2000 |
Children 16 mos–7 years (n = 10), adults 21–34 years (n = 7), elderly ≥ 67 years (n = 5) |
16S rRNA abundance |
Not assessed |
Greater abundance of Enterobacteria in children compared with adults |
Hopkins et al. [4] |
2006 |
Healthy adults between 20 and 50 years (n = 85), healthy adults, and elderly >60 years (n = 145) |
Fluoresence in situ hybridization of 16S rRNA genes |
Greater abundance of Bacteroides and Prevotella in males |
Greater abundance of Enterobacteria in the elderly |
Mueller et al. [8] |
2007 |
Infants (n = 150), adults 25–35 years (n = 54), elderly 80–82 years (n = 45) |
qPCR and fluorescence in situ hybridization of 16S rRNA genes specific for A. muciniphila
|
Not assessed |
Decreased abundance of A. muciniphila, a type of mucin-degrading bacteria in the intestinal tract, in the elderly |
Collado et al. [9] |
2009 |
Adults 18–31 years (n = 17), institutionalized elderly 78–94 years (n = 17) |
Denaturing gradient gel electrophoresis and qPCR |
Not assessed |
Greater abundance of Bacteroides and decreased abundance of Bifidobacteria in the elderly |
Zwielehner et al. [10] |
2013 |
Male (n = 123) and female (n = 132) nonobese diabetic germ-free and pathogen-free mice |
16S rRNA gene amplicon sequencing |
Intestinal communities were distinct among male and female mice |
Sex-specific differences in the intestinal community were most apparent in adult mice |
Markle et al. [7] |