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Rimskaya-Korsakova, N.

Publications and source records attributed to Rimskaya-Korsakova, N..

4 recordsLinked to original sources

Photosymbiotic algae acquisition and their interactions with the acoel Convolutriloba macropyga

Symbiosis with photosynthetic microbes is widespread in marine animals, with various symbiont transmission modes and localisation within the host. Here, we characterise the association between the acoel Convolutriloba macropyga and its photosymbionts, identified as Tetraselmis green algae based on rbcL gene phylogenetic analysis. Symbionts are transmitted vertically to asexual offspring and acquired horizontally by juveniles after sexual reproduction. Embryos develop to aposymbiotic juveniles that ingest Tetraselmis through the mouth. Confocal microscopy shows an increase in algae number within juveniles and in their presence at the body wall. Transmission electron microscopy reveals that symbionts lose flagella and theca. In adults, symbionts are extracellular at the body periphery, but can be intracellular within the parenchyma, in contrast with previously described acoel photosymbionts. This likely reflects different host-symbiont interactions, with algae potentially performing photosynthesis and nutrient exchange at the periphery, while undergoing transport or digestion in the parenchyma. Comparative transcriptomics between symbiotic adults and aposymbiotic juveniles shows an enrichment of amino acid synthesis, lipid metabolism, and osmotic and oxidative stress responses in symbiotic adults. Our data shows that algal symbionts engage with host tissues in distinct ways, inside or outside host cells, highlighting a previously unappreciated spatial complexity in host-algae interactions. HighlightsO_LITetraselmis algae are taken up by Convolutriloba macropyga juveniles C_LIO_LIAlgal symbionts in juveniles lose theca and flagella, proliferate, and move to the body wall C_LIO_LISymbionts are extracellular at the body wall and can be intracellular in the parenchyma C_LIO_LIAmino acid synthesis, lipid metabolism, osmoregulation and stress responses are activated in symbiotic adults C_LI

zoology↗

The ancient metazoan cytoplasmic intermediate filament protein, Cilin, shapes cilia arrangement and tissue architecture

The emergence of animal multicellularity demanded novel cytoskeletal systems to support cellular architecture and tissue integrity. Cytoplasmic intermediate filaments (cIFs) are essential components of this scaffold, yet their evolutionary origins remain obscure. Here, we identify and characterize a lamin-derived, bona fide cIF protein in a ctenophore--a sister lineage to all other extant animals. We name this protein Cilin. Unlike nuclear lamins, Cilin lacks a nuclear localization signal and instead localizes predominantly to motile ciliary structures, including comb plates, the aboral organ, and sperm flagella, indicating a central role in ciliary architecture and function. Remarkably, Cilin is also present in non-ciliated cells, suggesting early functional diversification of cIFs in animal evolution. Phylogenetic and structural analyses position Cilin within an ancestral class of intermediate filament proteins, homologous to cnidarian and bilaterian nematocilins and lamin-tail-domain-containing (LMNTD) proteins. In humans, LMNTD proteins are enriched in ciliated epithelia and spermatids, pointing to a deeply conserved role in cilia-associated functions. These findings establish cilins as the earliest lamin-derived cytoplasmic intermediate filament proteins in metazoans, likely contributing to both ciliary function and the emergence of multicellular tissue organization.

cell biology↗

Loss of immune signalling pathways and increased pathogen susceptibility associated to photosymbiosis in acoels

BackgroundHost immunity plays an important role in coral symbiosis with dinoflagellates. Photosymbiosis (the association between animal hosts and photosynthetic endosymbionts) has evolved multiple times within animals, e.g. within acoels, which are soft-bodied marine invertebrates whose immunity remains so far undescribed. ResultsOur predicted proteome searches show that acoels lack immune signal transduction genes commonly conserved in animals. Their loss in acoels predates the occurrence of photosymbiosis in this clade. Immune challenges with the coral pathogen and bleaching agent, Vibrio coralliilyticus, increase acoel mortality and decrease symbiont numbers in adults of the photosymbiotic acoel Convolutriloba macropyga. Mortality in aposymbiotic C. macropyga juveniles or aposymbiotic species Hofstenia miamia is not affected. Ultrastructural studies of immune challenged animals by Transmission Electron Microscopy show damages at the cellular and organelle level, as well as a degradation of potential pathogens by the host. In situ hybridisation and differential gene expression analysis point to some areas of interaction between Pattern Recognition Receptors and microbes, as well as to the involvement of acoel-specific or uncharacterised genes. ConclusionsBased on our findings, photosymbiosis evolution in acoels could have been favoured by the loss of immune signalling pathways. Photosymbiosis in acoels seems to increase susceptibility to pathogen exposure and is disrupted by pathogens. Our data also suggests the possibility of a novel molecular immune response specific to acoels.

evolutionary biology↗

The hologenome of Osedax frankpressi reveals the genetic interplay for the symbiotic digestion of vertebrate bone

The marine annelid Osedax has evolved a unique heterotrophic symbiosis that allows it to feed exclusively on sunken bones. Yet, the genetic and physiological principles sustaining this symbiosis are poorly understood. Here we show that Osedax frankpressi has a small, AT-rich genome shaped by extensive gene loss. While the Oceanospirillales endosymbiont of Osedax is enriched in genes for carbohydrate and nitrogen metabolism, O. frankpressi has undergone genetic changes to accommodate bone digestion, including the expansion of matrix metalloproteases, and a loss of pathways to synthesize amino acids that are abundant in collagen. Unlike other symbioses, however, innate immunity genes required to acquire and control the endosymbionts are reduced in O. frankpressi. These findings reveal Osedax has evolved an alternative genomic toolkit to bacterial symbiosis where host-symbiont co-dependence has favoured genome simplicity in the host to exploit the nutritionally unbalanced diet of bones. TeaserGenome reduction and adaptations for collagen digestion underpin the symbiosis of Osedax worms to exploit decaying bones.

genomics↗