Development of a standardized approach for environmental microbiota investigations related to asthma development in children

被引:8
|
作者
Fujimura, Kei E. [1 ]
Rauch, Marcus [1 ]
Matsui, Elizabeth [2 ]
Iwai, Shoko [1 ]
Calatroni, Agustin [3 ]
Lynn, Henry [3 ]
Mitchell, Herman [3 ]
Johnson, Christine C. [4 ]
Gern, James E. [5 ]
Togias, Alkis [6 ]
Boushey, Homer A. [7 ]
Kennedy, Suzanne [3 ]
Lynch, Susan V. [1 ]
机构
[1] Univ Calif San Francisco, Div Gastroenterol, San Francisco, CA 94143 USA
[2] Johns Hopkins Univ, Sch Med, Div Pediat Allergy & Immunol, Baltimore, MD 21287 USA
[3] Rho Fed Syst Div Inc, Chapel Hill, NC 27517 USA
[4] Henry Ford Hlth Syst, Div Allergy & Immunol, Dept Publ Hlth Sci, Dept Internal Med, Detroit, MI 48202 USA
[5] Univ Wisconsin, Sch Med & Publ Hlth, Dept Pediat & Med, Madison, WI 53792 USA
[6] NIAID, Bethesda, MD 20814 USA
[7] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
Dust microbiome; Standardized sampling; Phylogenetic microarray; 454-Pyrosequencing; GUT MICROBIOME; DIVERSITY; EXPOSURE; ALLERGY; RISK;
D O I
10.1016/j.mimet.2012.08.016
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Standardized studies examining environmental microbial exposure in populations at risk for asthma are necessary to improve our understanding of the role this factor plays in disease development. Here we describe studies aimed at developing guidelines for high-resolution culture-independent microbiome profiling, using a phylogenetic microarray (PhyloChip), of house dust samples in a cohort collected as part of the NIH-funded Inner City Asthma Consortium (ICAC). We demonstrate that though extracted DNA concentrations varied across dust samples, the majority produced sufficient 16S rRNA to be profiled by the array. Comparison of array and 454-pyrosequencing performed in parallel on a subset of samples, illustrated that increasingly deeper sequencing efforts validated greater numbers of array-detected taxa. Community composition agreement across samples exhibited a hierarchy in concordance, with the highest level of agreement in replicate array profiles followed by samples collected from adjacent 1 x 1 m(2) sites in the same room, adjacent sites with different sized sampling quadrants (1 x 1 and 2 x 2 m(2)), different sites within homes (living and bedroom) to lowest in living room samples collected from different homes. The guidelines for sample collection and processing in this pilot study extend beyond PhyloChip based studies of house-associated microbiota, and bear relevance for other microbiome profiling approaches such as next-generation sequencing. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:231 / 239
页数:9
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