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Updated: Aug 5, 2026

Whole Genome Sequencing for Rapid Characterization of Rabies Virus Using Nanopore Technology
Published on: August 18, 2023
Differences in codon usage between host-species-specific rabies virus clades are driven by non-GC3 nucleotide
Rowan Durrant1,2, Jonathan Dushoff2,3,4, Matthew Arnold1,5
1Boyd Orr Centre for Population and Ecosystem Health, School of Biodiversity, One Health & Veterinary Medicine, College of Medical, Veterinary & Life Sciences, University of Glasgow, Glasgow G12 8QQ, United Kingdom.
Rabies virus (RABV) codon usage varies between bat and carnivore hosts, driven by dinucleotide content and host immune pressures. Bat-associated RABV may face stronger host antiviral protein selection.
Area of Science:
- Virology
- Genomics
- Evolutionary Biology
Background:
- Rabies virus (RABV) exhibits codon usage bias influenced by nucleotide content, translation efficiency, and host immune selection.
- Previous studies on RABV codon usage have primarily focused on broad viral clades.
- RABV infects diverse mammalian hosts, with clades often associated with specific host species.
Purpose of the Study:
- To investigate differences in dinucleotide content and codon usage bias between host-associated RABV clades.
- To identify the factors driving these codon usage variations within RABV.
- To explore potential host immune selection pressures shaping RABV evolution.
Main Methods:
- Analysis of publicly available RABV nucleoprotein gene sequences.
- Comparative analysis of dinucleotide composition (e.g., CpG content) across different RABV clades.
- Investigation of codon usage patterns and their correlation with host association.
Main Results:
- Codon usage variation was most pronounced between bat- and carnivore-associated RABV clades.
- Specific dinucleotides (C1, GA3, GT3) significantly influenced codon usage patterns.
- Carnivore-associated RABV clades showed higher CpG content than bat-associated clades.
- Bat-associated RABV sequences had fewer predicted zinc-finger antiviral protein binding motifs than expected.
Conclusions:
- Host-associated codon usage differences in RABV are linked to dinucleotide content and host immune pressures.
- Bat-associated RABV clades may experience elevated selection from host zinc-finger antiviral proteins.
- Further research is needed to elucidate the specific mechanisms of host antiviral protein interactions with RABV.
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