Ornuma Pittayabumrung, Chanvit Leelayuwat, Amornrat V Romphruk, Piyapong Simtong
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Therefore, we aimed to develop a single-tube multiplex PCR-sequence specific primer (multiplex PCR-SSP) to detect <i>RHD</i> variant alleles commonly found in serologically D- phenotype individuals in a Thai population.</p><p><strong>Methods: </strong>In total, 205 blood samples with a serologically D- phenotype were tested using a single-tube multiplex PCR-SSP targeted <i>RHD</i> exons 1, 4, 7, 10, and c.1227G>A in <i>RHD</i> exon 9 in combination with a hybrid <i>Rhesus box</i>, and results were confirmed by direct DNA sequencing.</p><p><strong>Results: </strong>In a single-tube multiplex PCR-SSP, three patterns of amplified <i>RHD</i> exons were observed: total deletion of the <i>RHD</i> gene, Asian-type DEL, and <i>RHD-CE-D</i> hybrid. The allele frequencies of <i>RHD*01N.01</i>, <i>RHD*01EL.01</i>, and <i>RHD-CE-D</i> hybrid were 83.4%, 12.9%, and 2%, respectively. All of the Asian-type DEL samples present the <i>RHCE*C/E</i> allele (predicted RhCE phenotype: C/E+).</p><p><strong>Conclusion: </strong>This study successfully established a simple and reliable molecular diagnostic platform for analyzing <i>RHD</i> variant alleles commonly found in serologically D- phenotype individuals in a Thai population. This technique could enable broader <i>RHD*01EL.01</i> (Asian-type DEL) analyses in high-prevalence areas such as Thailand and other countries in East and Southeast Asia, serving as an example for blood bank routine settings.</p>","PeriodicalId":23252,"journal":{"name":"Transfusion Medicine and Hemotherapy","volume":"52 3","pages":"169-177"},"PeriodicalIF":1.9000,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12140609/pdf/","citationCount":"0","resultStr":"{\"title\":\"Single-Tube Multiplex PCR-SSP for the Detection of RHD Variant Alleles Commonly Found in Serologically D- Phenotype Individuals in a Thai Population.\",\"authors\":\"Ornuma Pittayabumrung, Chanvit Leelayuwat, Amornrat V Romphruk, Piyapong Simtong\",\"doi\":\"10.1159/000544107\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>The molecular basis of the <i>RHD</i> gene found in serologically D- phenotype individuals differs with race/ethnicity. Therefore, we aimed to develop a single-tube multiplex PCR-sequence specific primer (multiplex PCR-SSP) to detect <i>RHD</i> variant alleles commonly found in serologically D- phenotype individuals in a Thai population.</p><p><strong>Methods: </strong>In total, 205 blood samples with a serologically D- phenotype were tested using a single-tube multiplex PCR-SSP targeted <i>RHD</i> exons 1, 4, 7, 10, and c.1227G>A in <i>RHD</i> exon 9 in combination with a hybrid <i>Rhesus box</i>, and results were confirmed by direct DNA sequencing.</p><p><strong>Results: </strong>In a single-tube multiplex PCR-SSP, three patterns of amplified <i>RHD</i> exons were observed: total deletion of the <i>RHD</i> gene, Asian-type DEL, and <i>RHD-CE-D</i> hybrid. The allele frequencies of <i>RHD*01N.01</i>, <i>RHD*01EL.01</i>, and <i>RHD-CE-D</i> hybrid were 83.4%, 12.9%, and 2%, respectively. 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引用次数: 0
摘要
在血清学上D-表现型个体中发现的RHD基因的分子基础因种族/民族而异。因此,我们的目标是开发一种单管多重pcr序列特异性引物(多重PCR-SSP)来检测泰国人群中血清学上D-表型个体中常见的RHD变异等位基因。方法:采用单管多重PCR-SSP技术,结合杂交恒河猴箱,针对RHD外显子1、4、7、10和c.1227G> a,检测205份血清学上D-表型的血样,并通过直接DNA测序证实结果。结果:在单管多重PCR-SSP中,观察到RHD基因扩增外显子的三种模式:RHD基因完全缺失、亚洲型DEL和RHD- ce - d杂交。RHD*01N的等位基因频率。01, RHD * 01 el。RHD-CE-D杂种分别为83.4%、12.9%和2%。所有亚洲型DEL样本均存在RHCE*C/E等位基因(预测的RHCE表型为C/E+)。结论:本研究成功建立了一个简单可靠的分子诊断平台,用于分析泰国人群血清学D-表型个体中常见的RHD变异等位基因。该技术可实现更宽的RHD*01EL.01(亚洲型DEL)分析在高流行地区,如泰国和其他东亚和东南亚国家,作为血库常规设置的一个例子。
Single-Tube Multiplex PCR-SSP for the Detection of RHD Variant Alleles Commonly Found in Serologically D- Phenotype Individuals in a Thai Population.
Introduction: The molecular basis of the RHD gene found in serologically D- phenotype individuals differs with race/ethnicity. Therefore, we aimed to develop a single-tube multiplex PCR-sequence specific primer (multiplex PCR-SSP) to detect RHD variant alleles commonly found in serologically D- phenotype individuals in a Thai population.
Methods: In total, 205 blood samples with a serologically D- phenotype were tested using a single-tube multiplex PCR-SSP targeted RHD exons 1, 4, 7, 10, and c.1227G>A in RHD exon 9 in combination with a hybrid Rhesus box, and results were confirmed by direct DNA sequencing.
Results: In a single-tube multiplex PCR-SSP, three patterns of amplified RHD exons were observed: total deletion of the RHD gene, Asian-type DEL, and RHD-CE-D hybrid. The allele frequencies of RHD*01N.01, RHD*01EL.01, and RHD-CE-D hybrid were 83.4%, 12.9%, and 2%, respectively. All of the Asian-type DEL samples present the RHCE*C/E allele (predicted RhCE phenotype: C/E+).
Conclusion: This study successfully established a simple and reliable molecular diagnostic platform for analyzing RHD variant alleles commonly found in serologically D- phenotype individuals in a Thai population. This technique could enable broader RHD*01EL.01 (Asian-type DEL) analyses in high-prevalence areas such as Thailand and other countries in East and Southeast Asia, serving as an example for blood bank routine settings.
期刊介绍:
This journal is devoted to all areas of transfusion medicine. These include the quality and security of blood products, therapy with blood components and plasma derivatives, transfusion-related questions in transplantation, stem cell manipulation, therapeutic and diagnostic problems of homeostasis, immuno-hematological investigations, and legal aspects of the production of blood products as well as hemotherapy. Both comprehensive reviews and primary publications that detail the newest work in transfusion medicine and hemotherapy promote the international exchange of knowledge within these disciplines. Consistent with this goal, continuing clinical education is also specifically addressed.