Exploring the Fasciola hepatica tegument proteome

被引:96
作者
Wilson, R. Alan [1 ]
Wright, Janelle M. [2 ]
de Castro-Borges, William [1 ,3 ]
Parker-Manuel, Sophie J. [1 ]
Dowle, Adam A. [4 ]
Ashton, Peter D. [1 ]
Young, Neil D. [5 ]
Gasser, Robin B. [5 ]
Spithill, Terry W. [2 ,6 ,7 ]
机构
[1] Univ York, Dept Biol, Ctr Immunol & Infect, York YO10 5DD, N Yorkshire, England
[2] Charles Sturt Univ, Sch Anim & Vet Sci, Wagga Wagga, NSW 2650, Australia
[3] Univ Fed Ouro Preto, Dept Ciencias Biol, BR-35400000 Ouro Preto, MG, Brazil
[4] Univ York, Dept Biol, Technol Facil, Ctr Excellence Mass Spectrometry, York YO10 5DD, N Yorkshire, England
[5] Univ Melbourne, Dept Vet Sci, Parkville, Vic 3052, Australia
[6] La Trobe Univ, Dept Agr Sci, Bundoora, Vic 3083, Australia
[7] La Trobe Univ, Ctr AgriBiosci, Bundoora, Vic 3083, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
Fasciola hepatica; Liver fluke; Tegument proteome; Excretory-secretory proteins; Tandem mass spectrometry; Morphology; Vomitus; ADULT SCHISTOSOMA-MANSONI; CATHEPSIN-L PROTEINASES; THIN-TAIL SHEEP; LEUCINE AMINOPEPTIDASE; IN-VITRO; SURFACE-MEMBRANES; IMMUNE-RESPONSE; INFECTION; VACCINATION; PROTECTION;
D O I
10.1016/j.ijpara.2011.08.003
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
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.
引用
收藏
页码:1347 / 1359
页数:13
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