Inflammation Drives Dysbiosis and Bacterial Invasion in Murine Models of Ileal Crohn's Disease

被引:151
作者
Craven, Melanie [1 ]
Egan, Charlotte E. [2 ]
Dowd, Scot E. [3 ]
McDonough, Sean P. [4 ]
Dogan, Belgin [1 ]
Denkers, Eric Y. [2 ]
Bowman, Dwight [2 ]
Scherl, Ellen J. [5 ]
Simpson, Kenneth W. [1 ]
机构
[1] Cornell Univ, Coll Vet Med, Dept Clin Sci, Ithaca, NY 14853 USA
[2] Cornell Univ, Coll Vet Med, Dept Microbiol & Immunol, Ithaca, NY 14853 USA
[3] MR DNA Mol Res, Shallowater, TX USA
[4] Cornell Univ, Coll Vet Med, Dept Pathol, Ithaca, NY 14853 USA
[5] Cornell Univ, Weill Cornell Med Coll, Jill Roberts Inflammatory Bowel Dis Ctr, Div Gastroenterol & Hepatol, New York, NY 10021 USA
关键词
ESCHERICHIA-COLI STRAINS; CD4(+) T-LYMPHOCYTES; BOWEL-DISEASE; E; COLI; TOXOPLASMA-GONDII; ORAL INFECTION; ADHERENT; NOD2; MUCOSA; MICROBIOTA;
D O I
10.1371/journal.pone.0041594
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background and Aims: Understanding the interplay between genetic susceptibility, the microbiome, the environment and the immune system in Crohn's Disease (CD) is essential for developing optimal therapeutic strategies. We sought to examine the dynamics of the relationship between inflammation, the ileal microbiome, and host genetics in murine models of ileitis. Methods: We induced ileal inflammation of graded severity in C57BL6 mice by gavage with Toxoplasma gondii, Giardia muris, low dose indomethacin (LDI;0.1 mg/mouse), or high dose indomethacin (HDI;1 mg/mouse). The composition and spatial distribution of the mucosal microbiome was evaluated by 16S rDNA pyrosequencing and fluorescence in situ hybridization. Mucosal E. coli were enumerated by quantitative PCR, and characterized by phylogroup, genotype and pathotype. Results: Moderate to severe ileitis induced by T. gondii (day 8) and HDI caused a consistent shift from > 95% Gram + Firmicutes to > 95% Gram - Proteobacteria. This was accompanied by reduced microbial diversity and mucosal invasion by adherent and invasive E. coli, mirroring the dysbiosis of ileal CD. In contrast, dysbiosis and bacterial invasion did not develop in mice with mild ileitis induced by Giardia muris. Superimposition of genetic susceptibility and T. Gondii infection revealed greatest dysbiosis and bacterial invasion in the CD-susceptible genotype, NOD2(-/-), and reduced dysbiosis in ileitis-resistant CCR2(-)/- mice. Abrogating inflammation with the CD therapeutic anti-TNF-alpha-mAb tempered dysbiosis and bacterial invasion. Conclusions: Acute ileitis induces dysbiosis and proliferation of mucosally invasive E. coli, irrespective of trigger and genotype. The identification of CCR2 as a target for therapeutic intervention, and discovery that host genotype and therapeutic blockade of inflammation impact the threshold and extent of ileal dysbiosis are of high relevance to developing effective therapies for CD.
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页数:10
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