Molecular evidence for distinct modes of nutrient acquisition between visceral and neurotropic schistosomes of birds

Sci Rep. 2019 Feb 4;9(1):1347. doi: 10.1038/s41598-018-37669-2.

Abstract

Trichobilharzia species are parasitic flatworms (called schistosomes or flukes) that cause important diseases in birds and humans, but very little is known about their molecular biology. Here, using a transcriptomics-bioinformatics-based approach, we explored molecular aspects pertaining to the nutritional requirements of Trichobilharzia szidati ('visceral fluke') and T. regenti ('neurotropic fluke') in their avian host. We studied the larvae of each species before they enter (cercariae) and as they migrate (schistosomules) through distinct tissues in their avian (duck) host. Cercariae of both species were enriched for pathways or molecules associated predominantly with carbohydrate metabolism, oxidative phosphorylation and translation of proteins linked to ribosome biogenesis, exosome production and/or lipid biogenesis. Schistosomules of both species were enriched for pathways or molecules associated with processes including signal transduction, cell turnover and motility, DNA replication and repair, molecular transport and/or catabolism. Comparative informatic analyses identified molecular repertoires (within, e.g., peptidases and secretory proteins) in schistosomules that can broadly degrade macromolecules in both T. szidati and T. regenti, and others that are tailored to each species to selectively acquire nutrients from particular tissues through which it migrates. Thus, this study provides molecular evidence for distinct modes of nutrient acquisition between the visceral and neurotropic flukes of birds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bird Diseases / genetics
  • Bird Diseases / parasitology
  • Birds / genetics
  • Birds / parasitology
  • Cercaria / classification
  • Cercaria / genetics
  • Cercaria / pathogenicity
  • Computational Biology
  • DNA, Helminth / classification
  • DNA, Helminth / genetics*
  • Ducks / genetics
  • Ducks / parasitology
  • Humans
  • Nutrients
  • Phylogeny*
  • Schistosomatidae / genetics*
  • Schistosomatidae / pathogenicity
  • Schistosomiasis / genetics*
  • Schistosomiasis / parasitology
  • Trematoda / classification
  • Trematoda / genetics
  • Trematoda / pathogenicity

Substances

  • DNA, Helminth