疟原虫感染诱导宿主脾脏m6A表观转录组重编程研究

Abstract

N 6 -Methyladenosine (m 6 A), the most abundant mammalian mRNA modification, has been reported to modulate various viral infections. Although it has been confirmed that RNA modifications can also modulate the replication and development of different parasites, the role of the RNA epitranscriptome in the regulation of host response post parasite infection remains to be elucidated. Here we report host spleen m 6 A epitranscriptome landscapes induced by different strains of the malaria parasite Plasmodium yoelii . We found that malaria parasite infection dramatically changes host spleen m 6 A mRNA modification and gene expression. Additionally, malaria parasite infection reprograms host immune response pathways by regulating the m 6 A modification enzymes. Collectively, our study is the first characterization of host spleen m 6 A methylome triggered by malaria parasite infections, and our data identify m 6 A modifications as significant transcriptome-wide marks during host-parasite interactions. We demonstrate that host mRNA methylation machinery can sense and respond to malaria parasite infections, and provide new insights into epitranscriptomic mechanisms underlying parasite-induced pathogenesis.