Description:
<jats:title>Abstract</jats:title><jats:p>Malaria is one of the most severe infectious diseases affecting humans and it is caused by protozoan pathogens of the species <jats:italic>Plasmodium</jats:italic> (spp.). The malaria parasite <jats:italic>Plasmodium</jats:italic> is characterized by a complex, multistage life cycle that requires tight gene regulation which allows for host invasion and defense against host immune responses. Unfortunately, the mechanisms regulating gene expression during <jats:italic>Plasmodium</jats:italic> infection remain largely elusive, though several lines of evidence implicate a major involvement of non‐coding RNAs (ncRNAs). The ncRNAs have been found to play a key role in regulating transcriptional and post‐transcriptional events in a broad range of organisms including <jats:italic>Plasmodium</jats:italic>. In <jats:italic>Plasmodium</jats:italic> ncRNAs have been shown to regulate key events in the multistage life cycle and virulence ability. Here we review recent progress involving ncRNAs (microRNAs, long non‐coding RNAs, and circular RNAs) and their role as regulators of gene expression during <jats:italic>Plasmodium</jats:italic> infection in human hosts with focus on the possibility of using these molecules as biomarkers for monitoring disease status. We also discuss the surprising function of ncRNAs in mediating the complex interplay between parasite and human host and future perspectives of the field.</jats:p><jats:p>This article is categorized under:<jats:list list-type="simple">
<jats:list-item><jats:p>RNA in Disease and Development > RNA in Disease</jats:p></jats:list-item>
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