Julien Andreani1*†
Frederik Schulz2†
Fabrizio Di Pinto1
Anthony Levasseur1
Tanja Woyke2
Bernard La Scola1*- 1Aix-Marseille Université, IRD, APHM, MEPHI, IHU Méditerranée Infection, Marseille, France
- 2DOE Joint Genome Institute, Lawrence Berkeley National Laboratory, Berkeley, CA, United States
Since the discovery of Mimivirus, viruses with large genomes encoding components of the translation machinery and other cellular processes have been described as belonging to the nucleocytoplasmic large DNA viruses. Recently, genome-resolved metagenomics led to the discovery of more than 40 viruses that have been grouped together in a proposed viral subfamily named Klosneuvirinae. Members of this group had genomes of up to 2.4Mb in size and featured an expanded array of translation system genes. Yet, despite the large diversity of the Klosneuvirinae in metagenomic data, there are currently only two isolates available. Here, we report the isolation of a novel giant virus known as Fadolivirus from an Algerian sewage site and provide morphological data throughout its replication cycle in amoeba and a detailed genomic characterization. The Fadolivirus genome, which is more than 1.5Mb in size, encodes 1,452 predicted proteins and phylogenetic analyses place this viral isolate as a near relative of the metagenome assembled Klosneuvirus and Indivirus. The genome encodes for 66 tRNAs, 23 aminoacyl-tRNA synthetases and a wide range of transcription factors, surpassing Klosneuvirus and other giant viruses. The Fadolivirus genome also encodes putative vacuolar-type proton pumps with the domains D and A, potentially constituting a virus-derived system for energy generation. The successful isolation of Fadolivirus will enable future hypothesis-driven experimental studies providing deeper insights into the biology of the Klosneuvirinae.
Introduction
In 2003, with the first description of Mimivirus (La Scola, 2003), viruses were revealed to be more complex entities than previously thought and with extraordinary properties, e.g., numerous tRNAs, aminoacyl-tRNA synthetases (aaRS) and themselves being infected by virophages (La Scola et al., 2008; Gaia et al., 2014). In terms of capsid size, as well as gene content, this first discovery created a paradigm shift and shattered extant viral definition (Forterre, 2016; Colson et al., 2017). 18years later, giant viruses with ovoid forms, even larger genome sizes, and viruses with no capsid have been discovered with the successive isolations of Pandoraviruses (Philippe et al., 2013; Antwerpen et al., 2015; Aherfi et al., 2018; Legendre et al., 2018), Pithoviruses (Legendre et al., 2014; Levasseur et al., 2016), Cedratviruses (Andreani et al., 2016; Bertelli et al., 2017; Silva et al., 2018; Rodrigues et al., 2018a; Boudjemaa et al., 2020), and Orpheovirus (Andreani et al., 2018). In addition, the description of Meelsvirus revealed that these potential viruses can take extremely varied forms and are associated with a complex formation of their capsids (Shinn and Bullard, 2018). These large viruses share a common origin and a novel name has been proposed: Nucleocytoviricota (replacing the term nucleocytoplasmic large DNA viruses (NCLDV; Koonin et al., 2020).
In parallel, advances in (meta) genomic sequencing of viruses expanded rapidly (Verneau et al., 2016; Schulz et al., 2017, 2018, 2020; Wilson et al., 2017; Moniruzzaman et al., 2020a,b). In 2017, a metagenomic study reported the detection and genome reconstruction of four new viruses affiliated with the Mimiviridae which encoded expanded protein biosynthesis components, Klosneuvirus, Indivirus, Catovirus, and Hokovirus, proposed as a sub-family, Klosneuvirinae (Schulz et al., 2017). Just 1year later, the diversity of this unexplored viral group was further expanded with the discovery of seven additional metagenome assembled viruses from soil (Schulz et al., 2018) and the first isolate affiliated with the Klosneuvirinae, Bodo saltans virus (Deeg et al., 2018). In contrast to many other members of the Klosneuvirinae, Bodo saltans virus encodes for only two functional aminoacyl-tRNA synthetases (aaRS) and no tRNA. In the meantime, two novel members of the Mimiviridae were isolated, Tupanvirus soda lake and Tupanvirus deep ocean, possessing 70 tRNA and 20 aaRS, and similar and slightly more complete translational components than the metagenomic Klosneuvirus (Abrahão et al., 2018). Tupanviruses do not group with the Klosneuvirinae but with the Megamimivirinae, sharing a hypothetical ancestor with the three lineages of Mimiviruses A, B, and C (Rodrigues et al., 2018b). The first isolate of the Klosneuvirinae that had an expanded set of translation system genes was the icosahedral virus in Vermamoeba vermiformis, named Yasminevirus (Bajrai et al., 2019). Its genome is one of the largest in the Mimiviridae with 2.1Mb and possesses various components of a complete translation system. The discovery of these viruses has opened up new perspectives regarding their evolution in relation to eukaryotes. Recently, metagenomic has revealed the widespread presence of energy metabolism encoded in the Nucleocytoviricota, such as photosynthesis genes and enzymes playing roles in glycolysis among others (Schulz et al., 2020; Moniruzzaman et al., 2020a).
In this study, we report the isolation and detailed description of the closest relative of the metagenomic Klosneuvirus from an Algerian sewage sample, representing the third viral isolate of the Klosneuvirinae. Our study provides information on the viral replicative cycle and host range, as well as its phylogeny and genomic features, revealing a more complete picture of the Klosneuvirinae. Our isolate contributes toward establishing an experimental framework of viral strains that may be used to study the biology of this diverse subfamily of the Mimiviridae.
Materials and Methods
Sample Collection and Virus Isolation
Samples from which the virus was isolated were part of a study aiming to evaluate giant virus diversity in north-west Algeria (Boudjemaa et al., 2020). Briefly, a sample was collected from sewage in Sidi Bel Abbès (Algeria) on the September 1, 2017. As previously reported (Geballa-Koukoulas et al., 2020, 2021), we used Vermamoeba vermiformis stain CDC19 as cell support. The amoebae were harvested after 48h of culture in peptone yeast extract glucose medium (Eurobio, France) when a concentration of 1.106 amoebae/mL was reached. Cells were then rinsed twice in homemade Page’s Amoeba Saline and pelleted at 700×g for 10min. The amoebae were then resuspended in the starvation medium (Reteno et al., 2015). A cell suspension of 500μl per well was distributed onto a 24-well plate. The samples were vortexed, and 50μl was added to each well. Remaining wells served as negative controls. The plate was incubated at 30°C for 4days in order to monitor any potential cytopathic effect. This co-culture was repeated twice in the same order.
Host Range Survey
Multiple hosts were tested by inoculation of Fadolivirus on Vermamoeba vermiformis (ATCC® 50237, initial support of isolation), Vermamoeba vermiformis strain chuv172, Acanthamoeba castellanii strain Neff (ATCC® 30010), Acanthamoeba polyphaga strain Linc-AP1, Acanthamoeba royreba strain Oak ridge (ATCC® 30884), Disctyostelium discoideum (ATCC® 44841), the flagellated alga Tetraselmis sp. (IHU isolate), and the protist Cafeteria roenbergensis (IHU isolate). The lytic events were monitored by observations under an inverted microscope, as described for Tupanvirus (Abrahão et al., 2018), for 5days.
Flow Cytometry Analyses
According to previously described protocols (Khalil et al., 2016; Andreani et al., 2017), we centrifuged the viral supernatant at 700× g for 10min, added a 1:100 SYBR green dye dilution (SYBR green I nucleic acid gel stain; Molecular Probes, Life Technologies), and then heated the mixture at 80°C for 3min. Stained viral populations were acquired on a BD LSR Fortessa (BD Biosciences) cytometer and compared with previously recorded gates for known viral isolates on FlowJo software.
Electron Microscopy Observations
We used protocols similar to previous studies (Andreani et al., 2016, 2017) for embedding and transmission electron microscopy. The only difference was the infection time points at which the samples were collected. The time points were 0, 4, 8, 12, 16, 20, 24, and 36h post-infection. Microscopy was performed using a Tecnai G20 electron microscope (FEI, Germany) operating at 200keV, and the size of the particles was measured using ImageJ.1
Viral Production and Purity Control
We successively inoculated diluted viral supernatant on V. vermiformis at a dilution factor of 10 in order to clone the virus before its production. End point dilution was assessed for 5days and the lysis was controlled by inverted microscopy. For the production and purification processes, 15 flasks of 150cm2 (Corning®, Corning, NY, United States) were infected. After 4days, we filtrated all the supernatants from flasks using 0.8μm filters. The filtrate supernatant was then pelleted using the Beckman coulter® Optima™ XPN-80 - IVD (Beckman, France) at 50,000×g for 30min. A 25% sucrose gradient was used for the final purification step. After finalizing production, we extracted DNA by using the EZ1 Advanced XL device (Qiagen, Courtaboeuf, France).
Genome Sequencing and Genome Assembly
Genomic DNA of Fadolivirus was sequenced on the MiSeq platform (Illumina Inc., San Diego, CA, United States) using a paired end strategy. In order to pool the sample with 18 other genomic projects for sequencing, a barcoded library was created using the Nextera XT DNA sample prep kit (Illumina). In detail, Fadolivirus gDNA was quantified using a Qubit assay using the high sensitivity kit (Life technologies, Carlsbad, CA, United States). DNA concentration was 5.7ng/μl. To prepare the paired end library, the gDNA was diluted to provide 1ng of input. The “tagmentation” step fragmented and tagged the DNA. A limited cycle PCR amplification (12cycles) completed the tag adapters and introduced dual-index barcodes. After purification on AMPure XP beads (Beckman Coulter Inc., Fullerton, CA, United States, the libraries were normalized on specific beads according to the Nextera XT protocol (Illumina). Normalized barcoded libraries were then pooled into a single library for sequencing on the MiSeq. The pooled single strand library was loaded onto the reagent cartridge and the instrument along with the flow cell. Automated cluster generation and paired end sequencing with dual index reads were performed in a single 39-h run in 2×250-bp. A total of 8.5Gb of Fadolivirus genomic sequence was obtained from a 927,000 cluster density per mm2 with a cluster passing quality control filters of 94.1% (16,738,000 clusters). Within this run, the index representation for this virus was determined to represent 6.8%. To improve the Fadolivirus assembly, a MinIon Oxford Nanopore run was performed.
The Oxford Nanopore approach was performed on 1D genomic DNA sequencing using the MinIon device and SQK-LSK108 kit. The sequencing library was constructed using 1.5μg genomic DNA previously extracted without fragmentation and end repair. Adapters were ligated to both ends of genomic DNA. After purification on AMPure XP beads (Beckman Coulter Inc., Fullerton, CA, United States), the library was quantified by a Qubit assay with the high sensitivity kit (Life technologies, Carlsbad, CA, United States). Approximately 20ng of the tethered library was loaded on the flow cell via the SpotON port. 317 active pores were detected for sequencing and the WIMP workflow was chosen for live bioinformatics analysis. After 36h of run time and end life of the flow cell, 13,136 raw reads were generated. The software EPI2ME lead to 13,122 analyzed viral sequence reads totaling 30.3Mb, with an average length of 2,305kb and a maximum read length of 32,328bp.
Paired-end Illumina reads and Minion reads were de novo assembled using the hybridSPAdes algorithm (Antipov et al., 2016). We obtained two scaffolds representing a total size of 1,595,395bp with an average read coverage of 121-fold for the first scaffold and 102-fold for the second.
Genome Analysis
Gene predictions were computed using Prodigal (Hyatt et al., 2010). We deleted 49 predicted proteins of fewer than 50 amino acids, or which had abnormal tri-dimensional folding (from 50 to 99 amino acids), as detected by Phyre2 (Kelley et al., 2015). Protein blast was performed against the non-redundant (nr) protein database. Annotation was performed using a combination of Interpro https://www.ebi.ac.uk/interpro/search/sequence-search version 69.0, a CD-search tool online (Marchler-Bauer and Bryant, 2004) and delta-blastp (Boratyn et al., 2012). tRNA prediction was computed online (Lowe and Chan, 2016) with the eukaryotic model parameter.
Comparative Genomics
Orthofinder (v2.4; Emms and Kelly, 2015) was used to infer orthogroups from published genomes of representatives of all established Mimiviridae lineages and estimated high-quality giant virus metagenomes assembled genomes affiliated with the Klosneuvirinae. Further, Interproscan (v5.0; Jones et al., 2014) was employed to assign PFAM-A domains (v33.0; El-Gebali et al., 2019) to giant virus proteins. GenoplotR (Guy et al., 2010) was used to visualize genome synteny of conserved blocks that were inferred with Mauve (v2.4; Darling et al., 2004) in pairwise comparisons between genomes of selected members of the Mimiviridae and Fadolivirus.
Genome Deposition Into Data Repository
The two scaffolds of Fadolivirus IHUMI-VV54 are available on the NCBI website under accession numbers MT418680.1 and MT418681.1.
Phylogenetic Analysis—Species Tree
To infer the phylogenetic position of Fadolivirus in the Mimiviridae, five conserved NCLDV proteins (Yutin et al., 2009) were selected: DNA polymerase elongation subunit family B (NCVOG0038), D5-like helicase-primase (NCVOG0023), packaging ATPase (NCVOG0249), and DNA or RNA helicases of superfamily II (NCVOG0076) and Poxvirus Late Transcription Factor VLTF3-like (NCVOG0262), and identified with hmmsearch (version 3.1b2, hmmer.org). Protein sequences were extracted and aligned using mafft-lins (Katoh and Standley, 2016). Gapped columns in alignments (<10% sequence information) and columns with low information content were removed from the alignment with trimal (v1.4; Capella-Gutiérrez et al., 2009). Protein alignments were then concatenated to a supermatrix and a species tree of the Mimiviridae was built with IQ-tree (v2.03) with LG + F + R6 (Nguyen et al., 2015). The species tree was then visualized using iTOL v6 online (Letunic and Bork, 2016).
Phylogenetic Analysis - Protein Trees
Phylogenetic analyses for ATPases were conducted as follows. Blastp was used to find 39 close homologous proteins, and amino acid sequences were then aligned using the MUSCLE program (Edgar, 2004). The Mega 6.0 software was used with standard parameters using the maximum likelihood method with 1,000 bootstrap replicates and the Jones–Taylor–Thornton model for amino acid substitution. Phylogenetic trees were then visualized using iTOL v6 online (Letunic and Bork, 2016).
Results
Isolation of a Novel Giant Virus and Host Range Test
Co-culture steps were performed on 64 samples on the amoeba Vermamoeba vermiformis strain CDC19 (Boudjemaa et al., 2020). Cell lysis was observed using an inverted optical microscope, with obvious lysis in well 54. Flow cytometry allowed us to detect a single novel population in our gating strategy (Khalil et al., 2016), with a high value of fluorescence compared to the side scatter fluorescence (Figure 1). We tried to infect various potential alternate hosts with this virus, specifically Vermamoeba vermiformis strain chuv172, Acanthamoeba castellanii strain Neff, Acanthamoeba polyphaga strain Linc-AP1, Acanthamoeba royreba strain Oak ridge, Dictyostelium discoideum, the flagellated alga Tetraselmis sp., and the protist Cafeteria roenbergensis. Fadolivirus was only able to infect Vermamoeba vermiformis strain CDC19, suggesting a narrow host range. No cytopathic effects were observed using optical microscopy for any of these potential hosts.
Figure 1. Observation of virus isolate VV54 sample on flow cytometry superimposed with that of other known viral isolates. Flow cytometry dot plot showing different viral profiles, in SSC (side scatter) versus FITC (Fluorescein isothiocyanate) SYBR green DNA contents, distinguishable at the levels of capsid shape (optical properties) and DNA components. For the sample VV54, the single viral population (Fadolivirus) is shown in red. For comparison, gates from previous isolates of other viral strains are shown.
Ultrastructure of Fadolivirus and Replication Cycle
Fadolivirus particles are icosahedral with a diameter of about 300nm (n=21) on ultrathin sections. Multiple layers of high-density electrons (proteinaceous) were visible comparable to those described for Mimivirus, Yasminevirus and Bodo saltans virus (Deeg et al., 2018; Bajrai et al., 2019). The replication cycle of Fadolivirus showed classical NCLDV stages of infection and replication in V. vermiformis and small-sized fibrils were sometimes distinguishable in the periphery of the viral particles, as observed in Yasminevirus. Briefly, the replication cycle begins with the virus entry by phagocytosis. Next, particles escape the phagosomal process. DNA delivery occurs in the amoeba cytoplasm via the apex of the icosahedral virus (Figures 2A,B). After cytoplasmic liberation of the virus, an eclipse phase is observed. After 12h, viral factories are assembled within some amoeba (Figure 2C) and 16h post-infection (Figure 2D), nearly all cells present a well-established viral factory. While the Fadolivirus factory resembles that described for Mimivirus (Suzan-Monti et al., 2007), we found a singular element in the filling of the capsid. Indeed, after the synthesis of the icosahedral structure by the factory, the pseudo-ovoidal structure becomes increasingly dense and round inside this neo-formed capsid (Figures 2F,G). This step seems to be different compared to observations in Mimivirus. Finally, this gives the particle its mature aspect with a highly dense core. At 20h post-infection (Figure 2E) and 24h post-infection (Figure 2H), the host cells’ cytoplasm is fully occupied by newly synthesized virions. Cell burst begins 24h post-infection and is completed 36h after the viral infection.
Figure 2. Ultrathin section of the replication cycle of Fadolivirus IHUMI-VV54. Scale bars are indicated under each panel. (A, B) were observed during viral entry at 0h and two hours post-infection. (C) Represents a section of Vermamoeba vermiformis 12h post-infection. (D) High magnification of a viral factory 16h post-infection. (E) New virus produced 20h post-infection. (F, G) White arrows indicate icosahedral capsid with ovoid points intra-capsidic localization. (H) Intra-cytoplasmic viruses observed 24h post-infection.
Genomic Features of Fadolivirus
The Fadolivirus genome assembled into two scaffolds with a total length of 1,595,395bp (with 1,573,504bp for scaffold 1 and 21,891bp for scaffold 2; Table 1), encoding 1,452 genes of which 1,428 were on the larger scaffold, here referred to as the major scaffold. A megablast of the major scaffold against the nucleotide collection in the NCBI database revealed matches to Indivirus, Klosneuvirus, Catovirus, and Tupanviruses. A whole genome alignment showed that numerous blocks were conserved between Fadolivirus, Klosneuvirus KNV1 and Indivirus ILV1 (Figure 3). However, when aligned to the genome of Bodo saltans virus, the proportion of shared sequences decreased notably (data not shown).
Table 1. Morphological and genome characteristics of members of selected Klosneuvirinae and Tupanviruses.
Figure 3. Block synteny comparison between Fadolivirus and other Klosneuvirinae genomes. Conserved genomic regions (Mauve conserved blocks) between Fadolivirus and its closest relatives, Klosneuvirus and Indivirus. Contigs in Indivirus and Klosneuvirus have been reordered based on the Fadolivirus genome. For comparison, conserved regions are also shown between selected members of the proposed subfamily Megamimivirinae, including Tupanviruses.
A blastp comparison of Fadolivirus proteins to the NCBI nonredundant database (nr) revealed the presence of 256 ORFans without any matches in nr (≈17,6% of all predicted proteins), 552 hits with Klosneuvirus KNV1 (≈38% of all predicted proteins), 223 with Indivirus ILV1 (≈15,4% of all predicted proteins), 24 with Catovirus CTV1, 21 with Hokovirus HKV1 and 24 with Tupanvirus strain deep ocean, 23 with Tupanvirus soda lake, and only 59 with other viruses. We also obtained 111 best hits to eukaryotic and 151 to bacterial and archaeal proteins. Based on the results of this analysis, it becomes evident that the gene content of Fadolivirus is most similar to that of Klosneuvirus. The Fadolivirus genome encodes 66 tRNAs that belong to 19 different types and represent 35 different anticodons (Table 1; Supplementary Material S1). Twenty-five were described for the Klosneuvirus KNV1 genome and only one for Indivirus ILV1 (Table 1). Similar to what has been described for other Klosneuvirinae (Schulz et al., 2017, 2018), Fadolivirus encoded a comprehensive set of translation system components consisting of various translation initiation factors (eIF4G, F, eIF-5A, B for example), elongation factors (aef-2), and a termination factor (Rho domain).
As previously observed in members of the Klosneuvirinae and in particular in Bodo saltans virus, there were numerous gene duplication events (102 clusters with than two proteins) in the Fadolivirus genome of which only 18 clusters had predicted functions. Thirteen of the duplicated genes were homologous to the capsid protein. More detailed analyses revealed that two ORFs encoded a putative major capsid protein (MCP) split by 35 nucleotides and six others were predicted to represent other MCP (Supplementary Material S1). The in-depth in silico analysis further led to the exclusion of a putative capsid which was predicted as a probable Zinc finger (NCBI QKF94282.1) domain containing protein. No other Klosneuvirinae genome encodes that many (11) capsid proteins. Other conserved NCLDV hallmark genes (Koonin and Yutin, 2010) were also present in multiple copies in the Fadolivirus genome, including the protein predicted to encode the VV-D5 helicase homologues and the A32 packaging ATPase and mRNA capping enzyme with three and four copies, respectively.
In contrast to other members of the Klosneuvirinae, Fadolivirus encodes proteins that may play a role in modulation of host cell processes (as for BAG domain-containing protein), vesicular transport as the soluble N-ethylmaleimide-sensitive factor (NSF), pyrimidine metabolism (dihydroorotate dehydrogenase 1A, orotidine 5′-phosphate decarboxylase), transcription and catabolism (putative transcriptional regulator ICP4, regulator of protease activity HflC), in the vitamin K metabolism (vitamin K epoxide reductase and vitamin K dependent gamma-carboxylases (VKGC)), efflux protein (small multidrug resistance protein (multidrug transporter EmrE), in the channel formation (major intrinsic protein, and two predicted proteins in the peptidoglycan synthesis (D-ala-D-ala ligase).
We also retrieved a V21 virophage-like protein (initially described in the Sputnik virophage) that had recently been suggested to play a similar function to transcription factor, as found in other giant virus genomes such as Orpheovirus IHUMI-LCC2 (Andreani et al., 2018). However, no virophage was isolated together with Fadolivirus. Fadolivirus encodes a homolog of Cyclophilin, a chaperone with a role in protein folding (Barik, 2018), yet its role in the Fadolivirus biology remains currently unclear. In the Acanthamoeba polyphaga Mimivirus, phosphodiesterase activity was not found (Thai et al., 2008). The Fadolivirus genome also contains three genes annotated as cytochromes (one as 5b, two as P450) and two probable lactonases. Cytochrome has recently been shown to have a broad distribution in DNA viruses and may be involved in cholesterol/sterol synthesis (Lamb et al., 2019).
Fadolivirus Genes Involved in Energy Metabolism
The Fadolivirus genome annotation revealed multiple sequences annotated as putative ATPase subunits and proteins associated with electron transfer with a blue copper enzyme and a putative cytochrome 5b (see previous section). This cytochrome sequence is a probable nitrate reductase (NADH) protein (Chamizo-Ampudia et al., 2017) in the Fadolivirus genome. We identified six proteins associated with proton pumps containing ATPase domains. However, these genes were not co-located in the genome of Fadolivirus. A more detailed phyre2 analysis of these 6 proteins revealed that two of them were indeed predicted as v-type proton ATPase subunit D (QKF94710.1) with 100% confidence and 28% identity with the Yeast V-ATPase state 3 (PDB database 3J9V), and with the other states 1 and 2. This protein could be a vacuolar proton pump hydrolyzing the ATP to ADP (Balakrishna et al., 2015; Zhao et al., 2015). For the protein QKF93735.1, it presents known homologies with vacuolar ATP synthase subunit A by DELTA-blast. This potential subunit A is shared with other giant viruses in Klosneuvirinae, and the predicted subunit D is divergent compared to the eukaryotes (Figure 4).
Figure 4. Maximum-likelihood representation built with the Jones–Taylor–Thornton method with 1,000 bootstrap replication based on 286 aligned positions. 39 eukaryote sequences were downloaded as best hit with ATPase from Fadolivirus.
Genomic Diversity Across Klosneuvirinae and Phylogenetic Position of Fadolivirus
In the species tree of the Klosneuvirinae, Fadolivirus branched in a monophyletic clade with Klosneuvirus, Barrevirus and Indivirus (Figure 5). This result corresponded well with the complimentary best hit analysis described above. Genomes of members of this clade have a similar GC content of around 30% and genomes of Fadolivirus and Klosneuvirus express a similar genome size with approximately 1.5Mb, while Indivirus and Barrevirus have much smaller genomes of under 1Mb. Yasminevirus, another isolated member of the Klosneuvirinae branches divergent from Fadolivirus in the species tree and groups together with Dasosvirus. The third isolate of the Klosneuvirinae, Bodo saltans virus, groups in its own distinct clade. Genomic features and hallmarks that are found in Fadolivirus and Yasminevirus but not in Bodo saltans virus are aaRS. Clusters of orthologous proteins make it possible to observe significant diversity between Mimiviridae (Figure 6). There were 12 protein families that are almost exclusively found in the Klosneuvirus/Fadolivirus clade and 4 families that are widespread in the Klosneuvirinae but absent in members of the Klosneuvirus/Fadolivirus clade. Seventy-three orthologs are exclusively shared between Klosneuvirus and Fadolivirus; however, only 20 orthologs are exclusively shared between Fadolivirus, Klosneuvirus and Yasminevirus.
Figure 5. Phylogenetic position of Fadolivirus in the Mimiviridae and genome features. Maximum-likelihood phylogenetic tree (IQ-tree LG + F + R6) of the Mimiviridae inferred from a concatenated protein alignment of five core nucleocytoplasmic virus orthologous genes (NCVOGs; Yutin et al., 2009). Branches in orange represent viral isolates, and branches in black represent previously published metagenome-assembled genomes. The tree is rooted at the proposed viral subfamily Mesomimivirinae.Colored stars next to the tree indicate environmental origin. Bars next to the tree show genome features such as genome size, GC content and total number of proteins that contain aminoacyl-tRNA synthetase (aaRS)-related Pfam domain. Further, the presence/absence matrix next to the tree indicates protein families that are present in Fadolivirus and its closest relatives but absent in other members of the Mimiviridae; and protein families that are present in more than 30% of viral genomes in the Mimiviridae but not in Fadolivirus and its closest relatives. Stacked bars show the total count and annotation of pfam domains present in each of these protein families.
Figure 6. Orthologous genes shared by viruses in the Klosneuvirinae and some Mimiviridae. Connected lines highlight viruses sharing at least 10 orthologous genes. The bars at the top panel show the total number of shared orthologs between viruses that share at least 10 orthogroups. The bars in the right panel indicate the total number of shared orthogroups between visualized groups of viral genomes (connected by lines in the same row).
Discussion
Fadolivirus is a new viral isolate with up to 1.59 Mbp, belonging to the sub-family Klosneuvirinae. Its replicative cycle in V. vermiformis is comparable to other NCLDVs that have been described, such as Yasminevirus (Bajrai et al., 2019). Fadolivirus shows significant proximity to Klosneuvirus KNV1, virus described by a previous metagenomic study (Schulz et al., 2017), by phylogenetic analysis and by genomic comparison. However, even though these metagenomes assembled viral genomes were of estimated high completeness and low contamination, their hosts and the capacity of each virus to have multiple hosts often remain elusive. Co-occurrence study in Tara Oceans tried to identify probable hosts but their analyses identified families of virus with their probable host in Eukaryotes such as the dominance of Mimiviridae in relation with Alveolata, Opisthokonta, Rhizaria, and Stramenopiles (Meng et al., 2021). Further, based on detection of horizontal gene transfer events in members of the Klosneuvirinae have been suggested to infect Anthoathecata, fungi, arthropods, and various protists including slime molds (Schulz et al., 2020). Indeed, at this time, among amoeba only Tupanviruses have been shown to infect various protists with a similar pattern in A. castellanii and in V. vermiformis (Abrahão et al., 2018; Silva et al., 2019). Fadolivirus, contrary to earlier predictions, seemed to be rather host specific as it was only able to replicate in V. vermiformis (strain CDC19) and not in the Vermamoeba strain chuv172. Fadolivirus was also unable to infect any of the other diverse protists that we used in our infection experiments. However, our data are limited to the 8 different protists that were used in the infection experiments. Fadolivirus presents a near complete translation system similar to the ones described in Klosneuvirus (Schulz et al., 2017) and Tupanvirus (Abrahão et al., 2018). Moreover, Fadolivirus has additional copies of tRNA synthetases (Asx, Glutaminyl and Ile-lysidine tRNAsynthetases). However, a histidine tRNA synthetase was not found in its genome. It remains unclear whether this absence could lead to a restricted host range that we observed for Fadolivirus. Further analyses will be necessary to provide a more comprehensive overview of potential hosts for this virus. In particular, virus-encoded transcription factors have been proven as being key proteins in members of the Mimiviridae during infection of their amoeba host (Bekliz et al., 2018). The presence of translation system genes in Mimiviruses, Tupanviruses, Cafeteria roenbergensis virus, and Klosneuvirinae including Yasminevirus and Bodo saltans virus and combined with the paucity of these genes in the common ancestor of these viruses highlights that such an expanded genetic complement was acquired multiple times and independently in a lineage-specific style of evolution (Schulz et al., 2017; Koonin and Yutin, 2018; Bäckström et al., 2019).
The surprising features of this virus reside in the presence of predicted subunits A and D of ATPase. The first description of vacuolar (H+)-ATPase highlights the close proximity of V and F-type of ATPase D in their catalytic function (Nelson et al., 1995). Recently, during a giant viral infection, it was shown that the shift of the carbonaceous biomass of the host concerned 6–17% for viral production, probably due to a Cedratvirus (Kördel et al., 2021). This observation underlined the fact that viral production requires a greater production of energy by the infected cells. Further, active glycolysis and tricarboxylic acid cycles were identified by metagenomic studies (Moniruzzaman et al., 2020a; Ha et al., 2021) and some proteins were also found in Pandoravirus (Aherfi et al., 2020) and could have a confirmed functional activity such as the isocitrate dehydrogenase protein. Concerning the predicted ATPase subunit A, it is also present in some Klosneuvirinae. We could hypothesize that the presence of a more complete system for energy generation system in the ancestor of the Klosneuvirinae indicates that the involved genes have been lost in some viral lineages, or those sequences could be highly divergent in ways that are currently not identified by our bioinformatics comparisons. However, for the subunit D this protein is only present for Fadolivirus and could have been acquired from eukaryotes. Nevertheless, in this study we did not perform transcriptomic and proteomic analyses on these putative ATPase subunits; this constitutes a limitation to demonstrate their functional activity.
Meanwhile, novel viruses have been described and appeared as smaller DNA viruses among NCLDV with high speciation to their hosts (Boratto et al., 2020; Subramaniam et al., 2020). Their descriptions bring new opportunities to understanding the diversity and evolution across Nucleocytoviricota, and energy systems genes such as the ones observed in Fadolivirus would appear to play a major role during infection by giant viruses.
Data Availability Statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
Author Contributions
JA, FS, and BL designed the study and experiments. JA performed cytometry acquisition. JA and FDP performed electron microscopy. JA, FS, and AL performed bioinformatics analyses. JA, FS, TW, and BL wrote the manuscript. All authors approved the final manuscript.
Funding
This work was supported by the French Government under the “Investissements d’avenir” (Investments for the Future) programme managed by the Agence Nationale de la Recherche (ANR, fr: National Agency for Research) (reference: Méditerranée Infection 10-IAHU-03). Parts of this study were performed by the US Department of Energy Joint Genome Institute, a DOE Office of Science User Facility and made use of resources of the National Energy Research Scientific Computing Center, both supported by the Office of Science of the US Department of Energy under Contract no. DE-AC02–05CH11231.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Acknowledgments
The authors would like to thank Claire Andréani for her help with the first English correction.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmicb.2021.719703/full#supplementary-material
Footnotes
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Keywords: Vermamoeba vermiformis, giant virus, translation components, Mimiviridae, ATPase subunits, Klosneuvirinae, Fadolivirus
Citation: Andreani J, Schulz F, Di Pinto F, Levasseur A, Woyke T and La Scola B (2021) Morphological and Genomic Features of the New Klosneuvirinae Isolate Fadolivirus IHUMI-VV54. Front. Microbiol. 12:719703. doi: 10.3389/fmicb.2021.719703
Edited by:
Frank O'Neill Aylward, Virginia Tech, United StatesReviewed by:
Masaharu Takemura, Tokyo University of Science, JapanFelipe Hernandes Coutinho, Consejo Superior de Investigaciones Científicas (CSIC), Spain
Copyright © 2021 Andreani, Schulz, Di Pinto, Levasseur, Woyke and La Scola. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Bernard La Scola, bernard.la-scola@univ-amu.fr; Julien Andreani, miaguiabidou@gmail.com
†These authors have contributed equally to this work and share first authorship