5 research outputs found

    Understanding the evolution of immune genes in jawed vertebrates

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    Driven by co-evolution with pathogens, host immunity continuously adapts to optimize defence against pathogens within a given environment. Recent advances in genetics, genomics and transcriptomics have enabled a more detailed investigation into how immunogenetic variation shapes the diversity of immune responses seen across domestic and wild animal species. However, a deeper understanding of the diverse molecular mechanisms that shape immunity within and among species is still needed to gain insight into-and generate evolutionary hypotheses on-the ultimate drivers of immunological differences. Here, we discuss current advances in our understanding of molecular evolution underpinning jawed vertebrate immunity. First, we introduce the immunome concept, a framework for characterizing genes involved in immune defence from a comparative perspective, then we outline how immune genes of interest can be identified. Second, we focus on how different selection modes are observed acting across groups of immune genes and propose hypotheses to explain these differences. We then provide an overview of the approaches used so far to study the evolutionary heterogeneity of immune genes on macro and microevolutionary scales. Finally, we discuss some of the current evidence as to how specific pathogens affect the evolution of different groups of immune genes. This review results from the collective discussion on the current key challenges in evolutionary immunology conducted at the ESEB 2021 Online Satellite Symposium: Molecular evolution of the vertebrate immune system, from the lab to natural populations

    Proteomic-based evidence for adult neurogenesis in birds and mammals as indicated from cerebrospinal fluid

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    Adult neurogenesis is the life-long process of neural stem cell proliferation, differentiation into neurons, migration, and incorporation into the existing neuronal circuits. After decades of research, it is now widely accepted that mammals and birds retain the capacity to regenerate neurons even after their subadult ontogeny. Cerebrospinal fluid participates in the regulation of the neurogenic niches of the vertebrate brain through signaling pathways not fully elucidated. Proteomic studies of cerebrospinal fluid have the potential to allow the in-depth characterization of its molecular composition. Comparative studies help to delineate those pathways that are universally critical for the regulation of neurogenesis in adulthood. In this review, we performed literature-based data mining in studies using liquid chromatography-tandem mass spectroscopy that analyzed cerebrospinal fluid samples from healthy adult humans (Homo sapiens); mice (Mus musculus); sheep (Ovis aries); chickens (Gallus gallus); and two parrot species, the budgerigar (Melopsittacus undulatus) and cockatiel (Nymphicus hollandicus). We identified up to 911 proteins represented in cerebrospinal fluid, involved in various pathways regulating adult neurogenesis. However, only 196 proteins were common across humans, mice, and birds. Pathway components involved in nervous system development, cell migration, and axonal guidance were commonly evident in all species investigated so far. Extensive bioinformatic analysis revealed that the universally over-represented pathways involved L1 cell adhesion molecule protein interactions, cell-adhesion molecules, signals regulating extracellular matrix remodeling, regulation of insulin growth factor signaling, axonal guidance, programmed cell death, immune signaling, and post-translational modifications. Most of the reported proteins are part of extracellular vesicles enriched in cerebrospinal fluid. However, the information presently available is still highly fragmentary, and far more questions persist than are answered. Technological advances will allow cerebrospinal fluid comparative proteomic research to delve into the fundamental processes of adult neurogenesis and eventually translate this research into any regenerative interventions

    Supplementary Methods and Results from Cannabinoid receptor 2 evolutionary gene loss makes parrots more susceptible to neuroinflammation

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    In vertebrates, cannabinoids modulate neuroimmune interactions through two cannabinoid receptors (CNRs) conservatively expressed in the brain (CNR1, syn. CB1) and in the periphery (CNR2, syn. CB2). Our comparative genomic analysis indicates several evolutionary losses in the CNR2 gene that is involved in immune regulation. Notably, we show that the CNR2 gene pseudogenised in all parrots (Psittaciformes). This CNR2 gene loss occurred due to chromosomal rearrangements. Our positive selection analysis suggests the absence of any specific molecular adaptations in parrot CNR1 that would compensate for the CNR2 loss in the modulation of the neuroimmune interactions. Using transcriptomic data from the brains of birds with experimentally induced sterile inflammation we highlight possible functional effects of such a CNR2 gene loss. We compare the expression patterns of CNR and neuroinflammatory markers in CNR2-deficient parrots (represented by the budgerigar, Melopsittacus undulatus and five other parrot species) with CNR2-intact passerines (represented by the zebra finch, Taeniopygia guttata). Unlike in passerines, stimulation with lipopolysaccharide resulted in the parrots in neuroinflammation linked with a significant upregulation of expression in proinflammatory cytokines (including interleukin 1 beta, IL1B and IL6) in the brain. Our results indicate the functional importance of the CNR2 gene loss for increased sensitivity to brain inflammation

    Supplementary Data from Cannabinoid receptor 2 evolutionary gene loss makes parrots more susceptible to neuroinflammation

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    Table S21: Putative presence or absence of given immune gene (based on GO term: “negative regulation of inflammatory response“, GO:0050728) based on Avian Immunome database (AVIMM, Mueller et. al. 2020). Chicken gene annotation is used. Gene – gene name abbreviation, Description – full gene name. Putative presence or absence of given gene is shown for each species by the name of database where sequence was retrieved or NA, respectively. Data in AVIMM were retrieved from the following public repositories: ENSEMBL, Uniprot or The Bird 10,000 Genomes project (b10k). The following avian species were included: parrots (Melopsittacus undulatus, Eolophus roseicapillus, Probosciger aterrimus, Amazona guildingii, Agapornis roseicollis, Nestor notabilis) and passerines (Corvus moneduloides, Ficedula albicollis, Hirundo rustica, Lepidothrix coronata, Lonchura striata, Molothrus ater, Parus major, Passer domesticus, Serinus canaria, Sturnus vulgaris, Taeniopygia guttata, Zonotrichia albicollis, Zosterops hypoxanthus). Reference: Mueller RC, Mallig N, Smith J et al. Avian Immunome DB: an example of a user-friendly interface for extracting genetic information. BMC Bioinformatics 2020;21:1–16.. Table S22: Gene expression data. RT-qPCR Cp values for individual genes investigated; E1-3 = experiment 1-3
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