Molecular Detection and Conventional Identification of Leishmania Species in Reservoir Hosts of Zoonotic Cutaneous Leishmaniasis in Fars Province, South of Iran
Background: The objectives of our research were to search for Leishmania species in rodents in Fars province, south of Iran, and to compare molecular with conventional methods for detecting these para-sites. Methods: Rodents were captured using live traps and screened for Leishmania species using...
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Tehran University of Medical Sciences
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doaj-c687baa79f6140a2b960a72c948899002021-04-02T13:05:02ZengTehran University of Medical SciencesIranian Journal of Parasitology1735-70202008-238X2013-06-0182Molecular Detection and Conventional Identification of Leishmania Species in Reservoir Hosts of Zoonotic Cutaneous Leishmaniasis in Fars Province, South of IranA Mirzaei0S Rouhani1Pa Kazerooni2M Farahmand3P Parvizi4Molecular Systematic Laboratory, Parasitology Department, Pasteur Institute of Iran, Tehran, Iran AND Medical Faculty, Ilam University of Medical Sciences, Ilam, Iran.Parasitology Department, Medical Faculty, Shahid Beheshti University of Medical Sciences, IranShiraz University of Medical Sciences, Shiraz, IranMolecular Systematic Laboratory, Parasitology Department, Pasteur Institute of Iran, Tehran, IranMolecular Systematic Laboratory, Parasitology Department, Pasteur Institute of Iran, Tehran, Iran Background: The objectives of our research were to search for Leishmania species in rodents in Fars province, south of Iran, and to compare molecular with conventional methods for detecting these para-sites. Methods: Rodents were captured using live traps and screened for Leishmania species using molecular and conventional methods, including the taking of smears from each ear. Nested PCR was employed to detect Leishmania in rodents by amplifying a region of the ribosomal RNA amplicon of Leishmania (ITS1- 5.8S rRNA-ITS2) that is species-specific by DNA sequence. Results: Totally, 122 rodents were captured. Leishmania parasites were detected using the nested PCR and three conventional methods (direct smear, NNN culture and Balb/C inoculation. 41 (33.6%) out of 122 rodents had Leishmania infections (34 Meriones lybicus and 7 M. persicus). All PCR products of the ITS-rDNA gene were sequenced. Sequence analysis revealed that 28 out of 41 positive samples were Leishma-nia major. Thirteen sequences were unreadable and therefore not identified. Conclusion: At least two gerbil species common in Fars ZCL foci, M. lybicus and M. persicus, are acquir-ing infections of L. major and may be reservoir hosts of one predominant parasite haplotype. Most infec-tions were detected molecularly not by conventional methods, because most rodents died in the traps. https://ijpa.tums.ac.ir/index.php/ijpa/article/view/494ITS-ribosomal DNAIranLeishmania majorNested PCRsRodents |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
A Mirzaei S Rouhani Pa Kazerooni M Farahmand P Parvizi |
spellingShingle |
A Mirzaei S Rouhani Pa Kazerooni M Farahmand P Parvizi Molecular Detection and Conventional Identification of Leishmania Species in Reservoir Hosts of Zoonotic Cutaneous Leishmaniasis in Fars Province, South of Iran Iranian Journal of Parasitology ITS-ribosomal DNA Iran Leishmania major Nested PCRs Rodents |
author_facet |
A Mirzaei S Rouhani Pa Kazerooni M Farahmand P Parvizi |
author_sort |
A Mirzaei |
title |
Molecular Detection and Conventional Identification of Leishmania Species in Reservoir Hosts of Zoonotic Cutaneous Leishmaniasis in Fars Province, South of Iran |
title_short |
Molecular Detection and Conventional Identification of Leishmania Species in Reservoir Hosts of Zoonotic Cutaneous Leishmaniasis in Fars Province, South of Iran |
title_full |
Molecular Detection and Conventional Identification of Leishmania Species in Reservoir Hosts of Zoonotic Cutaneous Leishmaniasis in Fars Province, South of Iran |
title_fullStr |
Molecular Detection and Conventional Identification of Leishmania Species in Reservoir Hosts of Zoonotic Cutaneous Leishmaniasis in Fars Province, South of Iran |
title_full_unstemmed |
Molecular Detection and Conventional Identification of Leishmania Species in Reservoir Hosts of Zoonotic Cutaneous Leishmaniasis in Fars Province, South of Iran |
title_sort |
molecular detection and conventional identification of leishmania species in reservoir hosts of zoonotic cutaneous leishmaniasis in fars province, south of iran |
publisher |
Tehran University of Medical Sciences |
series |
Iranian Journal of Parasitology |
issn |
1735-7020 2008-238X |
publishDate |
2013-06-01 |
description |
Background: The objectives of our research were to search for Leishmania species in rodents in Fars province, south of Iran, and to compare molecular with conventional methods for detecting these para-sites.
Methods: Rodents were captured using live traps and screened for Leishmania species using molecular and conventional methods, including the taking of smears from each ear. Nested PCR was employed to detect Leishmania in rodents by amplifying a region of the ribosomal RNA amplicon of Leishmania (ITS1- 5.8S rRNA-ITS2) that is species-specific by DNA sequence.
Results: Totally, 122 rodents were captured. Leishmania parasites were detected using the nested PCR and three conventional methods (direct smear, NNN culture and Balb/C inoculation. 41 (33.6%) out of 122 rodents had Leishmania infections (34 Meriones lybicus and 7 M. persicus). All PCR products of the ITS-rDNA gene were sequenced. Sequence analysis revealed that 28 out of 41 positive samples were Leishma-nia major. Thirteen sequences were unreadable and therefore not identified.
Conclusion: At least two gerbil species common in Fars ZCL foci, M. lybicus and M. persicus, are acquir-ing infections of L. major and may be reservoir hosts of one predominant parasite haplotype. Most infec-tions were detected molecularly not by conventional methods, because most rodents died in the traps.
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topic |
ITS-ribosomal DNA Iran Leishmania major Nested PCRs Rodents |
url |
https://ijpa.tums.ac.ir/index.php/ijpa/article/view/494 |
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