Association of FCγRIIA (CD32) polymorphism with susceptibility to brucellosis

Background: Brucellosis is the major bacterial zoonoses of global importance caused by Brucella spps. FCγRIIA receptor plays a central role in phagocytosis of IgG2-opsonized bacteria. FCγRIIA exhibits allelic polymorphisms with different capacities for binding IgG2 and phagocytosis. Cells expressing...

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Main Authors: Zahra Hosseini khah, Zohreh Bahadori, Alireza Rafiei, Mehrdad Hajilooi
Format: Article
Language:English
Published: Mazandaran University of Medical Sciences and Health Services 2014-08-01
Series:Research in Molecular Medicine
Subjects:
Online Access:http://rmm.mazums.ac.ir/browse.php?a_code=A-10-25-3&slc_lang=en&sid=1
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author Zahra Hosseini khah
Zohreh Bahadori
Alireza Rafiei
Mehrdad Hajilooi
author_facet Zahra Hosseini khah
Zohreh Bahadori
Alireza Rafiei
Mehrdad Hajilooi
author_sort Zahra Hosseini khah
collection DOAJ
description Background: Brucellosis is the major bacterial zoonoses of global importance caused by Brucella spps. FCγRIIA receptor plays a central role in phagocytosis of IgG2-opsonized bacteria. FCγRIIA exhibits allelic polymorphisms with different capacities for binding IgG2 and phagocytosis. Cells expressing Fc γ RIIa-H131, bind more efficiently to complexes of IgG2 than those expressing the Fc γ RII A -R131 variant. The purpose of this study was to evaluate the association of FCγRIIA polymorphisms with susceptibility to or severity of brucellosis. Materials and Methods: In this study, we evaluated FCγRIIA polymorphisms (R/R131, R/H131, H/H131) in 67 patients with brucellosis and 67 age, sex and geographical matched healthy volunteers. FCγRIIA genotyping was performed by using a sequence-specific primer polymerase chain reaction (SSP-PCR). Results: The comparison of the FCγRIIA genotypes distribution in patients with brucellosis and controls showed a higher frequency in FCγRIIA-R/R131 homozygosity in patients than controls (47.8% vs. 28.4%). Logistic regression analysis showed that there is a significant correlation between R/R131 genotype and brucellosis (OR=2.3, 95%CI=1.3-4.2, P=0.04). Although the frequency of the FCγRIIA-R/R131 was higher in patients with chronic brucellosis compared with acute brucellosis, we did not find any statistically significant differences (53.8% vs. 46.3%, P=0.65). Conclusion: The result of this study showed that the homozygous genotype of FCγRIIA-R/R131 in patients with brucellosis may be associated with susceptibility to brucellosis as a genetic risk factor.
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spelling doaj.art-c27b05d5cf834c5aa4a8d41e2486c2952022-12-22T00:08:31ZengMazandaran University of Medical Sciences and Health ServicesResearch in Molecular Medicine2322-13482322-133X2014-08-01231723Association of FCγRIIA (CD32) polymorphism with susceptibility to brucellosisZahra Hosseini khah0Zohreh Bahadori1Alireza Rafiei2Mehrdad Hajilooi3 1Molecular and Cell Biology Research Center, Mazandaran University of Medical Sciences, Mazandaran, Iran 2Department of Microbiology, Faculty of Basic Sciences, Islamic Azad University, Tehran, Iran 1Molecular and Cell Biology Research Center, Mazandaran University of Medical Sciences, Mazandaran, Iran 3Department of Immunology, Faculty of Medicine, Hamedan University of Medical Sciences, Hamedan, Iran Background: Brucellosis is the major bacterial zoonoses of global importance caused by Brucella spps. FCγRIIA receptor plays a central role in phagocytosis of IgG2-opsonized bacteria. FCγRIIA exhibits allelic polymorphisms with different capacities for binding IgG2 and phagocytosis. Cells expressing Fc γ RIIa-H131, bind more efficiently to complexes of IgG2 than those expressing the Fc γ RII A -R131 variant. The purpose of this study was to evaluate the association of FCγRIIA polymorphisms with susceptibility to or severity of brucellosis. Materials and Methods: In this study, we evaluated FCγRIIA polymorphisms (R/R131, R/H131, H/H131) in 67 patients with brucellosis and 67 age, sex and geographical matched healthy volunteers. FCγRIIA genotyping was performed by using a sequence-specific primer polymerase chain reaction (SSP-PCR). Results: The comparison of the FCγRIIA genotypes distribution in patients with brucellosis and controls showed a higher frequency in FCγRIIA-R/R131 homozygosity in patients than controls (47.8% vs. 28.4%). Logistic regression analysis showed that there is a significant correlation between R/R131 genotype and brucellosis (OR=2.3, 95%CI=1.3-4.2, P=0.04). Although the frequency of the FCγRIIA-R/R131 was higher in patients with chronic brucellosis compared with acute brucellosis, we did not find any statistically significant differences (53.8% vs. 46.3%, P=0.65). Conclusion: The result of this study showed that the homozygous genotype of FCγRIIA-R/R131 in patients with brucellosis may be associated with susceptibility to brucellosis as a genetic risk factor.http://rmm.mazums.ac.ir/browse.php?a_code=A-10-25-3&slc_lang=en&sid=1Brucellosis FCγRIIA Polymorphism
spellingShingle Zahra Hosseini khah
Zohreh Bahadori
Alireza Rafiei
Mehrdad Hajilooi
Association of FCγRIIA (CD32) polymorphism with susceptibility to brucellosis
Research in Molecular Medicine
Brucellosis
FCγRIIA
Polymorphism
title Association of FCγRIIA (CD32) polymorphism with susceptibility to brucellosis
title_full Association of FCγRIIA (CD32) polymorphism with susceptibility to brucellosis
title_fullStr Association of FCγRIIA (CD32) polymorphism with susceptibility to brucellosis
title_full_unstemmed Association of FCγRIIA (CD32) polymorphism with susceptibility to brucellosis
title_short Association of FCγRIIA (CD32) polymorphism with susceptibility to brucellosis
title_sort association of fcγriia cd32 polymorphism with susceptibility to brucellosis
topic Brucellosis
FCγRIIA
Polymorphism
url http://rmm.mazums.ac.ir/browse.php?a_code=A-10-25-3&slc_lang=en&sid=1
work_keys_str_mv AT zahrahosseinikhah associationoffcgriiacd32polymorphismwithsusceptibilitytobrucellosis
AT zohrehbahadori associationoffcgriiacd32polymorphismwithsusceptibilitytobrucellosis
AT alirezarafiei associationoffcgriiacd32polymorphismwithsusceptibilitytobrucellosis
AT mehrdadhajilooi associationoffcgriiacd32polymorphismwithsusceptibilitytobrucellosis