TY - JOUR
T1 - Identification of membrane-bound and secreted proteins from Echinococcus granulosus by signal sequence trap
AU - Rosenzvit, Mara C.
AU - Zhang, Wenbao
AU - Motazedian, Hossein
AU - Smyth, Danielle
AU - Pearson, Mark
AU - Loukas, Alex
AU - Jones, Malcolm K.
AU - McManus, Donald P.
PY - 2006/1/1
Y1 - 2006/1/1
N2 - The signal sequence trap technique was applied to identify genes coding for secreted and membrane bound proteins from Echinococcus granulosus, the etiologic agent of cystic hydatid disease. An E. granulosus protoscolex cDNA library was constructed in the AP-PST vector such that randomly primed cDNAs were fused with a placental alkaline phosphatase reporter gene lacking its endogenous signal peptide. E. granulosus cDNAs encoding a functional signal peptide were selected by their ability to rescue secretion of alkaline phosphatase by COS-7 cells that had been transfected with the cDNA library. Eighteen positive clones were identified and sequenced. Their deduced amino acid sequences showed significant similarity with amino acid transporters, Krebs cycle intermediates transporters, presenilins and vacuolar protein sorter proteins. Other cDNAs encoded secreted proteins without homologues. Three sequences were transcribed antisense to E. granulosus expressed sequence tags. All the mRNAs were expressed in protoscoleces and adult worms, but some of them were not found in oncospheres. The putative E. granulosus secreted and membrane bound proteins identified are likely to play important roles in the metabolism, development and survival in the host and represent potential targets for diagnosis, drugs and vaccines against E. granulosus.
AB - The signal sequence trap technique was applied to identify genes coding for secreted and membrane bound proteins from Echinococcus granulosus, the etiologic agent of cystic hydatid disease. An E. granulosus protoscolex cDNA library was constructed in the AP-PST vector such that randomly primed cDNAs were fused with a placental alkaline phosphatase reporter gene lacking its endogenous signal peptide. E. granulosus cDNAs encoding a functional signal peptide were selected by their ability to rescue secretion of alkaline phosphatase by COS-7 cells that had been transfected with the cDNA library. Eighteen positive clones were identified and sequenced. Their deduced amino acid sequences showed significant similarity with amino acid transporters, Krebs cycle intermediates transporters, presenilins and vacuolar protein sorter proteins. Other cDNAs encoded secreted proteins without homologues. Three sequences were transcribed antisense to E. granulosus expressed sequence tags. All the mRNAs were expressed in protoscoleces and adult worms, but some of them were not found in oncospheres. The putative E. granulosus secreted and membrane bound proteins identified are likely to play important roles in the metabolism, development and survival in the host and represent potential targets for diagnosis, drugs and vaccines against E. granulosus.
KW - Developmental expression
KW - Echinococcus granulosus
KW - Membrane bound proteins
KW - Secreted proteins
KW - Signal sequence trap
UR - http://www.scopus.com/inward/record.url?scp=30044442929&partnerID=8YFLogxK
U2 - 10.1016/j.ijpara.2005.09.001
DO - 10.1016/j.ijpara.2005.09.001
M3 - Article
C2 - 16229848
AN - SCOPUS:30044442929
SN - 0020-7519
VL - 36
SP - 123
EP - 130
JO - International Journal for Parasitology
JF - International Journal for Parasitology
IS - 1
ER -