Comparison of the Diagnostic Performance of Antigen B Purified from Sheep Hydatid Cyst Fluid (HCF) with Commercial ELISA Kit


Cite item

Full Text

Abstract

Introduction::Cystic echinococcosis (CE) is a zoonotic parasitic disease caused by the metacestode of Echinococcus granulosus. CE is a health problem in Middle Eastern countries, such as Iran. The purpose of this study was to purify subunit 8 KDa antigen B from crude sheep hydatid cyst fluid (HCF) and compare its sensitivity and specificity with a commercial human ELISA kit (PT-Hydatid-96).

Methods::28 sera samples were collected from hydatid cyst patients who had surgery for a hydatid cyst and had their disease confirmed by pathology after the surgery. Furthermore, 35 samples of healthy individuals with no history of hydatid cysts were collected, as were nine serum samples from parasite-infected non-CE patients. HCF was obtained from sheep fertile cysts at a Sari slaughterhouse and used as an antigen. In an indirect ELISA test, the B antigen was employed, and the results were compared to those from a commercial ELISA kit.

Results::The results of this study were analyzed using the Kappa test. The commercial ELISA kit showed 17 cases (23.6%) positive, 44 cases (61.1%) negative, and 11 cases (15.3%) borderline. B antigen showed that 18 (25%), 43 (59.7 %), and 11 (15.3%) were positive, negative, and borderline, respectively. One sample (1.4% of 72 total samples) of 35 serum samples from healthy individuals was positive using B antigen-based ELISA. In addition, all nine serum samples from parasite-infected non-CE patients were negative for both tests. The sensitivity and specificity of the commercial ELISA kit have been evaluated at 60.7% and 100%, respectively. For B antigenbased ELISA, these values are 64.3 and 97.7%, respectively.

Conclusion::Antigen B produced from hydatid cyst fluid is a promising option for serological identification of hydatid cysts in both infected and healthy individuals. In an indirect ELISA test, hydatid fluid antigen could be used as a precise source of detection.

About the authors

Tahereh Galeh

Department of Parasitology, School of Medicine, Mazandaran University of Medical Sciences

Email: info@benthamscience.net

Mahdi Fakhar

Department of Parasitology, School of Medicine, Mazandaran University of Medical Sciences

Email: info@benthamscience.net

Majid Harandi

Department of Parasitology, School of Medicine, Kerman University of Medical Sciences

Email: info@benthamscience.net

Shirzad Gholami

Department of Parasitology, School of Medicine, Mazandaran University of Medical Sciences

Author for correspondence.
Email: info@benthamscience.net

Fatemeh Darzi

Department of Parasitology, School of Medicine, Mazandaran University of Medical Sciences

Email: info@benthamscience.net

Hossein Asgarian-Omran

Department of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran, Mazandaran University of Medical Sciences

Email: info@benthamscience.net

Shahabeddin Sarvi

Department of Parasitology, School of Medicine, Mazandaran University of Medical Sciences

Email: info@benthamscience.net

Reza Valadan

Department of Immunology, School of Medicine, Mazandaran University of Medical Sciences

Email: info@benthamscience.net

Maryam Hataminejad

Department of Parasitology, School of Medicine, Mazandaran University of Medical Sciences

Email: info@benthamscience.net

Sabah Mayahi

Doctor of Molecular Medicine, School of Medicine, Mazandaran University of Medical Sciences

Email: info@benthamscience.net

Seyyed Shariatzadeh

Department of Parasitology, Mazandaran University of Medical Sciences

Email: info@benthamscience.net

Toktam Abbasi

Student in Medical Laboratory Sciences, School of Paramedics, Islamic Azad University Tehran Medical Sciences

Email: info@benthamscience.net

References

  1. Thompson A, Deplazes P, Lymbery A. Preface. Adv Parasitol 2017; 95: xiii-v. doi: 10.1016/S0065-308X(17)30009-X PMID: 28131367
  2. Rokni M. Echinococcosis /hydatidosis in Iran. Iran J Parasitol 2009; 4(2)
  3. Thompson R, McManus D. Aetiology: Parasites and life-cycles. In: WHO/OIE manual on echinococcosis in humans and animals: a public health problem of global concern. 2001; pp. 1-16.
  4. Parija SC, Pramodhini S. Echinococcosis. In: Textbook of Parasitic Zoonoses. Springer 2022; pp. 353-68. doi: 10.1007/978-981-16-7204-0_33
  5. Pal M, Alemu HH, Marami LM, Garedo DR, Bodena EB. Cystic echincoccoosis: A comprehensive review on life cycle, epidemiology, pathogenesis, clinical Spectrum, diagnosis, public health and economic implications, treatment, and control. Int J Clin Exp Med Res 2022; 6(2): 131-41. doi: 10.26855/ijcemr.2022.04.005
  6. Brunetti E, Kern P, Vuitton DA. Expert consensus for the diagnosis and treatment of cystic and alveolar echinococcosis in humans. Acta Trop 2010; 114(1): 1-16. doi: 10.1016/j.actatropica.2009.11.001 PMID: 19931502
  7. Hosch W, Junghanss T, Stojkovic M, Brunetti E, Heye T, Kauffmann GW. Metabolic viability assessment of cystic echinococcosis using high‐field 1H MRS of cyst contents. NMR Biomed 2008; 21(7): 734-54.
  8. Abbasi B, Akhavan R, Ghamari KA, et al. Computed tomography and magnetic resonance imaging of hydatid disease: A pictorial review of uncommon imaging presentations. Heliyon 2021; 7(5): e07086. doi: 10.1016/j.heliyon.2021.e07086 PMID: 34095581
  9. El-Shazly AM, Saad RM, Belal US, Sakr T, Zakae HA. Evaluation of ELISA and IHAT in serological diagnosis of proven cases of human hydatidosis. J Egypt Soc Parasitol 2010; 40(2): 531-8. PMID: 21246959
  10. Vola A, Manciulli T, De Silvestri A, et al. Diagnostic performances of commercial ELISA, indirect hemagglutination, and western blot in differentiation of hepatic echinococcal and non-echinococcal lesions: A retrospective analysis of data from a single referral centre. Am J Trop Med Hyg 2019; 101(6): 1345-9. doi: 10.4269/ajtmh.19-0556 PMID: 31674293
  11. Aydin Y, Altuntas B, Kaya A, Ulas AB, Uyanik MH, Eroglu A. The availability of echinococcus IgG ELISA for diagnosing pulmonary hydatid cysts. Eurasian J Med 2018; 50(3): 144-7. doi: 10.5152/eurasianjmed.2018.16104 PMID: 30515031
  12. Siracusano A, Margutti P, Delunardo F, et al. Molecular cross-talk in host–parasite relationships: The intriguing immunomodulatory role of Echinococcus antigen B in cystic echinococcosis. Int J Parasitol 2008; 38(12): 1371-6. doi: 10.1016/j.ijpara.2008.06.003 PMID: 18692060
  13. Mohammadzadeh T, Sako Y, Sadjjadi SM, Sarkari B, Ito A. Comparison of the usefulness of hydatid cyst fluid, native antigen B and recombinant antigen B8/1 for serological diagnosis of cystic echinococcosis. Trans R Soc Trop Med Hyg 2012; 106(6): 371-5. doi: 10.1016/j.trstmh.2012.01.012 PMID: 22472966
  14. Folle AM, Kitano ES, Lima A, et al. Characterisation of antigen B protein species present in the hydatid cyst fluid of Echinococcus canadensis G7 genotype. PLoS Negl Trop Dis 2017; 11(1): e0005250. doi: 10.1371/journal.pntd.0005250 PMID: 28045899
  15. Pagnozzi D, Tamarozzi F, Roggio AM, et al. Structural and immunodiagnostic characterization of synthetic antigen B subunits from Echinococcus granulosus and their evaluation as target antigens for cyst viability assessment. Clin Infect Dis 2018; 66(9): 1342-51. doi: 10.1093/cid/cix1006 PMID: 29149256
  16. Oriol R, Oriol C, Williams JF, Pérez Esandi MV. Purification of lipoprotein antigens of Echinococcus granulosus from sheep hydatid fluid. Am J Trop Med Hyg 1971; 20(4): 569-74. doi: 10.4269/ajtmh.1971.20.569 PMID: 5568124
  17. Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 1976; 72(1-2): 248-54. doi: 10.1016/0003-2697(76)90527-3 PMID: 942051
  18. Siles-Lucas M, Casulli A, Conraths F, Müller N. Laboratory diagnosis of Echinococcus spp. in human patients and infected animals. Adv Parasitol 2017; 96: 159-257.
  19. Ahn CS, Han X, Bae YA, et al. Alteration of immunoproteome profile of Echinococcus granulosus hydatid fluid with progression of cystic echinococcosis. Parasit Vectors 2015; 8(1): 10. doi: 10.1186/s13071-014-0610-7 PMID: 25566682
  20. Rogan MT, Craig PS, Zeyhle E, Romig T, Lubano GM, Deshan L. Evaluation of a rapid dot-elisa as a field test for the diagnosis of cystic hydatid disease. Trans R Soc Trop Med Hyg 1991; 85(6): 773-7. doi: 10.1016/0035-9203(91)90451-4 PMID: 1801352
  21. Wen H, Craig PS. Immunoglobulin G subclass responses in human cystic and alveolar echinococcosis. Am J Trop Med Hyg 1994; 51(6): 741-8. doi: 10.4269/ajtmh.1994.51.741 PMID: 7810806
  22. El-On J, Khaleel E, Malsha Y, et al. Echinococcus granulosus: A seroepidemiological survey in northern Israel using an enzyme-linked immunosorbent assay. Trans R Soc Trop Med Hyg 1997; 91(5): 529-32. doi: 10.1016/S0035-9203(97)90011-0 PMID: 9463658
  23. Fotoohi S, Hashemi Tabar GR, Borji H. Serodiagnosis of human hydatidosis with an ELISA developed based on antigens derived from sheep hydatid cysts and comparison with a commercial human ELISA kit. Asian Pac J Trop Med 2013; 6(9): 723-7. doi: 10.1016/S1995-7645(13)60126-1 PMID: 23827151
  24. Rafiei A, Craig PS. The immunodiagnostic potential of protoscolex antigens in human cystic echinococcosis and the possible influence of parasite strain. Ann Trop Med Parasitol 2002; 96(4): 383-9. doi: 10.1179/000349802125001195 PMID: 12171619
  25. Ghaffari-Far F, Dalimi AA, Zavvaran HA, Jalosian F. Detection of antibodies against hydatid cyst fluid antigens using immunoblot technique. SSU_Journals 2004; 12(2): 33-8.
  26. Maleki F, Sarafpoor S. Assessment of pure and B hydatid cyst fluid antigens for the diagnosis of hydatidosis. J Gorgan Uni Med Sci 2014; 16(2): 74-81.

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2024 Bentham Science Publishers