Ecdysozoan mitogenomics: evidence for a common origin of the legged invertebrates, the Panarthropoda

Ecdysozoa is the recently recognized clade of molting animals that comprises the vast majority of extant animal species and the most important invertebrate model organisms—the fruit fly and the nematode worm. Evolutionary relationships within the ecdysozoans remain, however, unresolved, impairing the correct interpretation of comparative genomic studies. In particular, the affinities of the three Panarthropoda phyla (Arthropoda, Onychophora, and Tardigrada) and the position of Myriapoda within Arthropoda (Mandibulata vs. Myriochelata hypothesis) are among the most contentious issues in animal phylogenetics. To elucidate these relationships, we have determined and analyzed complete or nearly complete mitochondrial genome sequences of two Tardigrada, Hypsibius dujardini and Thulinia sp. (the first genomes to date for this phylum); one Priapulida, Halicryptus spinulosus; and two Onychophora, Peripatoides sp. and Epiperipatus biolleyi; and a partial mitochondrial genome sequence of the Onychophora Euperipatoides kanagrensis. Tardigrada mitochondrial genomes resemble those of the arthropods in term of the gene order and strand asymmetry, whereas Onychophora genomes are characterized by numerous gene order rearrangements and strand asymmetry variations. In addition, Onychophora genomes are extremely enriched in A and T nucleotides, whereas Priapulida and Tardigrada are more balanced. Phylogenetic analyses based on concatenated amino acid coding sequences support a monophyletic origin of the Ecdysozoa and the position of Priapulida as the sister group of a monophyletic Panarthropoda (Tardigrada plus Onychophora plus Arthropoda). The position of Tardigrada is more problematic, most likely because of long branch attraction (LBA). However, experiments designed to reduce LBA suggest that the most likely placement of Tardigrada is as a sister group of Onychophora. The same analyses also recover monophyly of traditionally recognized arthropod lineages such as Arachnida and of the highly debated clade Mandibulata

Shotgun Mitogenomics Provides a Reference Phylogenetic Framework and Timescale for Living Xenarthrans

Xenarthra (armadillos, sloths, and anteaters) constitutes one of the four major clades of placental mammals. Despite their phylogenetic distinctiveness in mammals, a reference phylogeny is still lacking for the 31 described species. Here we used Illumina shotgun sequencing to assemble 33 new complete mitochondrial genomes, establishing Xenarthra as the first major placental clade to be fully sequenced at the species level for mitogenomes. The resulting data set allowed the reconstruction of a robust phylogenetic framework and timescale that are consistent with previous studies conducted at the genus level using nuclear genes. Incorporating the full species diversity of extant xenarthrans points to a number of inconsistencies in xenarthran systematics and species definition. We propose to split armadillos in two distinct families Dasypodidae (dasypodines) and Chlamyphoridae (euphractines, chlamyphorines, and tolypeutines) to better reflect their ancient divergence, estimated around 42 million years ago. Species delimitation within long-nosed armadillos (genus Dasypus) appeared more complex than anticipated, with the discovery of a divergent lineage in French Guiana. Diversification analyses showed Xenarthra to be an ancient clade with a constant diversification rate through time with a species turnover driven by high but constant extinction. We also detected a significant negative correlation between speciation rate and past temperature fluctuations with an increase in speciation rate corresponding to the general cooling observed during the last 15 million years. Biogeographic reconstructions identified the tropical rainforest biome of Amazonia and the Guianan shield as the cradle of xenarthran evolutionary history with subsequent dispersions into more open and dry habitats.Fil: Gibb, Gillian C.. Universite de Montpellier; Francia. Massey Universit; Nueva ZelandaFil: Condamine, Fabien L.. University of Gothenburg; Suecia. Universite de Montpellier; Francia. University of Alberta; CanadáFil: Kuch, Melanie. McMaster University; CanadáFil: Enk, Jacob. McMaster University; CanadáFil: Moraes Barros, Nadia. Universidade Do Porto; Portugal. Universidade de Sao Paulo; BrasilFil: Superina, Mariella. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; ArgentinaFil: Poinar, Hendrik N.. McMaster University; CanadáFil: Delsuc, Frederic. Universite de Montpellier; Franci

Mitogenomics reveals high synteny and long evolutionary histories of sympatric cryptic nematode species

Species with seemingly identical morphology but with distinct genetic differences are abundant in the marine environment and frequently co-occur in the same habitat. Such cryptic species are typically delineated using a limited number of mitochondrial and/or nuclear marker genes, which do not yield information on gene order and gene content of the genomes under consideration. We used next-generation sequencing to study the composition of the mitochondrial genomes of four sympatrically distributed cryptic species of the Litoditis marina species complex (PmI, PmII, PmIII, and PmIV). The ecology, biology, and natural occurrence of these four species are well known, but the evolutionary processes behind this cryptic speciation remain largely unknown. The gene order of the mitochondrial genomes of the four species was conserved, but differences in genome length, gene length, and codon usage were observed. The atp8 gene was lacking in all four species. Phylogenetic analyses confirm that PmI and PmIV are sister species and that PmIII diverged earliest. The most recent common ancestor of the four cryptic species was estimated to have diverged 16 MYA. Synonymous mutations outnumbered nonsynonymous changes in all protein-encoding genes, with the Complex IV genes (coxI-III) experiencing the strongest purifying selection. Our mitogenomic results show that morphologically similar species can have long evolutionary histories and that PmIII has several differences in genetic makeup compared to the three other species, which may explain why it is better adapted to higher temperatures than the other species

High-throughput monitoring of wild bee diversity and abundance via mitogenomics

1. Bee populations and other pollinators face multiple, synergistically acting threats, which have led to population declines, loss of local species richness and pollination services, and extinctions. However, our understanding of the degree, distribution and causes of declines is patchy, in part due to inadequate monitoring systems, with the challenge of taxonomic identification posing a major logistical barrier. Pollinator conservation would benefit from a high-throughput identification pipeline. 2. We show that the metagenomic mining and resequencing of mitochondrial genomes (mitogenomics) can be applied successfully to bulk samples of wild bees. We assembled the mitogenomes of 48 UK bee species and then shotgun-sequenced total DNA extracted from 204 whole bees that had been collected in 10 pan-trap samples from farms in England and been identified morphologically to 33 species. Each sample data set was mapped against the 48 reference mitogenomes. 3. The morphological and mitogenomic data sets were highly congruent. Out of 63 total species detections in the morphological data set, the mitogenomic data set made 59 correct detections (93�7% detection rate) and detected six more species (putative false positives). Direct inspection and an analysis with species-specific primers suggested that these putative false positives were most likely due to incorrect morphological IDs. Read frequency significantly predicted species biomass frequency (R2 = 24�9%). Species lists, biomass frequencies, extrapolated species richness and community structure were recovered with less error than in a metabarcoding pipeline. 4. Mitogenomics automates the onerous task of taxonomic identification, even for cryptic species, allowing the tracking of changes in species richness and istributions. A mitogenomic pipeline should thus be able to contain costs, maintain consistently high-quality data over long time series, incorporate retrospective taxonomic revisions and provide an auditable evidence trail. Mitogenomic data sets also provide estimates of species counts within samples and thus have potential for tracking population trajectories

Bulk de novo mitogenome assembly from pooled total DNA elucidates the phylogeny of weevils (Coleoptera: Curculionoidea)

Complete mitochondrial genomes have been shown to be reliable markers for phylogeny reconstruction among diverse animal groups. However, the relative difficulty and high cost associated with obtaining de novo full mitogenomes have frequently led to conspicuously low taxon sampling in ensuing studies. Here, we report the successful use of an economical and accessible method for assembling complete or near-complete mitogenomes through shot-gun next-generation sequencing of a single library made from pooled total DNA extracts of numerous target species. To avoid the use of separate indexed libraries for each specimen, and an associated increase in cost, we incorporate standard polymerase chain reaction-based “bait” sequences to identify the assembled mitogenomes. The method was applied to study the higher level phylogenetic relationships in the weevils (Coleoptera: Curculionoidea), producing 92 newly assembled mitogenomes obtained in a single Illumina MiSeq run. The analysis supported a separate origin of wood-boring behavior by the subfamilies Scolytinae, Platypodinae, and Cossoninae. This finding contradicts morphological hypotheses proposing a close relationship between the first two of these but is congruent with previous molecular studies, reinforcing the utility of mitogenomes in phylogeny reconstruction. Our methodology provides a technically simple procedure for generating densely sampled trees from whole mitogenomes and is widely applicable to groups of animals for which bait sequences are the only required prior genome knowledge

Mitochondrial genomes and the complex evolutionary history of the cercopithecine tribe Papionini

Die vorliegende Arbeit soll dazu beitragen, Unstimmigkeiten in den Verwandtschaftsverhältnissen innerhalb der Papionini, einem Stamm innerhalb der Altweltaffen (Cercopithecidae), zu klären. Die Papionini, die zusammen mit den Cercopithecini die Unterfamilie der Cercopithecinae bilden, beinhalten sieben Gattungen (Macaca, Cercocebus, Mandrillus, Lophocebus, Papio, Theropithecus, Rungwecebus) und 45 Arten. Sechs der sieben Gattungen kommen heute hauptsächlich in Afrika vor. Eine Ausnahme ist die Gattung Papio, die mit einer Art (P. hamadryas) auch in Südwest-Arabien vorkommt. Im Gegensatz zu den sechs hauptsächlich afrikanischen Gattungen hat die siebte Gattung (Macaca) nur ein kleines Verbreitungsgebiet im Norden Afrikas und kommt sonst hauptsächlich in Asien vor. Fossilfunde belegen allerdings, dass während des Plio- und Pleistozäns die Gattungen Macaca und Theropithecus auch in Europa vorkamen. Von der Gattung Theropithecus, die heute ausschließlich in Afrika beheimatet ist, wurden zudem auch Fossilien aus dem Pliozän im Norden Indiens gefunden. Die Verwandtschaftsbeziehungen innerhalb der Papionini wurden bisher mit Hilfe morphologischer und genetischer Merkmale untersucht, allerdings waren die Ergebnisse nicht immer übereinstimmend und es gibt immer noch viele Unklarheiten. Zum einen ist nicht eindeutig geklärt, wie die Gattungen Papio, Lophocebus und Theropithecus zu einander in Beziehung stehen. Zum anderen ist auch unklar, wie die einzelnen Pavianarten innerhalb der Gattung Papio mit einander verwandt sind. Außerdem sind auch die Verwandtschaftsverhältnisse zwischen und innerhalb der Artgruppen der Makaken nicht eindeutig geklärt. Um mehr Klarheit in die Evolution der Papionini zu bringen, habe ich im Rahmen dieser Arbeit drei Studien durchgeführt (Kapitel 2-4). Ziel dabei war es, Verwandtschaftsbeziehungen auf unterschiedlichen taxonomischen Ebenen (zwischen und innerhalb von Gattungen, sowie innerhalb einer Art) zu untersuchen. Dazu wurden komplette mitochondriale Genome von Vertretern der Papionini sequenziert und damit Phylogenien und Aufspaltungszeiten berechnet. Die Ergebnisse meiner Arbeit zeigen unter anderem drei Hauptkladen innerhalb der Papionini (Kapitel 2): 1) Papio, Theropithecus, Lophocebus; 2) Mandrillus, Cercocebus; 3) Macaca, wobei Macaca in der mitochondrialen Phylogenie näher mit Mandrillus und Cercocebus verwandt zu seien scheint und nicht wie erwartet, als Schwestergruppe der afrikanischen Papionini abgebildet wird; ein Ergebnis, das im Widerspruch zu nukleären und morphologischen Studien steht. Meine Arbeit zeigt auch, dass komplette mitochondriale Genome in manchen Fällen nicht ausreichen, um phylogenetische Beziehungen vollständig zu rekonstruieren. So bleibt weiterhin unklar wie die Gattungen Papio, Theropithecus und Lophocebus zueinander stehen (Kapitel 2). Außerdem zeigen die Ergebnisse Paraphylien für Mandrillus und Cercocebus (Kapitel 2), sowie innerhalb der Paviane (Kapitel 3). Die Paviane werden dabei gemäß ihrer geographischen Verbreitung und nicht nach ihrer taxonomischen Zugehörigkeit abgebildet, wodurch die meisten Pavian-Arten paraphyletisch sind. Der Grund für diese Baumtopologie ist sehr wahrscheinlich sekundärer Genfluss zwischen parapatrisch vorkommenden Pavian-Arten. In der dritten Studie (Kapitel 4), in der innerartliche Verwandtschaftsverhältnisse innerhalb einer südostasiatischen Makaken-Artgruppe (Macaca fascicularis) untersucht wurden, zeigt sich eine klare Unterteilung in eine kontinentale und eine insulare Klade. Sowohl die kontinentale, als auch die insulare Linie sind auf Sumatra zu finden, was für einen sekundären genetischen Austausch zwischen beiden Populationen spricht. Generell kann man sagen, dass komplette mitochondriale Genome robuste Phylogenien mit hoher statistischer Unterstützung ergeben, die eine gute Grundlage für künftige vergleichende Studien bilden. Die berechneten Aufspaltungszeiten stimmen weitestgehend mit vorherigen Studien überein, wobei sich die ermittelten Konfidenzintervalle verkleinert haben. Allerdings zeigt die Arbeit auch, dass Phylogenien basierend auf mitochondrialen Genomen keine hohe Auflösung erzielen wenn sich Taxa innerhalb kurzer Zeit voneinander trennten. Die hier gezeigten Paraphylien und die abweichenden Ergebnisse zu nukleären Studien wurden höchstwahrscheinlich durch sekundären genetischen Austausch hervorgerufen. Um Verwandtschaftsverhältnisse möglichst exakt rekonstruieren zu können, müssen neben der maternal-vererbten, mitochondrialen Linie noch paternal- und biparentalvererbte Merkmale in Betracht gezogen werden. Zu beachten ist in diesem Zusammenhang, dass ein bestimmter molekularer Marker immer nur eine mögliche Phylogenie von vielen wiedergibt

Exploring mitogenome evolution in Branchiopoda (Crustacea) lineages reveals gene order rearrangements in Cladocera

The class Branchiopoda, whose origin dates back to Cambrian, includes ~ 1200 species which mainly occupy freshwater habitats. The phylogeny and systematics of the class have been debated for long time, until recent phylogenomic analyses allowed to better clarify the relationships among major clades. Based on these data, the clade Anostraca (fairy and brine shrimps) is sister to all other branchiopods, and the Notostraca (tadpole shrimps) results as sister group to Diplostraca, which includes Laevicaudata + Spinicaudata (clam shrimps) and Cladoceromorpha (water fleas + Cyclestherida). In the present analysis, thanks to an increased taxon sampling, a complex picture emerges. Most of the analyzed mitogenomes show the Pancrustacea gene order while in several other taxa they are found rearranged. These rearrangements, though, occur unevenly among taxa, most of them being found in Cladocera, and their taxonomic distribution does not agree with the phylogeny. Our data also seems to suggest the possibility of potentially homoplastic, alternative gene order within Daphniidae

Mitogenomics of southern hemisphere blue mussels (Bivalvia: Pteriomorphia): Insights into the evolutionary characteristics of the Mytilus edulis complex

Marine blue mussels (Mytilus spp.) are widespread species that exhibit an antitropical distribution with five species occurring in the Northern Hemisphere (M. trossulus, M. edulis, M. galloprovincialis, M. californianus and M. coruscus) and three in the Southern Hemisphere (M. galloprovincialis, M. chilensis and M. platensis). Species limits in this group remain controversial, in particular for those forms that live in South America. Here we investigated structural characteristics of marine mussels mitogenomes, based on published F mtDNA sequences of Northern Hemisphere species and two newly sequenced South American genomes, one from the Atlantic M. platensis and another fr om the Pacific M. chilensis. These mitogenomes exhibited similar architecture to those of other genomes of Mytilus, including the presence of the Atp8 gene, which is missing in most of the other bivalves. Our evolutionary analysis of mitochondrial genes indicates that purifying selection is the predominant force shaping the evolution of the coding genes. Results of our phylogenetic analyses supported the monophyly of Pteriomorphia and fully resolved the phylogenetic relationships among its five orders. Finally, the low genetic divergence of specimens assigned to M. chilensis and M. platensis suggests that these South American marine mussels represent conspecific variants rather than distinct species.Link_to_subscribed_fulltex