Significance: Myxozoans are a diverse group of microscopic parasites that infect invertebrate and vertebrate hosts. The assertion that myxozoans are highly reduced cnidarians is supported by the presence of polar capsules, which resemble cnidarian stinging structures called “nematocysts.” Our study characterizes the genomes and transcriptomes of two distantly related myxozoan species, Kudoa iwatai and Myxobolus cerebralis , and another cnidarian parasite, Polypodium hydriforme . Phylogenomic analyses that use a broad sampling of myxozoan taxa confirm the position of myxozoans within Cnidaria with P. hydriforme as the sister taxon to Myxozoa. Analyses of myxozoan genomes indicate that the transition to the highly reduced body plan was accompanied by massive reduction in genome size, including depletion of genes considered hallmarks of animal multicellularity.

Hydroidolina is a group of hydrozoans that includes Anthoathecata, Leptothecata and Siphonophorae. Previous phylogenetic analyses show strong support for Hydroidolina monophyly, but the relationships between and within its subgroups remain uncertain. In an effort to further clarify hydroidolinan relationships, we performed phylogenetic analyses on 97 hydroidolinan taxa, using DNA sequences from partial mitochondrial 16S rDNA, nearly complete nuclear 18S rDNA and nearly complete nuclear 28S rDNA. Our findings are consistent with previous analyses that support monophyly of Siphonophorae and Leptothecata and do not support monophyly of Anthoathecata nor its component subgroups, Filifera and Capitata. Instead, within Anthoathecata, we find support for four separate filiferan clades and two separate capitate clades (Aplanulata and Capitatasensu stricto). Our data however, lack any substantive support for discerning relationships between these eight distinct hydroidolinan clades.

The diversity of hydrozoan life cycles, as manifested in the wide range of polyp, colony, and medusa morphologies, has been appreciated for centuries. Unraveling the complex history of characters involved in this diversity is critical for understanding the processes driving hydrozoan evolution. In this study, we use a phylogenetic approach to investigate the evolution of morphological characters in Hydrozoa. A molecular phylogeny is reconstructed using ribosomal DNA sequence data. Several characters involving polyp, colony, and medusa morphology are coded in the terminal taxa. These characters are mapped onto the phylogeny and then the ancestral character states are reconstructed. This study confirms the complex evolutionary history of hydrozoan morphological characters. Many of the characters involving polyp, colony, and medusa morphology appear as synapomorphies for major hydrozoan clades, yet homoplasy is commonplace.

Although aerobic respiration is a hallmark of eukaryotes, a few unicellular lineages, growing in hypoxic environments, have secondarily lost this ability. In the absence of oxygen, the mitochondria of these organisms have lost all or parts of their genomes and evolved into mitochondria-related organelles (MROs). There has been debate regarding the presence of MROs in animals. Using deep sequencing approaches, we discovered that a member of the Cnidaria, the myxozoan Henneguya salminicola, has no mitochondrial genome, and thus has lost the ability to perform aerobic cellular respiration. This indicates that these core eukaryotic features are not ubiquitous among animals. Our analyses suggest that H. salminicola lost not only its mitochondrial genome but also nearly all nuclear genes involved in transcription and replication of the mitochondrial genome. In contrast, we identified many genes that encode proteins involved in other mitochondrial pathways and determined that genes involved in aerobic respiration or mitochondrial DNA replication were either absent or present only as pseudogenes. As a control, we used the same sequencing and annotation methods to show that a closely related myxozoan, Myxobolus squamalis , has a mitochondrial genome. The molecular results are supported by fluorescence micrographs, which show the presence of mitochondrial DNA in M. squamalis , but not in H. salminicola. Our discovery confirms that adaptation to an anaerobic environment is not unique to single-celled eukaryotes, but has also evolved in a multicellular, parasitic animal. Hence, H. salminicola provides an opportunity for understanding the evolutionary transition from an aerobic to an exclusive anaerobic metabolism.

Understanding the nature and timing of metazoan origins is one of the most important, yet elusive, questions in evolutionary biology. Fossil data provide the most tangible evidence for the origin of early animal lineages, although additional evidence from molecular phylogenetics, molecular clock studies, and development has contributed to our current understanding. We review several lines of evidence to explore the nature and timing of early metazoan evolution and discuss how these data, when considered together, provide a more cohesive picture of the origin of animal diversity. We discuss how trace fossils and biomarkers provide compelling evidence for the origins of Bilateria and siliceous sponges. Using a molecular phylogenetic framework for metazoans, we discuss how fossils can be used to date the origin of clades. We use these fossil dates to perform a relaxed molecular clock analysis for estimating dates of nodes when no fossils are available. We also discuss current data from developmental biology that suggest that early metazoans possessed a sophisticated molecular toolkit for building complex body plans. We conclude that the best evidence for the origin of major metazoan lineages lies in the careful interpretation of the fossil record and that these data, when considered with phylogenetic and developmental evidence, support the notion that the Cambrian radiation is a real phenomenon that marks a critically important time in the history of life.