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Mouse Footpad Inoculation Model to Study Viral-Induced Neuroinflammatory Responses
Published on: June 14, 2020
Basic Science and Pathogenesis
Giuseppe D Ciccotosto1, Elly Bijlsma1, Stuart G Dashper1
1The University of Melbourne, Parkville, VIC, Australia.
Background:
We have previously shown that repeated oral inoculation of mice with bacteria that cause the chronic oral disease periodontitis resulted in brain infiltration and induction of Alzheimer's disease (AD)-like pathology. Here, we examined whether purified bacterial membrane vesicles (BMVs) from the oral pathobiont Porphyromonas gingivalis or oral commensal Neisseria oralis could enter the brain and cause pathology, without the need for an infection of the brain.
Methods:
Three experimental groups of 36 female C57BL/6 mice, were injected intravenously with 10 µg of purified BMVs from P. gingivalis or N. oralis, or an equal volume of vehicle alone (Control), through the tail vein on Days 1, 5, 8 and 11. Six mice from each group were killed on Days 2, 6, 12, 26, 40 and 55, then PBS perfused before their brains dissected. Immunohistochemistry analyses of 3 hemibrains per group, per timepoint, were probed for the presence of the BMVs, neuronal damage, neuroinflammation, AD-like pathology and immune system activation.
Result:
BMVs from both P. gingivalis and N. oralis were found within the brains after one injection. Detection of P. gingivalis MV positive cells peaked at two timepoints, at Days 6 and 26, whereas detection of N. oralis MV positive cells peaked at Day 26, 2 weeks after the final intravenous injection. By Day 55, the detection of cells positive for both BMVs had decreased to levels consistent with the BMVs being removed from the brains. There were similar levels of neuronal degeneration, Il-6 and IL-1β in the hippocampus between the three groups of mice over time, but only P. gingivalis MVs were able to induce microgliosis and astrogliosis in the hippocampus. There were no amyloid plaques detected in the brains, but phosphorylated Tau peaked significantly at Day 26 in the mice that received BMVs.
Conclusion:
BMVs from both N. oralis and P. gingivalis entered the brain from the bloodstream but caused different host responses. Upon cessation of BMV injection, the BMVs were naturally removed from the brain over time, suggesting that treatment of the source of the BMVs, namely periodontitis, would reduce exposure to brain pathology causing agents.
Insights
Bacterial membrane vesicles (BMVs) from oral bacteria can enter the brain and trigger Alzheimer's disease (AD)-like changes. Treating the source of these vesicles, like periodontitis, may reduce brain pathology.
Area of Science:
- Neuroscience
- Microbiology
- Immunology
Background:
- Previous studies linked periodontitis bacteria to Alzheimer's disease (AD)-like brain pathology.
- This study investigated if bacterial membrane vesicles (BMVs) from oral bacteria could induce brain pathology without direct infection.
Purpose of the Study:
- To determine if purified BMVs from Porphyromonas gingivalis and Neisseria oralis can cross the blood-brain barrier.
- To assess the neuropathological effects of these BMVs in a mouse model.
Main Methods:
- Female C57BL/6 mice received intravenous injections of BMVs from P. gingivalis, N. oralis, or vehicle.
- Brain tissue was analyzed at multiple time points using immunohistochemistry for BMVs, neuronal damage, neuroinflammation, and AD markers.
Main Results:
- BMVs from both species were detected in the brain after injection and were cleared by Day 55.
- P. gingivalis BMVs induced microgliosis and astrogliosis, while both BMVs showed similar levels of neuronal degeneration and inflammatory cytokines.
- Phosphorylated Tau levels increased significantly in BMV-treated mice, but amyloid plaques were not detected.
Conclusions:
- Oral bacterial BMVs can enter the brain and elicit distinct host responses.
- The clearance of BMVs suggests that targeting the source of these vesicles, such as periodontitis, could mitigate brain pathology.
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