Fig 1.
Schematic representation of the genomes of rhabdoviruses analysed.
The genomes are shown in (+) sense with arrows indicating the locations of ORFs ≥180 nt. The five common structural protein genes (N, P, M, G and L) are shaded in black. Orthologous genes or genes encoding structurally similar proteins are shaded in the same colour, including viroporin-like proteins which are shaded in yellow. ORFs for which no orthologous or structurally similar proteins could be identified are shaded in light grey. The viruses are grouped according to established genera, proposed new genera or unassigned species (see Fig. 2).
Fig 2.
ML phylogenetic tree of 100 rhabdovirus L protein sequences.
Branches are colour-coded according to known vector species, while the principal animal host species (where known) are shown by indicated symbols. Horizontal branch lengths are drawn to a scale of amino acid substitutions/site, and all bootstrap proportion values (BSP) ≥ 85% are shown by the * symbol. Newly proposed genera are indicated by a † symbol. Cytorhabdovirus, novirhabdovirus and nucleorhabdovirus outgroup sequences were excluded from the tree as they were too divergent to establish a reliable rooting. The tree is therefore rooted arbitrarily on one of two basal clades (genera Almendravirus and Bahiavirus) that comprise viruses isolated from mosquitoes.
Table 1.
Averages (standard deviation) of the actual lengths of each genome region (nt), and the normalized lengths relative to the length of the L gene.
Fig 3.
The relative length of sequences of known or predicted function and unknown function.
Sequences of known or predicted function include ORFs and transcriptional regulatory sequences. Sequences of unknown function include 5’- and 3’-UTRs within transcriptional units and IGRs between transcriptional units. Genomic leader sequences (up to the N gene TI sequence) and trailer sequences (beyond the L gene TTP sequence) were excluded from the analysis as the extreme terminal sequences of some viruses were not determined. The sequence lengths are provided for each virus in the data set but identified only by their genus assignment.
Fig 4.
Illustration of the similar structural characteristics of viroporin-like proteins.
The sequences illustrate predicted hydrophobic transmembrane domains (grey shaded) which are usually bounded by anchoring charged residues (black shaded), an N-terminal domain containing several large aromatic residues (F, Y, W), and a C-terminal domain containing a large number of basic residues (R, K, H) (bold and underlined). The proteins are assigned numbers according to our defined annotation rules and are grouped according to existing genera and new genera proposed in this paper.
Fig 5.
TURBS-like sequence motifs in the genomes of sripuviruses, curioviruses, hapaviruses and ephemeroviruses.
The motif features the sequence UGGGA (highlighted) flanked short stretches of anti-complementary sequence (single underlined) upstream of overlapping or adjacent initiation and termination codons (double underlined). Variations in the TURBS sequence (UGAGA) occur in CHOV, SMV and ARUV. The ORF junctions (M-Mx; U1-U1x; G-Gx; α1-α2) are indicated for each virus. No TURBS-like sequence was detected upstream of the adjacent initiation and termination codons at the GLOV G—U3 junction or the KOOLV α1-α2 junction.
Fig 6.
Number of alternative ORFs of various size ranges (nt) across the genome data set.
ORFs ≥ 90 nt were identified in each genome and the assembled set was grouped into size ranges (i.e., 90–149, 150–209, 210–269, etc). The total number of observations of ORFs in each size range is shown. All ORFs ≥180 nt (60 aa) are listed in S2 Table.
Fig 7.
A model for the evolution of rhabdovirus accessory genes.
The model accounts for accessory genes that emerge initially from small ORFs arising randomly through mutation in alternative reading frames within existing ORF or in 5’ or 3’UTRs within transcriptional units.