MicroRNA-146a Deficiency Protects against Listeria monocytogenes Infection by Modulating the Gut Microbiota

Chong-Tao Du1, Wei Gao2, Ke Ma3

  • 1Key Laboratory of Zoonosis, Ministry of Education, College of Veterinary Medicine, Jilin University, Changchun 130062, China. duct@jlu.edu.cn.

Insights

MicroRNA-146a (miR-146a) deficiency enhances resistance to Listeria monocytogenes infection by altering the gut microbiota composition. This suggests miR-146a regulates gut bacteria to control infection.

Area of Science:

  • Immunology
  • Microbiology
  • Genetics

Background:

  • Gut microbiota and microRNAs are crucial for host defense against infections.
  • The specific role of microRNA-146a (miR-146a) in Listeria monocytogenes infection and its interaction with the gut microbiota remains largely unknown.

Purpose of the Study:

  • To investigate whether miR-146a influences L. monocytogenes infection by modulating the gut microbiota.
  • To characterize the impact of miR-146a on host response and gut microbial composition during L. monocytogenes infection.

Main Methods:

  • Utilized wild-type and miR-146a-deficient mice and macrophages.
  • Assessed animal survival, cell death, bacterial clearance, and gut microbiota composition.
  • Employed high-throughput sequencing of 16S rRNA to analyze microbial communities.

Main Results:

  • L. monocytogenes infection upregulated miR-146a expression in vitro and in vivo.
  • miR-146a-deficient mice exhibited increased resistance to L. monocytogenes infection and reduced bacterial invasion/survival in macrophages.
  • Significant alterations in gut microbiota were observed in miR-146a-deficient mice, including decreased Proteobacteria and increased short-chain fatty acid producers.

Conclusions:

  • miR-146a deficiency confers protection against L. monocytogenes infection.
  • This protection is mediated through the regulation of gut microbiota composition.
  • Modulating miR-146a levels represents a potential strategy for controlling bacterial infections via the gut microbiome.

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