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The study of the oipA and dupA genes in Helicobacter pylori strains and their relationship with different gastroduodenal diseases

AIM: The purpose of this investigation was to determine the oipA and dupA genes of Helicobacter pylori isolates from west of Iran; Chaharmahalo Bakhtiyari region and find their relationship with the severity of the gastroduodenal diseases. BACKGROUND: Helicobacter pylori is an organism responsible f...

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Autores principales: Souod, Negar, Sarshar, Meysam, Dabiri, Hossein, Momtaz, Hassan, Kargar, Mohammad, Mohammadzadeh, Alireza, Abdi, Saeed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shaheed Beheshti University of Medical Sciences 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495424/
https://www.ncbi.nlm.nih.gov/pubmed/26171137
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author Souod, Negar
Sarshar, Meysam
Dabiri, Hossein
Momtaz, Hassan
Kargar, Mohammad
Mohammadzadeh, Alireza
Abdi, Saeed
author_facet Souod, Negar
Sarshar, Meysam
Dabiri, Hossein
Momtaz, Hassan
Kargar, Mohammad
Mohammadzadeh, Alireza
Abdi, Saeed
author_sort Souod, Negar
collection PubMed
description AIM: The purpose of this investigation was to determine the oipA and dupA genes of Helicobacter pylori isolates from west of Iran; Chaharmahalo Bakhtiyari region and find their relationship with the severity of the gastroduodenal diseases. BACKGROUND: Helicobacter pylori is an organism responsible for many gastroduodenal diseases. Many studies suggest that genetic diversity in H. pylori virulence factors such as oipA and dupA genes is high among isolates of different geographic regions and may cause more severe diseases. PATIENTS AND METHODS: In this cross-sectional study, gastric biopsy specimens were taken from 150 patients suffering from gastroduodenal diseases. The presence of ureC, dupA and oipA genes was tested by polymerase chain reaction (PCR). RESULTS: Overall, 123 (82%) H. pylori strains were isolated from 150 specimens. dupA gene was detected in 41 (33.33%) H.pylori-positive specimens. There was a reverse correlation between this gene and gastric cancer. The oipA gene was found in 88 (71.54%) samples and statistically there was no association between this gene and gastric disorders. As statistical analyses revealed, the presence of the dupA was more common in isolates with the oipA negative. CONCLUSION: Based on our findings, the presence of dupA gene can be considered as a marker for the onset of severe diseases. However, the oipA gene cannot be regarded for prediction of gastroenterology diseases. Meanwhile, extended molecular epidemiology researches in other populations are recommended.
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spelling pubmed-44954242015-07-13 The study of the oipA and dupA genes in Helicobacter pylori strains and their relationship with different gastroduodenal diseases Souod, Negar Sarshar, Meysam Dabiri, Hossein Momtaz, Hassan Kargar, Mohammad Mohammadzadeh, Alireza Abdi, Saeed Gastroenterol Hepatol Bed Bench Original Article AIM: The purpose of this investigation was to determine the oipA and dupA genes of Helicobacter pylori isolates from west of Iran; Chaharmahalo Bakhtiyari region and find their relationship with the severity of the gastroduodenal diseases. BACKGROUND: Helicobacter pylori is an organism responsible for many gastroduodenal diseases. Many studies suggest that genetic diversity in H. pylori virulence factors such as oipA and dupA genes is high among isolates of different geographic regions and may cause more severe diseases. PATIENTS AND METHODS: In this cross-sectional study, gastric biopsy specimens were taken from 150 patients suffering from gastroduodenal diseases. The presence of ureC, dupA and oipA genes was tested by polymerase chain reaction (PCR). RESULTS: Overall, 123 (82%) H. pylori strains were isolated from 150 specimens. dupA gene was detected in 41 (33.33%) H.pylori-positive specimens. There was a reverse correlation between this gene and gastric cancer. The oipA gene was found in 88 (71.54%) samples and statistically there was no association between this gene and gastric disorders. As statistical analyses revealed, the presence of the dupA was more common in isolates with the oipA negative. CONCLUSION: Based on our findings, the presence of dupA gene can be considered as a marker for the onset of severe diseases. However, the oipA gene cannot be regarded for prediction of gastroenterology diseases. Meanwhile, extended molecular epidemiology researches in other populations are recommended. Shaheed Beheshti University of Medical Sciences 2015 /pmc/articles/PMC4495424/ /pubmed/26171137 Text en ©2015 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
Souod, Negar
Sarshar, Meysam
Dabiri, Hossein
Momtaz, Hassan
Kargar, Mohammad
Mohammadzadeh, Alireza
Abdi, Saeed
The study of the oipA and dupA genes in Helicobacter pylori strains and their relationship with different gastroduodenal diseases
title The study of the oipA and dupA genes in Helicobacter pylori strains and their relationship with different gastroduodenal diseases
title_full The study of the oipA and dupA genes in Helicobacter pylori strains and their relationship with different gastroduodenal diseases
title_fullStr The study of the oipA and dupA genes in Helicobacter pylori strains and their relationship with different gastroduodenal diseases
title_full_unstemmed The study of the oipA and dupA genes in Helicobacter pylori strains and their relationship with different gastroduodenal diseases
title_short The study of the oipA and dupA genes in Helicobacter pylori strains and their relationship with different gastroduodenal diseases
title_sort study of the oipa and dupa genes in helicobacter pylori strains and their relationship with different gastroduodenal diseases
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495424/
https://www.ncbi.nlm.nih.gov/pubmed/26171137
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