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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Tehran University of Medical Sciences
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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.
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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 |
_version_ |
1724403578750107648 |