Biology subjects

Rusanova, A.

Publications and source records attributed to Rusanova, A..

6 recordsLinked to original sources

bioRxiv2026

Water-mass origin and transformation shapes seawater microbiomes in the northeastern Barents Sea and the St. Anna Trough

The St. Anna Trough region is a key Eurasian Arctic gateway connecting the northeastern Barents Sea, northern Kara Sea, and central Arctic Ocean. The region is characterized by complex hydrodynamics, with multiple water masses of local and Atlantic origin interacting and undergoing transformation. In this study, we investigated whether seawater microbiome composition correlates with water-mass origin and can be used to help delineate water masses. We collected 115 seawater samples representing major regional water masses - Arctic surface water, meltwater, cold dense water, Barents Sea branch water, the recently discovered Keldysh Current water, and mixed waters - and analyzed them using 16S rRNA gene amplicon sequencing. We found that microbiome composition closely followed water mass structure, which, together with thermohaline properties and depth, explained the majority (61.2%) of microbiome composition variation. Distinct microbial patterns were associated with Atlantic and Arctic water masses, except for the Arctic surface water, which lacked a distinct microbiome and resembled those of meltwater or the Keldysh Current microbiomes. Differential abundance and network analyses revealed characteristic bacterial markers: SAR11 (Clades Ia and IV), Roseibacillus, SV1-3 (Microbacteriaceae), SAR86 clade, and AEGEAN-169 marine group in the Keldysh Current; Halieaceae, Planktomarina, NS5 marine group, and Sulfitobacter in meltwater; SUP05 cluster, SAR86, SAR92, and SAR324 clade in cold dense water; Nitrincolaceae and Amylibacter in Barents Sea branch water; Flavobacteriaceae and Chitinophagales in mixed waters. These differences were driven primarily by shifts in relative abundance of widespread Arctic bacterial taxa rather than by differential prevalence of bacterial groups. Our results demonstrate that seawater microbiomes can serve as sensitive biological tracers of water mass origin and transformation in the Eurasian Arctic. Furthermore, the distinct Keldysh Current microbiome supports its recognition as a novel hydrographic feature and indicates its role as a biological corridor transporting Atlantic-associated biota eastward toward the Kara Sea. These findings suggest that "Atlantification" of Eurasian Arctic includes a microbial component, highlighting marine microbiomes as indicators of ongoing ecological changes in the Arctic Ocean.

microbiology↗

bioRxiv2025

Taxonomically different symbiotic communities of sympatric Arctic sponge species show functional similarity with specialization at species level

Marine sponges harbor diverse communities of associated organisms, including eukaryotes, viruses, and bacteria. Sponge associated microbiomes contribute to the health of the host organisms by defending them against invading bacteria and providing them with essential metabolites. Here we describe microbiomes of three sympatric species of cold-water marine sponges - Halichondria panicea, Halichondria sitiens, and Isodictya palmata - sampled over a period of six years at the White Sea. We identified the sponges as low microbial abundance species and detected stably associated bacteria that represent new taxa of sponge symbionts within Alpha- and Gammaproteobacteria. The sponges carried unique sets of unrelated species of symbiotic bacteria illustrating varying complexity of microbiomes. On a community level, sponge associated microbiomes shared common symbiotic features; they encoded multiple eukaryotic-like proteins, biosynthetic pathways, and transporters of amino acids and vitamins essential for sponges. On a species level, however, different classes of eukaryotic-like proteins and pathways were distributed between dominant and minor symbionts indicating specialization within microbiomes. Particularly, taurine and sulfoacetate metabolism pathways were associated exclusively with dominant symbionts in all three sponge species. Our study demonstrates strong functional convergence and co-evolution of microbiomes of sympatric cold-water sponge species with a distribution of functions between community members. Additionally, we observed dramatic shifts in compositions of sponge microbiomes coinciding with abnormally high water temperatures during the 2018 season, highlighting the vulnerability of cold-water ecosystems to global warming.

microbiology↗

bioRxiv2021

An interplay between viruses and bacteria associated with marine sponges from the White Sea revealed by metagenomics

Sponges are remarkable holobionts harboring extremely diverse microbial and viral communities. However, the interactions between the components within holobionts and between a holobiont and environment are largely unknown, especially for polar organisms. To investigate possible interactions within the sponge-associated communities and between them, we probed the microbiomes and viromes of cold-water sympatric sponges Isodictya palmata, Halichondria panicea, and Halichondria sitiens by 16S and shotgun metagenomics. We showed that the bacterial and viral communities associated with these White Sea sponges are species-specific and different from the surrounding water. Extensive mining of bacterial antiphage defense systems in the metagenomes revealed a variety of defense mechanisms. The abundance of defense systems was comparable in the metagenomes of the sponges and the surrounding water, thus distinguishing the White Sea sponges from those inhabiting the tropical seas. We developed a network-based approach for the combined analysis of CRISPR-spacers and protospacers. Using this approach, we showed that the virus-host interactions within the sponge-associated community are typically more abundant than the inter-community interactions. Additionally, we detected the occurrence of viral exchanges between the communities. Our work provides the first insight into the metagenomics of the three cold-water sponge species from the White Sea and paves the way for a comprehensive analysis of the interactions between microbial communities and associated viruses.

microbiology↗

bioRxiv2021

Interaction Between Transcribing RNA Polymerase and Topoisomerase I Prevents R-loop Formation in E. coli

Bacterial topoisomerase I (TopoI) removes excessive negative supercoiling and is thought to relax DNA molecules during transcription, replication and other processes. Using ChIP-Seq, we show that TopoI of Escherichia coli (EcTopoI) is co-localized, genome-wide, with RNA polymerase (RNAP) in transcription units. Treatment with transcription elongation inhibitor rifampicin leads to EcTopoI relocation to promoter regions, where RNAP also accumulates. When a 14 kDa RNAP-binding EcTopoI C-terminal domain (CTD) is overexpressed, co-localization of EcTopoI and RNAP along the transcription units is reduced. Pull-down experiments directly show that the two enzymes interact in vivo. Using ChIP-Seq and Topo-Seq, we demonstrate that EcTopoI is enriched and in and upstream (within up to 12-15 Kbs) of highly-active transcription units, indicating that EcTopoI relaxes negative supercoiling generated by transcription. Uncoupling of the RNAP-EcTopoI interaction by either overexpression of EcTopoI CTD or deletion of EcTopoI domains involved in the interaction is toxic for cells and leads to excessive negative plasmid supercoiling. Moreover, the CTD overexpression leads to R-loops accumulation genome-wide, indicating that the RNAP-EcTopoI interaction is required for prevention of R-loops formation. Article HighlightsO_LITopoI colocalizes genome-wide and interacts with RNAP in E. coli C_LIO_LIDisruption of the interaction between TopoI and RNAP decreases cells viability, leads to hypernegative DNA supercoiling, and R-loops accumulation C_LIO_LITopoI and DNA gyrase are enriched, respectively, upstream and downstream of transcription units in accordance with twin-domain model of Liu and Wang C_LIO_LITopoI recognizes its cleavage sites through a specific motif and by sensing negative supercoiling C_LI

molecular biology↗

bioRxiv2021

Timed global reorganization of protein synthesis during neocortex neurogenesis at codon resolution

Translation modulates the timing and amplification of gene expression after transcription. Brain development requires uniquely complex gene expression patterns, but large-scale measurements of translation directly in the prenatal brain are lacking. We measure the reactants, synthesis, and products of translation spanning mouse neocortex neurogenesis, and discover a transient window of dynamic regulation at mid-gestation. Timed translation upregulation of chromatin binding proteins like Satb2, which is essential for neuronal subtype differentiation, restricts protein expression in neuronal lineages despite broad transcriptional priming in progenitors. In contrast, translation downregulation of ribosomal proteins sharply decreases ribosome number, coinciding with a major shift in protein synthesis dynamics at mid-gestation. Changing levels of eIF4EBP1, a direct inhibitor of ribosomal protein translation, are concurrent with ribosome downregulation and controls Satb2 fate acquisition during neuronal differentiation. Thus, the refinement of transcriptional programs by translation is central to the molecular logic of brain development. Modeling of the developmental neocortex translatome is provided as an open-source searchable resource: https://shiny.mdc-berlin.de/cortexomics/.

neuroscience↗

bioRxiv2020

Olig3 acts as a master regulator of cerebellar development

The mature cerebellum controls motor skill precision and participates in other sophisticated brain functions that include learning, cognition and speech. Different types of GABAergic and glutamatergic cerebellar neurons originate in temporal order from two progenitor niches, the ventricular zone and rhombic lip, which express the transcription factors Ptf1a and Atoh1, respectively. However, the molecular machinery required to specify the distinct neuronal types emanating from these progenitor zones is still unclear. Here, we uncover the transcription factor Olig3 as a major determinant in generating the earliest neuronal derivatives emanating from both progenitor zones. In the rhombic lip, Olig3 regulates progenitor cell proliferation. In the ventricular zone, Olig3 safeguards Purkinje cell specification by curtailing the expression of Pax2, a transcription factor that we found to impose an inhibitory interneuron identity. Our work thus defines Olig3 as a key factor in cerebellar development.

neuroscience↗