- Research article
- Open Access
Comparative mitogenomics of Braconidae (Insecta: Hymenoptera) and the phylogenetic utility of mitochondrial genomes with special reference to Holometabolous insects
© Wei et al; licensee BioMed Central Ltd. 2010
- Received: 7 March 2010
- Accepted: 11 June 2010
- Published: 11 June 2010
Animal mitochondrial genomes are potential models for molecular evolution and markers for phylogenetic and population studies. Previous research has shown interesting features in hymenopteran mitochondrial genomes. Here, we conducted a comparative study of mitochondrial genomes of the family Braconidae, one of the largest families of Hymenoptera, and assessed the utility of mitochondrial genomic data for phylogenetic inference at three different hierarchical levels, i.e., Braconidae, Hymenoptera, and Holometabola.
Seven mitochondrial genomes from seven subfamilies of Braconidae were sequenced. Three of the four sequenced A+T-rich regions are shown to be inverted. Furthermore, all species showed reversal of strand asymmetry, suggesting that inversion of the A+T-rich region might be a synapomorphy of the Braconidae. Gene rearrangement events occurred in all braconid species, but gene rearrangement rates were not taxonomically correlated. Most rearranged genes were tRNAs, except those of Cotesia vestalis, in which 13 protein-coding genes and 14 tRNA genes changed positions or/and directions through three kinds of gene rearrangement events. Remote inversion is posited to be the result of two independent recombination events. Evolutionary rates were lower in species of the cyclostome group than those of noncyclostomes. Phylogenetic analyses based on complete mitochondrial genomes and secondary structure of rrnS supported a sister-group relationship between Aphidiinae and cyclostomes. Many well accepted relationships within Hymenoptera, such as paraphyly of Symphyta and Evaniomorpha, a sister-group relationship between Orussoidea and Apocrita, and monophyly of Proctotrupomorpha, Ichneumonoidea and Aculeata were robustly confirmed. New hypotheses, such as a sister-group relationship between Evanioidea and Aculeata, were generated. Among holometabolous insects, Hymenoptera was shown to be the sister to all other orders. Mecoptera was recovered as the sister-group of Diptera. Neuropterida (Neuroptera + Megaloptera), and a sister-group relationship with (Diptera + Mecoptera) were supported across all analyses.
Our comparative studies indicate that mitochondrial genomes are a useful phylogenetic tool at the ordinal level within Holometabola, at the superfamily within Hymenoptera and at the subfamily level within Braconidae. Variation at all of these hierarchical levels suggests that the utility of mitochondrial genomes is likely to be a valuable tool for systematics in other groups of arthropods.
- Mitochondrial Genome
- tRNA Gene
- Gene Rearrangement
- Codon Position
- Rich Region
Most animal mitochondrial genomes are about 16 Kb in size and contain 37 genes: 13 protein-coding genes, 22 transfer RNA genes (tRNA) and two ribosomal RNA genes (rRNA) . Additionally, an A+T-rich region is present which contains essential regulatory elements for transcription and replication. It is therefore referred to as the control region . Complete mitochondrial genomes provide good models for molecular evolution and abundant molecular markers for phylogenetic and population studies [3–6].
Because mitochondrial genomes are highly economized, with few intergenic regions, gene rearrangements are rare . However in some lineages they are more common. For example amongst arthropods, the following groups show significant gene rearrangements: Myriapoda , Hymenoptera , hemipteroids [9–11], Acari [12, 13], Araneae [14, 15], and Isopoda [16, 17]. These lineages therefore make ideal candidates for the study of gene rearrangement mechanisms [8, 18–21].
Mitogenomic studies of the Hymenoptera have revealed many interesting features: (i) gene arrangements are conserved in the basal Hymenoptera, i.e., the grade Symphyta, whereas frequent gene rearrangements are observed in the derived clade, Apocrita [8, 22] with approximately equal amounts of gene shuffling, inversion, and translocation ; (ii) tRNA positions are selectively neutral in all studied hymenopteran mitochondrial genomes ; (iii) various gene rearrangement mechanisms are necessary to explain the derived gene arrangement patterns in Hymenoptera [8, 24], whereas amongst vertebrates, most gene rearrangement events are best explained by tandem duplication ; (v) nucleotide substitution rates are extremely high in the mitochondrial genomes of three Nasonia (Hymenoptera: Chalcidoidea) species, about 30 times faster than nuclear protein-coding genes .
The number of hymenopteran mitochondrial genomes, though high relative to other taxa, is rather limited, especially in relation to the species-richness of the order [24, 26–31]. The characterization of more hymenopteran mitochondrial genomes has promise in answering evolutionary questions such as mechanisms of remote inversion events of gene rearrangement  and the variation of strand-specific compositional bias between Braconidae and Ichneumonidae [8, 32].
Here we sequenced seven complete mitochondrial genomes of members of Braconidae, representing the subfamilies, Doryctinae, Opiinae, Microgastrinae, Cheloninae, Aphidiinae, Macrocentrinae and Euphorinae. Braconidae was selected because it is one of the largest families in Hymenoptera, second only to Ichneumonoidea, and because no complete mitochondrial genome has been reported for the family, although one of the reported mitochondrial gene rearrangement hot spots has been examined in this family [8, 20]; Due to variation within the family, Braconidae is an ideal group to study the evolution of modes of parasitism . Members of the subfamily Doryctinae are mostly ectoparasitic idiobionts (the host does not recover after paralysis by an ovipositing wasp and the wasp larvae feeds immediately), whereas member of the other six subfamilies are endoparasitic koinobionts (the host recovers after oviposition and develops normally for some time before it is consumed by the parasitoid). Though many efforts have been focused on the phylogeny of Braconidae, it is still a problematic group with many unresolved relationships [34–41].
Holometabolous insects represent the most successful lineages of Metazoa with 11 orders encompassing more than half of all known animal species. However, the phylogenetic relationships among orders in holometabolous insects are still controversial. Studies based on morphology or single molecular markers are limited by character quantity and quality respectively [42, 43], whereas those based on complete mitochondrial genome sequences or nuclear genomes are limited by taxon sampling [44, 45].
In this study, we explored some evolutionary traits of braconid mitochondrial genomes, and consequently assessed the phylogenetic utility of mitogenomics at three hierarchical levels, i.e., Braconidae, Hymenoptera and Holometabola.
General description Braconidae mitochondrial genomes
General information of the mitochondrial genomes from Ichneumonoidea
Wei et al., 2009
Dowton et al., 2009
All genes identified in the seven mitochondrial genomes are typical animal mitochondrial genes with normal gene sizes. In all, 37 genes and an A+T-rich region were identified in the two completely sequenced mitochondrial genomes of S. agrili and C. vestalis. In the mitochondrial genome of M. camphoraphilus, a region spanning partial sequence of cob and nad1 was duplicated and inserted downstream of the rrnS - trnM - trnI - A+T-rich region and reversed. This is the first report of protein-coding gene sequence duplication in Hymenoptera mitochondrial genomes. The duplicated region led to the failure of amplification of the sequence further downstream.
All protein-coding genes start with ATN start codons and stop with TAA termination codons or truncated termination codons TA or T. Gene nad1 has been found to employ TTG as a start codon in some species of Hymenoptera, Coleoptera and Lepidoptera, thus minimizing intergenic spacing and avoiding overlap with adjacent genes [47–49], however, we did not discover TTG start codons in nad1 genes for any Braconidae.
Most transfer RNA (tRNA) genes have the usual cloverleaf structure and anticodons commonly found in insects. All trnK and trnS2 use TTT and TCT as anticodons rather than the normal CTT and GCT, respectively. The use of abnormal anticodons in these two tRNAs appears to be correlated with gene rearrangement .
The A+T-rich region is believed to be involved in the regulation of transcription and control of DNA replication, characterized by five elements: (1) a polyT stretch at the 5'end of the A+T-rich region, which may be involved in the control of transcription and/or replication initiation; (2) a [TA(A)]n-like stretch following the polyT stretch; (3) a stem and loop structure, which may be associated with the second strand-replication origin; (4) a TATA motif and a G (A)nT motif flanking the stem and loop structure and (5) a G+A rich sequence downstream of the stem and loop structure .
We compared gene rearrangement rates among braconid mitochondrial genomes in the region from cox1 to trnH, which was successfully sequenced in all seven species; gene rearrangement rates were unequal among them. Gene arrangement pattern was conserved in A. gifuensis and P. flava, and derived in the other five species. Of the two microgastroid species P. flava and C. vestalis [20, 41, 51], the former is conserved while the latter was markedly rearranged in gene pattern. In conclusion, mitochondrial gene rearrangement rate was not taxonomically correlated at our level of investigation of the Braconidae.
Gene rearrangement events comprise three classes, i.e., translocation, local inversion (inverted but remaining in the position), and shuffling with remote inversion (translocated and inverted) . All determined trnI and trnM were inverted and translocated, forming the arrangement pattern trnI(-) - trnM(-) - A+T-rich region - trnQ in S. agrili. D. longicaudata and C. vestalis, and trnM(-) - trnI(-) - A+T-rich region - trnQ in M. camphoraphilus.
In the three species S. agrili, D. longicaudata and C. vestalis, trnH was inverted and translocated (remote inversion) to the junction of cox2 and atp8. The arrangement pattern, trnD(-) - trnH - trnK or trnH(-) - trnD - trnK, has been found in many subfamilies of Braconidae. It has been reported that both the inversion of trnD and the remote inversion of trnH are independent evolutionary events in this family [8, 20]. In the two reported species of Doryctinae, Jarra phorocantha and Heterospilus sp., the ancestral arrangement pattern of trnK - trnD occurs , which suggests that the gene rearrangement event in S. agrili occurred after the origin of the subfamily.
Gene rearrangement mechanism
Mechanisms for the three classes of gene rearrangement events in hymenopteran mitochondrial genomes are widely discussed [8, 21]. Inter/intro mitochondrial genome combination is presumed to be the most plausible explanation for local inversions. trnY in C. vestalis is the only locally inverted gene in these seven braconid species, except for the region from trnE to cob in C. vestalis. The duplication/random loss model, and the intramitochondrial genome recombination and duplication/nonrandom loss model are possible mechanisms to explain translocation. Of these, intramitochondrial genome recombination is presumed to be more common. Shuffling is thought to be the result of duplication/random loss. The tRNA clusters trnW - trnC - trnY and trnK - trnD are frequently shuffled regions. trnD was not only shuffled but also inverted. This may have been the result of two independent events caused by separate mechanisms.
Since trnI, trnM and the A+T-rich region were all inverted, separated remote inversions would make the rearrangement in this region extremely complicated. Therefore, it is more likely that trnI and trnM were inverted simultaneously. Thus, before the inversion of this region, trnQ would have been shuffled to form an intermediate pattern of A+T-rich region - trnM - trnI - trnQ. We observed a trnM - trnI - trnQ arrangement pattern in the mitochondrial genome of Diadegma semiclausum, an Ichneumonidae, the sister-group of Braconidae . This suggests that trnM - trnI - trnQ is ancestral, and trnM - trnI - A+T-rich region is a derived pattern in Braconidae. Recombination is more likely to explain the inversion of A+T-rich region - trnM - trnI - trnQ based on the parsimony criterion.
(2) tRNA translocations. The six tRNA genes between nad3 and nad5 in their ancestral position are heavily rearranged. And the most apparently conserved order of this tRNA cluster is trnA - trnR - trnN, which indicates that the derived relative positions of these tRNA genes are most likely the result of translocations of trnF and trnE and shuffling of trnS2. Nevertheless, trnH may have been inverted and translocated to the junction of cox2 and atp8 before the large-scale inversion event. The most possible mechanisms of gene translocation and shuffling are recombination, rather than tandem duplication followed by deletion (TDRL), which might change the remnant order of tRNA and the neighbouring protein-coding genes.
(3) Small-scale translocations. Four gene boundaries, i.e., nad4 - nad5, trnT - nad4l, cox3 - trnG - nad3 and cob - nad6 - trnP, were translocated after the large-scale inversion at the junction of atp6 - trnS1. Although tRNA gene rearrangement is more frequent than that of protein-coding genes, translocation of three gene boundaries is more parsimonious than tRNA gene rearrangement. Recombination is also favoured in these small-scale translocation events, because neither pseudo-genes nor large intergenic spacers are present in the boundaries of these rearranged genes, which are the intermediate state of the TDRL model .
Braconidae mitochondrial genomes have high A+T content, a characteristic typical of other hymenopterans, with values from 82.4% to 87.2%.
Nucleotide composition of Ichneumonoidea mitochondrial genomes
Whole genome sequences
All protein-coding genes
Hassanin et al. (2005) suggested that strand asymmetry is best reflected in the GC skew. Hence, all braconid species in the present study show reversal of strand asymmetry, as in some other arthropods [16, 58–61], flatworms , brachiopods , echinoderms  and fish .
Inversion of replication origin located in the A+T-rich region would lead to reversal of strand asymmetry [16, 59, 66], which were proved by examination of regulatory elements in A+T rich region in three sequenced braconid mitochondrial genomes. Although further sampling is necessary the present evidence suggests that reversal of strand asymmetry and inversion of the A+T-rich region is a synapomorphy for members of Braconidae.
Phylogenomics of Braconidae
Subfamilies of braconid have traditionally been divided into two groups, cyclostomes and noncyclostomes [20, 35, 39]. These clades were firmly resolved in all our analyses of seven representative subfamilies. Aphidiinae was also recovered as sister-group to cyclostomes by Dowton (2002) and Zaldivar-Riverón (2006). Our results obviously support the sister group relationship between Aphidiinae and cyclostomes. Sampling of only seven of the 40 subfamilies of Braconidae may be the cause of the misplacement of Cheloninae in some analyses. Our analyses indicate that mitochondrial genome sequence data has the potential to resolve the phylogenetic relationships among braconid subfamilies with increased taxon sampling.
Phylogenomics of Holometabola with an emphasis on Hymenoptera
Monophyly of the seven in-group orders was recovered in most analysis. Hymenoptera was recovered at the base of all homometabolous lineages, except in most likelihood analyses based on amino acid and protein-coding positions, in which Hymenoptera and Lepidoptera were recovered as sister-groups with low support value. In this study, we included mitochondrial genome sequences from Neuroptera and Mecoptera for the first time. Mecoptera was recovered as a sister-group of Diptera. Neuropterida (Neuroptera + Megaloptera in this study) is supported across all analyses, forming the sister-group to (Diptera + Mecoptera), differing from the presently preferred sister-group relationship of Neuropterida and Coleoptera .
In the previous analysis using complete mitochondrial genome sequence data, the relationships among holometabolous orders were not well resolved [45, 68]. Here, increased taxon sampling generated more stable phylogenetic relationships. The basal position of Hymenoptera is congruent with the analysis based on whole nuclear genome sequences .
Within Hymenoptera, three species of Symphyta representing three superfamilies and three families and 17 species of Apocrita representing seven superfamilies and eight families were used in analysis. Symphyta was shown to be paraphyletic; Apocrita was monophyletic with Orussoidea as its sister-group. Two major clades were recovered within Apocrita: Stephanoidea + Proctotrupomorpha, and Ichneumonoidea + (Evanioidea + Aculeata). Proctotrupomorpha (Proctotrupoidea + Chalcidoidea in this study), Ichneumonoidea (Ichneumonidae + Braconidae) and Aculeata ((Eumeninae + Vespinae) + Apoidea) in this study) were strongly supported in all analysis. Evaniomorpha proposed in  was not recovered: Evanoidea was recovered as sister-group to Aculeata, while Stephanoidea was sister to Proctotrupomorpha. Ichneumonoidea was the sister group of (Evanoidea + Aculeata). All nodes among Hymenoptera were perfectly supported in BI analyses except that of Stephanoidea + Proctotrupomorpha. In the topology based on amino acid sequences using BI, Stephanoidea was recovered as the sister-group of (Ichneumonoidea + (Evanoidea + Aculeata)), with a low support value of 0.54. In all analyses the ancestral position of Nasonia vitripennis among three Nasonia species is supported, which is congruent with the analyses based on nuclear gene sequence data and phylogeny of Wolbachia bacteria that they host [26, 70].
Phylogenetic relationships among Hymenoptera at the superfamily level remain controversial . Many well accepted phylogenetic relationships were recovered, such as the sister group relationship between Orussoidea and Apocrita, Apocrita, Proctotrupomorpha, Aculeata (or Vespomorpha) [69, 72–78]. Evaniomorpha was frequently recovered as polyphyletic [71, 75, 76, 79]. Castro and Dowton (2006) recovered a similar relationship among Ichneumonoidea, Evaniidae and Aculeata. The difference is that a group including Stephanidae was sister to Aculeata.
Within Diptera, well established relationships were recovered in nearly all of the analyses. Suborder relationships within Coleoptera were less stable. Adephaga and Myxophaga were recovered as sister group and then sister to Polyphaga. However, Archostemata was either recovered as sister-group to Polyphaga, or to Adephaga. Monophyly of the suborder Polyphaga is recovered in most analyses with internal relationships of Cyphon + (Elateroidea + (Chaetosoma + (Tribolium+ (Priasilpha + (Anoplophora + Crioceris))))). The intraordinal relationships of Lepidoptera are also unstable among datasets and methods. BI analyses supported early divergent of Rhopalocera (Lycaenidae + Pieridae in this study) most ML and MP analyses supported that of Tortricidae (Tortricoidea). Monophyly of Bombycoidea (Saturniidae + (Sphingidae + Bombycidae) in this study) was firmly supported in most analysis. The position of Lepidoptera and its internal relationships is likely negatively affected that the small sample of all taxa all of which were restricted to the clade Apoditrysia. We will not discuss the relationships among Coleoptera and Lepidoptera further since phylogenetic relationships are not robustly supported. However, our results might be of service to future researchers.
In this study, we reported seven complete or nearly complete mitochondrial genomes representing seven subfamilies of Braconidae. Four sequenced A+T-rich regions were shown to be inverted, as reported for species of Philopteridae (Phthiraptera) and Aleyrodidae (Hemiptera). Reversal of strand asymmetry was found in all seven sequenced mitochondrial genomes, which is correlated with the inversion of the A+T-rich region, indicating that inversion of A+T-rich region might be a ground-plan feature of braconid mitochondrial genomes. Mitochondrial gene rearrangement rates differed markedly among Braconidae, revealing that gene rearrangement might be more diverse than that previously reported [8, 21, 22, 29]. Among different rearrangement events, remote inversion was common in Braconidae.
Noncyclostome species have a higher evolutionary rate in mitochondrial genome sequences than those of cyclostome species. Those species with high gene rearrangement rates also have high nucleotide sequence evolutionary rates.
Phylogenetic analysis using complete mitochondrial genomes sequences recovered most of the well corroborated phylogenetic relationships among major lineages of Braconidae, depending on the method and data matrix used. Cyclostomes and noncyclostomes were recovered in all analysis, and Aphidiinae was firmly recovered as be a sister-group to the cyclostomes.
Within Hymenoptera, many well accepted relationships, such as the paraphyly of Symphyta and Evaniomorpha, the sister-group relationship between Orussoidea and Apocrita, and the taxa Proctotrupomorpha, Ichneumonoidea and Aculeata, were recovered with high support values. New views among major groups in Hymenoptera are suggested, such as the sister-group relationship between Evaniidae and Aculeata. Within Diptera, relationships were very stable across analysis, but not stable among suborders of Coleoptera and major lineages of Lepidoptera.
Relationships among holometabolous orders were improved with the increase of sampling based on complete mitochondrial genome sequences and the recently suggested basal position of Hymenoptera was supported in most analysis.
In conclusion, complete mitochondrial genome data have obvious potential to infer phylogenetic relationships at the subfamily, family, ordinal levels.
DNA extraction, PCR amplification and sequencing
For each species, one male adult or a leg was homogenized in liquid nitrogen and total genomic DNA was extracted using the DNeasy tissue kit (Qiagen, Hilden, Germany) following manufacturer protocols.
A range of universal insect mitochondrial primers and hymenopteran mitochondrial primers modified from universal insect mitochondrial primers were used [40, 57, 80, 81]. When necessary, species-specific primers were designed based on sequenced fragments and combined in various ways to bridge gaps. PCR and sequencing reactions were conducted following Wei at al. (2009).
Protein-coding and rRNA genes were initially identified using BLAST searches in GenBank and subsequently by alignment with genes of other insects. Protein-coding genes were translated using invertebrate mitochondrial genetic code. The tRNA searches were carried out with tRNAscan-SE search server . The parameters for the tRNA scan were set for Mito/Chloromast as the source, and the Invertebrate Mito genetic code was used. When long tracts of non-coding sequence were apparent and tRNA genes were not detected using default settings, the cove cutoff score was reduced and the search repeated. Finally, those tRNA genes that could not be identified by tRNAscan-SE were inspected by eye. rRNA structures were constructed by comparison with those in other insects and algorithm-based methods as in [24, 49]. All secondary structures were drawn in XRNA (developed by B. Weiser and available at http://rna.ucsc.edu/rnacenter/xrna/xrna.html).
The software packages DnaSP 4.0 (Rozas et al. 2003) was used to compute the number of synonymous substitutions per synonymous site (Ks) and the number of nonsynonymous substitutions per nonsynonymous site (Ka) for each braconid mitochondrial genomes, using that of D. semiclausum or Enicospilus sp. as reference sequences.
For construction of the phylogenetic relationships among Braconidae, seven species with mitochondrial genomes sequenced in this study were used, representing seven subfamilies of Braconidae. D. semiclausum and Enicospilus sp., both Ichneumonidae, the family commonly accepted as the sister-group of the Braconidae, were employed as outgroups.
For construction of phylogenetic relationships among holometabolous insects, 69 species with complete or nearly complete mitochondrial genome sequences were used (Additional file 2). Twenty species were chosen from Hymenoptera, representing 10 superfamilies and 11 families . Among Braconidae, S. agrili representing the cyclostomes and C. vestalis representing the noncyclostomes were used. Twelve species in nine families of the Lepidoptera, 14 species in 14 families of Coleoptera and 14 species in nine families of Diptera were included. Additionally, three species of Neuroptera, three species of Megaloptera and one species of Mecoptera were used to improve the sampling of orders among Holometabola. Hydaropsis longirostris and Triatoma dimidiata (Hemiptera) were used as outgroup taxa.
Amino acid sequences of protein-coding genes were aligned independently using ClustalX version 2.0.7  with default parameters. Alignment of protein-coding genes was inferred from amino acid alignment using RevTrans . Regions especially in the boundaries of genes that were aligned ambiguously were excluded in MacClade ver4.06 . All protein-coding genes were concatenated following their ancestral order in insect mitochondrial genomes. Data were partitioned based on first, second and third codon positions.
Four datasets were employed in the phylogenetic analyses: amino acid sequence (aa), nucleotide sequences of first and second codon positions (Pos12), all codon positions (Pos123), first and second codon positions, and RY-coded (purines coded by R and pyrimidines coded by Y) third codon position (Pos12RY3) of all protein-coding genes. Gene nad2 was excluded in construction of the phylogenetic relationships of braconid subfamilies, because this gene failed to amplify in four of the seven braconid species.
Phylogenetic analyses were performed using Maximum Parsimony (MP) with PAUP* 4.0b10 , Maximum Likelihood (ML) with PhyML [87, 88], and Bayesian Inference (BI) with MrBayes v3.1.2 . The MP analyses were run with default heuristic search options except that 100 replicates of random stepwise additions were used. Bootstrap proportions (BPs) were obtained after 1000 replicates by using 10 replicates of random stepwise additions of taxa. Models of DNA substitution were estimated in Modeltest 3.7 . For ML, we used a GTR+I+G model for nucleotide sequences and MtArt model for amino acid sequences with all parameters estimated. For BI, we used GTR+I+G model for four-state nucleotide sequences and a two-state substitution model with parameter I+G for RY-coded third codon position. All Bayesian analyses were conducted with four independent Markov chains run for 1,000,000 to 5,000,000 metropolis-coupled MCMC generations, with tree sampling every 100 to 500 generations and a burn-in of 2500 trees.
We thank Professor He Jun-Hua for his identification of the specimens used in this study. Dr. Zhu Chao-Dong from China Academy of Sciences, the Computational Biology Service Unit from Cornell University which is partially funded by Microsoft Corporation helped to carry some computation work. We also thank two anonymous reviewers for their valuable comments and suggestions. Funding for this study was provided jointly by the National Science Fund for Distinguished Young Scholars (30625006), the 973 Program (2006CB102005), the National Science Foundation of China (No. 30970384, 30700063, 30499341), and the National Special Basic Research Funds (2006FY110500-3, 2006FY120100) to XXC and the NSF (EF-0337220) to MJS.
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