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RAPD-PCR reveals genetic polymorphism among Leishmania major strains from Tunisian patients
BACKGROUND: Zoonotic cutaneous leishmaniasis caused by Leishmania (L.) major is endemoepidemic in the Center and South of Tunisia. The clinical course of the disease varies widely among different patients and geographic regions. Although genetic diversity in L. major parasites has been suggested as...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4501292/ https://www.ncbi.nlm.nih.gov/pubmed/26170197 http://dx.doi.org/10.1186/s12879-015-1010-0 |
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author | Yazidi, Rihab Bettaieb, Jihene Ghawar, Wissem Jaouadi, Kaouther Châabane, Sana Zaatour, Amor Ben Salah, Afif |
author_facet | Yazidi, Rihab Bettaieb, Jihene Ghawar, Wissem Jaouadi, Kaouther Châabane, Sana Zaatour, Amor Ben Salah, Afif |
author_sort | Yazidi, Rihab |
collection | PubMed |
description | BACKGROUND: Zoonotic cutaneous leishmaniasis caused by Leishmania (L.) major is endemoepidemic in the Center and South of Tunisia. The clinical course of the disease varies widely among different patients and geographic regions. Although genetic diversity in L. major parasites has been suggested as a potential factor influencing their pathogenic variability, little information on genetic polymorphism among L. major strains is available in the literature. This work aimed to estimate the genetic variability within different isolates of L. major. METHODS: Our sample comprised 39 isolates (confirmed as L. major by restriction fragment length polymorphism typing) from patients experiencing the same clinical manifestations but living in different regions of Tunisia where L. major is endemic. Random amplified polymorphic DNA (RAPD) PCR marker polymorphism was estimated by calculating Nei and Li’s genetic distances and by an analysis of molecular variance (AMOVA). RESULTS: Analysis of the genetic diversity among the isolates revealed a high level of polymorphism (43 %) among them. AMOVA indicated that the highest variability (99 %) existed within the study regions. CONCLUSIONS: Our results revealed a heterogeneous genetic profile for L. major with similar clinical manifestations occurring within the different geographical regions. Additional L. major isolates from patients, insect vectors, and reservoir hosts from different endemic foci should be collected for further analysis. |
format | Online Article Text |
id | pubmed-4501292 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45012922015-07-15 RAPD-PCR reveals genetic polymorphism among Leishmania major strains from Tunisian patients Yazidi, Rihab Bettaieb, Jihene Ghawar, Wissem Jaouadi, Kaouther Châabane, Sana Zaatour, Amor Ben Salah, Afif BMC Infect Dis Research Article BACKGROUND: Zoonotic cutaneous leishmaniasis caused by Leishmania (L.) major is endemoepidemic in the Center and South of Tunisia. The clinical course of the disease varies widely among different patients and geographic regions. Although genetic diversity in L. major parasites has been suggested as a potential factor influencing their pathogenic variability, little information on genetic polymorphism among L. major strains is available in the literature. This work aimed to estimate the genetic variability within different isolates of L. major. METHODS: Our sample comprised 39 isolates (confirmed as L. major by restriction fragment length polymorphism typing) from patients experiencing the same clinical manifestations but living in different regions of Tunisia where L. major is endemic. Random amplified polymorphic DNA (RAPD) PCR marker polymorphism was estimated by calculating Nei and Li’s genetic distances and by an analysis of molecular variance (AMOVA). RESULTS: Analysis of the genetic diversity among the isolates revealed a high level of polymorphism (43 %) among them. AMOVA indicated that the highest variability (99 %) existed within the study regions. CONCLUSIONS: Our results revealed a heterogeneous genetic profile for L. major with similar clinical manifestations occurring within the different geographical regions. Additional L. major isolates from patients, insect vectors, and reservoir hosts from different endemic foci should be collected for further analysis. BioMed Central 2015-07-14 /pmc/articles/PMC4501292/ /pubmed/26170197 http://dx.doi.org/10.1186/s12879-015-1010-0 Text en © Yazidi et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Yazidi, Rihab Bettaieb, Jihene Ghawar, Wissem Jaouadi, Kaouther Châabane, Sana Zaatour, Amor Ben Salah, Afif RAPD-PCR reveals genetic polymorphism among Leishmania major strains from Tunisian patients |
title | RAPD-PCR reveals genetic polymorphism among Leishmania major strains from Tunisian patients |
title_full | RAPD-PCR reveals genetic polymorphism among Leishmania major strains from Tunisian patients |
title_fullStr | RAPD-PCR reveals genetic polymorphism among Leishmania major strains from Tunisian patients |
title_full_unstemmed | RAPD-PCR reveals genetic polymorphism among Leishmania major strains from Tunisian patients |
title_short | RAPD-PCR reveals genetic polymorphism among Leishmania major strains from Tunisian patients |
title_sort | rapd-pcr reveals genetic polymorphism among leishmania major strains from tunisian patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4501292/ https://www.ncbi.nlm.nih.gov/pubmed/26170197 http://dx.doi.org/10.1186/s12879-015-1010-0 |
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