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Tiny animals in various metazoan phyla inhabit the interstices between sand and/or gravel grains, and adaptive traits in their body plan, such as simplification and size reduction, have attracted research attention. Several possible explanations of how such animals colonized interstitial habitats have been proposed, but their adaptation to this environment has generally been regarded as irreversible. However, the actual evolutionary transitions are not well understood in almost all taxa. In the present study, we show reversible evolutionary shifts from interstitial to epibenthic habitats in the lineage of the polyclad flatworm genus Boninia. In addition, we establish two new species of this genus found from different microhabitats on a single beach in Okinawa Island, Japan: (i) the interstitial species Boninia uru sp. nov. from gravelly sediments and (ii) the epibenthic species Boninia yambarensis sp. nov. from rock undersurfaces. Our observations suggest that rigid microhabitat segregation exists between these two species. Molecular phylogenetic analyses based on the partial 18S and 28S rDNA sequences of the new Boninia species and four other congeners, for which molecular sequences were available in public databases [Boninia antillara (epibenthic), Boninia divae (epibenthic), Boninia neotethydis (interstitial), and an unidentified Boninia sp. (habitat indeterminate)], revealed that the two interstitial species (B. neotethydis and B. uru sp. nov.) were not monophyletic among the three epibenthic species. According to ancestral state reconstruction analysis, the last common ancestor of the analyzed Boninia species inhabited interstitial realms, and a shift to the epibenthic environment occurred at least once. Such an \"interstitial to noninterstitial\" evolutionary route seems to be rare among Animalia; to date, it has been reported only in acochlidian slugs in the clade Hedylopsacea. Our phylogenetic tree also showed that the sympatric B. uru sp. nov. and B. yambarensis sp. nov. were not in a sister relationship, indicating that they colonized the same beach independently rather than descended in situ from a common ancestor that migrated and settled at the beach.

Bithyniids are freshwater snails that play a crucial role in the transmission of various parasitic trematodes of medical and veterinary importance. In this study, we explored the prevalence of cercarial trematode infections in bithyniid snails from Thailand and examined the species diversity of both the intermediate snail hosts and parasite larvae. A total of 688 bithyniid snails were collected from diverse natural habitats at 24 locations in 16 provinces across 5 regions of Thailand. The presence of larval trematode infections was examined using the cercarial shedding method. Both the collected snails and the emerging cercariae were identified at the species level using a combination of morphological and molecular techniques. The mitochondrial COI and 16S rDNA sequences of bithyniid snails, along with the ITS2 sequences of cercariae, were obtained via PCR amplification and sequencing. Three species of bithyniid snails were identified in this study: Bithynia funiculata, Bithynia siamensis siamensis, and Hydrobioides nassa. Among these species, B. s. siamensis exhibited the highest population density, followed by B. funiculata and H. nassa. The overall rate of cercarial infection in the bithyniid snails was relatively low, at 1.45%. H. nassa snails had the highest infection prevalence, at 11.11%, while B. s. siamensis had a prevalence of 1.39%. Only the morphological type of the xiphidiocercariae was detected. BLASTn searches in GenBank and phylogenetic trees based on xiphidiocercariae were used to classify the samples into four different families spanning two superfamilies of digenean trematodes. The genera Plagiorchis, Prosthogonimus, Paralecithodendrium, and cercaria of Renicolidae are reported for the first time in B. s. siamensis. Plagiorchis and Paralecithodendrium are significant genera of zoonotic trematodes. These findings indicate that B. s. siamensis and H. nassa can act as the first intermediate hosts for various parasitic trematodes in Thailand.

Host-parasite associations have historically been considered compelling examples of coevolution and useful in examining cospeciation. However, modern molecular methods have revealed more complex dynamics than previously assumed, with host-switching events appearing commonly across taxa and challenging traditional views of strict coevolution in host-parasite relationships. Monogenean parasites are considered highly host-specific and have long served as models for probing evolution of host-parasite associations, particularly in differentiating geographic and phylogenetic patterns of parasite diversification. We investigated the phylogeographic patterns of monogenean ectoparasites associated with four species of characin fishes across Panama, Nicaragua, and Mexico. We hypothesize that parasite diversity and community structure are more strongly correlated with host species (suggesting cospeciation) than with geographic location (indicative of allopatric speciation). We found high genetic differentiation among parasites and their hosts across different locations. However, while geography explained the genetic structure of both host fishes and parasites, the observed patterns were neither congruent nor parallel. Parasite community structure and genetic similarity were consistently better explained by geographic location than by host species identity, although both factors played a significant role. Contrary to our predictions, we found no evidence of cospeciation. Instead, the diversification of these monogenean parasites appears to be primarily driven by their ability to switch hosts. At this taxonomical scale, host-switching is mediated by the geographical proximity of potential hosts, underscoring the importance of spatial factors in parasite evolution.

Nearly seven decades have passed since the first records of helminths in rodents in Slovakia were published. Thereafter, the number of documented helminth species within the territory of the country has steadily increased. This checklist compiles data from 34 sources, including 27 academic articles, five unpublished reports, and two conference proceedings produced between 1955 and early 2025. Following a critical review of each source, 73 nominal helminth species from 27 species of rodents, comprising 30 nematodes, 29 cestodes, 13 trematodes, and one acanthocephalan, were included in this checklist. Information on helminth diversity is absent for only two of the 29 rodent species registered in the Slovak Republic: Myocastor coypus and Arvicola scherman . Furthermore, our findings suggest that certain rodent species remain under-researched despite the presence of some information on their helminth fauna. This checklist lays the basis for future helminthological research on rodents in Slovakia. The raw dataset generated for this article is available in the Suppl. material 1.

Flatworms number among the most diverse invertebrate phyla and represent the most biomedically significant branch of the major bilaterian clade Spiralia, but to date, deep evolutionary relationships within this group have been studied using only a single locus (the rRNA operon), leaving the origins of many key clades unclear. In this study, using a survey of genomes and transcriptomes representing all free-living flatworm orders, we provide resolution of platyhelminth interrelationships based on hundreds of nuclear protein-coding genes, exploring phylogenetic signal through concatenation as well as recently developed consensus approaches. These analyses robustly support a modern hypothesis of flatworm phylogeny, one which emphasizes the primacy of the often-overlooked ‘microturbellarian’ groups in understanding the major evolutionary transitions within Platyhelminthes: perhaps most notably, we propose a novel scenario for the interrelationships between free-living and vertebrate-parasitic flatworms, providing new opportunities to shed light on the origins and biological consequences of parasitism in these iconic invertebrates.

Several studies have demonstrated parasitism by monogenoids in characiform fish in the Neotropics. During studies on the helminth fauna of curimatids from the Tocantins River, specimens of Eigenmann & Eigenmann, 1889 were examined and species of Hanek, Molnar & Fernando, 1974 were found. Species of the genus are characterized mainly by the complex shape of haptoral anchors with a modified dorsal anchor, composed by two subunits, dorsal-median and dorsal. To date, two species of are known to parasitize curimatid fishes: the type species Hanek, Molnar & Fernando, 1974 and (Suriano, 1980). During examination of specimens of collected in the Tocantins River, Embiral, Imperatriz, Maranhão State, Brazil, two new species of were found and are described herein. and are characterized by possessing the male copulatory organ formed by a long cirrus and a claw-shaped accessory piece, connected to the base of the male copulatory organ by a ligament. The new species differs from the two known congeneric species mainly by the morphology of the dorsal-median and dorsal subunits of the dorsal anchor. also differs from other species of the genus by the absence of the ventral bar and by the size and shape of the ventral bar. An amendment to the diagnosis of is provided to accommodate the new species. The present study increases the number of species to four and extends the occurrence of the genus to the Tocantins-Araguaia Basin.

Robust phylogenetic analysis based on transcriptomes of Xenoturbella and acoelomorph worms shows that Xenacoelomorpha is an early bilaterian lineage forming the sister group to Nephrozoa. Solving the Xenoturbella puzzle Lacking a centralized nervous system, coelom, anus and reproductive organs, the deep-sea flatworm Xenoturbella presents problems when it comes to its classification and teasing out its evolutionary history. Despite its simplicity, some of Xenoturbella 's features appear to align it among the deuterostomes, the group of animals that includes ourselves. If true, this implies either a radical simplification of the body plan or the acquisition of many key deuterostome features independently by the various deuterostome groups. Two papers in this issue tackle different aspects of Xenoturbella , but together, move the field on a notch. Greg Rouse et al . add four new deep-sea species of Xenoturbella from the eastern Pacific Ocean to the two already known from the Atlantic. Phylogenomic analysis aligns them at the base of the Protostomia or even as basal bilaterians — much as would be expected from their simple morphology and not invoking radical simplification. Andreas Hejnol and colleagues come to a broadly similar conclusion based on robust phylogenetic analysis using eleven transcriptomes of Xeonturbella and acoel worms. The position of Xenacoelomorpha in the tree of life remains a major unresolved question in the study of deep animal relationships 1 . Xenacoelomorpha, comprising Acoela, Nemertodermatida, and Xenoturbella , are bilaterally symmetrical marine worms that lack several features common to most other bilaterians, for example an anus, nephridia, and a circulatory system. Two conflicting hypotheses are under debate: Xenacoelomorpha is the sister group to all remaining Bilateria (= Nephrozoa, namely protostomes and deuterostomes) 2 , 3 or is a clade inside Deuterostomia 4 . Thus, determining the phylogenetic position of this clade is pivotal for understanding the early evolution of bilaterian features, or as a case of drastic secondary loss of complexity. Here we show robust phylogenomic support for Xenacoelomorpha as the sister taxon of Nephrozoa. Our phylogenetic analyses, based on 11 novel xenacoelomorph transcriptomes and using different models of evolution under maximum likelihood and Bayesian inference analyses, strongly corroborate this result. Rigorous testing of 25 experimental data sets designed to exclude data partitions and taxa potentially prone to reconstruction biases indicates that long-branch attraction, saturation, and missing data do not influence these results. The sister group relationship between Nephrozoa and Xenacoelomorpha supported by our phylogenomic analyses implies that the last common ancestor of bilaterians was probably a benthic, ciliated acoelomate worm with a single opening into an epithelial gut, and that excretory organs, coelomic cavities, and nerve cords evolved after xenacoelomorphs separated from the stem lineage of Nephrozoa.

The planarian Schmidtea mediterranea is an important model for stem cell research and regeneration, but adequate genome resources for this species have been lacking. Here we report a highly contiguous genome assembly of S. mediterranea , using long-read sequencing and a de novo assembler (MARVEL) enhanced for low-complexity reads. The S. mediterranea genome is highly polymorphic and repetitive, and harbours a novel class of giant retroelements. Furthermore, the genome assembly lacks a number of highly conserved genes, including critical components of the mitotic spindle assembly checkpoint, but planarians maintain checkpoint function. Our genome assembly provides a key model system resource that will be useful for studying regeneration and the evolutionary plasticity of core cell biological mechanisms. An improved genome assembly for Schmidtea mediterranea shows that the genome is highly polymorphic and repetitive, and lacks multiple genes encoding core components of cell biological mechanisms. Genome of a regenerating worm The flatworm Schmidtea mediterranea is an important model for regeneration. Jochen Rink, Eugene Myers and colleagues report an improved genome assembly for the planarian S. mediterranea using long-read sequencing and a new genome assembler called MARVEL. They find that the S. mediterranea genome is highly polymorphic and repetitive, and includes a novel class of giant retroelements. This improved genome assembly provides a useful resource for studying regeneration and the evolution of cell plasticity.

Flatworms can very rapidly attach to and detach from many substrates. In the presented work, we analysed the adhesive system of the marine proseriate flatworm Minona ileanae . We used light-, scanning- and transmission electron microscopy to analyse the morphology of the adhesive organs, which are located at the ventral side of the tail-plate. We performed transcriptome sequencing and differential RNA-seq for the identification of tail-specific transcripts. Using in situ hybridization expression screening, we identified nine transcripts that were expressed in the cells of the adhesive organs. Knock-down of five of these transcripts by RNA interference led to a reduction of the animal's attachment capacity. Adhesive proteins in footprints were confirmed using mass spectrometry and antibody staining. Additionally, lectin labelling of footprints revealed the presence of several sugar moieties. Furthermore, we determined a genome size of about 560 Mb for M. ileanae . We demonstrated the potential of Oxford Nanopore sequencing of genomic DNA as a cost-effective tool for identifying the number of repeats within an adhesive protein and for combining transcripts that were fragments of larger genes. A better understanding of the molecules involved in flatworm bioadhesion can pave the way towards developing innovative glues with reversible adhesive properties. This article is part of the theme issue ‘Transdisciplinary approaches to the study of adhesion and adhesives in biological systems’.