Volume 28, Issue 4 pp. 613-619
Gastroenterology

Decreased abundance of Faecalibacterium prausnitzii in the gut microbiota of Crohn's disease

Takehide Fujimoto

Takehide Fujimoto

Division of Mucosal Immunology, Graduate School

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Hirotsugu Imaeda

Hirotsugu Imaeda

Department of Medicine, Shiga University of Medical Science, Otsu, Japan

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Kenichiro Takahashi

Kenichiro Takahashi

Division of Mucosal Immunology, Graduate School

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Eiji Kasumi

Eiji Kasumi

Division of Mucosal Immunology, Graduate School

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Shigeki Bamba

Shigeki Bamba

Division of Mucosal Immunology, Graduate School

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Yoshihide Fujiyama

Yoshihide Fujiyama

Department of Medicine, Shiga University of Medical Science, Otsu, Japan

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Akira Andoh

Corresponding Author

Akira Andoh

Division of Mucosal Immunology, Graduate School

Correspondence

Dr Akira Andoh, Division of Mucosal Immunology, Graduate School, Shiga University of Medical Science, Seta Tukinowa, Otsu 520-2192, Japan. Email: [email protected]

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First published: 06 December 2012
Citations: 246
Declaration of conflicts of interest: The authors have no conflict of interests to declare in this study.

Abstract

Background and Aims

Dysbiosis is thought to be relevant to the etiology and pathogenesis of Crohn's disease (CD). In this study, we investigated the abundance of Faecalibacterium prausnitzii, as well as Bilophila wadsworthia, in the gut microbiota of Japanese CD patients.

Methods

Forty-seven CD patients and 20 healthy controls were enrolled. Abundance of F. prausnitzii in fecal samples was quantified by real-time polymerase chain reaction. The gut microbiota profile was evaluated by terminal restriction fragment length polymorphisms.

Results

The abundance of F. prausnitzii significantly decreased in CD patients compared with healthy subjects. B. wadsworthia was scarcely detected in the same samples. Among CD patients, the Crohn's Disease Activity Index, C-reactive protein levels, and erythrocyte sedimentation rate were significantly lower, and serum albumin levels were significantly higher in the high F. prausnitzii group compared with the low group. Terminal restriction fragment length polymorphisms analysis showed that fecal bacterial communities of CD patients differed from those of healthy individuals. The changes in simulated bacterial composition indicated that class Clostridia, including genus Faecalibacterium, was significantly less abundant in CD patients as compared with healthy individuals. The bacterial diversity measured by the Shannon Diversity Index was significantly reduced in CD patients compared with healthy individuals.

Conclusion

The decreased abundance of class Clostridia, including F. prausnitzii, may translate into a reduction of commensal bacteria-mediated, anti-inflammatory activities in the mucosa, which are relevant to the pathophysiology of CD. In contrast, the role of B. wadsworthia was suspected to be minimal.

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