Analysis of treatment effects on the microbial ecology of the human intestine

被引:39
作者
Engelbrektson, Anna L.
Korzenik, Joshua R.
Sanders, Mary Ellen
Clement, Brian G.
Leyer, Gregory
Klaenhammer, Todd R.
Kitts, Christopher L. [1 ]
机构
[1] Calif Polytech State Univ San Luis Obispo, Dept Biol Sci, Environm Biotechnol Inst, San Luis Obispo, CA 93407 USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Boston, MA 02115 USA
[3] Dairy & Food Culture Technol, Centennial, CO USA
[4] Univ Calif San Diego, Scripps Inst Oceanog, San Diego, CA 92103 USA
[5] Danisco USA, Madison, WI USA
[6] N Carolina State Univ, Raleigh, NC 27695 USA
关键词
terminal restriction fragment length polymorphism; probiotics; antibiotics; prebiotics; gastrointestinal microbiota;
D O I
10.1111/j.1574-6941.2006.00112.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A large number of studies have investigated gastrointestinal microbiota and changes in the gastrointestinal community. However, a concern in these studies is how best to assess changes in gastrointestinal community structure. This paper presents two different human trials where the fecal terminal restriction fragment length polymorphism data sets were analyzed to search for treatment effects. Principle components analysis and cluster analysis based on grouped data are compared with analysis of data by subject using distance coefficients. Comparison with baseline within an individual before grouping by treatment provided a clearer indication of treatment effects than did an evaluation of data grouped before analysis. In addition, a large within-subject sample size and multiple baseline samples are necessary to accurately analyze treatment effects.
引用
收藏
页码:239 / 250
页数:12
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