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CircRNA and miRNA expression analysis in livers of mice with infection. | LitMetric

AI Article Synopsis

  • Toxoplasmosis is a zoonotic disease caused by a parasite, and its effects on circRNAs and miRNAs in infected mouse livers during both acute and chronic stages are not well understood.
  • High-throughput RNA sequencing identified 265 differentially expressed circRNAs and 171 miRNAs during acute infection, and 97 circRNAs and 77 miRNAs in chronic infection, highlighting significant changes in gene expression.
  • Certain immune response-related gene functions and metabolic pathways were enriched during both infection stages, revealing key insights into the molecular mechanisms behind liver disease caused by Toxoplasmosis in mice.

Article Abstract

Toxoplasmosis is an important zoonotic parasitic disease caused by (). However, the functions of circRNAs and miRNAs in response to infection in the livers of mice at acute and chronic stages remain unknown. Here, high-throughput RNA sequencing was performed for detecting the expression of circRNAs and miRNAs in livers of mice infected with 20 cysts at the acute and chronic stages, in order to understand the potential molecular mechanisms underlying hepatic toxoplasmosis. Overall, 265 and 97 differentially expressed (DE) circRNAs were found in livers at the acute and chronic infection stages in comparison with controls, respectively. In addition, 171 and 77 DEmiRNAs were found in livers at the acute and chronic infection stages, respectively. Functional annotation showed that some immunity-related Gene ontology terms, such as "positive regulation of cytokine production", "regulation of T cell activation", and "immune receptor activity", were enriched at the two infection stages. Moreover, the pathways "Valine, leucine, and isoleucine degradation", "Fatty acid metabolism", and "Glycine, serine, and threonine metabolism" were involved in liver disease. Remarkably, DEcircRNA 6:124519352|124575359 was significantly correlated with DEmiRNAs mmu-miR-146a-5p and mmu-miR-150-5p in the network that was associated with liver immunity and pathogenesis of disease. This study revealed that the expression profiling of circRNAs in the livers was changed after infection, and improved our understanding of the transcriptomic landscape of hepatic toxoplasmosis in mice.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9646959PMC
http://dx.doi.org/10.3389/fcimb.2022.1037586DOI Listing

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