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A Convenient and Sensitive Kdna-Pcr for Screening of Leishmania Infantum Latent Infection Among Blood Donors in a Highly Endemic Focus, Northwestern Iran Publisher Pubmed



Asfaram S1, 2 ; Fakhar M2 ; Mohebali M3 ; Ziaei Hezarjaribi H2 ; Mardani A4 ; Ghezelbash B5 ; Akhoundi B3 ; Zarei Z3 ; Moazeni M6
Authors
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Authors Affiliations
  1. 1. Zoonoses Research Center (ZRC), Ardabil University of Medical Sciences, Ardabil, Iran
  2. 2. Toxoplasmosis Research Center, Communicable Diseases Institute, Iranian National Registry Center for Lophomoniasis and Toxoplasmosis, Mazandaran University of Medical Sciences, P.O Box: 48471-91971, Farah-Abad Road, Sari, Iran
  3. 3. Center for Research of Endemic Parasites of Iran (CREPI), Department of Parasitology, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Microbiology, Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran
  5. 5. Laboratory Hematology and Blood Bank, Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran
  6. 6. Invasive Fungi Research Center, Communicable Diseases Institute, Department of Medical Mycology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran

Source: Acta Parasitologica Published:2022


Abstract

Background: Recent global evidences showed that asymptomatic blood donor carriers of Leishmania infection will appear as a threat for blood transfusions recipients in endemic areas. As yet, there is no appropriate diagnostic procedure for detecting infection of blood donors in blood banks. Subjects and Methods: The present study was aimed to apply various current diagnostic tests among blood donors in an endemic area of visceral leishmaniasis (VL), Ardabil Province, northwestern Iran. Blood samples were gathered from 860 blood donors in endemic areas of the province between 2017 and 2018, at eight blood donation centers. These samples was assessed using microculture, serological (DAT and rK39-ICT) and molecular based (conventional kDNA-PCR and HRM-PCR) tests. Results: Of 860 eligible donors, 24 (2.8%) were seropositive for VL by DAT, and 388 (45%) were positive by kDNA-PCR. Moreover, 19 (19/860) were positive for both of them. Out of 19 subjects, 5.3% (1/19) was positive by rK39-ICT, 10.5% (2/19), and 79% (15/19) were detected positive in microculture and HRM-PCR methods, respectively. Nineteen donors were followed up for 2 years, of which 16 (84.2%) had a serological conversion, and 4 (21%) were positive by kDNA-PCR. The sensitivity of kDNA-PCR, and HRM-PCR procedures in detecting Leishmania parasite was found to be 98.7%, and 79%, respectively. Conclusions: Our findings justify the use of kDNA-PCR as a convenient and sensitive tool for screening subjects with leishmanial latent infection in blood banks at least in endemic regions. In these areas, however, a PCR-based test should be used to validate Leishmania infection among seropositive donors. © 2022, The Author(s) under exclusive licence to Witold Stefanski Institute of Parasitology, Polish Academy of Sciences.
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