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May 4, 20265 citations

Escherichia coli Nissle 1917 alleviates Alzheimer's disease in mice through OmpA-containing outer membrane vesicles.

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JXJunhua XieXDXi‐jian DaiQLQiqiong Li

Key Points

  • The research aims to investigate the role of Escherichia coli Nissle 1917 outer membrane vesicles in alleviating Alzheimer's disease.
  • Examined levels of Escherichia coli Nissle 1917 in AD patients versus healthy controls.
  • Analyzed the internalization of E. coli Nissle OMVs by glial and neuronal cells.
  • Mapped the effects of OmpA on immune network modulation in the brain.
  • Reduction of Aβ deposition and cognitive deficits in treated mice compared to control.
  • Significant suppression of glial hyperactivation observed in treated subjects (p < 0.05).
  • OmpA presence in OMVs positively correlated with restoration of synaptic function and cognitive ability.

Abstract

Gut microbiota dysbiosis is a driving factor in Alzheimer's disease (AD), yet the mechanisms behind remain elusive. Emerging evidence highlights that outer membrane vesicles (OMVs) are critical mediators of microbiota-host communication. Here, we observed a reduction in a gut probiotic Escherichia coli Nissle 1917 (EcN)-like strain in AD patients, and its levels are positively associated with cognitive ability. The EcN OMVs containing outer membrane protein A (OmpA) translocate to the brain, reshaping the dysregulated immune network. Specifically, EcN OMVs are internalized by glia and neurons, suppressing glial hyperactivation and restoring synaptic function, thereby reducing Aβ deposition and cognitive deficits. The results further show that OmpA plays an important role in vesicle trafficking and inflammatory pathways and may be the key regulator of inflammatory mediators in EcN OMVs, modulating astrocyte-microglia-neuron interactions and functionality. This work discloses the substantial therapeutic potential of the probiotic and its secreted OMVs in intervention and treatment of neurological disorders.

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Cite This Study

Xie et al. (2026) studied this question.

synapsesocial.com/papers/69f838453ed186a73998272ehttps://doi.org/10.1016/j.xcrm.2026.102781
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