| Literature DB >> 33458259 |
Kentaro Tominaga1, Atsunori Tsuchiya1, Takeshi Mizusawa1, Asami Matsumoto2, Ayaka Minemura2, Kentaro Oka2, Motomichi Takahashi2, Tomoaki Yosida1, Yuzo Kawata1, Kazuya Takahashi1, Hiroki Sato1, Satoshi Ikarashi1, Kazunao Hayashi1, Ken-Ichi Mizuno1, Yosuke Tajima3, Masato Nakano3, Yoshifumi Shimada3, Hitoshi Kameyama3, Junji Yokoyama1, Toshifumi Wakai3, Shuji Terai1.
Abstract
It is reported that an increase in aerobic bacteria, a lack of short-chain fatty acids (SCFAs), and immune disorders in the diverted colon are major causes of diversion colitis. However, the precise pathogenesis of this condition remains unclear. The aim of the present study was to examine the microbiota, intestinal SCFAs, and immunoglobulin A (IgA) in the diverted colon. Eight patients underwent operative procedures for colostomies. We assessed the diverted colon using endoscopy and obtained intestinal samples from the diverted colon and oral colon in these patients. We analyzed the microbiota and SCFAs of the intestinal samples. The bacterial communities were investigated using a 16S rRNA gene sequencing method. The microbiota demonstrated a change in the proportion of some species, especially Lactobacillus, which significantly decreased in the diverted colon at the genus level. We also showed that intestinal SCFA values were significantly decreased in the diverted colon. Furthermore, intestinal IgA levels were significantly increased in the diverted colon. This study was the first to show that intestinal SCFAs were significantly decreased and intestinal IgA was significantly increased in the diverted colon. Our data suggest that SCFAs affect the microbiota and may play an immunological role in diversion colitis.Entities:
Keywords: AA, acetic acid; BA, butyric acid; DC, diversion colitis; Diversion colitis; IgA, immunoglobulin A; Immunoglobulin A; Microbiota; OA, organic acid; PA, propionic acid; SCFAs, short-chain fatty acids; Short-chain fatty acids
Year: 2020 PMID: 33458259 PMCID: PMC7797511 DOI: 10.1016/j.bbrep.2020.100892
Source DB: PubMed Journal: Biochem Biophys Rep ISSN: 2405-5808