Nuclear Elongation Factor-1 Gene A Molecular Marker for Iranian Sandfly Identification

Background: Elongation factor-1, a conserved nuclear protein coding gene was used to identify Iranian sandfly species. The phlebotomine sandfies are the vectors of the parasitic protozoan Leishmania, the causative agents of leishmaniasis, in Iran. Methods: Seven sets of primers were tried. PCR amp...

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Main Authors: P Parvizi, M Assmar
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2007-06-01
Series:Iranian Journal of Public Health
Subjects:
Online Access:https://ijph.tums.ac.ir/index.php/ijph/article/view/2115
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spelling doaj-46f56d3058ad4145a80b955a142e2ca52020-12-02T18:35:40ZengTehran University of Medical SciencesIranian Journal of Public Health2251-60852251-60932007-06-01362Nuclear Elongation Factor-1 Gene A Molecular Marker for Iranian Sandfly Identification P Parvizi0 M Assmar1 Background: Elongation factor-1, a conserved nuclear protein coding gene was used to identify Iranian sandfly species. The phlebotomine sandfies are the vectors of the parasitic protozoan Leishmania, the causative agents of leishmaniasis, in Iran. Methods: Seven sets of primers were tried. PCR amplification of elongation factor-1 was successfully achieved for all 14 species of Iranian sandflies that we caught, but different primers had to be used. Results: The aligned DNA sequences of 454 bp (without primers) of the gene had the most similarity to a coding region of the elongation factor-1 genes of D. melanogaster, as identified by a BLAST search of GenBank. Each Iranian species, except Phlebotomus caucasicus and P. mongolensis, had a unique combination of nucleotides, i.e. each had a diagnostic sequence. There were no diagnostic sequences for different geographical populations of the species in Iran. We found only a single copy of Ef-1 gene in most individual sandflies. However EF-1 gene was successfully amplified by PCR but, unfortunately, phylogenetic analysis showed that it might be multicopy in sandflies and so the markers could not be trusted. Conclusion: More highly polymorphic nuclear loci, like microsatellites, might be needed to distinguish morphologically indistinguishable females of the subgenus Paraphlebotomus, e.g. P. caucasiscus from P. mongolensis, in order to resolve their roles as vectors of Leishmania species in gerbils. https://ijph.tums.ac.ir/index.php/ijph/article/view/2115Elongation factor-1 (EF-1)
collection DOAJ
language English
format Article
sources DOAJ
author P Parvizi
M Assmar
spellingShingle P Parvizi
M Assmar
Nuclear Elongation Factor-1 Gene A Molecular Marker for Iranian Sandfly Identification
Iranian Journal of Public Health
Elongation factor-1 (EF-1)
author_facet P Parvizi
M Assmar
author_sort P Parvizi
title Nuclear Elongation Factor-1 Gene A Molecular Marker for Iranian Sandfly Identification
title_short Nuclear Elongation Factor-1 Gene A Molecular Marker for Iranian Sandfly Identification
title_full Nuclear Elongation Factor-1 Gene A Molecular Marker for Iranian Sandfly Identification
title_fullStr Nuclear Elongation Factor-1 Gene A Molecular Marker for Iranian Sandfly Identification
title_full_unstemmed Nuclear Elongation Factor-1 Gene A Molecular Marker for Iranian Sandfly Identification
title_sort nuclear elongation factor-1 gene a molecular marker for iranian sandfly identification
publisher Tehran University of Medical Sciences
series Iranian Journal of Public Health
issn 2251-6085
2251-6093
publishDate 2007-06-01
description Background: Elongation factor-1, a conserved nuclear protein coding gene was used to identify Iranian sandfly species. The phlebotomine sandfies are the vectors of the parasitic protozoan Leishmania, the causative agents of leishmaniasis, in Iran. Methods: Seven sets of primers were tried. PCR amplification of elongation factor-1 was successfully achieved for all 14 species of Iranian sandflies that we caught, but different primers had to be used. Results: The aligned DNA sequences of 454 bp (without primers) of the gene had the most similarity to a coding region of the elongation factor-1 genes of D. melanogaster, as identified by a BLAST search of GenBank. Each Iranian species, except Phlebotomus caucasicus and P. mongolensis, had a unique combination of nucleotides, i.e. each had a diagnostic sequence. There were no diagnostic sequences for different geographical populations of the species in Iran. We found only a single copy of Ef-1 gene in most individual sandflies. However EF-1 gene was successfully amplified by PCR but, unfortunately, phylogenetic analysis showed that it might be multicopy in sandflies and so the markers could not be trusted. Conclusion: More highly polymorphic nuclear loci, like microsatellites, might be needed to distinguish morphologically indistinguishable females of the subgenus Paraphlebotomus, e.g. P. caucasiscus from P. mongolensis, in order to resolve their roles as vectors of Leishmania species in gerbils.
topic Elongation factor-1 (EF-1)
url https://ijph.tums.ac.ir/index.php/ijph/article/view/2115
work_keys_str_mv AT pparvizi nuclearelongationfactor1geneamolecularmarkerforiraniansandflyidentification
AT massmar nuclearelongationfactor1geneamolecularmarkerforiraniansandflyidentification
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