Abstract

Insect thioester-containing protein (iTEP) is the most recently defined group among the thioester-containing protein (TEP) superfamily. TEPs are key components of the immune system, and iTEPs from flies and mosquitoes were shown to be major immune weapons. Initially characterized from insects, TEP genes homologous to iTEP were further described from several other invertebrates including arthropods, cniderians, and mollusks albeit with few functional characterizations. In the freshwater snail Biomphalaria glabrata, a vector of the schistosomiasis disease, the presence of a TEP protein (BgTEP) was previously described in a well-defined immune complex involving snail lectins (fibrinogen-related proteins) and schistosome parasite mucins (SmPoMuc). To investigate the potential role of BgTEP in the immune response of the snail, we first characterized its genomic organization and its predicted protein structure. A phylogenetic analysis clustered BgTEP in a well-conserved subgroup of mollusk TEP. We then investigated the BgTEP expression profile in different snail tissues and followed immune challenges using different kinds of intruders during infection kinetics. Results revealed that BgTEP is particularly expressed in hemocytes, the immune-specialized cells in invertebrates, and is secreted into the hemolymph. Transcriptomic results further evidenced an intruder-dependent differential expression pattern of BgTEP, while interactome experiments showed that BgTEP is capable of binding to the surface of different microbes and parasite either in its full length form or in processed forms. An immunolocalization approach during snail infection by the Schistosoma mansoni parasite revealed that BgTEP is solely expressed by a subtype of hemocytes, the blast-like cells. This hemocyte subtype is present in the hemocytic capsule surrounding the parasite, suggesting a potential role in the parasite clearance by encapsulation. Through this work, we report the first characterization of a snail TEP. Our study also reveals that BgTEP may display an unexpected functional dual role. In addition to its previously characterized anti-protease activity, we demonstrate that BgTEP can bind to the intruder surface membrane, which supports a likely opsonin role.

Highlights

  • Thioester-containing proteins (TEPs) are large secreted glycoproteins characterized by the presence of a unique intrachain β-cysteinyl-γ-glutamyl thioester bond [1]

  • BgTEP exhibits all the characteristics of known Insect thioester-containing protein (iTEP) family members, including a signal peptide (SP) for secretion, several predicted N-glycosylation sites, the canonical thioester motif (GCGEQ), the complement component domain, the Alpha2 macroglobulin receptor binding domain, and numerous cysteins such as the six C-terminal ones which are a signature of iTEPs [42]

  • BgTEP is composed of eight MG domains, a succession of several β-sheets related to the fibronectin type III domains, with insertions of a LNK domain nested into MG6 and a CUB domain (β-sheet domain), and of a thioester domain (TED) (α-helical thioester domain) between MG7 and MG8 (Figure 1A)

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Summary

Introduction

Thioester-containing proteins (TEPs) are large secreted glycoproteins characterized by the presence of a unique intrachain β-cysteinyl-γ-glutamyl thioester bond [1]. The canonical intrachain thioester bond (GCGEQ) was originally described in the human alpha-2-macroglobulin (A2M), pro­ tease inhibitor, and C3, a central component of the complement system [3]. The TEP superfamily is divided into two subfamilies displaying dis­ tinct functions, complement factors, and A2M [2], supported by the presence of anaphylatoxin (ANA) and C-terminal C345C domains only in members of the complement factor subfamily. The A2M subfamily comprises A2M, pregnancy zone protein-like (PZP), complement C3 and PZP A2M domain-containing 8 (CPAMD8), and cell surface glycoprotein CD109. Two other classes of TEP were recently discovered in insects: the insect thioester-containing protein (iTEP) [4] and the macroglobulin complement-related (Mcr) [5], which constitute a third subfamily inside TEP superfamily, based on the phylogenetic analysis [2]

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