Impact of natural occurring erap1 single nucleotide polymorphisms within mirna-binding sites on hcmv infection

Human cytomegalovirus (HCMV) is a beta-herpesvirus that causes serious problems in people with a compromised immune system, whereas it coexists asymptomatically within the host with a healthy immune system. Like other viruses, HCMV has adopted multiples strategies to manipulate the host's immune responses. Among them, expression of viral microRNAs (miRNAs) is one of the most intriguing. HCMV miR-UL112-5p and miR-US4-1 have been found to contribute to immune evasion by targeting the endoplasmic reticulum aminopeptidase 1 (ERAP1), a highly polymorphic key component of antigen processing. The current incomplete picture on the interplay between viral miRNAs and host immunity implies the need to better characterize the host genetic determinants. Naturally occurring single nucleotide polymorphisms (SNPs) within the miRNA binding sites of target genes may affect miRNA-target interactions. In this review, we focus on the relevance of 3 ' untranslated region (3 ' UTR)ERAP1SNPs within miRNA binding sites in modulating miRNA-mRNA interactions and the possible consequent individual susceptibility to HCMV infection. Moreover, we performed an in silico analysis using different bioinformatic algorithms to predictERAP1variants with a putative powerful biological function. This evidence provides a basis to deepen the knowledge on how 3 ' UTRERAP1variants may alter the mechanism of action of HCMV miRNAs, in order to develop targeted antiviral therapies.