Genomic Analysis of Sindbis Virus Reveals Uncharacterized Diversity within the Australasian Region, and Support for Revised SINV Taxonomy

• Published in: Viruses 2023-12, Vol.16 (1), p.7
• Main Authors: Michie, Alice, Ernst, Timo, Pyke, Alyssa T, Nicholson, Jay, Mackenzie, John S, Smith, David W, Imrie, Allison
• Format: Article
• Language: English
• Subjects: alphavirus; Amino acid sequence; Amino acids; Analysis; Animals; arbovirus; Argyle virus; Australia; Bird migration; Culicidae; Datasets; Disease; Distribution; Divergence; DNA sequencing; E2 gene; Epidemiology; Fourier transforms; Genes; Genomes; Genomic analysis; Genomics; Genotypes; Humans; Identification and classification; Mosquitoes; Nucleotide sequencing; Nucleotides; Phenotypes; Phylogenetics; Phylogeny; RNA viruses; Sindbis virus; Sindbis Virus - genetics; Surveillance; Taxonomic revision; Thomson’s Lake virus; Togaviridae; Varieties; Viral genetics; Viruses; Whole genome sequencing
• ISSN: 1999-4915; 1999-4915
• DOI: 10.3390/v16010007

Sindbis virus (SINV) is a widely dispersed mosquito-borne alphavirus. Reports of Sindbis disease are largely restricted to northern Europe and South Africa. SINV is frequently sampled in Australian mosquito-based arbovirus surveillance programs, but human disease has rarely been reported. Molecular epidemiological studies have characterized six SINV genotypes (G1-G6) based on E2 gene phylogenies, mostly comprising viruses derived from the African-European zoogeographical region and with limited representation of Australasian SINV. In this study, we conducted whole genome sequencing of 66 SINV isolates sampled between 1960 and 2014 from countries of the Australasian region: Australia, Malaysia, and Papua New Guinea. G2 viruses were the most frequently and widely sampled, with three distinct sub-lineages defined. No new G6 SINV were identified, confirming geographic restriction of these viruses to south-western Australia. Comparison with global SINV characterized large-scale nucleotide and amino acid sequence divergence between African-European G1 viruses and viruses that circulate in Australasia (G2 and G3) of up to 26.83% and 14.55%, respectively, divergence that is sufficient for G2/G3 species demarcation. We propose G2 and G3 are collectively a single distinct alphavirus species that we name Argyle virus, supported by the inapparent or mild disease phenotype and the higher evolutionary rate compared with G1. Similarly, we propose G6, with 24.7% and 12.61% nucleotide and amino acid sequence divergence, is a distinct alphavirus species that we name Thomson's Lake virus.