Dysbiosis of Fecal Microbiota From Complement 3 Knockout Mice With Constipation Phenotypes Contributes to Development of Defecation Delay

被引:21
作者
Choi, Yun Ju [1 ]
Kim, Ji Eun [1 ]
Lee, Su Jin [1 ]
Gong, Jeong Eun [1 ]
Son, Hong Joo [2 ]
Hong, Jin Tae [3 ]
Hwang, Dae Youn [1 ,4 ]
机构
[1] Pusan Natl Univ, Dept Biomat Sci, Coll Nat Resources & Life Sci, Life & Ind Convergence Res Inst,Program BK21 FOUR, Miryang, South Korea
[2] Pusan Natl Univ, Dept Life Sci & Environm Biochem, Coll Nat Resources & Life Sci, Life & Ind Convergence Res Inst, Miryang, South Korea
[3] Chungbuk Natl Univ, Coll Pharm, Cheongju, South Korea
[4] Pusan Natl Univ, Lab Anim Resources Ctr, Miryang, South Korea
基金
新加坡国家研究基金会;
关键词
complement C3; constipation; dysbiosis; fecal microbiota transplantation; C-kit; INFLAMMATORY-BOWEL-DISEASE; GUT-MICROBIOTA; CLOSTRIDIUM-DIFFICILE; COLONIC-MUCOSA; GEN; NOV; PATHOGENESIS; SUPPRESSION; ACTIVATION; EXPRESSION; PROBIOTICS;
D O I
10.3389/fphys.2021.650789
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Significant phenotypes for constipation were detected in complement 3 (C3) knockout (KO) mice, although no research has been conducted on an association with alteration of gut microbiota. To investigate the effects of dysbiosis on fecal microbiota from C3 KO mice with constipation, the composition of fecal microbiota was characterized in mid-colons of 16-week-old C3 KO mice, and their function for defecation delay development was examined after fecal microbiota transplantation (FMT) of C3 KO mice. Some significant alterations in constipation phenotypes, including stool parameters and histopathological structure, were detected in 16-week-old C3 KO mice compared to those of wild-type (WT) mice. Fecal microbiota of C3 KO mice exhibited decreases in Anaerocolumna, Caecibacterium, Christensenella, Kineothrix, and Oscillibacter populations and increases in Prevotellamassilia, Reuthenibacterium, Prevotella, Eubacterium, Culturomica, Bacteroides, and Muribaculum populations. In FMT study, key stool parameters, including weight and water content, were remarkably declined in a transplanted KO (KFMT) group of antibiotics-induced depletion of microbiota (AiDM)-WT and AiDM-KO mice, and a similar change was observed in fecal morphology. However, intestine length decreased in only the KFMT group of AiDM-WT mice compared with that of AiDM-KO mice. The mucosal layer and muscle thickness were commonly decreased in the KFMT group of AiDM-WT and AiDM-KO mice, and significant alterations in the crypt structure of Lieberkuhn and molecular regulators, including AQP8, C-kit, and 5-HT, were observed in the same group. Taken together, results of the present study indicate that dysbiosis of fecal microbiota from C3 KO mice with constipation phenotypes has a key role in the induction and regulation of defecation delay.
引用
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页数:16
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