Abstract

The molecules that mediate innate immunity are encoded by relatively few genes and exhibit broad specificity. Detailed annotation of the Pacific oyster (Crassostrea gigas) genome, a protostome invertebrate, reveals large-scale duplication and divergence of multigene families encoding molecules that effect innate immunity. Transcriptome analyses indicate dynamic and orchestrated specific expression of numerous innate immune genes in response to experimental challenge with pathogens, including bacteria, and a pathogenic virus. Variable expression of individual members of the multigene families encoding these genes also occurs during different types of abiotic stress (environmentally-equivalent conditions of temperature, salinity and desiccation). Multiple families of immune genes are responsive in concert to certain biotic and abiotic challenges. Individual members of expanded families of immune genes are differentially expressed under both biotic challenge and abiotic stress conditions. Members of the same families of innate immune molecules also are transcribed in developmental stage- and tissue-specific manners. An integrated, highly complex innate immune system that exhibits remarkable discriminatory properties and responses to different pathogens as well as environmental stress has arisen through the adaptive recruitment of tandem duplicated genes. The co-adaptive evolution of stress and innate immune responses appears to have an ancient origin in phylogeny.

Highlights

  • The molecules that mediate innate immunity are encoded by relatively few genes and exhibit broad specificity

  • EGF-toll/interleukin-1 receptor (TIR), proteins with epidermal growth factor (EGF) and TIR domains; NF-kB, nuclear factor-KappaB; RIG-I]-like receptors (RLRs), RIG-1-like receptor; MAVS, mitochondrial antiviral-signaling protein; MITA, transmembrane protein 173; IRF, interferon regulatory factor; TNF, tumor necrosis factor; TNFR, tumor necrosis factor receptor; TNF receptor-associated factors (TRAFs), TNF receptor associated factors; FADD, Fas-associated protein with Death domain; CRADD, Death domain-containing protein CRADD; EDARADD, cctodysplasin-A receptor-associated adapter protein; AP-1, activator protein 1; NACHT-leucine-rich repeat receptor (NLR), NOD-like receptor; SRCR, scavenger receptor cysteine-rich repeat protein; PGRP, peptidoglycan recognition proteins; GNBP, Gram-negative binding protein; CTLDC, C-lectin domain containing protein; FBGDC, fibrinogen-domain-containing proteins; C3, complement C3; C1q domain-containing (C1qDC), globular head C1q domain containing protein; MBP, mannose binding protein. * genes involved in both toll-like receptors (TLR) and RIG-I pathway

  • This study represents a comprehensive genomic and transcriptomic survey of innate immune molecules in the Pacific oyster, which have undergone adaptive evolution through tandem gene duplication and lineage-specific diversification that are an order of magnitude larger and more complex than seen in vertebrates

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Summary

Introduction

The molecules that mediate innate immunity are encoded by relatively few genes and exhibit broad specificity. A number of different genetic mechanisms increase the diversity and specificity of the innate response of invertebrates, including: massive alternative splicing of Down syndrome cell adhesion molecule in fruit fly (Drosophila melanogaster)[5], hypervariation and somatic variation in the fibrinogen-related proteins of the snail (Biomphalaria glabrata)[6] and high allelic diversity in the immunoglobulin (Ig) domains of amphioxus (Branchiostoma floridae) variable region-containing chitin-binding proteins[7] increase the diversity and specificity of the innate response of invertebrates In both sea urchin (Strongylocentrotus purpuratus) and amphioxus[8,9], the diversity and likely specificity of immunity is achieved through large-scale expansion and diversification of multigene families encoding innate immune genes. EGF-TIR, proteins with epidermal growth factor (EGF) and TIR domains; NF-kB, nuclear factor-KappaB; RLR, RIG-1-like receptor; MAVS, mitochondrial antiviral-signaling protein; MITA, transmembrane protein 173; IRF, interferon regulatory factor; TNF, tumor necrosis factor; TNFR, tumor necrosis factor receptor; TRAF, TNF receptor associated factors; FADD, Fas-associated protein with Death domain; CRADD, Death domain-containing protein CRADD; EDARADD, cctodysplasin-A receptor-associated adapter protein; AP-1, activator protein 1; NLR, NOD-like receptor; SRCR, scavenger receptor cysteine-rich repeat protein; PGRP, peptidoglycan recognition proteins; GNBP, Gram-negative binding protein; CTLDC, C-lectin domain containing protein; FBGDC, fibrinogen-domain-containing proteins; C3, complement C3; C1qDC, globular head C1q domain containing protein; MBP, mannose binding protein. * genes involved in both TLR and RIG-I pathway

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