4.6 Article

Predominance of Escherichia-Shigella in Gut Microbiome and Its Potential Correlation with Elevated Level of Plasma Tumor Necrosis Factor Alpha in Patients with Tuberculous Meningitis

期刊

MICROBIOLOGY SPECTRUM
卷 10, 期 6, 页码 -

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/spectrum.01926-22

关键词

tuberculous meningitis; gut microbiota; Escherichia-Shigella; TNF-alpha; claudin-5

资金

  1. National Natural Science Foundation of China [82072243]
  2. Research Cultivation Foundation of Capital Medical University [PYZ21166]
  3. Translational Cultivation Project of Beijing Chest Hospital
  4. Capital Medical University [SPY2021-15]

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This study compared the gut microbiota composition and blood cytokine levels of tuberculous meningitis (TBM) patients, pulmonary tuberculosis patients, and healthy controls. The results showed significant gut microbiota dysbiosis in TBM patients, characterized by a high proportion of Escherichia-Shigella species, as well as increased levels of tumor necrosis factor alpha (TNF-alpha) and interleukin 6 (IL-6) in the blood.
Tuberculous meningitis (TBM), the most lethal and disabling form of tuberculosis (TB), may be related to gut microbiota composition, warranting further study. Here we systematically compared gut microbiota compositions and blood cytokine profiles of TBM patients, pulmonary TB patients, and healthy controls. Notably, the significant gut microbiota dysbiosis observed in TBM patients was associated with markedly high proportions of Escherichia-Shigella species as well as increased blood levels of tumor necrosis factor alpha (TNF-alpha) and interleukin 6 (IL-6). Next, we obtained a fecal bacterial isolate from a TBM patient and administered it via oral gavage to mice in order to develop a murine gut microbiota dysbiosis model for use in exploring mechanisms underlying the observed relationship between gut microbial dysbiosis and TBM. Thereafter, cells of commensal Escherichia coli (E. coli) were isolated and administered to model mice by gavage and then mice were inoculated with Mycobacterium tuberculosis (M. tuberculosis). Subsequently, these mice exhibited increased blood TNF-alpha levels accompanied by downregulated expression of tight junction protein claudin-5, increased brain tissue bacterial burden, and elevated central nervous system inflammation relative to corresponding indicators in controls administered PBS by gavage. Thus, our results demonstrated that a signature dysbiotic gut microbiome profile containing a high proportion of E. coli was potentially associated with an increased circulating TNF-alpha level in TBM patients. Collectively, these results suggest that modulation of dysbiotic gut microbiota holds promise as a new strategy for preventing or alleviating TBM.

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