Abstract

Schistosoma mansoni and other Schistosoma sp. are multicellular parasitic helminths (worms) that infect humans and mammals worldwide. Infection by these parasites, which results in developmental maturation and sexual differentiation of the worms over a period of 5–6 weeks, induces antibodies to glycan antigens expressed in surface and secreted glycoproteins and glycolipids. There is growing interest in defining these unusual parasite-synthesized glycan antigens and using them to understand immune responses, their roles in immunomodulation, and in using glycan antigens as potential vaccine targets. A key problem in this area, however, has been the lack of information about the enzymes involved in elaborating the complex repertoire of glycans represented by the schistosome glycome. Recent availability of the nuclear genome sequences for Schistosoma sp. has created the opportunity to define the glycogenome, which represents the specific genes and cognate enzymes that generate the glycome. Here we describe the current state of information in regard to the schistosome glycogenome and glycome and highlight the important classes of glycans and glycogenes that may be important in their generation.

Highlights

  • Schistosomiasis is a debilitating vascular disease caused by an infection with parasitic helminths of the Schistosoma species

  • The identification of novel glycans synthesized by schistosomes and their unique functions as immunomodulators and recognition as antigens has raised awareness of their importance

  • The complementary elucidation of the genomes of Schistosoma species has opened the way to linking the glycogenome to the glycome, which has important consequences for the future of research in this area

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Summary

Deciphering the glycogenome of schistosomes

Are multicellular parasitic helminths (worms) that infect humans and mammals worldwide. Infection by these parasites, which results in developmental maturation and sexual differentiation of the worms over a period of 5–6 weeks, induces antibodies to glycan antigens expressed in surface and secreted glycoproteins and glycolipids. A key problem in this area, has been the lack of information about the enzymes involved in elaborating the complex repertoire of glycans represented by the schistosome glycome. Has created the opportunity to define the glycogenome, which represents the specific genes and cognate enzymes that generate the glycome. We describe the current state of information in regard to the schistosome glycogenome and glycome and highlight the important classes of glycans and glycogenes that may be important in their generation

INTRODUCTION
Gene ID
Findings
CONCLUSIONS
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