Genotyping for Dombrock blood group alleles in Northern Pakistani blood donors.

Q4 Medicine Immunohematology Pub Date : 2021-09-01 DOI:10.21307/immunohematology-2021-016
S A Jadoon, N Salamat, S A Khan, M S Yazdani, N Khatak, M A Naeem
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Abstract

Abstract Genotyping can be used to identify rare blood group antigens and to solve suspected blood group discrepancies, particularly when serologic methods are limited. Unfortunately, only a few such studies have been performed in Pakistan. The present study was conducted to determine the frequency of Dombrock blood group alleles by genotyping samples from blood donors from the north of Pakistan. Blood samples were taken with consent from 300 blood donors; DNA was extracted and tested for DO*01 and DO*02 alleles by sequence-specific primer polymerase chain reaction (PCR-SSP), followed by gel electrophoresis. Allele frequencies were calculated. The observed and expected genotype frequencies were compared using the χ 2 test. The allele frequencies for DO*01 and DO*02 were 0.40 and 0.60, respectively. Genotype frequencies were in Hardy-Weinberg equilibrium. This study in Pakistani blood donors provides Dombrock blood group allele frequencies by PCR-SSP. This approach is efficient and economical and can be applied in developing countries. The findings can contribute to the development of in-house red blood cell panels, identification of rare blood types, and establishment of a national rare blood donor program.
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巴基斯坦北部献血者Dombrock血型等位基因的基因分型。
基因分型可用于鉴定罕见的血型抗原和解决可疑的血型差异,特别是在血清学方法有限的情况下。不幸的是,在巴基斯坦只进行了几次这样的研究。本研究是通过对来自巴基斯坦北部献血者的样本进行基因分型来确定Dombrock血型等位基因的频率。在征得300名献血者同意的情况下采集血样;提取DNA,采用序列特异性引物聚合酶链反应(PCR-SSP)检测DO*01和DO*02等位基因,并进行凝胶电泳。计算等位基因频率。观察到的基因型频率与预期的基因型频率采用χ2检验进行比较。DO*01和DO*02的等位基因频率分别为0.40和0.60。基因型频率为Hardy-Weinberg平衡。本研究在巴基斯坦献血者中采用PCR-SSP提供了Dombrock血型等位基因频率。这种方法既有效又经济,可以在发展中国家应用。这一发现有助于发展内部红细胞小组,鉴定稀有血型,并建立一个国家稀有血液捐献计划。基因分型可用于鉴定罕见的血型抗原和解决可疑的血型差异,特别是在血清学方法有限的情况下。不幸的是,在巴基斯坦只进行了几次这样的研究。本研究是通过对来自巴基斯坦北部献血者的样本进行基因分型来确定Dombrock血型等位基因的频率。在征得300名献血者同意的情况下采集血样;提取DNA,采用序列特异性引物聚合酶链反应(PCR-SSP)检测DO*01和DO*02等位基因,并进行凝胶电泳。计算等位基因频率。观察到的基因型频率与预期的基因型频率采用χ2检验进行比较。DO*01和DO*02的等位基因频率分别为0.40和0.60。基因型频率为Hardy-Weinberg平衡。本研究在巴基斯坦献血者中采用PCR-SSP提供了Dombrock血型等位基因频率。这种方法既有效又经济,可以在发展中国家应用。这一发现有助于发展内部红细胞小组,鉴定稀有血型,并建立一个国家稀有血液捐献计划。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Immunohematology
Immunohematology Medicine-Medicine (all)
CiteScore
1.30
自引率
0.00%
发文量
18
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