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Molecular Characterization and Analysis of 16S Ribosomal DNA in Some Isolates of Demodex folicullorum

BACKGROUND: Demodicosis is one of the most prevalent skin diseases resulting from infestation by Demodex mites. This parasite usually inhabits in follicular infundibulum or sebaceous duct and transmits through close contact with an infested host. METHODS: This study was carried from September 2014 t...

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Autores principales: DANESHPARVAR, Afrooz, MOWLAVI, Gholamreza, MIRJALALI, Hamed, HAJJARAN, Homa, MOBEDI, Iraj, NADDAF, Saeed Reza, SHIDFAR, Mohammadreza, SADAT MAKKI, Mahsa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5527032/
https://www.ncbi.nlm.nih.gov/pubmed/28761482
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author DANESHPARVAR, Afrooz
MOWLAVI, Gholamreza
MIRJALALI, Hamed
HAJJARAN, Homa
MOBEDI, Iraj
NADDAF, Saeed Reza
SHIDFAR, Mohammadreza
SADAT MAKKI, Mahsa
author_facet DANESHPARVAR, Afrooz
MOWLAVI, Gholamreza
MIRJALALI, Hamed
HAJJARAN, Homa
MOBEDI, Iraj
NADDAF, Saeed Reza
SHIDFAR, Mohammadreza
SADAT MAKKI, Mahsa
author_sort DANESHPARVAR, Afrooz
collection PubMed
description BACKGROUND: Demodicosis is one of the most prevalent skin diseases resulting from infestation by Demodex mites. This parasite usually inhabits in follicular infundibulum or sebaceous duct and transmits through close contact with an infested host. METHODS: This study was carried from September 2014 to January 2016 at Tehran University of Medical Sciences, Tehran, Iran. DNA extraction and amplification of 16S ribosomal RNA was performed on four isolates, already obtained from four different patients and identified morphologically though clearing with 10% Potassium hydroxide (KOH) and microscopical examination. Amplified fragments from the isolates were compared with GeneBank database and phylogenetic analysis was carried out using MEGA6 software. RESULTS: A 390 bp fragment of 16S rDNA was obtained in all isolates and analysis of generated sequences showed high similarity with those submitted to GenBank, previously. Intra-species similarity and distance also showed 99.983% and 0.017, respectively, for the studied isolates. Multiple alignments of the isolates showed Single Nucleotide Polymorphisms (SNPs) in 16S rRNA fragment. Phylogenetic analysis revealed that all 4 isolates clustered with other D. folliculorum, recovered from GenBank database. Our accession numbers KF875587 and KF875589 showed more similarity together in comparison with two other studied isolates. CONCLUSION: Mitochondrial 16S rDNA is one of the most suitable molecular barcodes for identification D. folliculorum and this fragment can use for intra-species characterization of the most human-infected mites.
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spelling pubmed-55270322017-07-31 Molecular Characterization and Analysis of 16S Ribosomal DNA in Some Isolates of Demodex folicullorum DANESHPARVAR, Afrooz MOWLAVI, Gholamreza MIRJALALI, Hamed HAJJARAN, Homa MOBEDI, Iraj NADDAF, Saeed Reza SHIDFAR, Mohammadreza SADAT MAKKI, Mahsa Iran J Parasitol Original Article BACKGROUND: Demodicosis is one of the most prevalent skin diseases resulting from infestation by Demodex mites. This parasite usually inhabits in follicular infundibulum or sebaceous duct and transmits through close contact with an infested host. METHODS: This study was carried from September 2014 to January 2016 at Tehran University of Medical Sciences, Tehran, Iran. DNA extraction and amplification of 16S ribosomal RNA was performed on four isolates, already obtained from four different patients and identified morphologically though clearing with 10% Potassium hydroxide (KOH) and microscopical examination. Amplified fragments from the isolates were compared with GeneBank database and phylogenetic analysis was carried out using MEGA6 software. RESULTS: A 390 bp fragment of 16S rDNA was obtained in all isolates and analysis of generated sequences showed high similarity with those submitted to GenBank, previously. Intra-species similarity and distance also showed 99.983% and 0.017, respectively, for the studied isolates. Multiple alignments of the isolates showed Single Nucleotide Polymorphisms (SNPs) in 16S rRNA fragment. Phylogenetic analysis revealed that all 4 isolates clustered with other D. folliculorum, recovered from GenBank database. Our accession numbers KF875587 and KF875589 showed more similarity together in comparison with two other studied isolates. CONCLUSION: Mitochondrial 16S rDNA is one of the most suitable molecular barcodes for identification D. folliculorum and this fragment can use for intra-species characterization of the most human-infected mites. Tehran University of Medical Sciences 2017 /pmc/articles/PMC5527032/ /pubmed/28761482 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
DANESHPARVAR, Afrooz
MOWLAVI, Gholamreza
MIRJALALI, Hamed
HAJJARAN, Homa
MOBEDI, Iraj
NADDAF, Saeed Reza
SHIDFAR, Mohammadreza
SADAT MAKKI, Mahsa
Molecular Characterization and Analysis of 16S Ribosomal DNA in Some Isolates of Demodex folicullorum
title Molecular Characterization and Analysis of 16S Ribosomal DNA in Some Isolates of Demodex folicullorum
title_full Molecular Characterization and Analysis of 16S Ribosomal DNA in Some Isolates of Demodex folicullorum
title_fullStr Molecular Characterization and Analysis of 16S Ribosomal DNA in Some Isolates of Demodex folicullorum
title_full_unstemmed Molecular Characterization and Analysis of 16S Ribosomal DNA in Some Isolates of Demodex folicullorum
title_short Molecular Characterization and Analysis of 16S Ribosomal DNA in Some Isolates of Demodex folicullorum
title_sort molecular characterization and analysis of 16s ribosomal dna in some isolates of demodex folicullorum
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5527032/
https://www.ncbi.nlm.nih.gov/pubmed/28761482
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