Abstract

BackgroundDextran sulfate sodium (DSS) replicates ulcerative colitis (UC)-like colitis in murine models. However, the microbial characteristics of DSS-triggered colitis require further clarification. To analyze the changes in gut microbiota associated with DSS-induced acute and chronic colitis.MethodsAcute colitis was induced in mice by administering 3% DSS for 1 week in the drinking water, and chronic colitis was induced by supplementing drinking water with 2.5% DSS every other week for 5 weeks. Control groups received the same drinking water without DSS supplementation. The histopathological score and length of the colons, and disease activity index (DAI) were evaluated to confirm the presence of experimental colitis. Intestinal microbiota was profiled by 16S rDNA sequencing of cecal content.ResultsMice with both acute and chronic DSS-triggered colitis had significantly higher DAI and colon histopathological scores in contrast to the control groups (P < 0.0001, P < 0.0001), and the colon was remarkably shortened (P < 0.0001, P < 0.0001). The gut microbiota α-diversity was partly downregulated in both acute and chronic colitis groups in contrast to their respective control groups (Pielou index P = 0.0022, P = 0.0649; Shannon index P = 0.0022, P = 0.0931). The reduction in the Pielou and Shannon indices were more obvious in mice with acute colitis (P = 0.0022, P = 0.0043). The relative abundance of Bacteroides and Turicibacter was increased (all P < 0.05), while that of Lachnospiraceae, Ruminococcaceae, Ruminiclostridium, Rikenella, Alistipes, Alloprevotella, and Butyricicoccus was significantly decreased after acute DSS induction (all P < 0.05). The relative abundance of Bacteroides, Akkermansia, Helicobacter, Parabacteroides, Erysipelatoclostridium, Turicibacter and Romboutsia was also markedly increased (all P < 0.05), and that of Lachnospiraceae_NK4A136_group, Alistipes, Enterorhabdus, Prevotellaceae_UCG-001, Butyricicoccus, Ruminiclostridium_6, Muribaculum, Ruminococcaceae_NK4A214_group, Family_XIII_UCG-001 and Flavonifractor was significantly decreased after chronic DSS induction (all P < 0.05).ConclusionDSS-induced acute and chronic colitis demonstrated similar symptoms and histopathological changes. The changes in the gut microbiota of the acute colitis model were closer to that observed in UC. The acute colitis model had greater abundance of SCFAs-producing bacteria and lower α-diversity compared to the chronic colitis model.

Highlights

  • Dextran sulfate sodium (DSS) replicates ulcerative colitis (UC)-like colitis in murine models

  • disease activity index (DAI) scores were notably raised in the chronic colitis group relative to the control group (P < 0.0001) after 5 weeks

  • The acute colitis group demonstrated notably thinned intestinal mucosa in contrast to that seen in the chronic colitis group

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Summary

Introduction

Dextran sulfate sodium (DSS) replicates ulcerative colitis (UC)-like colitis in murine models. To analyze the changes in gut micro‐ biota associated with DSS-induced acute and chronic colitis. The dextran sodium sulfate (DSS)-stimulated colitis model mimics the pathological damage and symptoms of human UC [1], and is routinely used for studying the pathogenesis and pharmacodynamics of UC [2]. With the development of 16S rDNA sequencing, the DSS-induced colitis model been proven to be well-suited for analyzing colitis-associated microbial changes. DSS-induced acute and chronic colitis mimic histopathological damages associated with UC. In order to establish acute and chronic models of colitis in mice, either 3% or 2.5% DSS is added to the drinking water for varying durations [8, 9]

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