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Interferon-γ receptor-1 gene promoter polymorphisms and susceptibility for brucellosis in Makkah region
BACKGROUND: Genetic polymorphisms that affect the production levels of certain cytokines and/or their receptors may determine the risk, severity or protection in some infectious diseases like brucellosis. OBJECTIVES: The aim of this study was to investigate the association of certain known Interfero...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Makerere Medical School
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6354847/ https://www.ncbi.nlm.nih.gov/pubmed/30766581 http://dx.doi.org/10.4314/ahs.v18i4.36 |
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author | Ismael, AB Mergani, A Salim, A Mostafa, S Alkafaween, I |
author_facet | Ismael, AB Mergani, A Salim, A Mostafa, S Alkafaween, I |
author_sort | Ismael, AB |
collection | PubMed |
description | BACKGROUND: Genetic polymorphisms that affect the production levels of certain cytokines and/or their receptors may determine the risk, severity or protection in some infectious diseases like brucellosis. OBJECTIVES: The aim of this study was to investigate the association of certain known Interferon-γ Receptor-1 (IFN-γ R1) gene promoter polymorphisms and the susceptibility to infection with Brucellosis in Saudi population. METHODS: A cases-control association study was conducted in 69 individuals with human brucellosis and 94 healthy individuals. Genotyping of IFN-γ R1 — 56 C>T and IFN-γ R1 — 611 A>G polymorphism in both patients and healthy controls was done by PCR- restriction enzyme length polymorphisms (PCR-RFLP) and PCR- confronting two primer pairs (PCR-CTPP) methods and were assessed for potential associations with susceptibility for human brucellosis and their mode of penetrance. RESULTS: Interestingly, we have designed a PCR-CTPP system to be used for genotyping of IFN-γ R1 — 611 A > G polymorphism. The PCR-CTPP is an accurate method for genotyping of SNPs. Moreover, it is time-saving, inexpensive and easy to perform. CONCLUSION: Both tested polymorphisms, IFN-γ R1 — 56 C>T and IFN-γ R1 -611 A>G polymorphism had no role in genetic susceptibility to human brucellosis in the study population. The PCR-CTPP can be used for genotyping IFN-γ R1 — 611 A > G polymorphism and other types of mutation. |
format | Online Article Text |
id | pubmed-6354847 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Makerere Medical School |
record_format | MEDLINE/PubMed |
spelling | pubmed-63548472019-02-14 Interferon-γ receptor-1 gene promoter polymorphisms and susceptibility for brucellosis in Makkah region Ismael, AB Mergani, A Salim, A Mostafa, S Alkafaween, I Afr Health Sci Articles BACKGROUND: Genetic polymorphisms that affect the production levels of certain cytokines and/or their receptors may determine the risk, severity or protection in some infectious diseases like brucellosis. OBJECTIVES: The aim of this study was to investigate the association of certain known Interferon-γ Receptor-1 (IFN-γ R1) gene promoter polymorphisms and the susceptibility to infection with Brucellosis in Saudi population. METHODS: A cases-control association study was conducted in 69 individuals with human brucellosis and 94 healthy individuals. Genotyping of IFN-γ R1 — 56 C>T and IFN-γ R1 — 611 A>G polymorphism in both patients and healthy controls was done by PCR- restriction enzyme length polymorphisms (PCR-RFLP) and PCR- confronting two primer pairs (PCR-CTPP) methods and were assessed for potential associations with susceptibility for human brucellosis and their mode of penetrance. RESULTS: Interestingly, we have designed a PCR-CTPP system to be used for genotyping of IFN-γ R1 — 611 A > G polymorphism. The PCR-CTPP is an accurate method for genotyping of SNPs. Moreover, it is time-saving, inexpensive and easy to perform. CONCLUSION: Both tested polymorphisms, IFN-γ R1 — 56 C>T and IFN-γ R1 -611 A>G polymorphism had no role in genetic susceptibility to human brucellosis in the study population. The PCR-CTPP can be used for genotyping IFN-γ R1 — 611 A > G polymorphism and other types of mutation. Makerere Medical School 2018-12 /pmc/articles/PMC6354847/ /pubmed/30766581 http://dx.doi.org/10.4314/ahs.v18i4.36 Text en © 2018 Ismael et al. Licensee African Health Sciences. This is an Open Access article distributed under the terms of the Creative commons Attribution License (https://creativecommons.org/licenses/BY/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Ismael, AB Mergani, A Salim, A Mostafa, S Alkafaween, I Interferon-γ receptor-1 gene promoter polymorphisms and susceptibility for brucellosis in Makkah region |
title | Interferon-γ receptor-1 gene promoter polymorphisms and susceptibility for brucellosis in Makkah region |
title_full | Interferon-γ receptor-1 gene promoter polymorphisms and susceptibility for brucellosis in Makkah region |
title_fullStr | Interferon-γ receptor-1 gene promoter polymorphisms and susceptibility for brucellosis in Makkah region |
title_full_unstemmed | Interferon-γ receptor-1 gene promoter polymorphisms and susceptibility for brucellosis in Makkah region |
title_short | Interferon-γ receptor-1 gene promoter polymorphisms and susceptibility for brucellosis in Makkah region |
title_sort | interferon-γ receptor-1 gene promoter polymorphisms and susceptibility for brucellosis in makkah region |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6354847/ https://www.ncbi.nlm.nih.gov/pubmed/30766581 http://dx.doi.org/10.4314/ahs.v18i4.36 |
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