4.5 Article

Exploring the Fasciola hepatica tegument proteome

期刊

INTERNATIONAL JOURNAL FOR PARASITOLOGY
卷 41, 期 13-14, 页码 1347-1359

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.ijpara.2011.08.003

关键词

Fasciola hepatica; Liver fluke; Tegument proteome; Excretory-secretory proteins; Tandem mass spectrometry; Morphology; Vomitus

资金

  1. ARC/NHMRC Research Network for Parasitology, Australia
  2. Australian Society for Parasitology
  3. Charles Sturt University
  4. La Trobe University, Australia
  5. Australian Research Council (ARC)
  6. National Health and Medical Research Council (NHMRC)
  7. Melbourne Water Corporation, Australia
  8. Victorian Life Sciences Computation Initiative (VLSCI)
  9. IBM 'Collaboratory'

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The surface tegument of the liver fluke Fasciola hepatica is a syncytial cytoplasmic layer bounded externally by a plasma membrane and covered by a glycocalyx, which constitutes the interface between the parasite and its ruminant host. The tegument's interaction with the immune system during the fluke's protracted migration from the gut lumen through the peritoneal cavity and liver parenchyma to the lumen of the bile duct, plays a key role in the fluke's establishment or elimination. However, little is known about proteins of the tegument surface or its secretions. We applied techniques developed for the blood fluke, Schistosoma mansoni, to enrich a tegument surface membrane preparation and analyse its composition by tandem mass spectrometry using new transcript databases for F. hepatica. We increased the membrane and secretory pathway components of the final preparation to similar to 30%, whilst eliminating contaminating proteases. We identified a series of proteins or transcripts shared with the schistosome tegument including annexins, a tetraspanin, carbonic anhydrase and an orthologue of a host protein (CD59) that inhibits complement fixation. Unique to F. hepatica, we also found proteins with lectin, cubulin and von Willebrand factor domains plus 10 proteins with leader sequences or transmembrane helices. Many of these surface proteins are potential vaccine candidates. We were hampered in collecting tegument secretions by the propensity of liver flukes, unlike blood flukes, to vomit their gut contents. We analysed both the 'vomitus' and a second supernatant released from haematin-depleted flukes. We identified many proteases, some novel, as well as a second protein with a von Willebrand factor domain. This study demonstrates that components of the tegumental surface of F. hepatica can be defined using proteomic approaches, but also indicates the need to prevent vomiting if tegument secretions are to be characterised. Crown Copyright (C) 2011 Published by Elsevier Ltd. on behalf of Australian Society for Parasitology Inc. All rights reserved.

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