Min-Kyung Joo, Xiaoyang Ma, Jung-Woo Shin, Yoon-Jung Shin, Dong-Hyun Kim
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Lactococcus lactis and Bifidobacterium longum attenuate Clostridioides difficile- or Clostridium symbiosum-induced colitis and depression/anxiety-like behavior in male mice.
Clostridioides difficile causes severe colitis, which induces neuroinflammation and psychiatric disorder. In a preliminary study, we isolated Clostridium symbiosum from the stools of patients with ulcerative colitis. Therefore, we first examined whether oral infection with C. difficile or C. symbiosum could induce colitis and depression in male mice. Orally gavaged C. difficile or C. symbiosum caused diarrhea, bodyweight loss, depression/anxiety-like behavior, and tumor necrosis factor (TNF)-α and interleukin (IL)-6 overexpression in the colon and hippocampus in the pseudo-germ-free (PGF) and specific germ-free (SPF) mice. However, healthy volunteer microbiota-derived Lactococcus lactis P22 and/or Bifidobacterium longum P26 suppressed C. difficile or C. symbiosum growth and TNF-α expression in macrophage cells. They alleviated C. difficile- or C. symbiosum-induced bodyweight loss, diarrhea, and neurobehavioral changes in PGF and SPF mice, while reducing pro-inflammatory cytokines (IL-1β, IL-6, and TNF-α) levels in the colon and in the hippocampus. These findings suggest that C. difficile or C. symbiosum can cause colitis and depression/anxiety. Oral administration of P22 and/or P26 may alleviate gut bacteria-induced gut inflammation and depression/anxiety through the inhibition of their growth and inflammatory response.
期刊介绍:
Microbes and Infection publishes 10 peer-reviewed issues per year in all fields of infection and immunity, covering the different levels of host-microbe interactions, and in particular:
the molecular biology and cell biology of the crosstalk between hosts (human and model organisms) and microbes (viruses, bacteria, parasites and fungi), including molecular virulence and evasion mechanisms.
the immune response to infection, including pathogenesis and host susceptibility.
emerging human infectious diseases.
systems immunology.
molecular epidemiology/genetics of host pathogen interactions.
microbiota and host "interactions".
vaccine development, including novel strategies and adjuvants.
Clinical studies, accounts of clinical trials and biomarker studies in infectious diseases are within the scope of the journal.
Microbes and Infection publishes articles on human pathogens or pathogens of model systems. However, articles on other microbes can be published if they contribute to our understanding of basic mechanisms of host-pathogen interactions. Purely descriptive and preliminary studies are discouraged.