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Tracheophyte genomes keep track of the deep evolution of the Caulimoviridae

  • Scientific Reports 8, Article number: 572 (2018)
  • doi:10.1038/s41598-017-16399-x
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Endogenous viral elements (EVEs) are viral sequences that are integrated in the nuclear genomes of their hosts and are signatures of viral infections that may have occurred millions of years ago. The study of EVEs, coined paleovirology, provides important insights into virus evolution. The Caulimoviridae is the most common group of EVEs in plants, although their presence has often been overlooked in plant genome studies. We have refined methods for the identification of caulimovirid EVEs and interrogated the genomes of a broad diversity of plant taxa, from algae to advanced flowering plants. Evidence is provided that almost every vascular plant (tracheophyte), including the most primitive taxa (clubmosses, ferns and gymnosperms) contains caulimovirid EVEs, many of which represent previously unrecognized evolutionary branches. In angiosperms, EVEs from at least one and as many as five different caulimovirid genera were frequently detected, and florendoviruses were the most widely distributed, followed by petuviruses. From the analysis of the distribution of different caulimovirid genera within different plant species, we propose a working evolutionary scenario in which this family of viruses emerged at latest during Devonian era (approx. 320 million years ago) followed by vertical transmission and by several cross-division host swaps.


Although the field of viral metagenomics is rapidly expanding the repertoire of viral genome sequences available for evolutionary studies1, it only provides a picture of viral diversity over a very short geological time scale. However, viruses can leave molecular records in the genomes of their hosts in the form of endogenous viral elements (EVEs). EVEs are viral sequences that have been inserted in the nuclear genomes of their hosts by either active or passive integration mechanisms and in many cases have been retained for extended periods of time, sometimes millions of years. Although many EVEs are subject to sequence decay, it is common to be able to reconstruct ancestral viral genome sequences, particularly for high copy number EVEs, due to the random nature of the mutations that do occur. The study of EVEs does allow the evolution of viruses to be traced, much like a fossil record2. For example, the study of endogenous retroviruses has uncovered the extended diversity and host range of retroviruses, and has provided evidence that they have a marine origin, and that they developed in parallel with their vertebrate hosts more than 450 million years ago (MYA)3,4,5.

Plant EVEs were first discovered a little more than 20 years ago6 but have only received a fraction of the research attention directed towards EVEs in humans and other animals. Most characterized plant EVEs are derivatives of viruses in the family Caulimoviridae7. The Caulimoviridae is one of the five families of reverse-transcribing viruses or virus-like retrotransposons that occur in eukaryotes8, and is the only family of viruses with a double-stranded DNA genome that infects plants ( Unlike retroviruses, members of the Caulimoviridae do not integrate in the genome of their host as part of their replication cycle. However, caulimovirid DNA can be captured in the host genome, probably by illegitimate recombination mechanisms. In fact, five of the eight officially recognized genera of the Caulimoviridae have endogenous counterparts in at least one plant genome7,9.

Recently, Geering et al.10 showed that EVEs from an additional tentative genus of the Caulimoviridae, called ‘Florendovirus’, are widespread in the genomes of cultivated and wild angiosperms, and provided evidence for the oldest EVE integration event yet reported in plants, at 1.8 MYA10. Sister taxa relationships between florendoviruses in South American and Australian plants suggested Gondwanan links and a minimum age of 34 MYA for this virus genus based on estimates of when land bridges between these two continents were severed. About 65% of all angiosperm species that were examined contained endogenous florendoviruses and for five, these sequences constituted more than 0.5% of the total plant genome content. Another remarkable feature of the biology of florendoviruses was their extremely broad host range, which included both the primitive ANITA-grade angiosperms, as well as the more advanced mesangiosperms. Putative bipartite florendoviral genomes were also found, a unique characteristic for any viral retroelement.

Almost contemporaneously to the study of Geering et al.10, Mushegian and Elena9 interrogated plant genomes for the presence of 30 K viral movement protein (MP) homologues, a superfamily of proteins that is common to the Caulimoviridae and a diverse range of plant viruses with single-stranded RNA genomes. While some of the MPs that were detected were undoubtedly those of endogenous florendoviruses and other recognized taxa, some MPs appeared to derive from previously undescribed genera in the Caulimoviridae. In this and a subsequent study11, caulimovirid MPs were shown to be nearly universally distributed in angiosperm genomes but also, importantly, in the genomes or transcriptomes of conifers, ferns and club mosses, thus extending the host range of this family of viruses to non-flowering land plants.

The reverse transcriptase (RT) domain is the most conserved domain in the genome of viral retroelements and is used for classification12,13. The strong sequence conservation of this domain allows high quality alignments to be generated, even for distantly related taxa, and therefore searches for homologues in plant genomes is the most sensitive and informative method to assess whether endogenous caulimovirids occur in the first place, and then what diversity exists. In the following study, we provide evidence that almost every vascular land plant (Tracheophyta), even the most primitive species such as the club mosses (Lycopodiophyte), contain endogenous caulimovirids. By analyzing the distribution of different genera, we unveil a complex pattern of associations and propose a scenario in which the Caulimoviridae would have emerged approximately 320 million years ago.


Augmenting the diversity of known endogenous caulimovirids

A collection of RT domain sequences from known exogenous and endogenous caulimovirids was used to search for related sequences across the breadth of the Viridiplantae (four green algae, one moss, one club moss, four gymnosperms, and 62 angiosperms; Supplementary Table 1) using tBLASTn. Initially, over 8,400 protein-coding sequences were retrieved, all containing an RT domain with a best reciprocal hit against members of the Caulimoviridae, as opposed to the closely related Metaviridae (Ty3/Gypsy LTR retrotransposons). To provide a preliminary classification, sequences with at least 55% amino acid identity to each other were clustered and then iteratively added to our reference set of RT domain sequences to build a sequence similarity network. The successive networks were examined manually and representative sequences from each cluster were kept only when creating substantially divergent branches so as to cover an extended diversity of caulimovirid RTs with a core sequence assortment. While this network-based approach cannot be taken as phylogenetic reconstruction, it provided a practical method to explore diversity.

In the final sequence similarity network (Fig. 1), 17 groups with deep connections were identified, hereafter referred to as operational taxonomic units (OTUs). Remarkably, nine of these OTUs were distinct from recognized genera of the Caulimoviridae. Four of these novel OTUs were exclusively composed of sequences from gymnosperms, thereby confirming a significant host range extension for the Caulimoviridae. These OTUs were named Gymnendovirus 1 to 4. Two other novel OTUs were composed of RTs from various angiosperms and were named Xendovirus and Yendovirus. The last three novel OTUs were less populated, comprising sequences from one or two plant species (Petunia inflata and Petunia axillaris; Vitis vinifera; Glycine max; named species-wise: Petunia-, Vitis-, and Glycine-endovirus). This initial search therefore uncovered a significantly augmented diversity of caulimovirid RTs.

Figure 1
Figure 1

Augmented diversity of the Caulimoviridae. Core of asequence similarity network constructed using an alignment of amino acid reverse transcriptase (RT) sequences from reference genera, representative endogenous caulimovirids and Ty3/Gypsy LTR retrotransposons. The full network is available in Supplementary Fig. 1. Operational taxonomic units (OTUs) that do not correspond to recognized genera are highlighted by  dashed lime green outlines (referred to as novel OTUs). Each fill color corresponds to a different OTU, except for  novel OTUs that contain only one type of sequence, which are shaded dark grey and named after the host plant genome of origin (Petunia-, Vitis-, and Glycine-virus). *RT clustering at 55% amino acid identity groups, which has led to the lumping of the genera Cavemovirus and Solendovirus in a single OTU (OTU 8). **Sequences grouped in the Xendovirus OTU are paraphyletic after phylogenetic reconstruction (see Fig. 3).

Endogenous caulimovirid RT (ECRT) density across the Viridiplantae

To perform a more comprehensive search for ECRTs in our collection of plant genomes, we used the sequences from the final sequence similarity network (Fig. 1) to search for ECRT nucleotide sequences that do not necessarily retain uninterrupted open reading frames. Using tBLASTn, we detected 14,895 genomic loci representing high-confidence ECRT candidates. Remarkably, ECRTs were found in nearly all seed plants, ranging from gymnosperms (ginkgo and conifers) to angiosperms. Over one-thousand ECRTs were detected in each of the genome assemblies of the gymnosperms Picea glauca (white spruce) and Pinus taeda (loblolly pine), as well as from the solanaceous plant species Capsicum annuum (bell pepper) (Fig. 2A). In general, we observed a positive correlation between plant genome size and the number of ECRTs, although there were notable exceptions, such as the monocot Zea mays (maize), which has a relatively large genome at 2.1 Gb but no detectable ECRT. Five other seed plants from our sample also lacked ECRTs, including two other monocots (Zostera marina and Oryza brachyantha) and three dicots in the order Brassicales (Arabidopsis thaliana, Schrenkiella parvula and Carica papaya). When the number of ECRTs was normalized against genome size, Citrus sinensis (sweet orange) and Ricinus communis (castor bean) had the highest densities at 2.3 and 2 ECRTs per Mb, respectively (Fig. 2B). The primitive ANITA-grade angiosperm Amborella trichopoda also had a relatively high density of ECRTs (1 ECRT per Mb) compared to an average density of 0.2 ECRT per Mb across the 62 seed plant species that were examined.

Figure 2
Figure 2

Estimates of copy numbers and densities of endogenous caulimovirids (ECRTs) in different plant genomes. (A) Number of ECRTs found in each plant genome as a function of Log10 genome size, expressed in megabases (assembly gaps excluded). The logarithmic trendline indicates moderate correlation between the number of ECRTs and genome size (R2 = 0.544). (B) Density of ECRTs per megabase in each plant genome as a function of Log10 genome size, expressed in megabases (assembly gaps excluded). In (A) and (B), arrows indicate outliers andcorresponding plant species names.

Caulimovirid RTs also detected in ferns and a clubmoss

From the plant genomes examined thus far, ECRTs were detected in gymnosperm genomes but not in those from the spikemoss Selaginella moellendorffii and from the moss Physcomitrella patens, which belong to the more basal land plant divisions Lycophyta and Bryophyta, respectively. Monilophytes, including ferns (class Polypodiopsida), are a sister lineage to seed plants14,15, but no high quality genome assemblies are publicly available for these plants. However, six fern genomes have recently been sequenced at low coverage (approximately 0.4 to 2x genome size equivalent16 and we therefore screened these datasets for the presence of ECRTs. A total of twenty-one protein-coding ECRTs were detected in genomic contigs from five of the six fern species examined (Supplementary Table 1). Sequence similarity network reconstruction using representative fern ECRTs revealed that they form two novel OTUs that were named Fernendovirus 1 and 2 and numbered OTU #18 and 19, respectively (Supplementary Fig. 2).

Additional basal lineages of the Viridiplantae are represented in the 1,000 plant transcriptomes generated by the 1KP initiative17,15. From this dataset, we found two transcript contigs (2.4 and 2.8 kilobases long, respectively) in the fern Botrypus virginianus (identifier BEGM-2004510) and Lindsaea linearis (identifier NOKI-2097008), which contained ECRTs (Supplementary File 1). Remarkably, we identified one more transcript contig (identified as ENQF-2084799, 2 kb) that contained an ECRT in the clubmoss Lycopodium annotinum, which belongs to the Lycopoda, the most basal radiation of vascular plants (Tracheophyta). It is not possible to determine whether the mRNAs were transcribed from exogenous viruses or from EVEs.

Phylogenetic reconstruction

Complete or near complete viral genomes were reconstructed from each novel OTU except Fernendovirus 1 and 2 (Supplementary file 1). From the fern genomic data sets, we were able to reconstruct fragments of the Fernendovirus 1 and 2 genomes of sufficient size for phylogenetic analysis. We also used the complete genomes of the type species of the eight currently recognized genera in the family Caulimoviridae (Badnavirus, Caulimovirus, Cavemovirus, Petuvirus, Rosadnavirus, Solendovirus, Soymovirus and Tungrovirus), those of two unassigned viruses, Blueberry fruit drop-associated virus (BFDaV18) and Rudbeckia flower distortion virus (RuFDV19), and EVEs from the tentative genera Orendovirus20 and Florendovirus10. From this library of sequences, we aligned conserved protease, reverse transcriptase and ribonuclease H1 domains to build a maximum likelihood phylogenetic tree (Fig. 3). Importantly, all newly identified EVEs grouped within the Caulimoviridae with strong bootstrap support.

Figure 3
Figure 3

Phylogeny of the Caulimoviridae, as inferred using  maximum likelihood criteria and a multiple sequence alignment of protease, reverse transcriptase and ribonuclease H1 domain sequences from recognized (black) and putative (red) genera. Ty3/Gypsy LTR retrotransposons were designated as the outgroup. Bootstrap support values below 50% are not shown. Branch nodes were collapsed until only taxa at the genus level were illustrated. Viruses included in the analysis were as follows: Orendovirus - Aegilops tauschii virus and Brachypodium distachyon virus; Tungrovirus - Rice tungro bacilliform virus (Type and West Bengal isolates); Badnavirus - Commelina yellow mottle virus and Banana streak OL virus; Yendovirus - Capiscum annuum virus; Zendovirus - Fragaria vesca virus; Unassigned - Blueberry fruit drop-associated virus (BFDaV); Caulimovirus - Cauliflower mosaic virus and Figwort mosaic virus; Unassigned - Rudbeckia flower distortion virus (RuFDV); Soymovirus - Soybean chlorotic mottle virus and Peanut chlorotic streak virus; Solendovirus - Sweet potato vein clearing virus and Tobacco vein clearing virus; Cavemovirus - Cassava vein mosaic virus and Sweet potato collusive virus; Petuvirus - Petunia vein clearing virus; Rosadnavirus - Rose yellow vein virus; Florendovirus - Fragaria vesca virus and Mimulus guttatus virus; Gymnendovirus 1 - Pinus taeda gymnendovirus 1 and Picea glauca gymnendovirus 1; Gymnendovirus 2 - Pinus taeda gymnendovirus 2, Picea glauca gymnendovirus 2 and Ginkgo biloba gymnendovirus 2; Gymnendovirus 3 - Pinus taeda gymnendovirus 3; Gymnendovirus 4 - Pinus taeda gymnendovirus 4 and Picea glauca gymnendovirus 4; Fernendovirus 1: Cystopteris protrusa fernendovirus 1 contig 1, and the transcript scaffolds BEGM-2004510 from Botrypus virginianus, NOKI-2097008 from Lindsaea linearis, and ENQF-2084799 from Lycopodium annotinum; Fernendovirus 2 - Dipteris conjugata fernendovirus 2 Contigs 2, 4 and 1319. Clade A and B and the last common ancestor (LCA) of the Caulimoviridae are indicated with red arrows. The upper cladogram indicates the evolutionary relationships between major classes of vascular plants. At the intersection between both trees, colored boxes indicate the presence of either endogenous (green) or exogenous (blue) representatives of the Caulimoviridae.

In agreement with previous studies10, the tree revealed two sister clades, hereafter referred to as clade A and B (Fig. 3). Clade A comprised sequences from representatives of Xendovirus and Yendovirus OTUs and from members of the genera Caulimovirus, Soymovirus, Rosadnavirus, Solendovirus, Cavemovirus, Badnavirus, Tungrovirus and Orendovirus, as well as RuFDV and BFDaV. The Xendovirus OTU was found to be polyphyletic, hence a new taxon, Zendovirus, was created to accomodate the EVE from Fragaria vesca, while the EVE from Gossypium raimondii (cotton) was retained in Xendovirus. The Yendovirus OTU, comprising the EVE from Capsicum annuum (bell pepper), fell in the subclade comprising bacilliform-shaped viruses in the genera Badnavirus and Tungrovirus. The reconstructed genomes from novel OTUs found in single dicot species (Petunia-, Vitis-, and Glycine-endovirus) were discarded from the phylogenetic reconstruction as they significantly weakened the robustness of the tree. However, they unambiguously fell within clade A (data not shown).

Clade B comprised EVEs from the four gymnendovirus OTUs, the two fernendovirus OTUs, as well as representatives of the genus Petuvirus and the tentative genus Florendovirus. Gymnendovirus 2 EVEs were sister to all other clade B viruses, indicating that this group of viruses arose in gymnosperms. Interestingly, the angiosperm-infecting caulimovirids in this clade were polyphyletic, indicating independent origins and probable large host jumps of the most recent common ancestors. Fernendovirus 1 and 2 were monophyletic, and the club moss EVE placed within Fernendovirus 1. Again, the fernendoviruses appear to have arisen after a large host range swap of the most recent common ancestor.

ECRT distribution across seed plant genomes

To address the distribution of ECRTs in our collection of plant genomes, we determined the most likely position within the reference phylogenetic tree (Fig. 3) for the 14,895 sequences that we collected from using the pplacer program21. For this, we extracted sequences extending upstream and downstream of ECRT loci so as to retrieve contiguous fragments containing entire pol gene sequences (aspartic protease, RT and ribonuclease H1 domains). Using more relaxed length criteria, we extracted a total of 134 ECRT loci from the fern genomic data set that we also attempted to place on our reference tree.

Applying this strategy, we were able to classify a total of 13,834 ECRTs within specific OTUs (Fig. 4); the remaining ECRTs were placed on inner nodes of the reference tree. Overall, we observed striking differences between caulimovirid genera for both the number of ECRT loci and the number of plant species in which they were found. For instance, florendoviral RT loci were the most abundant, amounting to an overall total of 5,000 copies, and they were also found in the largest number of host species (46 of the 62 seed plant species that were screened). Petuviral RT loci were also well represented, with an overall total of 1,900 copies found in a total of 27/62 seed plant species, especially dicots. Among the novel OTUs, RTs classified as Yendovirus were found in the largest number of species, including monocots and dicots (Fig. 4).

Figure 4
Figure 4

Distribution of endogenous caulimovirid RTs (ECRTs) among the Euphyllophytes. The  cladogram on the left margin represents  the phylogeny of euphyllophyte species investigated in this study; the names of major branches and nodes are indicated. The cladogram on the upper margin, which represents virus phylogeny, is derived from Fig. 3. At the intersection of these two trees, the colored boxes indicate the number of ECRT loci from each virus genus in each plant genome. Abbreviations of virus genera are as follows: Pe (Petuvirus), Gy1 (Gymnendovirus 1), Gy2 (Gymnendovirus 2), Gy3 (Gymnendovirus 3), Gy4 (Gymnendovirus 4), Fe1 (Fernendovirus 1), Fe2 (Fernendovirus 2), Flo (Florendovirus), Soy (Soymovirus), Rud (Rudbeckia flower distortion virus), Cau (Caulimovirus), Blu (Blueberry fruit drop-associated virus), Zen (Zendovirus), Xen (Xendovirus), Yen (Yendovirus), CaS (Cavemovirus + Solendovirus), Ros (Rosadnavirus), Bad (Badnavirus), Tun (Tungrovirus), Ore (Orendovirus).

Most importantly, the analysis of distribution of ECRTs in plant genomes revealed striking differences between ferns, gymnosperms and angiosperms (Fig. 4). No single OTU spans more than one plant division. Fernendovirus 1 sequences were exclusively distributed in fern and club moss genomes or transcriptomes. Similarly, ECRT loci that were assigned to one of the four Gymnendovirus OTUswere confined to gymnosperms. The three conifer genomes contained a mixture of ECRTs from the four Gymnendovirus OTUs but only ECRTs that were classified as Gymnendovirus 2 were detected in Ginkgo biloba (Ginkgoales). Within angiosperms, there was a dichotomy in the distribution of OTUs between monocots and dicots. On the one hand, Yendovirus, Badnavirus, Orendovirus and Florendovirus ECRTs are common in monocots, with the tentative genus Orendovirus being the only one specific to monocots. On the other hand, Petuvirus, Florendovirus, Xendovirus, Cavemovirus/Solendovirus and Yendovirus ECRTs are widely distributed in dicots and Florendovirus and Yendovirus ECRTs are additionally found in monocots.


Endogenous viral elements are considered relics of past infections, and an extrapolation of the results from this study is that nearly every tracheophyte plant species in the world has at some point in its evolutionary history been subject to infection by at least one member of the family Caulimoviridae, as previously proposed by Mushegian and Elena9. This finding attests to the tremendous adaptability of the Caulimoviridae and also the large influence they have had on plant evolution, either as pathogens or as donors of novel genetic material to the plant genome.

The development of multicellularity in plants was likely a critical event in the emergence of the Caulimoviridae. Plants with rigid, cellulosic cell walls depend on plasmodesmata for the exchange of macromolecules22. The presence of a 30 K MP is an important feature of the Caulimoviridae that distinguishes it from the LTR retrotransposon family Metaviridae. This protein is crucial for the formation of systemic infection by allowing intercellular trafficking and phloem-loading of the viruses through increasing the size exclusion limit of plasmodesmata22,23. The most recent common ancestor of the Caulimoviridae possibly arose after a recombination between a LTR-retrotransposon and an ssRNA virus with a 30 K MP, and this new hybrid virus would have been able to colonize the Tracheophyta but not necessarily more primitive plant lineages due to differences in plasmodesmatal biology. Although algae contain plasmodesmata, which superficially resemble those of higher plants, they are not homologous structures24. Multicellular algae in the Charales, the closest relatives of land plants to have plasmodesmata, lack desmotubules that are continuous with the endoplasmic reticulum (ER), an anatomical feature that would likely limit intercellular trafficking of viruses that utilize the 30 K MP pathway. Furthermore, the true mosses (Bryophyta) do not have orthologues of the cysteine-rich receptor-like plasmodesmata-localized proteins that modulate cell trafficking in eudicots22.

The caulimovirid tree contained two major clades: clade A, comprising viruses that were found exclusively in mesangiosperm species and clade B, comprising viruses associated with all the major classes of Tracheophyta. Assuming the monophyly of clades A and B, the obtained plant-virus associations could be explained by the emergence of these viruses in a common ancestor of the gymnosperms and angiosperms followed by several major host swaps: in clade A, between monocots and dicots, and in clade B between gymnosperms and angiosperms in the case of florendoviruses and petuviruses (although the position of this latter genus in the tree is uncertain), and from gymnosperms to ferns and clubmoss in the case of fernendoviruses. Following this scenario, the Caulimoviridae could have emerged at the latest with the Spermatophyta, i.e. during the Devonian era, about 320 MYA25.

When recapitulating the distribution of EVEs in plant genomes, the known host range of exogenous viruses, and the phylogenetic relationships between caulimovirid OTUs and major groups of vascular plants (Fig. 3) to infer the evolutionary trajectories of plant-virus coevolution, we obtain a complex pattern of host-virus associations. At the OTU level, the host distributions of petu- and xendovirus, including dicots and the ANITA grade angiosperm (Amborella trichopoda) but not any of the monocot species, is suggestive of horizontal transfer. In addition, although vertical transmission is overall well supported by a co-evolutionary study of florendoviral EVEs and their host species10, it could not be confirmed for A. trichopoda. Together with the observation that A. trichopoda presents a high density of ECRTs (Fig. 2B), this may suggest that this species is permissive to infection by a range of caulimovirid genera and/or that it represents a hotbed for the emergence of caulimovirid genera, some of which swapped towards mesangiosperms. We however cannot rule out the possibility that petu- and xendovirus were lost in monocots.


Discovery and clustering of novel caulimovirid OTUs

We built a library containing an assortment of amino acid (aa) sequences from 54 RT domains including four from Retroviridae, six from Ty3/Gypsy LTR retrotransposons, 41 from eight different genera of Caulimoviridae (Florendovirus, Caulimovirus, Tungrovirus, Cavemovirus, Solendovirus, Badnavirus, Soymovirus, and Petuvirus), two from Picea glauca, and the one from the DIRS-1 element. We compared this library to a collection of 72 genome assemblies from the Viridiplantae (listed in Supplementary Table 1) using tBLASTn with default parameters (except –e option set to 1e−5). The hit genomic loci were merged when overlapping and their coordinates were extended 120 bases upstream and downstream. Extended hit loci were translated and the protein sequences of length > = 200aa were compared to the initial RT library using BLASTp with default parameters (except −e = 1e−5). Queries with best alignment score against Caulimoviridae over at least 170 residues were selected for further analysis. For each plant species, the selected set of RT aa sequences were clustered following sequence similarity using the UCLUST program26 with identity threshold set at 80%. The longest sequence from each resulting cluster was considered as the representative sequence and it was appended to the initial RT library. To detect potential false positives, each set of sequences (each consisting of the initial RT library and cluster representatives from one species) was aligned using MUSCLE followed by filtering of lower fit sequences using two rounds of trimAl v1.227 to remove poorly aligned sequences (–resoverlap 0.75–seqoverlap 50) separated by one round to remove gaps from the alignment (–gt 0.5). The representative sequences from each plant species that passed this selection were combined into a single file and appended to the initial RT library to be clustered with UCLUST using an identity threshold of 55%. At this level of similarity, aa RT sequences from every genus in the Caulimoviridae was separated except those from Cavemovirus and Solendovirus.

Starting with the first cluster, one or more sequences presenting high quality alignment and containing several conserved residues as determined contextually for each cluster were then manually selected to be representative of the diversity observed within each cluster. The following clusters were processed similarly while keeping the representative sequences selected from previously processed clusters. Clusters containing ECRT sequences from only one plant species were analyzed only when they contained at least three sequences. After processing each cluster individually, a total of 56 ECRT sequences detected here and 20 RT from known genera were selected for their remarkable divergence. Together with four RT sequences from Ty3/Gypsy LTR retrotransposons, these combined sequences (hereafter referred to as “diverse library”) were aligned with the GUIDANCE228 program using MAFFT29 to generate bootstrap supported MSA and to remove columns (–colCutoff) with confidence score below 0.95 (16/244 columns removed in the RT sequence from CaMV). The resulting MSA was then used to build the sequence similarity network shown in Fig. 1 and Supplementary Fig. 1 with SplitsTree4 30 applying the NeighborNet method with uncorrected P distance model and 1,000 bootstrap tests. Manual analysis of this network enabled the discrimination of 17 distinct groups sharing deep connections among caulimovirid sequences.

In response to the discovery of several novel OTUs, we repeated ECRT mining in plant genomes using the diverse library as query. This second search was also designed to be more sensitive as it took into account DNA sequences instead of uninterrupted ORFs. The workflow was identical to the one employed for the initial search until obtaining the set of extended hit loci. These were directly compared to the diverse library using BLASTx with default parameters (except −e = 1e−5). Queries with a best alignment score against any member of the Caulimoviridae with an alignment length above 80% of subject length (set generically to 576 bp considering an average size of RT domains of 240 aa) were selected for phylogenetic placement.

Phylogenetic analysis

Fragments of virus sequence were assembled using CodonCode aligner 6.0.2 using default settings or using VECTOR NTI Advance 10.3.1 (Invitrogen) operated using default settings, except that the values for maximum clearance for error rate and maximum gap length were increased to 500 and 200, respectively.

Phylogenetic reconstruction was performed using the contiguous nucleotide sequences corresponding to the protease, reverse transcriptase and ribonuclease H domains. Whole sequences  of representatives of the different genera of the Caulimoviridae and Ty3/Gypsy LTR retrotransposons were first globally aligned using MAFFT v7.3 29. The core genomes were extracted and then locally re-aligned using MAFFT. The GTRGAMMA model of evolution was selected after examination of the alignment with pmodeltest v1.4 (from ETE 3 package31). Phylogenetic inference with maximum likelihood (ML) criteria was then performed using RaxML v8.232 under the predicted model with 500 ML bootstrap replicates.

The resulting tree was then used as a reference to classify the ECRT loci mined from plant genomes. We first added query sequences from each plant species separately to the reference alignment and aligned each library using Mafft v7.3 (with options–addfragment, –keeplength and by reordering). The most likely placement of each ECRT sequence on the reference tree was then tested using pplacer v1.1 alpha1921 with the option (–keep-at-most 1), which allows one placement to be kept for each query sequence. The python package Taxit was used to construct a reference package which we used to run pplacer.

Data availability

The datasets and scripts generated during the current study are available from the corresponding author on request.

Additional Information

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We thank Mark Tepfer for critical reading of a previous version of this manuscript. PYT was funded by the Guadeloupe Region and the European Regional Development Fund.

Author information


  1. URGI, INRA, Université Paris-Saclay, 78026, Versailles, France

    • Seydina Issa Diop
    • , Françoise Alfama-Depauw
    • , Mikaël Loaec
    •  & Florian Maumus
  2. Queensland Alliance for Agriculture and Food Innovation, The University of Queensland, GPO Box 267, Brisbane, Queensland, 4001, Australia

    • Andrew D. W. Geering
  3. UMR AGAP, CIRAD, INRA, SupAgro, 97130, Capesterre Belle-Eau, France

    • Pierre-Yves Teycheney


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S.D., A.D.W.G., and F.M. performed research; F.A-D. and M.L. provided the research environment; S.D., A.D.W.G., P.Y.T., and F.M. analyzed the data; A.D.W.G., P.Y.T., and F.M. wrote the manuscript with contributions from S.D.; F.M. designed the research.

Competing Interests

The authors declare that they have no competing interests.

Corresponding author

Correspondence to Florian Maumus.

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