Abstract

The evolution of TLR-mediated innate immunity is a fundamental question in immunology. Here, we report the characterization and functional analysis of four TLR members in the lophotrochozoans Crassostrea gigas (CgTLRs). All CgTLRs bear a conserved domain organization and have a close relationship with TLRs in ancient non-vertebrate chordates. In HEK293 cells, every CgTLR could constitutively activate NF-κB responsive reporter, but none of the PAMPs tested could stimulate CgTLR-activated NF-κB induction. Subcellular localization showed that CgTLR members have similar and dual distribution on late endosomes and plasma membranes. Moreover, CgTLRs and CgMyD88 mRNA show a consistent response to multiple PAMP challenges in oyster hemocytes. As CgTLR-mediated NF-κB activation is dependent on CgMyD88, we designed a blocking peptide for CgTLR signaling that would inhibit CgTLR-CgMyD88 dependent NF-κB activation. This was used to demonstrate that a Vibrio parahaemolyticus infection-induced enhancement of degranulation and increase of cytokines TNF mRNA in hemocytes, could be inhibited by blocking CgTLR signaling. In summary, our study characterized the primitive TLRs in the lophotrocozoan C . gigas and demonstrated a fundamental role of TLR signaling in infection-induced hemocyte activation. This provides further evidence for an ancient origin of TLR-mediated innate immunity.

Highlights

  • Understanding the evolution of Toll-like receptor (TLR)mediated innate immunity or ancient function of Toll-like Receptors (TLRs) is an intriguing topic in immunology, due to their essential role in host defense of diverse organisms [1,2]

  • The results showed that the vertebrata TLR family has a much higher level divergence than that within mollusk and arthropod groups

  • We studied the role of TLRs in the immune response of a mollusk species (C. gigas; which is a member of the lophotrocozoans, a sister group of ecdysozoans), to provide insights into origin and emergence of TLR-mediated innate immune

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Summary

Introduction

Understanding the evolution of Toll-like receptor (TLR)mediated innate immunity or ancient function of TLRs is an intriguing topic in immunology, due to their essential role in host defense of diverse organisms [1,2]. In Drosophila Toll receptors contribute to the activation of NF-κB through the conserved adaptor Myd; this is associated with an increased resistance to infection which has led to the suggestion that TLR-mediated innate responses share a common ancient ancestry. Contrary to mammalian TLRs whose function is specific to innate immunity, Drosophila and C. elegans Tolls are recognized as key regulators of embryonic development; this role is independent of NF-κB activation [7,8]. It is not clear whether the TLR-mediated innate immune response results from a common ancient ancestor or from independent co-option in different lineages

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