Table 1.
Group | Method, microbiota analyzed | Diagnostic criteria and subjects | Finding | Reference | |
---|---|---|---|---|---|
IBS | Q-PCR, fecal microbiome | Rome II, n = 27 | ↓ Lactobacillus spp. in IBS-D subjects | Malinen et al. (2005) | |
BS-D (n = 12), IBS-C (n = 9), IBS-A (n = 6) | ↑ Veillonella spp. in IBS-C | ||||
Culture/DGGE, fecal microbiome | Rome II, n = 26 | Increased number of aerobes in IBS patients | Mättö et al. (2005) | ||
BS-D (n = 12), IBS-C (n = 9), IBS-A (n = 5) | Temporal instability in IBS patients revealed by DGGE | ||||
Q-PCR, Phylogenic Microarray, fecal microbiome | Rome II, n = 62 IBS-D (n = 25), IBS-C (n = 18), IBS-A (n = 19) | ↑ Ratio of the Firmicutes to Bacteroidetes in IBS | Rajilic-Stojanovic et al., 2011) | ||
↑ in numbers of Dorea, Ruminococcus, and Clostridium spp. in IBS | |||||
↓ Bacteroidetes in IBS | |||||
↓ Bifidobacterium and Faecalibacterium spp. | |||||
↓ Average number of methanogens in IBS | |||||
Fractionation/16S rRNA gene cloning and sequencing, Q-PCR, fecal microbiome | Rome II, n = 24 | Significant differences in Coprococcus, Collinsella, and Coprobacillus Phyla in the IBS group compared to controls | Kassinen et al. (2007) | ||
IBS-D (n = 10), IBS-C (n = 8), IBS-A (n = 6) | |||||
DGGE, fecal microbiome | Rome II, n = 47 | Significant difference between IBS and healthy controls | Codling et al. (2010) | ||
No sub-typing | Significantly more variation in microbiota of healthy volunteers than that of IBS patients | ||||
FISH, fecal and duodenal microbiome | Rome II, n = 41 | ↓ Bifidobacteria in IBS subjects compared to healthy controls | Kerckhoffs et al. (2009) | ||
IBS-D (n = 14) IBS-C (n = 11) IBS-A (n = 16) | |||||
Q-PCR, fecal microbiome | Rome II and III, n = 26 | ↑ Veillonella and Lactobacillus in IBS | Tana et al. (2010) | ||
IBS-D (n = 8) IBS-C (n = 11) IBS-A (n = 7) | |||||
IBD | FISH adapted to flow cytometry, fecal microbiota | Active CD (n = 13) | Clostridium coccoides was reduced in UC | Sokol et al. (2006) | |
Active UC (n = 13) | C. leptum group was reduced in CD | ||||
IC (n = 5), HS (n = 13). | Bacteroides group was more abundant in IC | ||||
16S rRNA DGGE analysis, fecal microbiota | Active CD (n = 5) Inactive CD (n = 11), HS (n = 18) | ↓ Temporal stability of dominant species for all Crohn’s disease patients | Scanlan et al. (2006) | ||
Bifidobacterium spp. were similar in all samples | |||||
Clostridiales and Bacteroidales communities are altered in Crohn’s disease | |||||
DGGE, Q-PCR, fecal microbiota | CD (n = 68) Unaffected relatives (n = 84), HS (n = 55) |
CD vs. unaffected relatives | Joossens et al. (2011) | ||
↓ Dialister invisus, an uncharacterized species of Clostridium cluster XIVa, Faecalibacterium prausnitzii and Bifidobacterium adolescentis | |||||
↑ Ruminococcus gnavus | |||||
Unaffected relatives vs. HS | |||||
↓ Collinsella aerofaciens and member of the Escherichia coli–Shigella group | |||||
↑ Ruminococcus torques | |||||
T-RFLP analysis16S rRNA gene, Q-PCR, ileal and rectal biopsies | Monozygotic twin pairs that were discordant (n = 6) or concordant (n = 4) for CD, HS (n = 6) | Predominantly ileal CD vs. co-twins and CD localized in the colon | Willing et al. (2009) | ||
↓ Faecalibacterium prausnitzii | |||||
↑ Escherichia coli | |||||
16S rRNA gene sequencing, mucosal biopsies | Inflamed and non-inflamed intestinal tissue from 6 CD (n = 12), 6 UC (n = 12), HS (n = 5) | ↓ Mucosal microbial diversity in IBD | Walker et al. (2011) | ||
↓ Firmicutes in IBD samples and ↑ Bacteroidetes | |||||
↑ Enterobacteriaceae in CD only significant differences in microbial community structure between inflamed and non-inflamed mucosal sites | |||||
rRNA sequence analysis and Q-PCR | UC (n = 61), CD (n = 68) | ↓ Bacteroidetes and Lachnospiraceae in IBD | Frank et al. (2007) | ||
HS (n = 61) | ↑ Actinobacteria and Proteobacteria in IBD | ||||
Obesity | Pyrosequencing, cecal contents | Ob/Ob mice | ↑ Firmicutes | Turnbaugh et al. (2006) | |
↓ Firmicute to Bacteroides ratio | |||||
16S rRNA sequencing, cecal contents | Ob/Ob mice | ↓ Bacteroidetesob/ob animals | Ley et al. (2005) | ||
↑ Firmicutes | |||||
16S rRNA sequencing | Human | ↓ Bacteroides in obesity | Ley et al. (2006b) | ||
↑ Bacteroides during calorie restriction | |||||
Q-PCR, MALDI-TOF spectral analysis, fecal microbiota | Human | Bifidobacterium animalis and Methanobrevibacter smithii were associated with normal bodyweight | Million et al. (2011) | ||
Lactobacillus reuteri was associated with obesity | |||||
Autism | Q-PCR, fecal microbiota | Autistic (n = 15), HS (n = 8) | ↑ Clostridium bolteae and Clostridium clusters I and XI in autistic children | Song et al. (2004) | |
↓ Clostridium cluster XIVab in autistic children | |||||
16S rRNA gene sequencing and culture, fecal microbiota Gastric and duodenal sampling | Autistic (n = 13), HS (n = 8) | Fecal samples | Finegold et al. (2002) | ||
Children with autism had nine species of Clostridium not found in controls | |||||
Control children had three species of Clostridium not found in autistic children Gastric and duodenal Specimens | |||||
No non-spore-forming anaerobes and microaerophilic bacteria from controls significant numbers of non-spore-forming anaerobes and microaerophilic bacteria in children with autism | |||||
Pyrosequencing, fecal microbiota | Autistic (n = 33) Non-affected siblings (n = 7), HS (n = 8) |
↑ Increased diversity and richness in the autistic gastrointestinal microbiome | Finegold et al. (2010) | ||
↑ Bacteroidetes in the severely autistic group | |||||
↑ Firmicutes in the control group | |||||
↑ Desulfovibrio species and Bacteroides vulgatus autistic children |
IBS-D, diarrhea predominant IBS; IBS-C, constipation predominant IBS; IBS-A, alternating IBS; UC, ulcerative colitis; CD, Crohn’s disease; IC, infectious colitis; HS, healthy subjects; DGGE, denaturing gradient gel electrophoresis; Q-PCR, quantitative PCR; FISH, fluorescent in situ hybridization; T-RFLP, terminal restriction length polymorphism.