Detection Cell-Free DNA (cfDNA) Using Nested-PCR as a Diagnosis Tool for Human Fascioliasis Infection

Background: we aimed to detect fasciola specific deoxyribonucleic acid (dna) by nested-pcr assay on human stool and urine samples and compare the results with the respective elisa diagnostic assay. methods: overall, 206 clinically suspected cases of fascioliasis were enrolled in the study. blood samples were collected from all the patients, and serum samples were isolated. elisa assay, using fasciola somatic antigen (sa), was carried out to detect anti fasciola antibodies for the collected sera. dna was randomly extracted from 25 stool and 10 urine samples of seropositive individuals and was evaluated by conventional pcr and nested pcr methods. the nested-pcr results were confirmed by sequencing the 430 bp region of ribosomal itsi gene. stool and urine samples from patients with different parasitic diseases and 25 stool samples from healthy individuals served as controls. urine samples were collected from 10 healthy controls as well. results: fascioliasis was detected by elisa in 24.8% of the individuals. of these, 25 seropositive patients were randomly assigned to the study. fasciola dna was identified in the stool samples of 96% of seropositive patients by nested pcr but ova of fasciola was detected by parasitology methods in only 20% of seropositive cases. fasciola dna was identified in 90% of the urine samples by nested pcr. no cross-reactions were ob-served with other parasites. conclusion: detection of cfdna in stool and urine samples has high accuracy and thus can be used for the diagnosis of fasciola infection in human.