Cargando…

A rapid and sensitive assay to identify HLA-DQ2/8 risk alleles for celiac disease using real-time PCR method

AIM: To perform a simple, rapid and sensitive Real-time PCR based SYBR Green method to determine the human leukocyte antigen (HLA)-DQ 2/8 alleles in celiac disease (CD) patients. BACKGROUND: Many molecular techniques are available to determine the HLA-DQ2 and DQ8 alleles, but they are too expensive...

Descripción completa

Detalles Bibliográficos
Autores principales: Mashayekhi, Kazem, Rostami-Nejad, Mohammad, Amani, Davar, Rezaei-Tavirani, Mostafa, Mohaghegh-Shalmani, Hamid, Zali, Mohammad Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shaheed Beheshti University of Medical Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6040037/
https://www.ncbi.nlm.nih.gov/pubmed/30013750
_version_ 1783338785679867904
author Mashayekhi, Kazem
Rostami-Nejad, Mohammad
Amani, Davar
Rezaei-Tavirani, Mostafa
Mohaghegh-Shalmani, Hamid
Zali, Mohammad Reza
author_facet Mashayekhi, Kazem
Rostami-Nejad, Mohammad
Amani, Davar
Rezaei-Tavirani, Mostafa
Mohaghegh-Shalmani, Hamid
Zali, Mohammad Reza
author_sort Mashayekhi, Kazem
collection PubMed
description AIM: To perform a simple, rapid and sensitive Real-time PCR based SYBR Green method to determine the human leukocyte antigen (HLA)-DQ 2/8 alleles in celiac disease (CD) patients. BACKGROUND: Many molecular techniques are available to determine the HLA-DQ2 and DQ8 alleles, but they are too expensive and have many steps that make them difficult to use. METHODS: To determine the HLA-DQ 2/8 alleles we have developed a new real-time PCR assay, using SYBR Green technique with melting curve analysis on genomic DNA isolated from 75 CD patients and 94 healthy controls. The specific primers to examine HLA-DQA1*05, HLA-DQB1*02 and HLA-DQB1*0302 alleles were used and results were compared with commercially available kits. RESULTS: Using this method, the presence of HLA-DQ2 and HLA-DQ8 alleles were determined with sensitivity and specificity 80% and 100% respectively and compared to low resolution commercially available kits, the results of this method were more efficient. The frequency of DQ2 and DQ8 in patients was 76% and 29%, respectively and overall 96% of patients were carries DQ2 and/or DQ8 alleles. CONCLUSION: The result of this study showed that Real-time PCR using SYBR Green method with melting curve analysis has good efficiency to identify the HLA-DQ2/8 risk alleles.
format Online
Article
Text
id pubmed-6040037
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Shaheed Beheshti University of Medical Sciences
record_format MEDLINE/PubMed
spelling pubmed-60400372018-07-16 A rapid and sensitive assay to identify HLA-DQ2/8 risk alleles for celiac disease using real-time PCR method Mashayekhi, Kazem Rostami-Nejad, Mohammad Amani, Davar Rezaei-Tavirani, Mostafa Mohaghegh-Shalmani, Hamid Zali, Mohammad Reza Gastroenterol Hepatol Bed Bench Original Article AIM: To perform a simple, rapid and sensitive Real-time PCR based SYBR Green method to determine the human leukocyte antigen (HLA)-DQ 2/8 alleles in celiac disease (CD) patients. BACKGROUND: Many molecular techniques are available to determine the HLA-DQ2 and DQ8 alleles, but they are too expensive and have many steps that make them difficult to use. METHODS: To determine the HLA-DQ 2/8 alleles we have developed a new real-time PCR assay, using SYBR Green technique with melting curve analysis on genomic DNA isolated from 75 CD patients and 94 healthy controls. The specific primers to examine HLA-DQA1*05, HLA-DQB1*02 and HLA-DQB1*0302 alleles were used and results were compared with commercially available kits. RESULTS: Using this method, the presence of HLA-DQ2 and HLA-DQ8 alleles were determined with sensitivity and specificity 80% and 100% respectively and compared to low resolution commercially available kits, the results of this method were more efficient. The frequency of DQ2 and DQ8 in patients was 76% and 29%, respectively and overall 96% of patients were carries DQ2 and/or DQ8 alleles. CONCLUSION: The result of this study showed that Real-time PCR using SYBR Green method with melting curve analysis has good efficiency to identify the HLA-DQ2/8 risk alleles. Shaheed Beheshti University of Medical Sciences 2018 /pmc/articles/PMC6040037/ /pubmed/30013750 Text en ©2018 RIGLD, Research Institute for Gastroenterology and Liver Diseases This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Mashayekhi, Kazem
Rostami-Nejad, Mohammad
Amani, Davar
Rezaei-Tavirani, Mostafa
Mohaghegh-Shalmani, Hamid
Zali, Mohammad Reza
A rapid and sensitive assay to identify HLA-DQ2/8 risk alleles for celiac disease using real-time PCR method
title A rapid and sensitive assay to identify HLA-DQ2/8 risk alleles for celiac disease using real-time PCR method
title_full A rapid and sensitive assay to identify HLA-DQ2/8 risk alleles for celiac disease using real-time PCR method
title_fullStr A rapid and sensitive assay to identify HLA-DQ2/8 risk alleles for celiac disease using real-time PCR method
title_full_unstemmed A rapid and sensitive assay to identify HLA-DQ2/8 risk alleles for celiac disease using real-time PCR method
title_short A rapid and sensitive assay to identify HLA-DQ2/8 risk alleles for celiac disease using real-time PCR method
title_sort rapid and sensitive assay to identify hla-dq2/8 risk alleles for celiac disease using real-time pcr method
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6040037/
https://www.ncbi.nlm.nih.gov/pubmed/30013750
work_keys_str_mv AT mashayekhikazem arapidandsensitiveassaytoidentifyhladq28riskallelesforceliacdiseaseusingrealtimepcrmethod
AT rostaminejadmohammad arapidandsensitiveassaytoidentifyhladq28riskallelesforceliacdiseaseusingrealtimepcrmethod
AT amanidavar arapidandsensitiveassaytoidentifyhladq28riskallelesforceliacdiseaseusingrealtimepcrmethod
AT rezaeitaviranimostafa arapidandsensitiveassaytoidentifyhladq28riskallelesforceliacdiseaseusingrealtimepcrmethod
AT mohagheghshalmanihamid arapidandsensitiveassaytoidentifyhladq28riskallelesforceliacdiseaseusingrealtimepcrmethod
AT zalimohammadreza arapidandsensitiveassaytoidentifyhladq28riskallelesforceliacdiseaseusingrealtimepcrmethod
AT mashayekhikazem rapidandsensitiveassaytoidentifyhladq28riskallelesforceliacdiseaseusingrealtimepcrmethod
AT rostaminejadmohammad rapidandsensitiveassaytoidentifyhladq28riskallelesforceliacdiseaseusingrealtimepcrmethod
AT amanidavar rapidandsensitiveassaytoidentifyhladq28riskallelesforceliacdiseaseusingrealtimepcrmethod
AT rezaeitaviranimostafa rapidandsensitiveassaytoidentifyhladq28riskallelesforceliacdiseaseusingrealtimepcrmethod
AT mohagheghshalmanihamid rapidandsensitiveassaytoidentifyhladq28riskallelesforceliacdiseaseusingrealtimepcrmethod
AT zalimohammadreza rapidandsensitiveassaytoidentifyhladq28riskallelesforceliacdiseaseusingrealtimepcrmethod