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. 2011 Dec 7;2:94. doi: 10.3389/fphys.2011.00094

Table 1.

Studies which have shown altered fecal and mucosal microbiome in disease states.

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.