Please use this identifier to cite or link to this item:
http://elar.urfu.ru/handle/10995/141653
Title: | Circadian Rhythm Perturbation Aggravates Gut Microbiota Dysbiosis in Dextran Sulfate Sodium-Induced Colitis in Mice |
Authors: | Amara, J. Itani, T. Hajal, J. Bakhos, J. -J. Saliba, Y. Aboushanab, S. A. Kovaleva, E. G. Fares, N. Mondragon, A. C. Miranda, J. M. |
Issue Date: | 2024 |
Publisher: | Multidisciplinary Digital Publishing Institute (MDPI) |
Citation: | Amara , J., Itani, T., Hajal, J., Bakhos, J-J., Saliba, Y., Aboushanab, S., Kovaleva, E., Fares, N., Mondragon, A. C., & Miranda, J. (2024). Circadian Rhythm Perturbation Aggravates Gut Microbiota Dysbiosis in Dextran Sulfate Sodium-Induced Colitis in Mice. Nutrients, 16(2), [247]. https://doi.org/10.3390/nu16020247 |
Abstract: | Circadian rhythm disruption is increasingly considered an environmental risk factor for the development and exacerbation of inflammatory bowel disease. We have reported in a previous study that nychthemeral dysregulation is associated with an increase in intestinal barrier permeability and inflammation in mice with dextran sulfate sodium (DSS)-induced colitis. To investigate the effect of circadian rhythm disruption on the composition and diversity of the gut microbiota (GM), sixty male C57BL/6J mice were initially divided to two groups, with the shifted group (n = 30) exposed to circadian shifts for three months and the non-shifted group (n = 30) kept under a normal light–dark cycle. The mice of the shifted group were cyclically housed for five days under the normal 12:12 h light–dark cycle, followed by another five days under a reversed light–dark cycle. At the end of the three months, a colitis was induced by 2% DSS given in the drinking water of 30 mice. Animals were then divided into four groups (n = 15 per group): sham group non-shifted (Sham-NS), sham group shifted (Sham-S), DSS non-shifted (DSS-NS) and DSS shifted (DSS-S). Fecal samples were collected from rectal content to investigate changes in GM composition via DNA extraction, followed by high-throughput sequencing of the bacterial 16S rRNA gene. The mouse GM was dominated by three phyla: Firmicutes, Bacteroidetes and Actinobacteria. The Firmicutes/Bacteroidetes ratio decreased in mice with induced colitis. The richness and diversity of the GM were reduced in the colitis group, especially in the group with inverted circadian rhythm. Moreover, the GM composition was modified in the inverted circadian rhythm group, with an increase in Alloprevotella, Turicibacter, Bacteroides and Streptococcus genera. Circadian rhythm inversion exacerbates GM dysbiosis to a less rich and diversified extent in a DSS-induced colitis model. These findings show possible interplay between circadian rhythm disruption, GM dynamics and colitis pathogenesis. © 2024 by the authors. |
Keywords: | BACTERIAL DIVERSITY CIRCADIAN RHYTHM DSS-INDUCED COLITIS DYSBIOSIS GUT MICROBIOTA ANIMALS BACTEROIDETES CIRCADIAN RHYTHM COLITIS DEXTRAN SULFATE DYSBIOSIS FIRMICUTES GASTROINTESTINAL MICROBIOME MALE MICE MICE, INBRED C57BL RNA, RIBOSOMAL, 16S BACTERIAL RNA DRINKING WATER RNA 16S DEXTRAN SULFATE RNA 16S ACTINOBACTERIA ALLOPREVOTELLA ANIMAL EXPERIMENT ANIMAL MODEL ARTICLE BACTERIAL COLONIZATION BACTEROIDES CIRCADIAN RHYTHM CLINICAL PROTOCOL CONTROLLED STUDY DEXTRAN SULFATE SODIUM-INDUCED COLITIS DNA EXTRACTION DYSBIOSIS EXPERIMENTAL DESIGN FECES ANALYSIS FIRMICUTES GENUS HIGH THROUGHPUT SEQUENCING INTESTINE FLORA LIGHT DARK CYCLE MALE MICROBIAL COMMUNITY MOUSE NONHUMAN PHYLUM SAMPLE SHAM PROCEDURE SHANNON INDEX SIMPSON INDEX SPECIES COMPOSITION SPECIES DIVERSITY SPECIES RICHNESS STREPTOCOCCUS ANIMAL BACTEROIDETES C57BL MOUSE CIRCADIAN RHYTHM COLITIS DYSBIOSIS GENETICS |
URI: | http://elar.urfu.ru/handle/10995/141653 |
Access: | info:eu-repo/semantics/openAccess cc-by |
SCOPUS ID: | 85183263287 |
WOS ID: | 001151267600001 |
PURE ID: | 52297935 |
ISSN: | 2072-6643 |
DOI: | 10.3390/nu16020247 |
metadata.dc.description.sponsorship: | Research Council of the Saint Joseph University-Faculty of Medicine; Ministry of Education and Science of the Russian Federation, Minobrnauka, (FPH86); Ministry of Education and Science of the Russian Federation, Minobrnauka The research funding from the Ministry of Science and Higher Education of the Russian Federation (Ural Federal University Program of Development within the Priority-2030 Program), Grant FPH86, is gratefully acknowledged. This work was partly supported by the Research Council of the Saint Joseph University-Faculty of Medicine. |
RSCF project card: | Research Council of the Saint Joseph University-Faculty of Medicine; Ministry of Education and Science of the Russian Federation, Minobrnauka, (FPH86); Ministry of Education and Science of the Russian Federation, Minobrnauka The research funding from the Ministry of Science and Higher Education of the Russian Federation (Ural Federal University Program of Development within the Priority-2030 Program), Grant FPH86, is gratefully acknowledged. This work was partly supported by the Research Council of the Saint Joseph University-Faculty of Medicine. |
Appears in Collections: | Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
2-s2.0-85183263287.pdf | 2,48 MB | Adobe PDF | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.