Identification of Leishmania donovani in blood of experimentally infected rats by quantitative real-time PCR

The present study has been carried out at the Department of Microbiology and Parasitology, College of Veterinary Medicine/Al-Qadisiyah University to diagnose the visceral leishmaniasis molecular technique (Quantitative real-time polymerase chain reaction). The experimental study includes fourth Wist...

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Main Authors: Noor Idan Jarad, Ghaidaa Abbas Jasim
Format: Article
Language:English
Published: College of Veterinary Medicine 2018-12-01
Series:Al-Qadisiyah Journal of Veterinary Medicine Sciences
Online Access:http://www.qu.edu.iq/journalvm/index.php/vm_journal/article/view/511
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spelling doaj-0d3c20db2e094b4c82fca9439a1c05552020-11-24T22:43:29ZengCollege of Veterinary MedicineAl-Qadisiyah Journal of Veterinary Medicine Sciences 1818-57462313-44292018-12-011729910410.29079/vol17iss2art511Identification of Leishmania donovani in blood of experimentally infected rats by quantitative real-time PCRNoor Idan Jarad0Ghaidaa Abbas Jasim1Department of Microbiology and Parasitology, College of Veterinary Medicine, University of Al-Qadisiyah, IraqDepartment of Microbiology and Parasitology, College of Veterinary Medicine, University of Al-Qadisiyah, IraqThe present study has been carried out at the Department of Microbiology and Parasitology, College of Veterinary Medicine/Al-Qadisiyah University to diagnose the visceral leishmaniasis molecular technique (Quantitative real-time polymerase chain reaction). The experimental study includes fourth Wistar female rats (weighted 250 ± 2 g.) were injected by blood from an infected patient in the peritoneal cavity, after 8-10 days of experimental infection, blood samples had been collected directly from the heart in order to diagnose the infection by using quantitative real-time polymerase chain reaction. Quantitative Real-Time PCR qPCR technique was used for amplification of the conserved region in the GAPDH gene that was used for the detection of Leishmania donovani in blood samples of rats. It shows the Amplification of genomic DNA template concentrations of Leishmania donovani during reaction with syber dye inside the apparatus under threshold cycle, also shows the melting peak of Leishmania donovani genomic DNA template concentrations is demonstrate the specialization of Leishmania donovani genomic DNA amplification in a single peak for all samples. http://www.qu.edu.iq/journalvm/index.php/vm_journal/article/view/511
collection DOAJ
language English
format Article
sources DOAJ
author Noor Idan Jarad
Ghaidaa Abbas Jasim
spellingShingle Noor Idan Jarad
Ghaidaa Abbas Jasim
Identification of Leishmania donovani in blood of experimentally infected rats by quantitative real-time PCR
Al-Qadisiyah Journal of Veterinary Medicine Sciences
author_facet Noor Idan Jarad
Ghaidaa Abbas Jasim
author_sort Noor Idan Jarad
title Identification of Leishmania donovani in blood of experimentally infected rats by quantitative real-time PCR
title_short Identification of Leishmania donovani in blood of experimentally infected rats by quantitative real-time PCR
title_full Identification of Leishmania donovani in blood of experimentally infected rats by quantitative real-time PCR
title_fullStr Identification of Leishmania donovani in blood of experimentally infected rats by quantitative real-time PCR
title_full_unstemmed Identification of Leishmania donovani in blood of experimentally infected rats by quantitative real-time PCR
title_sort identification of leishmania donovani in blood of experimentally infected rats by quantitative real-time pcr
publisher College of Veterinary Medicine
series Al-Qadisiyah Journal of Veterinary Medicine Sciences
issn 1818-5746
2313-4429
publishDate 2018-12-01
description The present study has been carried out at the Department of Microbiology and Parasitology, College of Veterinary Medicine/Al-Qadisiyah University to diagnose the visceral leishmaniasis molecular technique (Quantitative real-time polymerase chain reaction). The experimental study includes fourth Wistar female rats (weighted 250 ± 2 g.) were injected by blood from an infected patient in the peritoneal cavity, after 8-10 days of experimental infection, blood samples had been collected directly from the heart in order to diagnose the infection by using quantitative real-time polymerase chain reaction. Quantitative Real-Time PCR qPCR technique was used for amplification of the conserved region in the GAPDH gene that was used for the detection of Leishmania donovani in blood samples of rats. It shows the Amplification of genomic DNA template concentrations of Leishmania donovani during reaction with syber dye inside the apparatus under threshold cycle, also shows the melting peak of Leishmania donovani genomic DNA template concentrations is demonstrate the specialization of Leishmania donovani genomic DNA amplification in a single peak for all samples.
url http://www.qu.edu.iq/journalvm/index.php/vm_journal/article/view/511
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