Abstract:Tuatara (Sphenodon punctatus) are one of the most phylogenetically isolated species and provide a unique host system to study virus evolution. While the tuatara genome, sequenced in 2020, revealed many endogenous viral elements, we know little of the exogenous viruses that infect tuatara. We performed a metatranscriptomics study of tuatara cloaca samples from a wild population on Takapourewa (Stephens Island), Aotearoa New Zealand. From these data we identified 49 potentially novel viral species that spanned 2… Show more
“…It is remarkable that the genome of the virus we call MaTV because its genome was found first in maize and its ancestor teosinte, in Mexico, was also found in the cloaca of a tuatara on the tiny uninhabited island of Takpourewa (also known as Stephens Island) in New Zealand (Table 1), a wildlife refuge on which no crops are cultivated (East et al, 1995). Moreover, BCaTV and ZLaTV sequences, first described in kohlrabi and Manchurian wild rice, respectively, in China (Yang et al, 2022) were also found in the Asian long-horned tick in China (Ni et al, 2023) and in the cloaca of a tuatara in New Zealand (Waller et al, 2022). These wide distributions suggest these viruses may have wide host ranges, and perhaps rather cryptic symptomatology.…”
Section: Discussionmentioning
confidence: 99%
“…to MaTV (Lappe et al, 2022). Like the MaTV genome, all eleven of these genomes were discovered in metagenomics sequencing projects using Illumina sequencing (Shi et al, 2016;Chiapello et al, 2020;Waller et al, 2022;Yang et al, 2022;Ni et al, 2023). As discussed below, all of the genomes were misannotated because ORFs were assumed to begin with an AUG codon.…”
Section: Identification Of Viruses Similar Tomentioning
SummaryTombusviridaeis a large family of single-stranded, positive-sense RNA plant viruses with uncapped, non-polyadenylated genomes encoding 5-7 open reading frames (ORFs). Previously, we discovered, by high-throughput sequencing of maize and teosinte RNA, a novel genome of a virus we call Maize-associated tombusvirus (MaTV). Here we determined the precise termini of the MaTV genome by using 5’ and 3’ rapid amplification of cDNA ends (RACE). In GenBank, we discovered eleven other nearly complete viral genomes with MaTV-like genome organizations and related RNA-dependent RNA polymerase (RdRp) sequences. These genomes came from diverse plant, fungal, invertebrate and vertebrate organisms, and some have been found in multiple organisms across the globe. The available 5’ untranslated regions (UTRs) of these genomes are remarkably long: at least 438 to 727 nucleotides (nt), in contrast to those of other tombusvirids, which are <150 nt. Moreover these UTRs contain 6 to 12 AUG triplets that are unlikely to be start codons, because - with the possible exception of MaTV - there are no large or conserved ORFs in the 5’ UTRs. Such features suggest an internal ribosome entry site (IRES), but we found no conserved secondary structures. In the 50 nt upstream of and adjacent to the ORF1 start codon, the 5’ UTR was cytosine-rich and guanosine-poor. As in most tombusvirids, ORF2 (RdRp gene) appears to be translated by in-frame ribosomal readthrough of the ORF1 stop codon. Indeed, in all twelve genomes we identified RNA structures known in other tombusviruses to facilitate this readthrough. ORF5 is predicted to be translated by readthrough of the ORF3 (coat protein gene) stop codon as in genusLuteovirus. The resulting readthrough domains are highly divergent. ORF4 overlaps with ORF3 and may initiate with a non-AUG start codon. We also found no obvious 3’ cap-independent translation elements, which are present in other tombusvirids. The twelve genomes diverge sufficiently from other tombusvirids to warrant classification in a new genus. Because they contain two leaky stop codons and a potential leaky start codon, we propose to name this genusRimosavirus(rimosa= leaky in Latin).
“…It is remarkable that the genome of the virus we call MaTV because its genome was found first in maize and its ancestor teosinte, in Mexico, was also found in the cloaca of a tuatara on the tiny uninhabited island of Takpourewa (also known as Stephens Island) in New Zealand (Table 1), a wildlife refuge on which no crops are cultivated (East et al, 1995). Moreover, BCaTV and ZLaTV sequences, first described in kohlrabi and Manchurian wild rice, respectively, in China (Yang et al, 2022) were also found in the Asian long-horned tick in China (Ni et al, 2023) and in the cloaca of a tuatara in New Zealand (Waller et al, 2022). These wide distributions suggest these viruses may have wide host ranges, and perhaps rather cryptic symptomatology.…”
Section: Discussionmentioning
confidence: 99%
“…to MaTV (Lappe et al, 2022). Like the MaTV genome, all eleven of these genomes were discovered in metagenomics sequencing projects using Illumina sequencing (Shi et al, 2016;Chiapello et al, 2020;Waller et al, 2022;Yang et al, 2022;Ni et al, 2023). As discussed below, all of the genomes were misannotated because ORFs were assumed to begin with an AUG codon.…”
Section: Identification Of Viruses Similar Tomentioning
SummaryTombusviridaeis a large family of single-stranded, positive-sense RNA plant viruses with uncapped, non-polyadenylated genomes encoding 5-7 open reading frames (ORFs). Previously, we discovered, by high-throughput sequencing of maize and teosinte RNA, a novel genome of a virus we call Maize-associated tombusvirus (MaTV). Here we determined the precise termini of the MaTV genome by using 5’ and 3’ rapid amplification of cDNA ends (RACE). In GenBank, we discovered eleven other nearly complete viral genomes with MaTV-like genome organizations and related RNA-dependent RNA polymerase (RdRp) sequences. These genomes came from diverse plant, fungal, invertebrate and vertebrate organisms, and some have been found in multiple organisms across the globe. The available 5’ untranslated regions (UTRs) of these genomes are remarkably long: at least 438 to 727 nucleotides (nt), in contrast to those of other tombusvirids, which are <150 nt. Moreover these UTRs contain 6 to 12 AUG triplets that are unlikely to be start codons, because - with the possible exception of MaTV - there are no large or conserved ORFs in the 5’ UTRs. Such features suggest an internal ribosome entry site (IRES), but we found no conserved secondary structures. In the 50 nt upstream of and adjacent to the ORF1 start codon, the 5’ UTR was cytosine-rich and guanosine-poor. As in most tombusvirids, ORF2 (RdRp gene) appears to be translated by in-frame ribosomal readthrough of the ORF1 stop codon. Indeed, in all twelve genomes we identified RNA structures known in other tombusviruses to facilitate this readthrough. ORF5 is predicted to be translated by readthrough of the ORF3 (coat protein gene) stop codon as in genusLuteovirus. The resulting readthrough domains are highly divergent. ORF4 overlaps with ORF3 and may initiate with a non-AUG start codon. We also found no obvious 3’ cap-independent translation elements, which are present in other tombusvirids. The twelve genomes diverge sufficiently from other tombusvirids to warrant classification in a new genus. Because they contain two leaky stop codons and a potential leaky start codon, we propose to name this genusRimosavirus(rimosa= leaky in Latin).
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