Journal Home
Search for

Volume 12, Issue 6, Pages e49-e59 (November 2008)


View previous. 25 of 54 View next.

Asparaginyl endopeptidase from the carcinogenic liver fluke, Opisthorchis viverrini, and its potential for serodiagnosis

Thewarach LahaaCorresponding Author Informationemail address, Jittiyawadee Sripaa, Banchob Sripab, Mark Pearsonc, Leon Triboletc, Sasithorn Kaewkesa, Paiboon Sithithaworna, Paul J. Brindleyd, Alex Loukasc

Received 24 January 2008; received in revised form 5 March 2008; accepted 18 March 2008. published online 11 July 2008.

Summary 

Objectives

To isolate and characterize an asparaginyl endopeptidase from the carcinogenic liver fluke, Opisthorchis viverrini, and evaluate its expression profile, biochemical activity, and potential as an immunodiagnostic antigen.

Methods

The full length mRNA encoding an asparaginyl endopeptidase (family C13), Ov-aep-1, was isolated by immunoscreening of a cDNA bacteriophage library of adult O. viverrini using sera from patients infected with O. viverrini. Investigation of Ov-aep-1 transcripts in developmental stages of the parasite, and phylogenetic analysis, immunohistochemical localization, and recombinant protein expression and enzymology were employed to characterize the Ov-AEP-1 protein. Immunoblotting was used to assess the potential of this enzyme for immunodiagnosis of human opisthorchiasis.

Results

Ov-AEP-1 is characteristic of the C13 cysteine protease family. Ov-aep-1 transcripts were detected in adult and juvenile worms, eggs, and metacercariae. Phylogenetic analysis indicated that Ov-AEP-1 is closely related to homologous proteins in other trematodes. Recombinant Ov-AEP-1 was expressed in bacteria in inclusion bodies and refolded to a soluble form. Excretory–secretory (ES) products derived from adult O. viverrini and refolded recombinant Ov-AEP-1 both displayed catalytic activity against the diagnostic tripeptide substrate, Ala–Ala–Asn-aminomethylcoumarin. Rabbit antiserum raised to recombinant Ov-AEP-1 identified the native AEP-1 protease in both somatic extract and ES products of adult worms. Anti-Ov-AEP-1 IgG immunolocalized the anatomical site of expression to the gut of the fluke, implying a physiological role in digestion of food or activation of other digestive enzymes. Recombinant Ov-AEP-1 was recognized by serum antibodies from patients with opisthorchiasis but not other helminth infections, with a sensitivity and specificity of 85% and 100%, respectively. The positive and negative predictive values are 100% and 67%, respectively.

Conclusions

The liver fluke, O. viverrini, has a gut-localized asparaginyl endopeptidase. Refolded recombinant Ov-AEP-1 is catalytically active and has potential for immunodiagnosis of human opisthorchiasis.

Corresponding Editor: Timothy Barkham, Tan Tock Seng, Singapore

a Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand

b Department of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

c Division of Infectious Diseases, Queensland Institute of Medical Research, Brisbane, Queensland, Australia

d Department of Microbiology, Immunology and Tropical Medicine, George Washington University Medical Center, Washington, DC, USA

Corresponding Author InformationCorresponding author. Tel.: +66 43 348 387; fax: +66 43 202475.

PII: S1201-9712(08)01360-X

doi:10.1016/j.ijid.2008.03.033


View previous. 25 of 54 View next.