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Comparative Evaluation of Real-Time Pcr and Elisa for the Detection of Human Fascioliasis Publisher Pubmed



Bakhshipour F1 ; Zibaei M1 ; Rokni MB2, 3 ; Miahipour A1 ; Firoozeh F4 ; Beheshti M5 ; Beikzadeh L6 ; Alizadeh G7 ; Aryaeipour M2 ; Raissi V2
Authors
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Authors Affiliations
  1. 1. Department of Parasitology and Mycology, School of Medicine, Alborz University of Medical Sciences, Karaj, Iran
  2. 2. Department of Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Center for Research of Endemic Parasites of Iran, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Microbiology, School of Medicine, Alborz University of Medical Sciences, Karaj, Iran
  5. 5. Department of Virology, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
  6. 6. Department of Medical Laboratory Sciences, Faculty of Para-Medicine, Alborz University of Medical Sciences, Karaj, Iran
  7. 7. Department of Parasitology and Mycology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran

Source: Scientific Reports Published:2024


Abstract

Fascioliasis is a zoonotic parasitic infection caused by Fasciola species in humans and animals. Despite significant advances in vaccination and new therapeutic agents, little attention has been paid to validating methods for the diagnosis of fascioliasis in humans. Serological techniques are convenient assays that significantly improves the diagnosis of Fasciola infection. However, a more sensitive method is required. The aim of this study was to compare the Real-Time PCR technique with the indirect-ELISA for the detection of Fasciola hepatica in human. Using a panel of sera from patients infected with Fasciola hepatica (n = 51), other parasitic infections (n = 7), and uninfected controls (n = 12), we optimized an ELISA which employs an excretory–secretory antigens from F. hepatica for the detection of human fascioliasis. After DNA extraction from the samples, molecular analysis was done using Real-Time PCR technique based on the Fasciola ribosomal ITS1 sequence. Of 70 patient serum samples, 44 (62.86%) samples were identified as positive F. hepatica infection using ELISA and Real-Time PCR assays. There was no cross-reaction with other parasitic diseases such as toxoplasmosis, leishmaniasis, taeniasis, hydatidosis, trichinosis, toxocariasis, and strongyloidiasis. The significant difference between the agreement and similarity of the results of patients with indirect ELISA and Real-Time PCR was 94.4% and 99.2%, respectively (Cohen’s kappa ≥ 0.7; P = 0.02). Based on the Kappa agreement findings, the significant agreement between the results of ELISA and Real-Time PCR indicates the accuracy and reliability of these tests in the diagnosis of F. hepatica in humans. © The Author(s) 2024.