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Updated: Feb 10, 2026

A Tissue Displacement-based Contusive Spinal Cord Injury Model in Mice
Published on: June 18, 2017
Gut-lung axis perturbation and Bifidobacterium potential after spinal cord injury in humans and mice
Yuanqing Ding1, Xingyu Chen1, Yiming Tao1
1Department of Neurosurgery, National Center for Neurological Disorders, Neurosurgical Institute of Fudan University, Shanghai Clinical Medical Center of Neurosurgery, Shanghai Key Laboratory of Brain Function and Restoration and Neural Regeneration, Huashan Hospital, Fudan University, Shanghai 200040, P.R. China.
Abstract:
Spinal cord injury (SCI) predisposes patients to severe respiratory complications. Integrating clinical observations with a mouse model, we identified gut-lung axis perturbation as a key mechanism. SCI increased the similarity between gut and lung microbial communities, consistent with cross-compartment convergence driven by intestinal dysbiosis. Fecal microbiota transplantation from SCI donors reproduced this convergence in healthy recipients. Crucially, oral Bifidobacterium supplementation restored intestinal community structure, reduced gut-lung similarity, and attenuated pulmonary inflammation following an Escherichia coli challenge. These findings indicate that SCI disrupts gut-lung compartmentalization and that augmenting beneficial gut taxa mitigates downstream pulmonary consequences. Microbiota-targeted strategies therefore warrant evaluation as adjuncts to reduce post-SCI respiratory risk.
Insights
Spinal cord injury (SCI) disrupts the gut-lung axis, increasing microbial similarity. Supplementing beneficial gut bacteria like Bifidobacterium can restore balance and reduce lung inflammation after SCI.
Area of Science:
- Microbiome research
- Immunology
- Neuroscience
Background:
- Spinal cord injury (SCI) frequently leads to severe respiratory complications.
- The gut-lung axis, a bidirectional communication pathway, is crucial for maintaining homeostasis.
- Dysbiosis in the gut microbiome is increasingly recognized as a factor in systemic inflammation.
Purpose of the Study:
- To investigate the role of gut-lung axis perturbation in respiratory complications following SCI.
- To identify microbial mechanisms linking SCI to pulmonary inflammation.
- To evaluate the therapeutic potential of modulating the gut microbiome.
Main Methods:
- Utilized a mouse model of SCI alongside clinical observations.
- Analyzed gut and lung microbial communities using sequencing techniques.
- Performed fecal microbiota transplantation (FMT) experiments.
- Administered oral Bifidobacterium supplementation and challenged with Escherichia coli.
Main Results:
- SCI induced significant convergence between gut and lung microbial communities, indicating disrupted compartmentalization.
- FMT from SCI donors replicated this microbial convergence in healthy recipients.
- Oral Bifidobacterium supplementation restored gut microbial structure, reduced gut-lung microbial similarity, and attenuated pulmonary inflammation.
Conclusions:
- SCI disrupts the integrity of the gut-lung axis, promoting microbial cross-contamination.
- Targeting the gut microbiome, specifically by augmenting beneficial taxa like Bifidobacterium, can mitigate pulmonary inflammation post-SCI.
- Microbiota-based strategies represent a promising avenue for reducing respiratory risks associated with spinal cord injury.
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