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HLA Class II (DRB1 and DQB1) Polymorphism in Omanis | OMICS International
ISSN: 2161-0991
Journal of Transplantation Technologies & Research

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HLA Class II (DRB1 and DQB1) Polymorphism in Omanis

Khalid Rashid Albalushi1,2, Mohamed Hichem Sellami3*, Hamad AlRiyami2, Mathew Varghese2, Mohamed Kamel Boukef1 and Slama Hmida1,3

1Faculty of Pharmacy, University of Monastir, Tunisia

2Department of Genetics, Sultan Qaboos University. Tunisia

3Department of Immunohaematology, National Blood Transfusion Centre of Tunis, Tunisia

*Corresponding Author:
Mohamed Hichem Sellami
Department of Immuno-Haematology
The National Blood Transfusion Centre of Tunis
13 Rue Djbel Lakhdar-Bab Saadoun 1006
Tunis-Tunisia
Tel: +216 71.561.920, +216 71.573.884
Fax: + 216 71.562.957
E-mail: [email protected]

Received Date: Jun 13, 2014,Accepted Date: July 25, 2014; Published Date: July 27, 2014

Citation: Albalushi KR, Sellami MH, AlRiyami H, Varghese M, Boukef MK, et al. (2014) HLA Class II (DRB1 and DQB1) Polymorphism in Omanis. J Transplant Technol Res 4: 134. doi: 10.4172/2161-0991.1000134

Copyright: © 2014 Albalushi KR, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Abstract

The HLA class II polymorphism of 254 healthy unrelated Omanis was analyzed by PCR-SSP method, and the detected frequencies were compared to those reported in 20 other populations. The most frequent HLA class II DRB1 alleles were DRB1*16, DRB1*03 and DRB1*15 with frequencies of 0.315, 0.224 and 0.106 respectively, while the most frequent DQB1 alleles were DQB1*05 and DQB1*02 with frequencies of 0.366 and 0.283 respectively. The haplotype analysis revealed that DRB1*03-DQB1*02 was the most common HLA class II haplotype with linkage disequilibrium (a frequency of 0.206). Compared with other populations, our result, deduced from the analysis of genetic distances and the construction of neighbour joining dendrogram, indicates that Omanis are related to Mediterranean and West-Asian populations. This fact might be explained by several historic and socio-geographic factors if we consider on the long history of this population.

Keywords

HLA class II; Linkage disequilibrium; Polymorphism; Omanis

Introduction

The HLA system is the most polymorphic genetic system described in humans and consists of several closely linked loci [1-4]. All HLA loci map to the short arm of chromosome 6 (6.p21) and were classified in two major HLA classes: class I (A, -B, -C, -E, -F, -G and -H) and class II (DRA, -DRB, -DQA1, -DQB1, -DPA1, -DPB1, -DMA, -DMB, -DOA and -DOB) [1,5]. Others non-HLA genes and pseudogenes have been also reported of which some loci were grouped in a third HLA class (HLA class III) [1]. More than 9,000 alleles characterising HLA polymorphism have been documented in the IMGT/HLA database (release 3.9.0) of which 1,122 alleles (14.3%) were described in the most recent common and well-documented HLA alleles catalogue [6]. The high degree of polymorphism of the HLA system has proved a useful tool in tracing the migration of ancient human populations as well as studying the ethnic composition of the present day populations [7,8]. Thus, it had been reported that some HLA alleles and haplotypes are frequent only in specific populations due to several social and historic factors [9].

Oman is an Arabic country occupying the south eastern corner of the Arabian Peninsula. The History of Oman is very rich due to its strategic position on the borders of the Indian Ocean area and the Arabian Gulf. As reported by Paul Lunde in “Oman: A history”, the coast of Oman was occupied by Persians early in its history [10]. The Persian control was extended for 10 centuries until the arrival of Islam (from 3rd century BC to 7th century AD) and exerted by two other Iranian dynasties, the Parthians and the Sassanids. Oman territories have also experienced the arrival of tribes from Marib (Yemen) during the pre-Islamic time in a strategy to control the lucrative incense trade [11]. With the advent of Islam, the Omani population was enriched with other tribes [10]. Thus, it is clear that Omanis were in regular contact with other ethnic groups during all ages and that this has led to the genetic heterogeneity of this population.

Studying HLA polymorphism in various populations can enrich the international HLA database which is very useful in clinical practices and in anthropological studies [5]. Thus, we decided to conduct this basic genetic study in order to investigate the HLA class II system polymorphism in Omani population which is an Arabic population occupying the south eastern corner of the Arabian Peninsula.

To date, few studies investigating the HLA polymorphism in Omanis have been published [12-14]. Here we present a study of HLA Class II polymorphism of Omanis using a molecular approach.

Materials and Methods

Informed consent was obtained from all participants, and approval was obtained from the ethical committee for scientific and medical research of the College of Medicine and Health Sciences at Sultan Qaboos University (Sultanate of Oman) for performing this study.

Study subjects: A total of 254 healthy and unrelated normal blood donors (149 men and 105 women) were randomly selected from the Omani population (from all regions of the Sultanate) to perform this study. The origin of the other populations used for the interethnic comparison is detailed in (Table 1) [15].

Population Sample size
Omanis-currentstudy 254
Iran.Azeri  100
Iran.Baloch  100
Iran.Kurd  100
Ashkenazi.Jews.pop2  132
Gaza.Palestinian  165
Iranian.Jews  101
Lebanon.pop.2  191
India.Uttar.Pradesh  202
Algeria.pop.2  106
Ethiopia.Amhara  98
Ethiopia.Oromo  83
Morocco  96
Tunisia.Jerba.Berber  55
Tunisia.Matmata.Berber  81
Tunisia.pop.3  104
Turkey.pop.2 228
Bangladesh.Dhaka.Bangalee 141
Pakistan.Baloch 66
Pakistan.Brahui 104
Pakistan.Karachi.Parsi 91

Table 1: Populations used for measurement of genetic distances [15].

Molecular HLA class II typing: HLA-DRB1 and -DQB1 molecular genotyping was carried out using the PCR-SSP method according to manufacturer’s specifications (Dynal Allset Gold SSP, Life Technologies Corp).

Statistical analysis: HLA-DRB1/DQB1 allele and haplotype frequencies; Hardy-Weinberg equilibrium for each locus; and relative linkage disequilibrium (D’) between these loci were calculated by applying the expectation-maximization (EM) algorithm (Arlequin program V3.5.12) [16]. Standard deviations (SD), for both alleles and haplotypes frequencies (HF), were obtained by a bootstrap procedure [16].

Omani HLA-DRB1 and -DQB1 allele frequencies were compared with other Mediterranean and Asian population’s frequencies in order to investigate the relatedness between these populations. In this analysis, we used only HLA-DRB1 allele frequencies because some of the populations used lacked some HLA-DQB1 data. Phylogenetic tree (dendrogram) was constructed with allele frequencies by applying the Neighbor-Joining (NJ) method with the standard genetic distances (SGD) [17,18], using the Dispan software which contains the GNKDST and TREEVIEW application [19,20].

Results

Hardy-Weinberg test analysis showed that all alleles at the DRB1 and DQB1 loci are in equilibrium (p values are, respectively, 0.27 and 0.13).

HLA class II allele frequencies: The allele analysis showed the presence of 11 variants at the HLA-DRB1 locus of which DRB1*16 and DRB1*03 were the most frequent in Omanis (Table 2). Except the DRB1*03 allele which is frequent in all populations, DRB1*16 variant is a common allele among the Southeast Asian peoples such as in Malaysia (28%), Papua New guinea (28%) and Vietnam (19.2%) and in South American peoples such as in Brazil (37%), Colombia (38%), Mexico (30.9%) [15]. The third frequent HLA-DRB1 allele in Omanis was the DRB1*15 which is a common allele between several ethnic groups [15].

DRB1 locus No. subjects with allele Allele frequency S.D.1 DQB1 locus No. subjects with allele Allele frequency S.D.
DRB1*01 2 0.004 0.003 DQB1*02 138 0.283 0.019
DRB1*03 112 0.224 0.018 DQB1*03 78 0.163 0.015
DRB1*04 47 0.096 0.013 DQB1*04 13 0.026 0.007
DRB1*07 34 0.067 0.011 DQB1*05 164 0.366 0.021
DRB1*09 2 0.004 0.003 DQB1*06 76 0.161 0.016
DRB1*11 40 0.083 0.012        
DRB1*12 5 0.01 0.004        
DRB1*13 32 0.063 0.011        
DRB1*14 14 0.028 0.007        
DRB1*15 52 0.106 0.013        
DRB1*16 148 0.315 0.021        

Table 2: HLA-DRB1 and –DQB1 allele frequencies in the Omani population

For the HLA-DQB1 locus, 5 alleles were detected in which DQB1*05 and DQB1*02 are the most frequent alleles in Omanis (Table 2). HLA-DQB1*05 is a relatively frequent allele in some Southeast Asian peoples, e.g. Malaysia “pop 2” (37.1%) and in Pakistan “Baloch” (34%) whereas a very lower frequency of this allele was reported in several Amerindian peoples, e.g. Mexico, Brazil, Argentina [15]. In contrast to DQB1*05, the HLA-DQB1*02 is a common allele in several populations although it was detected with high frequency in some Mediterranean populations, e.g. in Spain « Arratia Valley Basque » (48%), Israel « Libyan Jews » (33.3%), Morocco « pop 2 » (30.6%), France « Rennes pop 3 » (24%) and Turkey « pop 2 » (23.8%) [15].

The phylogenetic analysis showed that Omanis are closer to West-Asian and Mediterranean peoples (Figure 1) than to others populations, which was more evident in (Table 3), reporting SGD between the selected populations.

transplantation-technologies-research-dendrogram-omanis-genetic

Figure 1: Neighbour-joining dendrogram showing relatedness between Omanis and some neighbouring populations. Standard genetic distances (SGD) were calculated by using HLA-DRB1 allele frequencies. Data from other populations were taken from references detailed in (Table 1). Bootstrap values from 1000 replicates are shown.

Population HLA-DRB1 (SGD)
Pakistan.Brahui 0.158
Pakistan.Baloch 0.233
Tunisia.pop3 0.328
Iran.Baloch 0.384
Iran.Kurd 0.424
Algeria.pop2 0.467
Iran.Azeri 0.52
Tunisia.Matmata.Berber 0.569
Gaza.Palestinian 0.574
Morocco 0.618
Ashkenazi.Jews.pop2 0.629
Lebanon.pop2 0.656
Ethiopia.Oromo 0.671
India.Uttar.Pradesh 0.676
Turkey.pop2 0.68
Pakistan.Karachi.Parsi 0.751
Bangladesh.Dhaka.Bangalee 0.805
Ethiopia.Amhara 0.805
Tunisia.Jerba.Berber 0.848
Iranian.Jews 0.885

Table 3: Standard genetic distances (SGD) between Omanis and 20 other populations.

HLA-DRB1-DQB1 haplotype frequencies and linkage disequilibria: The most dominant HLA-DRB1_DQB1 haplotypes in Omanis are DRB1*16_DQB1*05 (HF 31.3%, D’ 0.03, p>0.023) and DRB1*03_DQB1*02 (20.6%), but the most dominant HLA-DRB1_DQB1 haplotype with linkage disequilibrium is the DRB1*03_DQB1*02 (Table 4). At this level, it should be mentioned that HLA-DRB1*16_DQB1*05 is found in 27.3% of Papua New Guinean peoples and in 15% of Pakistani “Brahui”; and HLA-DRB1*03_DQB1*02 is found in some Mediterranean peoples such as in Tunisians “Gabes” (15%), Israel “Arabs “ (9.6%) and Moroccans “pop 2” (9.3%) [15].

Haplotype No. subjects with haplotype Frequency S.D.1 D’ value p value for significance of D’
DRB1*16-DQB1*05 158 0.313 0.02 0.093 0.023
DRB1*03-DQB1*02 104 0.206 0.018 0.228 0.01
DRB1*15-DQB1*06 46 0.09 0.013 0.106 0.044
DRB1*04-DQB1*03 39 0.077 0.012 0.037 0.006
DRB1*11-DQB1*03 35 0.071 0.012 0.01 0.035
DRB1*07-DQB1*02 31 0.064 0.011 0.051 0.018
DRB1*13-DQB1*06 28 0.055 0.011 0.003 0.009
DRB1*14-DQB1*05 13 0.026 0.007 0.009 0.083
DRB1*03-DQB1*04 8 0.016 0.006 0.091 0.011
DRB1*15-DQB1*05 8 0.016 0.005 0.107 0.029
DRB1*11-DQB1*06 5 0.012 0.005 0.007 0.047
DRB1*04-DQB1*02 5 0.01 0.005 0.008 0.055
DRB1*04-DQB1*04 5 0.01 0.005 0.008 0.039

Table 4: HLA-DRB1-DQB1 haplotype frequencies and linkage disequilibrium values (D’) in the Omani population.

Discussion

The HLA class II allele analysis showed that the frequent HLA-DRB1 variants in Omanis, (Table 1) are those that are common in some Southeast Asian and Mediterranean populations especially the HLA-DRB1*16, -DRB1*15 and -DRB1*03 variants [2gfgf1-24]. The same findings were also observed when analysing the HLA-DQB1 locus [22-25]. Thus, it seems likely that there is an HLA allele admixture between Omanis and Mediterranean-West Asian peoples. This finding was supported when analysing HLA class II haplotypes. We revealed that the predominant haplotypes, with significant linkage disequilibrium, in Omanis, e.g. HLA-DRB1*03-DQB1*02 is also predominant in some Mediterranean peoples such as Tunisians, Israel “Arabs” and Moroccans [22,26,27]. Accordingly, we believe that these findings provide some evidence that Omanis are close to Mediterranean and West-Asian populations. This proposal might be explained by several historic and socio-geographic factors if we consider the long history of this region [10].

The possible relatedness of Omanis to Mediterranean and West-Asian populations is not surprising in view of the above cited reasons. Any genetic overlapping between Omanis and West-Asian peoples is likely to be correlated with interethnic marriages during the Persian domination of the coast of Oman early in history. The same theory may also be valid to explain the relatedness of Omanis to Mediterranean peoples and we think that some Mediterranean groups who came to Oman for trade were finally settled down in the region [10]. This possibility may be reinforced by the importance of Oman territories as an ancient economic and military area. In fact, Oman is located in a strategic region that links the ancient Fertile Crescent or “The Cradle of Civilization” to the Indian Ocean area and it is in the same time a very appropriate location to control sea incense trade routes between the Arabian Gulf, Gulf of Oman and Indian Ocean [11]. So, it is quite normal to be colonized by major forces such as Persians followed by tribes of Marib, Portuguese and Ottomans that leaded to an admixture of the Omani’s genetic patrimony.

This work will help to further investigate the relatedness between Omanis and others middle east populations. Furthermore, such studies will be helpful in making an Arabic HLA allele frequency database that would prove useful in clinical practices especially in bone marrow and solid organ transplantation.

Acknowledgment

We thank all technicians from the Genetics Department at the College of Medicine and Health Sciences (Sultan Qaboos University, Sultanate of Oman) and from the National Blood Transfusion Centre of Tunis (Tunisia) for their valuable technical assistance.

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