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

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