 30-224 天),评估了个体微生物组的纵向变化。这种采样策略产生了 11174 个初级样本,其中 12479 个 DNA 样本被提交给 4 个中心进行宏基因组测序。我们的临床设计和明确的参考队列为微生物组研究奠定了基础。