AUTHOR=Yu Pei-Lun , Wu Rui , Cao San-Jie , Wen Yi-Ping , Huang Xiao-Bo , Zhao Shan , Lang Yi-Fei , Zhao Qin , Lin Ju-Chun , Du Sen-Yan , Yu Shu-Min , Yan Qi-Gui 

TITLE=Pseudorabies virus exploits N6-methyladenosine modification to promote viral replication

JOURNAL=Frontiers in Microbiology

VOLUME=14

YEAR=2023

URL=https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2023.1087484

DOI=10.3389/fmicb.2023.1087484

ISSN=1664-302X

ABSTRACT=<sec><title>Introduction</title><p>Pseudorabies virus (PRV) is the pathogenic virus of porcine pseudorabies (PR), belonging to the <italic>Herpesviridae</italic> family. PRV has a wide range of hosts and in recent years has also been reported to infect humans. N<sup>6</sup>-methyladenosine (m<sup>6</sup>A) modification is the major pathway of RNA post-transcriptional modification. Whether m<sup>6</sup>A modification participates in the regulation of PRV replication is unknown.</p></sec><sec><title>Methods</title><p>Here, we investigated that the m<sup>6</sup>A modification was abundant in the PRV transcripts and PRV infection affected the epitranscriptome of host cells. Knockdown of cellular m<sup>6</sup>A methyltransferases METTL3 and METTL14 and the specific binding proteins YTHDF2 and YTHDF3 inhibited PRV replication, while silencing of demethylase ALKBH5 promoted PRV output. The overexpression of METTL14 induced more efficient virus proliferation in PRV-infected PK15 cells. Inhibition of m<sup>6</sup>A modification by 3-deazaadenosine (3-DAA), a m<sup>6</sup>A modification inhibitor, could significantly reduce viral replication.</p></sec><sec><title>Results and Discussion</title><p>Taken together, m<sup>6</sup>A modification played a positive role in the regulation of PRV replication and gene expression. Our research revealed m<sup>6</sup>A modification sites in PRV transcripts and determined that m<sup>6</sup>A modification dynamically mediated the interaction between PRV and host.</p></sec>