Parallel analysis of miRNAs and mRNAs suggests distinct regulatory networks in Crassostrea gigas infected by Ostreid herpesvirus 1

• Published in: BMC Genomics
• Main Authors: Rosani Umberto, Abbadi Miriam, Green Timothy, Bai Chang-Ming, Turolla Edoardo, Arcangeli Giuseppe, Wegner K. Mathias, Venier Paola
• Other Authors: Rosani, Umberto, Abbadi, Miriam, Green, Timothy, Bai, Chang-Ming, Turolla, Edoardo, Arcangeli, Giuseppe, Wegner K., Mathia, Venier, Paola
• Format: Article in Journal/Newspaper
• Language: English
• Published: BioMed Central (BMC) Part of Springer Nature 2020
• Subjects: oyster; miRNA; OsHV-1; ADAR; C. gigas; miRNAome; Crassostrea gigas
• Online Access: http://hdl.handle.net/11577/3350559; https://doi.org/10.1186/s12864-020-07026-7; https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-020-07026-7

Background: Since 2008, the aquaculture production of Crassostrea gigas was heavily affected by mass mortalities associated to Ostreid herpesvirus 1 (OsHV-1) microvariants worldwide. Transcriptomic studies revealed the major antiviral pathways of the oyster immune response while other findings suggested that also small non-coding RNAs (sncRNA) such as microRNAs might act as key regulators of the oyster response against OsHV-1. To explore the explicit connection between small non-coding and protein-coding transcripts, we performed paired whole transcriptome analysis of sncRNA and messenger RNA (mRNA) in six oysters selected for different intensities of OsHV-1 infection. Results: The mRNA profiles of the naturally infected oysters were mostly governed by the transcriptional activity of OsHV-1, with several differentially expressed genes mapping to the interferon, toll, apoptosis, and pro-PO pathways. In contrast, miRNA profiles suggested more complex regulatory mechanisms, with 15 differentially expressed miRNAs (DE-miRNA) pointing to a possible modulation of the host response during OsHV-1 infection. We predicted 68 interactions between DE-miRNAs and oyster 3′-UTRs, but only few of them involved antiviral genes. The sncRNA reads assigned to OsHV-1 rather resembled mRNA degradation products, suggesting the absence of genuine viral miRNAs. Conclusions: We provided data describing the miRNAome during OsHV-1 infection in C. gigas. This information can be used to understand the role of miRNAs in healthy and diseased oysters, to identify new targets for functional studies and, eventually to disentangle cause and effect relationships during viral infections in marine mollusks.