Abstract

The recent reclassification of the Riboviria, and the introduction of multiple new taxonomic categories including both subfamilies and subgenera for coronaviruses (family Coronaviridae, subfamily Orthocoronavirinae), represents a major shift in how official classifications are used to designate specific viral lineages. While the newly defined subgenera provide much-needed standardization for commonly cited viruses of public health importance, no method has been proposed for the assignment of subgenus based on partial sequence data, or for sequences that are divergent from the designated holotype reference genomes. Here, we describe the genetic variation of a 387 nt region of the coronavirus RNA-dependent RNA polymerase (RdRp), which is one of the most used partial sequence loci for both detection and classification of coronaviruses in molecular epidemiology. We infer Bayesian phylogenies from more than 7000 publicly available coronavirus sequences and examine clade groupings relative to all subgenus holotype sequences. Our phylogenetic analyses are largely coherent with whole-genome analyses based on designated holotype members for each subgenus. Distance measures between sequences form discrete clusters between taxa, offering logical threshold boundaries that can attribute subgenus or indicate sequences that are likely to belong to unclassified subgenera both accurately and robustly. We thus propose that partial RdRp sequence data of coronaviruses are sufficient for the attribution of subgenus-level taxonomic classifications and we supply the R package, MyCoV, which provides a method for attributing subgenus and assessing the reliability of the attribution.

Highlights

  • Coronaviruses are widely studied for their impact on human and animal health [1], as well as their broad diversity and host/reservoir associations

  • Separation of the inferred tree topologies into monophyletic clades based on the positions of reference holotype sequences produced logical and well-­ supported groupings that covered the majority of coronavirus diversity explored to date by RNA-d­ ependent RNA polymerase (RdRp) sequencing (Figs 1 and 2)

  • Unclassified deltacoronaviruses were all from bird species in Oceania, and many unclassified alpha- and betacoronaviruses originated in bat species that are exclusively found in Central and South America (Fig. S1, available in the online version of this article)

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Summary

Introduction

Coronaviruses are widely studied for their impact on human and animal health [1], as well as their broad diversity and host/reservoir associations. Numerous molecular studies have identified a wealth of coronavirus diversity harboured by diverse animal hosts [1,2,3,4,5,6,7,8,9], and phylogenetic analysis of sequence data from these studies is helping to increase our understanding of many aspects of disease ecology and evolution [10,11,12] This includes the role of reservoir hosts in disease maintenance and transmission [3, 4, 6, 13,14,15], the evolutionary origins of human-i­nfecting coronaviruses

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