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Identification of RNA Virus-Derived RdRp Sequences in Publicly Available Transcriptomic Data Sets
Ingrida Olendraite1, Katherine Brown1, Andrew E Firth1
1Division of Virology, Department of Pathology, Addenbrookes Hospital, University of Cambridge, Cambridge, United Kingdom.
Molecular Biology and Evolution
|April 4, 2023
Summary
Researchers expanded the known diversity of RNA viruses by mining public transcriptomic data. They developed 77 Hidden Markov Model profiles for RNA-dependent RNA polymerase (RdRp) to discover new viral sequences.
Area of Science:
- Virology
- Bioinformatics
- Genomics
Background:
- RNA viruses are diverse and infect most eukaryotic organisms, but only a small fraction of their species have been catalogued.
- Discovering novel RNA virus sequences is crucial for understanding viral diversity and host interactions.
- Existing methods for virus discovery can be costly and limited in scope.
Purpose of the Study:
- To cost-effectively expand the catalogued diversity of RNA virus sequences.
- To develop a robust method for identifying RNA viruses in large-scale genomic datasets.
- To provide a valuable resource for the virus discovery community.
Main Methods:
- Mining publicly available transcriptomic datasets.
- Developing 77 family-level Hidden Markov Model (HMM) profiles for the viral RNA-dependent RNA polymerase (RdRp) gene.
- Searching the NCBI Transcriptome Shotgun Assembly (TSA) database using the developed RdRp HMM profiles.
Main Results:
- Identification of 5,867 contigs encoding RNA virus RdRps or fragments thereof.
- Analysis of the diversity, taxonomic classification, phylogeny, and host associations of the identified viral sequences.
- Successful expansion of the known RNA virus sequence diversity.
Conclusions:
- The study significantly expands the known diversity of RNA viruses.
- The 77 curated RdRp HMM profiles serve as a valuable resource for future virus discovery efforts.
- This approach offers a cost-effective strategy for cataloguing novel RNA virus sequences.
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