4.7 Article

Interaction between gut microbiota dysbiosis and lung infection as gut-lung axis caused by Streptococcus suis in mouse model

Journal

MICROBIOLOGICAL RESEARCH
Volume 261, Issue -, Pages -

Publisher

ELSEVIER GMBH
DOI: 10.1016/j.micres.2022.127047

Keywords

Gut microbiota dysbiosis; Streptococcus suis; gut -lung axis; Alveolar macrophage

Categories

Funding

  1. Opening Subject of Key Laboratory of Prevention and Control Agents for Animal Bacteriosis, Ministry of Agriculture and Rural Affairs
  2. Hubei Provincial Key Laboratory of Animal Pathogenic Microbiology [KLPCAAB-2019-02, KLPCAAB-2021-02]
  3. Fundamental Research Funds for the Central Universities [2662020DKPY001]

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Streptococcus suis is a zoonotic pathogen that affects the pig farming industry globally. This study found that S. suis can cause damage and inflammation in the intestinal tissue after lung infection. It was also discovered that gut microbiota dysbiosis worsens lung injury during the infection. This research provides new theoretical basis for the treatment of related lung diseases.
Streptococcus suis (S. suis) is an important zoonotic pathogen threatening the global pig farming industry. It causes respiratory and digestive tract infections simultaneously in pigs. The balanced gut microbiota not only affects the local mucosal immune response but also involves the regulation of the immune status of the distant lung tissues that is termed as gut-lung axis. Whether S. suis affects the gut during lung infection and how does the intestinal microbial disturbance play role in the development of lung infection during S. suis exposure is not clear yet. Therefore, in the current study, we constructed the animal model using six-week-old mice (N = 48) divided into four groups with S. suis serotype 2 (SS2)-induced lung infection and the antibiotic treated gut microbiota dysbiosis. By means of various techniques (like HE staining, RT-qPCR, Western Blot and ELISA and viability detection) we explored that S. suis can concurrently cause intestinal tissue damage and inflammation after lung infection. Moreover, gut microbiota dysbiosis changes the balance of Th1/Th2 cells that aggravates lung injury during the infection. Thus, gut-lung axis of the communication between the gut microbiota and lung infection was established through the spleen and blood. In addition, intestinal dysbacteriosis can affect alveolar macrophage activity for a long time and the balance of gut microbiota plays an important role in lung infection caused by S. suis. Hence, this study clarified the pulmonary infection caused by SS2 from the perspective of the intestinal microbiota providing novel theoretical basis for the treatment of related lung diseases.

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