Nematode microRNAs can Individually Regulate Interferon Regulatory Factor 4 and mTOR in Differentiating T Helper 2

Julien Soichot1, Nathalie Guttmann1, Hubert Rehrauer2

  • 1Institute of Parasitology, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland.

Insights

Nematode-secreted microRNAs (miRNAs) can suppress host immune cell differentiation and function. Specific parasite miRNAs, like Hpo-miR-71-5p, target key immune pathways, potentially impairing the host response to parasitic infections.

Area of Science:

  • Immunology
  • Molecular Biology
  • Parasitology

Background:

  • Parasitic nematodes employ sophisticated immune evasion strategies, including the release of molecules like microRNAs (miRNAs).
  • Parasite-derived miRNAs are implicated in modulating host immune responses, but isolating their specific effects is challenging.
  • Understanding how nematode miRNAs impact host immunity is crucial for developing new therapeutic strategies against helminth infections.

Purpose of the Study:

  • To investigate the effects of nematode-secreted miRNAs on the in vitro differentiation of Th2 lymphocytes and macrophages.
  • To identify specific nematode miRNAs and their host targets involved in immune modulation.
  • To assess the potential of parasite miRNAs to impair host innate and adaptive immunity.

Main Methods:

  • Exposure of immune cells to nematode-derived miRNAs from models of gastrointestinal infections (Heligmosomoides polygyrus bakeri, Trichuris muris, Ascaris suum).
  • Analysis of signaling pathways (e.g., interferon gamma, IL-2/STAT5, mTOR) and gene targets (e.g., Irf4, Mtor) affected by specific miRNAs.
  • Assessment of cytokine levels in macrophages and incorporation of miRNAs into host protein complexes.

Main Results:

  • Hpo-miR-71-5p downregulated interferon gamma, IL-2/STAT5, and mTOR signaling pathways.
  • Interferon regulatory factor 4 (Irf4) was validated as a target of Hpo-miR-71-5p, and Mtor as a target of Asu-miR-791-3p.
  • Nematode miRNAs were shown to persist in host cells and can be incorporated into Argonaute complexes, suggesting functional integration.

Conclusions:

  • Nematode-derived miRNAs can impair both innate and adaptive immune responses.
  • Hpo-miR-71-5p, a non-mammalian miRNA, interacts with host pathways critical for anthelmintic immunity.
  • The subtle but synergistic effects of multiple nematode miRNAs highlight a significant mechanism of host immune modulation by parasites.

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