4.5 Review

Implications of Microorganisms in Alzheimer's Disease

Journal

CURRENT ISSUES IN MOLECULAR BIOLOGY
Volume 44, Issue 10, Pages 4584-4615

Publisher

MDPI
DOI: 10.3390/cimb44100314

Keywords

Alzheimer's disease; neuroinflammation; neurodegeneration; inhibitors; gut microbiota; beta-secretase; gamma-secretase; blood-brain barrier

Funding

  1. Hallym University Research Fund
  2. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [NRF-2020R1I1A3074575]

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Alzheimer's disease is a deadly brain disorder characterized by brain shrinkage and dementia. Studies have found evidence of fungal and bacterial infections in the brain tissue of AD patients, which may contribute to neuroinflammation and neurodegeneration. Pathogens such as herpes simplex virus and periodontal bacteria can cross the blood-brain barrier and play a role in the onset of AD.
Alzheimer's disease (AD) is a deadly brain degenerative disorder that leads to brain shrinkage and dementia. AD is manifested with hyperphosphorylated tau protein levels and amyloid beta (A beta) peptide buildup in the hippocampus and cortex regions of the brain. The nervous tissue of AD patients also contains fungal proteins and DNA which are linked to bacterial infections, suggesting that polymicrobial infections also occur in the brains of those with AD. Both immunohistochemistry and next-generation sequencing (NGS) techniques were employed to assess fungal and bacterial infections in the brain tissue of AD patients and non-AD controls, with the most prevalent fungus genera detected in AD patients being Alternaria, Botrytis, Candida, and Malassezia. Interestingly, Fusarium was the most common genus detected in the control group. Both AD patients and controls were also detectable for Proteobacteria, followed by Firmicutes, Actinobacteria, and Bacteroides for bacterial infection. At the family level, Burkholderiaceae and Staphylococcaceae exhibited higher levels in the brains of those with AD than the brains of the control group. Accordingly, there is thought to be a viscous cycle of uncontrolled neuroinflammation and neurodegeneration in the brain, caused by agents such as the herpes simplex virus type 1 (HSV1), Chlamydophila pneumonia, and Spirochetes, and the presence of apolipoprotein E4 (APOE4), which is associated with an increased proinflammatory response in the immune system. Systemic proinflammatory cytokines are produced by microorganisms such as Cytomegalovirus, Helicobacter pylori, and those related to periodontal infections. These can then cross the blood-brain barrier (BBB) and lead to the onset of dementia. Here, we reviewed the relationship between the etiology of AD and microorganisms (such as bacterial pathogens, Herpesviridae viruses, and periodontal pathogens) according to the evidence available to understand the pathogenesis of AD. These findings might guide a targeted anti-inflammatory therapeutic approach to AD.

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