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Comparing Genome Sequencing Methods to Reconstruct the Spread of Piscine Myocarditis Virus in Ireland
Andrew J Tighe1,2,3, Jens Carlsson2, Neil M Ruane1
1Marine Institute, Oranmore, Co. Galway, Ireland.
Abstract:
Piscine myocarditis virus (PMCV), a double-stranded RNA virus, is the causative agent of cardiomyopathy syndrome (CMS) in Atlantic salmon Salmo salar, which was first reported in Ireland in 2012. PMCV continues to be a disease threat to Atlantic salmon aquaculture in Ireland, and as such, it is of growing importance to understand how the virus spreads. Genetic sequences allow for transmission pathways to be examined, with whole genomes providing the most accurate information. In this study, whole genome sequencing has been applied to Irish strains of PMCV, in doing so revealing how > 80% of the genetic diversity of the virus lies outside the commonly sequenced open reading frames (ORFs). Second, this paper examines the effectiveness of incorporating a MinION sequencing approach into routine diagnostics by comparing a MinION generated genome to the corresponding sequence generated via Illumina MiSeq. The results showed the MinION genome shared 99.59% identity with the Illumina genome, and while this accuracy may be sufficient for studies such as pathogen identification and deeper evolutionary questions, it was shown to be insufficient for accurately tracking viral transmission pathways. Finally, comparing Irish and Faroese sequences reveals that some strains of PMCV in Ireland may originate from wild fish.
Insights
Piscine myocarditis virus (PMCV) genetic diversity is largely outside its coding regions. While MinION sequencing is accurate for identification, it’s insufficient for tracking PMCV transmission pathways in Atlantic salmon.
Area of Science:
- Virology
- Aquaculture
- Genomics
Background:
- Piscine myocarditis virus (PMCV) causes cardiomyopathy syndrome (CMS) in Atlantic salmon.
- PMCV poses a significant disease threat to salmon aquaculture in Ireland.
- Understanding PMCV transmission is crucial for disease management.
Purpose of the Study:
- To analyze the whole genome diversity of Irish PMCV strains.
- To evaluate the utility of MinION sequencing for PMCV diagnostics and transmission studies.
- To investigate the origins of PMCV strains in Ireland.
Main Methods:
- Whole genome sequencing of Irish PMCV strains.
- Comparison of MinION and Illumina MiSeq sequencing platforms.
- Phylogenetic analysis of PMCV sequences from Ireland and the Faroe Islands.
Main Results:
- Over 80% of PMCV genetic diversity resides outside commonly sequenced open reading frames (ORFs).
- MinION sequencing achieved 99.59% identity to Illumina MiSeq, sufficient for pathogen identification but not transmission tracking.
- Comparison with Faroese strains suggests some Irish PMCV strains may originate from wild fish.
Conclusions:
- PMCV genetic diversity is extensive and located in non-coding regions.
- MinION sequencing offers a viable option for PMCV identification but requires higher accuracy for transmission pathway analysis.
- Wild fish populations may be a source of PMCV introduction into farmed salmon.
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