Molecular Characterization and Sequencing of a Gene Encoding Mannose Binding Protein in an Iranian Isolate of Acanthamoeba castellanii as a Major Agent of Acanthamoeba keratitis

Background: Acanthamoeba castellanii is the important cause of amoebic keratitis in Iran. The key molecule in pathogene­sis of Acanthamoeba keratitis is Mannose Binding Protein (MBP) led to adhesion of amoeba to corneal epithelium. Subse­quent to adhesion other cytopathic effects occur. The goal of...

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Main Authors: M Niyyati, S Rezaie, F Rahimi, M Mohebali, AH Maghsood, SH Farnia, M Rezaeian
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2008-06-01
Series:Iranian Journal of Public Health
Subjects:
Online Access:https://ijph.tums.ac.ir/index.php/ijph/article/view/2050
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author M Niyyati
S Rezaie
F Rahimi
M Mohebali
AH Maghsood
SH Farnia
M Rezaeian
author_facet M Niyyati
S Rezaie
F Rahimi
M Mohebali
AH Maghsood
SH Farnia
M Rezaeian
author_sort M Niyyati
collection DOAJ
description Background: Acanthamoeba castellanii is the important cause of amoebic keratitis in Iran. The key molecule in pathogene­sis of Acanthamoeba keratitis is Mannose Binding Protein (MBP) led to adhesion of amoeba to corneal epithelium. Subse­quent to adhesion other cytopathic effects occur. The goal of this study was to identify the molecular characterization of a gene encoding MBP in an Iranian isolate of A.castellanii in order to pave the way for further investigations such as new therapeu­tic advances or immunization. Methods: A.castellanii was cultured on non nutrient agar. Extraction of DNA was performed by phenol-chloroform method. After designing a pair of primer for the gene encoding MBP, PCR analysis was performed. Finally, the PCR prod­uct has been sequenced and the result submitted to the gene data banks. Results: An MBP gene of 1081 nucleotides was sequenced. This fragment contained three introns and encodes a protein with 194 amino acids. Homology search by Blast program showed a significant homology with the MBP gene in gene data banks (96%). Besides, the identity of amino acids with the other MBPs in gene data banks was about 86%. Conclusion: We isolated and sequenced a gene fragment encoding MBP in an Iranian isolate of A.castellanii. Molecular characteri­zation of this important gene is the first step in pursuing researches such as developing better therapeutic agents, im­mu­nization of population at risk or even developing a diagnostic tool by PCR techniques.
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spelling doaj.art-9f6419f36f3b4e6490b0d057fdca88d82022-12-21T17:44:32ZengTehran University of Medical SciencesIranian Journal of Public Health2251-60852251-60932008-06-01372Molecular Characterization and Sequencing of a Gene Encoding Mannose Binding Protein in an Iranian Isolate of Acanthamoeba castellanii as a Major Agent of Acanthamoeba keratitis M Niyyati0 S Rezaie1 F Rahimi2 M Mohebali3 AH Maghsood4 SH Farnia5 M Rezaeian6 Background: Acanthamoeba castellanii is the important cause of amoebic keratitis in Iran. The key molecule in pathogene­sis of Acanthamoeba keratitis is Mannose Binding Protein (MBP) led to adhesion of amoeba to corneal epithelium. Subse­quent to adhesion other cytopathic effects occur. The goal of this study was to identify the molecular characterization of a gene encoding MBP in an Iranian isolate of A.castellanii in order to pave the way for further investigations such as new therapeu­tic advances or immunization. Methods: A.castellanii was cultured on non nutrient agar. Extraction of DNA was performed by phenol-chloroform method. After designing a pair of primer for the gene encoding MBP, PCR analysis was performed. Finally, the PCR prod­uct has been sequenced and the result submitted to the gene data banks. Results: An MBP gene of 1081 nucleotides was sequenced. This fragment contained three introns and encodes a protein with 194 amino acids. Homology search by Blast program showed a significant homology with the MBP gene in gene data banks (96%). Besides, the identity of amino acids with the other MBPs in gene data banks was about 86%. Conclusion: We isolated and sequenced a gene fragment encoding MBP in an Iranian isolate of A.castellanii. Molecular characteri­zation of this important gene is the first step in pursuing researches such as developing better therapeutic agents, im­mu­nization of population at risk or even developing a diagnostic tool by PCR techniques.https://ijph.tums.ac.ir/index.php/ijph/article/view/2050Mannose Binding ProteinAcanthamoebaKeratitisIran
spellingShingle M Niyyati
S Rezaie
F Rahimi
M Mohebali
AH Maghsood
SH Farnia
M Rezaeian
Molecular Characterization and Sequencing of a Gene Encoding Mannose Binding Protein in an Iranian Isolate of Acanthamoeba castellanii as a Major Agent of Acanthamoeba keratitis
Iranian Journal of Public Health
Mannose Binding Protein
Acanthamoeba
Keratitis
Iran
title Molecular Characterization and Sequencing of a Gene Encoding Mannose Binding Protein in an Iranian Isolate of Acanthamoeba castellanii as a Major Agent of Acanthamoeba keratitis
title_full Molecular Characterization and Sequencing of a Gene Encoding Mannose Binding Protein in an Iranian Isolate of Acanthamoeba castellanii as a Major Agent of Acanthamoeba keratitis
title_fullStr Molecular Characterization and Sequencing of a Gene Encoding Mannose Binding Protein in an Iranian Isolate of Acanthamoeba castellanii as a Major Agent of Acanthamoeba keratitis
title_full_unstemmed Molecular Characterization and Sequencing of a Gene Encoding Mannose Binding Protein in an Iranian Isolate of Acanthamoeba castellanii as a Major Agent of Acanthamoeba keratitis
title_short Molecular Characterization and Sequencing of a Gene Encoding Mannose Binding Protein in an Iranian Isolate of Acanthamoeba castellanii as a Major Agent of Acanthamoeba keratitis
title_sort molecular characterization and sequencing of a gene encoding mannose binding protein in an iranian isolate of acanthamoeba castellanii as a major agent of acanthamoeba keratitis
topic Mannose Binding Protein
Acanthamoeba
Keratitis
Iran
url https://ijph.tums.ac.ir/index.php/ijph/article/view/2050
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