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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/30942
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dc.contributor.advisorBercik, Premysl-
dc.contributor.authorClements, Charlotte-
dc.date.accessioned2025-01-23T20:19:34Z-
dc.date.available2025-01-23T20:19:34Z-
dc.date.issued2025-
dc.identifier.urihttp://hdl.handle.net/11375/30942-
dc.description.abstractMajor depressive disorder (MDD) is highly prevalent in our society, with many patients poorly responding to the available treatments. Accumulating evidence suggests that gut microbiota may be causally linked to depression, by interacting with the host immune or neural systems. Fecal microbiota transplantation (FMT) is a technique used to study disorders of the gut-brain axis by transplanting fecal microbiota of patients and healthy controls into germ-free mice to produce the phenotype of interest. With studies suggesting increased IL-6 among individuals with MDD, an FMT animal model of MDD was created using stool microbiota from MDD patients with the highest levels of serum IL-6 and age/sex-matched healthy controls with low serum IL-6. Our results provide evidence of elevated serum IL-6 correlating with increased presence of anxiety and depressive-like behavior. Six bacteria genera Acetanaerobacterium (p=0.0230), Bifidobacterium (p=0.0309), Blautia (p=0.0386), Candidatus soleaferrea (p=0.0446), Roseburia (p=0.0169), and Ruminococcus (p=0.0290) correlated with ileum tissue IL-6 concentration. There was a positive correlation between ileum and serum IL-6 concentrations (p=0.0108). Finally, using immunofluorescence we found an increased expression of IL-6 in the neural cells in the hippocampus and amygdala, among the MDD mice. Thus, this study demonstrates that alterations in gut microbiota correlate with intestinal tissue IL-6, which then correlate with serum IL-6 and elevated brains IL-6 in mice with MDD microbiota, as well as altered behaviors among mice with high serum IL-6. Overall, these results support the notion that IL-6 plays an important role in MDD, connecting gut microbiota to the brain.en_US
dc.language.isoen_USen_US
dc.subjectMajor Depressive Disorder, Interleukin-6, Microbiota, Gut-Brain Axis, Inflammation, Fecal Microbiota Transplanten_US
dc.titleMicrobiota Related Production of IL-6 as a Mechanism Underlying Symptoms in Patients with Major Depressive Disorderen_US
dc.typeThesisen_US
dc.description.degreetypeThesisen_US
dc.description.degreeMaster of Science (MSc)en_US
dc.description.layabstractAnimal models play a key role in scientific research as they provide a deeper understanding of how disease develop and how they can be treated. In this study an animal model of Major Depressive Disorder (MDD) was created by transferring human bacteria from patients with MDD or healthy volunteers (HV) into germ-free mice. Depressive-like behavior developed in mice colonized with gut bacteria from some, but not all, patients. Compared to their age and sex-matched controls, mice with microbiota from patients 1 and 2 displayed depressive-like behavior in the Tail Suspension Test (TST), and mice with microbiota from all patients tended to have abnormal behavior in the Sucrose Preference Test. The proinflammatory marker, serum interleukin-6 (IL-6) levels of colonized mice revealed a trend towards increased MDD behaviours among mice with high serum IL-6, independent of donor type. Analysis of fecal samples revealed significant differences in relative abundance of bacteria between MDD and HV donor groups; furthermore, five types of bacteria significantly correlate with intestinal tissue IL-6 concentration. Lastly, immunofluorescence imaged expression of IL-6 in the brain revealed a higher percentage of cells expressing IL-6 in MDD mice compared to HV. Overall, the results suggest the peripheral proinflammatory cytokine IL-6 concentration correlates with the presence of depressive-like behaviors; furthermore, correlations among bacteria, intestinal, and brain IL-6 concentration were identified. This study provides a potential explanation for how bacteria in the human gut relates to MDD behaviors through the concentration of IL-6.en_US
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