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Western Blot Analysis of Leishmania infantum Antigens in Sera of Patients with Visceral Leishmaniasis
BACKGROUND: Visceral leishmaniasis (VL) is endemic in the northwest and south of Iran. Untreated cases of VL could cause death. The aim of the present study was to evaluate the diagnostic performance of western blotting to detect a specific immunodominant proteins pattern for Leishmania infantum inf...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6511593/ https://www.ncbi.nlm.nih.gov/pubmed/31123464 |
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author | HEIDARI, Soudabeh GHARECHAHI, Javad MOHEBALI, Mehdi AKHOUNDI, Behnaz MIRSHAHVALADI, Shahab AZARIAN, Bahareh HAJJARAN, Homa |
author_facet | HEIDARI, Soudabeh GHARECHAHI, Javad MOHEBALI, Mehdi AKHOUNDI, Behnaz MIRSHAHVALADI, Shahab AZARIAN, Bahareh HAJJARAN, Homa |
author_sort | HEIDARI, Soudabeh |
collection | PubMed |
description | BACKGROUND: Visceral leishmaniasis (VL) is endemic in the northwest and south of Iran. Untreated cases of VL could cause death. The aim of the present study was to evaluate the diagnostic performance of western blotting to detect a specific immunodominant proteins pattern for Leishmania infantum infection using human sera infected with VL. METHODS: We studied a panel of 122 cryopreserved human serum samples from the leishmaniasis Research Laboratory, Tehran University of Medical Sciences, Tehran, Iran from 2010 to 2017. Serum samples were collected from visceral (Group I, n: 43) and cutaneous leishmaniasis (CL) (Group II, n: 8) patients, healthy individuals from endemic (Group III, n: 13) and non-endemic (Group IV, n: 16) areas for VL, and patients with other infectious diseases (Group V, n: 42). Total antigens were prepared from the Iranian strain of L. infantum promastigote form. RESULTS: In western blotting method, 34 protein bands of 14 to 163 kDa were recognized using the sera of VL patients. The polypeptide fractions with the highest frequency including 29, 51, and 62 kDa fractions were detected using 81.4%, 79%, and 81.4% of the sera, respectively. These bands were not detected using the sera of the negative control. Moreover, 19–23, 27, 31–35, 143–163, and 109 kDa fractions were detected specifically using the sera of the patients with VL. CONCLUSION: This technique could be a primary step for further exploration of VL immunodominant antigens for cloning (or any technique) further investigations for future planning. |
format | Online Article Text |
id | pubmed-6511593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Tehran University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-65115932019-05-23 Western Blot Analysis of Leishmania infantum Antigens in Sera of Patients with Visceral Leishmaniasis HEIDARI, Soudabeh GHARECHAHI, Javad MOHEBALI, Mehdi AKHOUNDI, Behnaz MIRSHAHVALADI, Shahab AZARIAN, Bahareh HAJJARAN, Homa Iran J Parasitol Original Article BACKGROUND: Visceral leishmaniasis (VL) is endemic in the northwest and south of Iran. Untreated cases of VL could cause death. The aim of the present study was to evaluate the diagnostic performance of western blotting to detect a specific immunodominant proteins pattern for Leishmania infantum infection using human sera infected with VL. METHODS: We studied a panel of 122 cryopreserved human serum samples from the leishmaniasis Research Laboratory, Tehran University of Medical Sciences, Tehran, Iran from 2010 to 2017. Serum samples were collected from visceral (Group I, n: 43) and cutaneous leishmaniasis (CL) (Group II, n: 8) patients, healthy individuals from endemic (Group III, n: 13) and non-endemic (Group IV, n: 16) areas for VL, and patients with other infectious diseases (Group V, n: 42). Total antigens were prepared from the Iranian strain of L. infantum promastigote form. RESULTS: In western blotting method, 34 protein bands of 14 to 163 kDa were recognized using the sera of VL patients. The polypeptide fractions with the highest frequency including 29, 51, and 62 kDa fractions were detected using 81.4%, 79%, and 81.4% of the sera, respectively. These bands were not detected using the sera of the negative control. Moreover, 19–23, 27, 31–35, 143–163, and 109 kDa fractions were detected specifically using the sera of the patients with VL. CONCLUSION: This technique could be a primary step for further exploration of VL immunodominant antigens for cloning (or any technique) further investigations for future planning. Tehran University of Medical Sciences 2019 /pmc/articles/PMC6511593/ /pubmed/31123464 Text en Copyright© Iranian Society of Parasitology & Tehran University of Medical Sciences http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article HEIDARI, Soudabeh GHARECHAHI, Javad MOHEBALI, Mehdi AKHOUNDI, Behnaz MIRSHAHVALADI, Shahab AZARIAN, Bahareh HAJJARAN, Homa Western Blot Analysis of Leishmania infantum Antigens in Sera of Patients with Visceral Leishmaniasis |
title | Western Blot Analysis of Leishmania infantum Antigens in Sera of Patients with Visceral Leishmaniasis |
title_full | Western Blot Analysis of Leishmania infantum Antigens in Sera of Patients with Visceral Leishmaniasis |
title_fullStr | Western Blot Analysis of Leishmania infantum Antigens in Sera of Patients with Visceral Leishmaniasis |
title_full_unstemmed | Western Blot Analysis of Leishmania infantum Antigens in Sera of Patients with Visceral Leishmaniasis |
title_short | Western Blot Analysis of Leishmania infantum Antigens in Sera of Patients with Visceral Leishmaniasis |
title_sort | western blot analysis of leishmania infantum antigens in sera of patients with visceral leishmaniasis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6511593/ https://www.ncbi.nlm.nih.gov/pubmed/31123464 |
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