Figures
Abstract
The Indianmeal moth, Plodia interpunctella (Lepidoptera: Pyralidae), is a common pest of stored goods with a worldwide distribution. The complete genome sequence for a larval pathogen of this moth, the baculovirus Plodia interpunctella granulovirus (PiGV), was determined by next-generation sequencing. The PiGV genome was found to be 112, 536 bp in length with a 44.2% G+C nucleotide distribution. A total of 123 open reading frames (ORFs) and seven homologous regions (hrs) were identified and annotated. Phylogenetic inference using concatenated alignments of 36 baculovirus core genes placed PiGV in the “b” clade of viruses from genus Betabaculovirus with a branch length suggesting that PiGV represents a distinct betabaculovirus species. In addition to the baculovirus core genes and orthologues of other genes found in other betabaculovirus genomes, the PiGV genome sequence contained orthologues of the bidensovirus NS3 gene, as well as ORFs that occur in alphabaculoviruses but not betabaculoviruses. While PiGV contained an orthologue of inhibitor of apoptosis-5 (iap-5), an orthologue of inhibitor of apoptosis-3 (iap-3) was not present. Instead, the PiGV sequence contained an ORF (PiGV ORF81) encoding an IAP homologue with sequence similarity to insect cellular IAPs, but not to viral IAPs. Phylogenetic analysis of baculovirus and insect IAP amino acid sequences suggested that the baculovirus IAP-3 genes and the PiGV ORF81 IAP homologue represent different lineages arising from more than one acquisition event. The presence of genes from other sources in the PiGV genome highlights the extent to which baculovirus gene content is shaped by horizontal gene transfer.
Citation: Harrison RL, Rowley DL, Funk CJ (2016) The Complete Genome Sequence of Plodia Interpunctella Granulovirus: Evidence for Horizontal Gene Transfer and Discovery of an Unusual Inhibitor-of-Apoptosis Gene. PLoS ONE 11(7): e0160389. https://doi.org/10.1371/journal.pone.0160389
Editor: Miguel Lopez-Ferber, Ecole des Mines d'Alès, FRANCE
Received: May 7, 2016; Accepted: July 18, 2016; Published: July 29, 2016
This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
Data Availability: The nucleotide sequence data reported in this paper are available from GenBank (accession number KX151395).
Funding: This work was supported by funding from the National Institute of General Medical Sciences (https://www.nigms.nih.gov), grant number P20 GM103429, awarded to CJF. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Viruses of family Baculoviridae infect insects of orders Lepidoptera, Diptera, and Hymenoptera [1, 2]. These viruses are characterized as having relatively large (80–180 kbp), circular, double-stranded DNA genomes that are packaged into rod-shaped, cylindrical capsids, which in turn are surrounded by a lipid envelope. Another key feature of these viruses is the formation of distinctive occlusion bodies consisting of a single highly-expressed viral protein (polyhedrin or granulin) assembled into a protective paracrystalline matrix around the enveloped virions.
Baculoviruses of genera Alphabaculovirus and Betabaculovirus, identified from moth and butterfly larvae, have received the most attention from researchers. Alphabaculovirus occlusion bodies (also referred to as polyhedra) are large polyhedral-shaped structures (0.15 to 15 μm) that contain multiple virions, often with >1 nucleocapsid per unit envelope [2]. Alphabaculoviruses, also known as nucleopolyhedroviruses (NPVs), can also productively infect insect cell lines derived from their hosts. This feature has facilitated much basic research on NPVs as well as the development of selected NPVs (such as Autographa californica multiple nucleopolyhedrovirus, or AcMNPV) into expression vectors [3]. Betabaculoviruses, also known as granuloviruses (GVs), differ by producing significantly smaller ovocylindrical occlusion bodies (approximately 0.13 x 0.5 μm) that contain a single virion [2]. There have been far fewer reports of successful infection of a cell line by a GV [4], and research with GVs has lagged behind that of NPVs.
A granulovirus reported to infect larvae of the Indianmeal moth, Plodia interpunctella, was first described in 1968 [5]. Study of this virus, Plodia interpunctella granulovirus (PiGV), led to the creation and recognition of the species Plodia interpunctella granulosis virus (later renamed as Plodia interpunctella granulovirus) in family Baculoviridae in 1982 [6].
P. interpunctella is a prevalent and cosmopolitan pest of stored grains, nuts, and other dried foodstuffs. As a consequence, research on PiGV was carried out to evaluate it as a potential alternative to chemical insecticides for controlling infestations of P. interpunctella [7–10]. This research culminated in the registration of PiGV as a biopesticide [11]. PiGV was also the subject of study in early research on the molecular biology of baculovirus structural proteins and virion assembly [12–14]. Finally, PiGV and P. interpunctella have been developed into a model system for understanding the ecology and evolution of infectious disease, particularly with respect to factors affecting pathogen transmission [15–18], host susceptibility [19–22], host dynamics [23, 24], and response to infection [25–27].
As of this writing, complete or partial DNA sequence data for > 50 betabaculovirus isolates have been deposited in GenBank, including the open reading frame (ORF) of a PiGV chitinase gene (GenBank accession no. KP864638). To fully characterize the genome of PiGV, we isolated and sequenced genomic DNA isolated from PiGV granules. The complete PiGV genome sequence was determined, and analysis of this sequence suggests that the species Plodia interpunctella granulovirus is distinct from other species of Betabaculovirus. Our analysis highlighted the remarkable degree to which this virus has acquired genes from other sources.
Materials and Methods
Virus DNA isolation
PiGV stocks were obtained from the USDA-ARS Manhattan, KS laboratory where PiGV biopesticide and molecular biology research took place during the 1970s and 1980s [28, 29]. This PiGV isolate was obtained from D. K. Hunter (USDA-ARS, Fresno, CA) in 1972, and originated with the isolate characterized by Arnott and Smith [5]. The virus was propagated in P. interpunctella larvae, separated from cell debris using a sucrose cushion, then purified using sucrose gradients [30]. Purified PiGV granules were solubilized in 0.1 M sodium carbonate and DNA was extracted from occluded virus as previously described [31, 32].
Genome sequencing and assembly
Genomic DNA was sequenced as previously described [32] except that the DNA was fragmented and the MID tags added at University of Florida Interdisciplinary Center for Biotechnology Research (Gainesville, FL). Sequencing reads from a Roche 454 GS Junior instrument were sorted and assembled using the SeqMan NGEN V3.0 assembler program (Lasergene; DNASTAR, Inc., Madison, WI) with default parameters. PCR and Sanger dideoxy sequencing were carried out to close gaps in the alignment and resolve or confirm regions with ambiguous sequences or unusual features, including 17 N8+ homopolymer regions. The Lasergene SeqManPro (version 12) sequence editor was used to prepare the final contig of the consensus genome sequence. The PiGV genome sequence generated for this study has been deposited in GenBank with the accession number KX151395.
ORF and homologous repeat region (hr) annotation
ORFs identified in the PiGV genome sequence were annotated if they were >50 codons in length and were evolutionarily conserved with other viral or non-viral ORFs, as ascertained by BLASTp. ORFs which did not yield a significant match by BLASTp (e.g. no matches with e-values <0.010) were annotated if they did not overlap a larger ORF by >75 bp and if they were predicted to be protein-encoding by both the fgenesV (http://linux1.softberry.com/berry.phtml) and ZCURVE_V [33] algorithms. In accordance with the convention for numbering baculovirus ORFs, the ORF encoding granulin was designated as ORF1, and the adenine of the granulin ORF start codon was designated as nt 1 of the genome.
Homologous region (hr) sequences were identified using the pattern- and repeat-finding functions of the LaserGene GeneQuest program (DNASTAR), Tandem Repeats Finder [34], and REPuter [35]. Individual repeats from the hrs were aligned using Clustal W in LaserGene MegAlign (DNASTAR), and the alignment and repeat consensus sequence were displayed with BOXSHADE (http://www.ch.embnet.org/software/BOX_form.html).
Sequence comparison and phylogeny
Shared synteny between PiGV and Plutella xylostella granulovirus K1 (PlxyGV-K1) [36], Cydia pomonella granulovirus isolate M1 (CpGV-M1; [37], and Pieris rapae granulovirus isolate Wuhan (PiraGV-Wuhan; [38] was determined by constructing gene parity plots [39].
To identify genetic differences between the PiGV genome reported in this study and the PiGV transcriptome sequences reported by [40], pairwise alignment was carried out between the PiGV genome sequence and the PiGV transcriptome contigs located at http://afterparty.bio.ed.ac.uk/study/show/2194070 [40].
The relationship of PiGV to other baculoviruses was inferred from the concatenated alignments of 36 of 37 putative baculovirus core genes [41]. An alignment of P6.9 amino acid sequences was not included in the analysis, as ORF31 of the gammabaculovirus Neodiprion abietis nucleopolyhedrovirus (NeabNPV) does not encode a p6.9 homologue and no complete p6.9 ORF has not been identified in the NeabNPV genome. In addition, the homologue of the ac78 core gene in NeabNPV is not ORF46 as reported by Garavaglia et al., but is instead an unannotated ORF extending from nt 42344←42628 in the NeabNPV genome. The amino acid sequence specified by this unannotated ORF was used in the AC78 alignment. The baculovirus core gene amino acid alignments were concatenated using BioEdit 7.1.3 [42].
In addition, amino acid sequence alignments were assembled with additional individual PiGV ORFs of interest (PiGV ORF11, ORF15, ORF18, and ORF81) and related viral and non-viral homologues of these ORFs.
In all cases, amino acid sequences were aligned by Clustal W using LaserGene MegAlign (DNASTAR) with default parameters, except for desmoplakin (AC66), AC78, PiGV ORF15, ORF18, and ORF81. For these alignments, the multiple and pairwise alignment penalties were reduced from 10 to 5 and the multiple alignment gap length penalty was reduced from 0.2 to 0.1 to compensate for the lower degree of conservation among the sequences of these proteins. Phylogenetic trees were constructed with the minimum evolution (ME) method using MEGA6 [43] with 500 bootstrap replicates. A phylogenetic tree was also inferred from the same alignment by maximum likelihood using either MEGA6 (for the individual PiGV ORF alignments) or RAxML 7.7.1 [44] (for the concatenated core gene alignment). MEGA6 was used to identify the best-fitting evolutionary models to use with these analyses and to calculate the gamma shape parameter for site rate differences.
The sequences used for phylogenetic inference are listed in S1 Table.
Results and Discussion
Properties of the PiGV genome
Assembly of 454 and Sanger dideoxy sequencing data yielded a genome of 112, 536 bp with a coverage of 53.9 X (Fig 1). The size is lower than the mean GV genome size of 123,464 (n = 18), though this average is skewed by the inclusion of the unusually large Helicoverpa armigera GV (HearGV) and Xestia c-nigrum GV (XecnGV) genomes [45, 46]. The PiGV genome is closest in size to that of Cryptophebia leucotreta GV (CrleGV), which is 110, 907 bp [47]. The PiGV nucleotide distribution, at 44.2% G+C, is closest to that of Clostera anachoreta granulovirus-HBHN (ClanGV-HBHN; [48]) at 44.4% G+C. Up to 123 ORFs were annotated for the PiGV genome, with 64 in the sense direction and 59 in the antisense direction (Fig 1, S2 Table).
ORFs are represented by arrows, with the position and direction of the arrow indicating ORF position and orientation. Each ORF is designated by a number or, in the case of conserved or well-characterized baculovirus orthologues, a name. Categories of ORFs are indicated in the figure. Homologous repeat regions (hrs) are represented by red boxes.
Seven homologous repeat regions (hrs) were identified in the PiGV genome. These hrs consist of 1–3 imperfect palindromes ranging in size from 49 to 83 bp and bound by inverted repeats with the consensus sequence TGATGACGAA (Fig 2). The consensus sequence of the PiGV hr terminal repeats did not closely match the consensus terminal sequence found to be conserved among the hrs of five GVs [49]. However, six of the seven PiGV hrs are located in positions that are conserved among other GV genomes for hrs, such as next to CpGV ORF cp5 (hr1), between sod and p74 (hr3), upstream of p47 (hr4), within vp91 (hr5), next to dna ligase (hr6), and within lef-8 (hr7) [45]; Fig 1, S2 Table). Some hrs of CpGV and CrleGV have been found to act as origins of DNA replication in C. pomonella tissue culture-based assays [49, 50], and it seems likely that PiGV hrs perform the same function in PiGV-infected P. interpunctella cells.
Nucleotide positions of the repeats in the genome sequence are indicated. Identical nucleotides occupying >50% of aligned positions are shaded in black, and nucleotides of the same class as conserved nucleotides (containing either a purine or pyrimidine base) are shaded in gray. Nucleotides in the repeat consensus sequence are denoted by uppercase letters for positions in the alignment with completely identical residues, and lowercase letters for positions in the alignment with a majority of identical residues. The conserved 10-bp inverted terminal repeat sequence is indicated by boxes surrounding the aligned sequence at each end.
Relationships to other baculoviruses
Blastp queries with the conceptual amino acid sequences of PiGV ORFs yielded the highest-scoring matches with ORFs from a wide variety of betabaculoviruses, including isolates of CpGV, CrleGV, Agrotis segetum granulovirus (AgseGV), Choristoneura occidentalis granulovirus (ChocGV), Clostera anastomosis granulovirus-A (ClanGV-A, or CaLGV) and -B (ClanGV-B), Lacanobia oleracea granulovirus (LaolGV), Pieris rapae granulovirus (PiraGV), Phthorimaea operculella granulovirus (PhopGV), Epinotia aporema granulovirus (EpapGV), Erinnyis ello granulovirus (ErelGV), Spodoptera frugiperda granulovirus (SpfrGV), and Spodoptera litura granulovirus (SpltGV) (S2 Table). PiGV ORF1, encoding granulin, was the most conserved gene, exhibiting a 94.4% amino acid sequence similarity with the encoded granulin of CrleGV. Other ORFs encoding granulovirus homologues exhibited amino acid similarities ranging from 28.4% (PiGV ORF38, mmp) to 89.7% (PiGV ORF46, ubiquitin), with an average amino acid similarity of 54.8%.
Phylogenetic inference with concatenated amino acid sequence alignments of 36 of the 37 currently accepted baculovirus core genes [41] confirmed that PiGV is a virus of genus Betabaculovirus (Fig 3). Miele and co-workers [51] proposed that betabaculoviruses occurred in two distinct groups, clade a and clade b. The ME phylogenetic tree (Fig 3) supports this division, but inference with ML placed PlxyGV outside of these two clades (data not shown). PiGV occurs in clade b, the support for its position among the other clade b granuloviruses is relatively weak with ME/ML bootstrap values of 74/-. The PiGV core gene concatemer is separated from other clade b sequences by long branch lengths and does not appear to be closely related to any particular GV.
The phylogenetic tree was constructed from the concatenated alignments of 36 baculovirus core gene amino acid sequences using the minimum-evolution (ME) method. Taxon genera are indicated with colored text background. Both the group I and II clades of genus Alphabaculovirus and the a and b clades of Betabaculovirus are indicated with brackets. Bootstrap values >50% for both ME and maximum likelihood (ML) analysis are indicated for each interior branch (ME/ML). In addition to PiGV (indicated by a red arrow), virus taxa and accession numbers used in the analysis are as indicated in S1 Table.
Gene parity plot analysis was carried out to visualize the synteny between the genomes of PiGV and two other clade b granuloviruses (CpGV-M1 and PiraGV-Wuhan). Gene order in the PiGV genome was also compared with that of a clade a granulovirus that has a genome of a comparable size (PlxyGV; 100,999 bp). Although the gene content differences between PiGV and PlxyGV were visibly more numerous than those between PiGV and the clade b GVs, the degree of synteny was not noticeably different (Fig 4).
Plots show the ORF content and order of the PiGV genome (x-axis) with that of (A) CpGV, (B) PiraGV, and (C) PlxyGV (y-axes). Each point in the plot represents an ORF. ORFs present in only one of the compared genomes appear on the axis corresponding to the virus in which they are present.
Recently, the transcriptome of P. interpunctella larvae infected with PiGV and harvested at 24 hours post-infection (hr p. i.) was reported [40]. The authors of this study identified contigs of granulovirus origin (ascertained by BLAST alignment with the sequence of PlxyGV) and concluded that they had assembled viral sequence data from the infected P. interpunctella transcriptome amounting to an estimated 44% of the PiGV genome. Comparison of the PiGV genome with the viral contigs assembled from transcriptomic data [40] revealed that the virus used by McTaggart and co-workers is the same virus reported here. Transcriptome reads from this project assembled into eleven contigs that aligned with PiGV nt 2841–7436, 10664–13710, 18056–27589, 29803–34735, 64189–69653, 70348–71408, 72086–77471, and 79003–96283, for a total of 51, 303 bp or 45.6% of the genome. Two of the transcriptome contigs consist of an inverted repeat of the same sequence–for example, nt 1→ 4891 of contig comp66738_c0_seq1 aligns with the antisense strand of PiGV genome nt 88851←93740, while nt 4808→9698 of the same contig aligns with the sense strand of the same region of PiGV (nt 88851→93740). PCR with PiGV genomic DNA and primers that annealed close to the inversion points in these contigs failed to produce amplimers, indicating that the inversions in these contigs were the result of erroneous assembly. These contigs may have led McTaggart and co-workers to conclude that there were inversions of the PiGV genome sequence relative to that of PlxyGV in a dot-plot of the PiGV-derived sequence vs. the PlxyGV genome sequence, [40]. Our gene parity plot analysis does not support the presence of large-scale inversions in the PiGV genome relative to the genome of PlxyGV.
Alignment of the consensus PiGV genome and the McTaggart et al. viral transcriptomic sequences revealed a total of 66 substitutions (28 synonymous, 26 nonsymonymous, and 12 intergenic), for a rate of 1.3 substitutions/kbp (Table 1). In addition, 23 indels (12 intergenic and 11 located within ORFs) were detected. Thirty-six of the substitutions and six of the indels in Table 1 also were found in a minority of the 454 genome sequence reads, ranging in frequency from 10% (indel at nt 12508) to 48.8% (C to T substitution at nt 90715) with an average frequency of 27.9%. Of the 11 indels in ORFs, 10 of them were in-frame and 1 resulted in a frameshift within PiGV ORF14. This ORF is an orthologue of p49 (AcMNPV ORF ac142), which appears to be required for virus production [52, 53]. The indel in p49, which increases a homopolymer repeat from A8 to A9, is present in 10% of the 454 genome sequence reads, suggesting that it corresponds to a minor genotype that may be dependent on P49 supplied in trans.
Gene content
The PiGV genome contained all 37 of the core genes proposed for Baculoviridae by Garavaglia et al. [41](Fig 1). Several non-core genes conserved among all members of Alphabaculovirus and Betabaculovirus were also found in the PiGV genome, including granulin, pk-1, ac13, ac23, dbp, lef-6, ubiquitin, pp31, lef-11, ac38, fp25k, lef-3, ac75, tlp, p12, ac106/107, ac108, ac110, p24, pep, me53, ac145, ac146, and ie-1. Two genes claimed by Garavaglia et al. to be conserved among betabaculoviruses, gp37 and exon0, were not found in PiGV. These genes also do not occur in the genomes of SpfrGV-VG008, ErelGV, or in isolates of AgseGV.
The remaining ORFs in the PiGV genome consist of (a) ORFs with homologues among granuloviruses (S2 Table) and (b) ORFs with no granulovirus homologues (Table 2). Among the former class of ORFs is PiGV ORF11, which had the most significant blastp match with an ORF from isolates of Bombyx mori bidensovirus, the sole species of the recently-created virus family Bidnaviridae [54]. Other homologues have been described from a handful of granulovirus genomes, including those of CrleGV-CV3, ChocGV, Clostera anastomosis granulovirus B (ClasGV-B), and ErelGV. A homologue has also been identified in the genome of Perigonia lusca single nucleopolyhedrovirus (PeluSNPV). The encoded amino acid sequences of these genes also share similarity with amino acid sequences of the NS3 gene found in isolates of the densovirus species Lepidopteran ambidensovirus 1. Phylogenetic inference of these sequences grouped the densovirus sequences together as well as the two copies of the homologue found in ErelGV with strong bootstrap support (Fig 5). PiGV ORF11 was grouped with the bidensovirus sequences, and homologues from ClasGV-B and PeluSNPV were grouped together with moderate bootstrap support, while there was no significant bootstrap support for the positions of the other homologues. From the phylogeny, it appears that homologues of the densovirus/bidensovirus NS3 sequences appeared in baculovirus genomes as a result of independent acquisition events. This conclusion is consistent with that drawn by Ardisson-Araújo et al. [55] from their analysis of a smaller data set. An alternative hypothesis for the presence of NS3 homologues in the betabaculovirus genomes involves a single ancient acquisition event followed by sequence divergence. The NS3 homologue in PeluSNPV may be due to horizontal gene transmission from a granulovirus, or it may point to an NS3 gene acquisition that predated the divergence of alphabaculoviruses and betabaculoviruses. In either case, for this hypothesis, one would also have to stipulate that the NS3 gene was subsequently lost from most baculovirus lineages. With regard to the possible functional significance of these genes, Junonia coenia densovirus NS3 was shown to be required for viral DNA replication [56], while BmDNV-Zhenjiang NS3 was shown to interact with a transgelin homologue and a serine protein precursor in B. mori BmN cells [57]. It is unclear what role, if any, the baculovirus homologues of these genes possess in the baculovirus life cycle.
ME phylogram inferred from the alignment of NS3 homologue amino acid sequences are shown with bootstrap values (>50%) at interior branches for ME and ML analysis (ME/ML) where they occur. In addition to PiGV (indicated by a red arrow), virus taxa are as indicated in S1 Table. Family and/or genus of each taxon is indicated with a color-coded text background.
ORFs with alphabaculovirus homologues.
Four PiGV ORFs–ORF9, ORF15, ORF18, and ORF103 –encode sequences that only exhibit significant sequence similarity to alphabaculovirus ORFs.
ORF9 encodes an amino acid sequence with significant similarity to dUTPases (dut) from a number of sources. Although the granuloviruses AgseGV, EpapGV, ErelGV, and SpfrGV-VG008 also encode dut homologues, none of these GV dUTPase sequences appeared in a BLASTp search with PiGV ORF9 as a query sequence. The only baculovirus homologue that appeared as a match to ORF9 by blastp was that of Spodoptera frugiperda multiple nucleopolyhedrovirus (SfMNPV). This result suggests that the dut homologues in the PiGV genome and other GV genomes are a consequence of a separate gene acquisition events. Recent comprehensive analyses of baculovirus dut gene phylogeny [58, 59] supports this hypothesis, in one case finding that the dut genes present in baculovirus genomes are the product of at least nine horizontal gene transfer events [59].
Both ORF15 and ORF18 encode homologues of the AcMNPV ORF ac11. Homologues of this gene have only been found in all group I alphabaculoviruses and a selection of group II alphabaculoviruses. Phylogenetic inference of relationships among ac11 homologues points to two well-supported clades of group I alphabaculovirus sequences (Fig 6). The homologues from PiGV and the group II alphabaculoviruses occur outside these clades and are separated by long branch lengths, suggesting that these homologues have diverged extensively from each other and/or are the results of horizontal gene transfer. ORF15 and ORF18, which only share 26% amino acid sequence identity with each other, are grouped together but with no significant degree of support. Two homologues of the same gene in the same genome could arise from a single acquisition event followed by gene duplication and sequence divergence. However, given the degree of sequence divergence between the ORF15 and ORF18 sequences, and in the absence of reports of ac11 homologues in other granulovirus genomes, it seems more likely that ORF15 and ORF18 resulted from independent acquisition events. In cells infected with an AcMNPV ac11 knockout mutant bacmid-generated virus, both nucleocapsid egress from the nucleus and intranuclear envelopment of nucleocapsids were absent, suggesting an essential role for ac11 in those particular steps in virion morphogenesis [60]. It is unclear if the PiGV homologues play a similar role in PiGV-infected cells.
ME phylogram inferred from the alignment of AcMNPV ac11 homologue amino acid sequences are shown with bootstrap values (>50%) at interior branches for ME and ML analysis (ME/ML) where they occur. Virus taxa and accession numbers used in the analysis are as indicated in S1 Table. The PiGV ac11 homologues are highlighted in yellow, and the group I alphabaculovirus sequences are indicated by a bracket.
Finally PiGV ORF103 encodes a homologue of an ORF annotated in isolates of Lymantria dispar multiple nucleopolyhedrovirus (LdMNPV), Lymantria xylina nucleopolyhedrovirus (LyxyNPV), and isolates of the nudivirus species Heliothis zea nudivirus. Although the annotation for the LdMNPV 5–6 isolate genome indicates that this is a homologue of AcMNPV ac4 [61], blastp and HMMER [62] queries with PiGV ORF103 and the LdMNPV orthologue sequences did not yield matches with ac4 or any other baculovirus gene.
ORFs encoding inhibitor of apoptosis (IAP) homologues.
Inhibitors of apoptosis (IAPs) are functionally diverse proteins that were originally identified in baculoviruses as inhibitors of host cell apoptosis [63–67]. They were subsequently found in both eukaryotic organisms and in other DNA viruses. IAPs are recognized by the presence of at least one baculoviral IAP repeat (BIR) domain, which mediates protein interaction. Baculovirus IAPs also contain a copy of a Really Interesting New Gene (RING) domain in the C-terminus.
Clem (2015) [67] identified 6 distinct groups of IAP-encoding genes found in baculovirus genomes. The genes iap-1, iap-2, and iap-4 have been found only in alphabaculoviruses, while iap-5 and iap-6 genes are found exclusively in betabaculoviruses. Genes of the iap-3 group are found among alphabaculoviruses, betabaculoviruses, and gammabaculoviruses.
In the PiGV genome, ORF101 was identified as an iap-5 orthologue. However, no orthologue for iap-3 or iap-6 was found. Instead, a second iap homologue encoded by PiGV ORF81 was identified that did not appear to correspond to any of the baculovirus iap groups described by Clem (2015) [67]. A blastp query with the ORF81 amino acid sequence yielded 189 matching sequences that included mostly IAP sequences from insects of orders Diptera (flies and mosquitoes), Hymenoptera (ants and wasps), Hemiptera (true bugs), with additional matches with a few sequences from Coleoptera (beetles), Isoptera (termites), and Dictyoptera (cockroaches). No baculovirus IAP sequences were among these matches, and only one IAP sequence from a moth, Galleria mellonella (order Lepidoptera; Genbank accession no. ACV04797, expected value of 2e-13), occurred in the results of the query. G. mellonella, like P. interpunctella, is classified in the family Pyralidae. A tBlastn search of the McTaggart et al. [40] P. interpunctella transcriptome contigs with the sequences of the G. mellonella IAP and an IAP from the pyralid moth Amyelois transitella (Genbank accession no. XP_013192077) failed to yield any matches. A search of the annotation for these contigs also failed to find any sequences identified as encoding inhibitors of apoptosis in the P. interpunctella transcriptome.
An examination of the ORF81 amino acid sequence revealed the existence of two BIR motifs and a C-terminal RING domain (Fig 7). ORF81 is thus similar to baculovirus IAP-1, IAP-3, and IAP-5, which also possess two BIRs and one RING domain. However, at 399 amino acids, the protein encoded by ORF81 was significantly larger than those encoded by baculovirus iap genes (which range from approximately 240–310 amino acids). Rather, the size of the ORF81 protein was more similar to that of insect cellular IAP homologues (Fig 7). Cellular insect IAPs possess an N-terminal leader sequence occurring prior to the first BIR repeat (BIR1) that is longer than the sequence upstream of BIR1 in baculovirus IAPs (Fig 7). In lepidopteran IAPs, leader sequence contains a mitogen-activated kinase (MAPK) degron motif (TPxxS) which mediates the turnover of cellular IAPs in baculovirus-infected cells [68]. The PiGV ORF81 protein does not possess an extended leader sequence; BIR1 in this protein begins at residue 3, 5, or 7 (depending on the specific conserved domain database that is consulted). Also, no sequences similar to the lepidopteran IAP degron, the caspase cleavage site, or the cellular IAP instability motifs identified by Vandergaast et al (2015) [68] are present in PiGV ORF81.
A schematic illustration of IAPs from PiGV, selected alphabaculoviruses (AcMNPV-C6, OpMNPV) and betabaculoviruses (CpGV), and insects. Lines representing the IAPs are drawn in proportion to the sizes of the proteins. The BIR domains are shown in green, the RING domain in orange, and the ubiquitin-association domain (UBA) of T. castaneum IAP-2 is shown in blue.
Phylogenetic inference was carried out with a selection of cellular IAPs with two copies of the BIR motif that exhibited significant sequence similarity with the PiGV ORF81 product by blastp, along with baculovirus IAPs of the iap-1, iap-3, and iap-5 classes (Fig 8). Many of the basal nodes of this tree did not possess ≥50% bootstrap support, but well-supported clades were obtained for the alphabaculovirus IAP-1 and betabaculovirus IAP-5 sequences, as well as sequences from insect orders Diptera, Hymenoptera, Hemiptera, and the moth species of families Noctuidae and Pyralidae. The single termite IAP sequence (from Zootermopsis nevadensis) grouped with the hemipteran sequences. While the group I alphabaculovirus IAP-3 sequences were grouped together, the bootstrap support for this clade was not strong. Other IAP-3 sequences from group II alphabaculoviruses and betabaculoviruses did not form a coherent clade, though some IAPs from closely related viruses (e.g. the Spodoptera and Agrotis spp. NPVs) occurred in terminal and sub-terminal branches that enjoyed good support. The results of this analysis are similar to a comprehensive phylogenetic analysis of IAPs from many different viral and cellular sources conducted by Thézé and coworkers [58], but different from the phylogenetic analysis carried out by Clem (2015) [67] exclusively with viral sequences in which the IAP-3 sequences all occurred in a single clade. PiGV ORF81 was placed in a group with IAP-3 sequences from Mamestra spp. NPVs and the IAP-3 from HearMNPV, which is closely related to the Mamestra spp. viruses [69]. Both ME and ML methods placed ORF81 in this clade, although the bootstrap value in the ML tree was only 43%. However, ORF81 and the NPV IAP sequences were separated by long branch lengths.
ML phylogram inferred from the alignment of baculovirus and insect amino acid sequences are shown with bootstrap values (>50%) at interior branches for ME and ML analysis (ME/ML) where they occur. Branches for alphabaculovirus IAP-1, betabaculovirus IAP-5, and group I alphabaculovirus IAP-3 sequences are collapsed, and the nodes for these classes of IAPs are indicated in the tree. The baculovirus genus or insect order for each taxon is indicated with color-coded text background. The virus and insect taxa and their accession numbers are as listed in S1 Table.
Phylogenetic analysis by Hughes [70] with a smaller set of baculovirus and host insect IAP sequences placed CpGV IAP-3 and four other NPV IAP-3 sequences in a group with three lepidopteran IAPs with a strong degree of support. While CpGV-M1 IAP-3 was also placed with lepidopteran IAPs in our analysis, the relationships of other viral IAP-3 sequences to the lepidopteran sequences is less clear (Fig 8). In addition to using fewer sequences, the analysis of Hughes also employed alignments of the BIR domain sequences only, which may account for some differences in the results. Nevertheless, it seems clear that the baculovirus IAP-1 and IAP-5 lineages are each due to single acquisition events. It is also possible that the baculovirus IAP-3 genes and the PiGV ORF81 IAP homologue are descended from a single ancient acquisition event followed by extensive sequence divergence, although these sequences do not occur in a single well-supported clade in the IAP phylogeny as is the case for the IAP-1 and IAP-5 sequences.
While some baculovirus IAPs of the IAP-3 group possess demonstrated anti-apoptotic activity, not all baculovirus IAPs have been shown to inhibit apoptosis when tested [66]. The IAPs with proven anti-apoptotic activity do not appear to function by directly binding and inhibiting the effector caspases that trigger apoptosis [71, 72], but instead bind to and stabilize cellular IAPs, which are degraded rapidly in response to baculovirus infection [68, 73]. Since both PiGV IAP-5 and ORF81 have short leader sequences with no degron or instability motifs, it is possible that they would inhibit apoptosis by the same mechanism.
Conclusions
The role of horizontal gene transfer in the evolution and adaptation of organisms has long been recognized [74]. Viruses in particular have been documented as mediators of horizontal gene transfer, and large DNA viruses in particular appear to be mosaics of genes from different sources [75, 76]. In particular, a recent study has provided evidence that baculoviruses may have served to shuttle transposons among different species of host moths [77]. Some environments hypothetically are more conducive to horizontal gene transfer than others. This is likely the case for the Indianmeal moth, P. interpunctella. As pests of stored grains and nuts in a wide range of climates and locations, larvae of P. interpunctella conceivably could encounter a wide variety of donor gene sources, including microorganisms. One can imagine opportunities for viruses and other microorganisms resident in P. interpunctella to acquire genes from a wide taxonomic range of donor genomes. In particular, exposure of P. interpunctella to the viruses of other insects that infest grains and nuts could conceivably account for the appearance of genes in the PiGV genome that are present in other distinct lineages of viruses, such as alphabaculoviruses and densoviruses. In support of this hypothesis, an analysis of gene homologues shared by baculoviruses and entomopoxviruses found that ORF xc138, originally identified in the XecnGV genome, was apparently transferred directly between entomopoxviruses and granuloviruses on two separate occasions [58]. The sequence of PiGV thus serves to further highlight the concept of viruses as agents for horizontal gene transfer, not only from a virus to a host [78], but to other viruses as well.
Supporting Information
S1 Table. Names, abbreviations, and GenBank accession numbers of taxa used in phylogenetic inference.
https://doi.org/10.1371/journal.pone.0160389.s001
(DOCX)
S2 Table. PiGV open reading frames (ORFs) and homologous repeat regions (hrs).
https://doi.org/10.1371/journal.pone.0160389.s002
(DOCX)
Acknowledgments
The authors would like to thank Jeff Lord (USDA-ARS) for providing a sample of PiGV and William McGaughey and Lee Bulla for information on the source of the PiGV isolate sequenced in this study. Equipment used for purification of the virus and viral DNA isolation was made possible from support by the Arkansas INBRE program, with a grant from the National Institute of General Medical Sciences, (NIGMS), P20 GM103429. Mention of trade names or commercial products in this publication is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the U.S. Department of Agriculture.
Author Contributions
Conceived and designed the experiments: RLH DLR CJF. Performed the experiments: DLR CJF. Analyzed the data: RLH DLR. Contributed reagents/materials/analysis tools: DLR CJF. Wrote the paper: RLH DLR CJF.
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