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Nath, R.

Publications and source records attributed to Nath, R..

5 recordsLinked to original sources

Amphibious Transitions Drive Lineage-Specific Diversification of Olfactory Receptors in Vertebrates

Olfactory receptors (ORs), which mediate chemical detection in vertebrates, constitute a highly dynamic and ecologically responsive gene family. While OR evolution has been well studied in fully terrestrial and aquatic lineages, its dynamics in amphibious vertebrates remain less explored. Species that occupy both aquatic and terrestrial habitats span a broad phylogenetic and ecological range--from amphibians to freshwater-dwelling mammals, semi-aquatic reptiles, and shoreline birds--and are subject to the functional demands of odour detection across two chemically disparate milieus. Here, we analysed OR gene repertoires across 230 vertebrate genomes, including 138 amphibious species. Our results show that OR repertoire expansion is not a uniform feature of terrestrial adaptation but is most pronounced in amphibious lineages, particularly those inhabiting freshwater systems, where chemically variable environments likely impose stronger selective pressures on olfaction. These expansions are primarily driven by lineage-specific expansions and correlate with ecologies that require sensing a wide range of chemical cues. While amphibious marine taxa possess larger OR repertoires than their fully marine relatives, they consistently exhibit fewer ORs than freshwater amphibious vertebrates. More broadly, species that rely on other sensory modalities--such as echolocation, electroreception, or vision--tend to exhibit reduced OR repertoires. Despite this diversity, several amphibious and terrestrial species within the same clade retain a small subset of shared OR genes, reflecting the retention of conserved OR orthologs--potentially those tuned to airborne odorants--across habitat transitions. However, overlap across clades is minimal, reflecting independent evolutionary responses to similar ecological pressures. Overall, our findings highlight amphibious lifestyles as key inflection points in vertebrate olfactory evolution--driving both OR repertoire expansion and divergence through the interplay of habitat complexity, sensory trade-offs, and lineage-specific constraints.

evolutionary biology↗

Genome of the Predatory Volute Melo melo Provides Insights into Adaptive Gene Family Diversification in a Basal Neogastropod Lineage

Neogastropods represent one of the most diverse and ecologically specialized lineages of marine mollusks, yet many of their early-diverging families remain genomically underexplored. Here, we present the first high-contiguity genome of a volutid species, the tropical predatory snail Melo melo, assembled using PacBio HiFi long reads. The final assembly spans 2.29 Gb with high contiguity (N50: 18.6 Mb) and completeness (BUSCO: 92.4%). Phylogenomic analyses place M. melo as an early-branching neogastropod lineage, supporting the basal position of Volutidae within the order. Comparative genomic analyses reveal expansions of gene families associated with digestion and nutrient metabolism (e.g., metallopeptidases), neurotoxicity (conotoxin-like genes), neurotransmission (ion channels), detoxification (cytochrome P450s and ABC transporters), and innate immunity (C1q and LRR-containing proteins), among others. These expansions are consistent with M. melos predatory behavior and adaptation to sediment-rich benthic habitats. Notably, M. melo lacks nacre-related genes but retains several biomineralization-related gene families previously implicated in shell and pearl formation, offering a genomic basis for investigating its distinctive non-nacreous phenotype. Orthology and CAFE analyses further reveal both conserved and lineage-specific dynamics of gene families across the analyzed gastropods. This study fills a key phylogenetic gap in molluscan genomics and establishes Melo melo as a valuable model for understanding the genomic basis of ecological adaptation and trait evolution in basal neogastropods.

genomics↗

Evolutionary Dynamics of Lineage-Specific Class-A GPCR Subsets Reveal Widespread Chemosensory Roles and Adaptations in Lophotrochozoa

Detecting external chemosensory cues via Class-A G protein-coupled receptors (GPCRs) is essential for behavioral and biological functions, influencing animal evolution and ecological adaptations. While well-studied in vertebrates and echinoderms, their role in major clades like Lophotrochozoa is less understood despite their remarkable ecological adaptations. Utilizing 238 lophotrochozoan genomes across eight phyla, we conducted a large-scale comparative genomics analysis to identify lineage-specifically expanded subsets (LSEs) of Class-A GPCRs adapted for chemoreception. Using phylogeny and orthology-based clustering, we differentiated these expansions from conserved orthogroups of endogenous ligand-binding GPCRs. LSEs correlated with adaptations to diverse habitats, with whole-genome duplications having limited impact. Across phyla, species in coastal, freshwater, and terrestrial habitats exhibited large and diverse LSEs, while those adapted to extreme deep-sea environments, parasitic lifestyles, or alternative chemosensory mechanisms showed consistent reductions. Sequence heterogeneity, positive selection, and ligand-binding pocket flexibility in these LSEs further underscored adaptations to environmental signals. These findings provide foundational insights into Class-A GPCR-mediated chemoreception across Lophotrochozoa. TeaserUnveiling correlations between lophotrochozoans habitat adaptations and lineage-specific changes in Class-A GPCR repertoire.

evolutionary biology↗

Optimization of conditions for conjugation of outer membrane vesicles of Salmonella Typhimurium with oral delivery systems using response surface method

BackgroundOuter membrane vesicles (OMVs) released from Salmonella Typhimurium can become the effective vaccine candidate. For efficient delivery through oral route, the OMVs are conjugated with some delivery systems. The current study was aimed at optimization of conditions required for conjugation of OMVs with nano- or microparticles for maximum entrapment of OMV in terms of protein concentration. MethodsThe OMVs of Salmonella Typhimurium were conjugated under three optimum conditions of pH, temperature and ratio (nanoparticles or microparticles: OMVs) predicted by response surface method. The efficiency of conjugation was determined by entrapment of OMVs in nano/microparticles. ResultThe pH and temperature were not influential conditions in case of conjugation of OMVs with chitosan nanoparticles (Ch-NP) and poly-lactide co-glycolide microparticles (PLG-MP) while they had influence in case of poly(anhydride) nanoparticles. In case of Ch-NP and PLG-MP, the optimum ratio for maximum entrapment was found to be 1:10 and 1:9 respectively. The optimum pH and temperature was found to be 7 and 24{degrees}C respectively for conjugation of poly(anhydride) nanoparticles. The optimized conditions did not alter the protein profile and immunogenic potential of conjugated vaccines.

biochemistry↗

Secretome of senescent hepatoma cells modulate macrophage polarization and neutrophil extracellular traps formation

Presence of dysfunctional senescent hepatocyte is a hallmark feature of cirrhosis. We now report the presence of senescent hepatocytes (p21 and p53 positive) in vicinity of infiltrated immune cells in hepatocellular carcinoma. Hence, we checked if senescent cells can alter fate of macrophage polarization and neutrophil extracellular trap (NETs) formation. Using an in vitro assay, senescence was induced in hepatoma cells (HepG2 and Huh7 cells) by doxorubicin treatment and senescent cell showed secretory phenotype with strong expression of cytokines (IL1{beta}, IL6, IL8 and IL13) as evaluated by Flow cytometry. The senescent secretome from hepatoma cells induced macrophage differentiation predominantly with M2 markers (CD80, CD86) while that of non-senescent cell induced M1 phenotype (CD163, CD206) as analysed by flow cytometry. Human hepatocellular carcinoma harbouring senescent hepatocytes showed presence of M2 macrophages, while M1 macrophages were predominant in non-tumorous region. Additionally, the senescent secretome from Huh7 cells (p53mut) enhanced the NETs formation, while HepG2 (p53+/+) secretome had an inhibitory affect In conclusion, the "pro-inflammatory" senescent secretome drives non-inflammatory type M2 macrophage polarization and modulate neutrophil traps thereby modulating the microenvironment towards tumor promotion. Targeting senescent hepatocyte secretome appears a promising therapeutic target in liver cancer in future. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=126 SRC="FIGDIR/small/423905v1_ufig1.gif" ALT="Figure 1"> View larger version (27K): org.highwire.dtl.DTLVardef@1df4256org.highwire.dtl.DTLVardef@7c4f53org.highwire.dtl.DTLVardef@13bfe80org.highwire.dtl.DTLVardef@1c1c4b5_HPS_FORMAT_FIGEXP M_FIG Work Highlight (Diagrammatic Representation). C_FIG

cancer biology↗