» Articles » PMID: 30281608

Evaluation of a Set of Refolded Recombinant Antigens for Serodiagnosis of Human Fascioliasis

Overview
Journal PLoS One
Date 2018 Oct 4
PMID 30281608
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Diagnosis of fascioliasis with high sensitivity and specificity antigens play a vital role in the management of the disease. Majority of commercial serological tests use F. hepatica native antigens and indicate wide diversities in test accuracy. Nowadays, recombinant antigens have been introduced as diagnostic reagents offer better test standardization. A combination of highly pure recombinant antigens associated with correct folding will leads to improve specificity and sensitivity of ELISA for diagnosis of Fascioliasis. In this article, Fasciola hepatica saposin-like protein 2 (SAP-2), ferritin protein (Ftn-1) and leucine aminopeptidase (LAP) recombinant antigens were considered as tools for the detection of F. hepatica immunoglobulin G antibodies in persons with chronic human fasciolasis. The recombinant antigens were obtained as fusion proteins, expressed in Escherichia coli and purified by immobilized metal affinity chromatography (IMAC). The refolding processes of denatured recombinant proteins were performed using dialysis method in the presence of chemical additives, and reduced/oxidized glutathione (in vitro). The immunoreactivity of the recombinant antigens was assessed individually and in a combination compared with excretory/secretory antigen (E/S) in an enzyme-linked immunosorbent assay (ELISA) test. The experiments were optimized using 213 serum samples from humans, including patients with chronic fascioliasis, patients with other parasitic diseases, and healthy subjects. The results indicated 95% sensitivity and 98% specificity for rtFhSAP-2, 96% sensitivity and 91% specificity for E/S, 80% and 83.3% for rtFhFtn-1, 84% and 88% for FhLAP, and also, 96% and 95% for combination of recombinant antigens, respectively. In conclusion, the results of this investigation showed that rtFhSAP-2 with the highest specificity and acceptable sensitivity has a considerable superiority compared to mentioned antigens and even in combination with these antigens in serodiagnosis of human fascioliasis.

Citing Articles

Recent Developments in Recombinant Proteins for Diagnosis of Human Fascioliasis.

Mirzadeh A, Jafarihaghighi F, Kazemirad E, Sabzevar S, Tanipour M, Ardjmand M Acta Parasitol. 2020; 66(1):13-25.

PMID: 32974849 DOI: 10.1007/s11686-020-00280-5.


Immunoproteomic Approach of Extracellular Antigens From Species Reveals Exclusive B-Cell Epitopes.

Moreira A, Oliveira M, Souza Silva L, Inacio M, Bailao A, Parente-Rocha J Front Microbiol. 2020; 10:2968.

PMID: 32117076 PMC: 7015227. DOI: 10.3389/fmicb.2019.02968.

References
1.
Espino A, Morales A, Delgado B, Rivera F, Figueroa O, Suarez E . Partial immunity to Fasciola hepatica in mice after vaccination with FhSAP2 delivered as recombinant protein or DNA construct. Ethn Dis. 2010; 20(1 Suppl 1):S1-17-23. PMC: 3260556. View

2.
Esteban J, Bargues M . Epidemiology of human fascioliasis: a review and proposed new classification. Bull World Health Organ. 1999; 77(4):340-6. PMC: 2557647. View

3.
Jayaraj R, Hales B, Viberg L, Pizzuto S, Holt D, Rolland J . A diagnostic test for scabies: IgE specificity for a recombinant allergen of Sarcoptes scabiei. Diagn Microbiol Infect Dis. 2011; 71(4):403-7. DOI: 10.1016/j.diagmicrobio.2011.09.007. View

4.
Gonzales Santana B, Dalton J, Vasquez Camargo F, Parkinson M, Ndao M . The diagnosis of human fascioliasis by enzyme-linked immunosorbent assay (ELISA) using recombinant cathepsin L protease. PLoS Negl Trop Dis. 2013; 7(9):e2414. PMC: 3777859. DOI: 10.1371/journal.pntd.0002414. View

5.
Figueroa-Santiago O, Delgado B, Espino A . Fasciola hepatica saposin-like protein-2-based ELISA for the serodiagnosis of chronic human fascioliasis. Diagn Microbiol Infect Dis. 2011; 70(3):355-61. PMC: 3260655. DOI: 10.1016/j.diagmicrobio.2011.03.016. View