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Detection of Circulatory E. Granulosus-Derived Cell-Free Dna in the Plasma and Urine of Human Cystic Echinococcosis Using an In-House Pcr: A Potential Promising Diagnostic Biomarker Publisher Pubmed



Habibi B1, 2 ; Gholami S1, 3 ; Bagheri A4 ; Fakhar M1, 3, 5 ; Torabi M6 ; Tabaripour R1, 2 ; Moradi A7
Authors
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Authors Affiliations
  1. 1. Toxoplasmosis Research Center, Communicable Diseases Institute, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran
  2. 2. Student Research Committee, Mazandaran University of Medical Sciences, Sari, Iran
  3. 3. Mazandaran Registry Center for Hydatid Cyst, Mazandaran University of Medical Sciences, Sari, Iran
  4. 4. Department of Clinical Biochemistry-Biophysics and Genetics, Immunogenetics Research Center, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran
  5. 5. Iranian National Registry Center for Lophomoniasis and Toxoplasmosis, Imam Khomeini Hospital, Mazandaran University of Medical Sciences, Sari, Iran
  6. 6. Baghiatallah Hospital, Baghiatallah University of Medical Sciences, Tehran, Iran
  7. 7. Department of General surgery Division of HPB and transplantation surgery, Tehran University of Medical Sciences, Tehran, Iran

Source: Molecular Biology Reports Published:2024


Abstract

Background: The diagnostic tool for identifying cystic echinococcosis (CE) patients at an early stage is currently lacking. However, circulatory cell-free DNA (cfDNA) has shown potential as a biomarker for parasitic infections and could be used for diagnosing CE. Research Design and methods: The plasma and urine samples were collected from 39 patients with confirmed CE through imaging and histopathological techniques. All plasma samples were tested for anti-echinococcal antibodies using a commercial ELISA test. Total plasma and urine cfDNA were extracted and an in-house PCR assay was developed to detect E. granulosus specific cfDNA in the samples of CE patients. Results: Out of the 39 patients, 30 tested positive for E. granulosus using serology, with a sensitivity of 76.9%. Moreover, the detection rates for the cfDNA were 79.5% in plasma samples and 58.97% in urine samples using the 80 bp COX1 gene. The plasma-based PCR and serology test showed the highest agreement (Kappa = 0.53). Conclusions: Plasma-based PCR has been found to be a reliable diagnostic tool for identifying CE patients at different cyst stages. It offers validity, speed, and sufficient sensitivity, making it an alternative to serology in diagnosing CE in endemic areas. © The Author(s), under exclusive licence to Springer Nature B.V. 2024.