Shihang Zhou1,2, Ming Liu3, Wanxin An2, Xiaohua Liang2, Weijian Yu2, Fengyuan Piao1. 1. Department of Occupational and Environmental Health, Dalian Medical University, Dalian, China. 2. Dalian Blood Center, Dalian, China. 3. Department of Cell Biology, Dalian Medical University, Dalian, China.
Abstract
BACKGROUND: Duffy blood group genotyping is useful to ensure transfusion safety and determine the association of Duffy blood group polymorphism with diseases, and therefore has its clinical significance. In order to improve the existing methods for genotyping of Duffy blood group, which normally require post-PCR manipulation, a new method was developed by using 5'-nuclease assay (NA) with TaqMan minor groove binding (MGB) probes. METHODS: Primers and TaqMan-MGB probes were designed and synthesized to genotype FY*A and FY*B alleles at Duffy blood group locus on a real-time PCR platform. A total of 120 samples were genotyped by using the new 5'-NA and conventional polymerase chain reaction with allele-specific primers (PCR-ASP). The results obtained by the two methods were compared. RESULTS: There was a complete concordance of results for all samples genotyped by 5'-NA and PCR-ASP. The retesting results of 5'-NA were consistent with those of the initial testing. The detection limit of 5'-NA was determined as 100 pg per reaction. The FY*A and FY*B allelic frequencies were 93.3% and 6.7% respectively in the Chinese Han population in Dalian. CONCLUSIONS: The 5'-NA for genotyping of Duffy blood group is simple, rapid, reliable, reproducible, sensitive, and high-throughput and is superior to PCR-ASP used in routine genotyping.
BACKGROUND: Duffy blood group genotyping is useful to ensure transfusion safety and determine the association of Duffy blood group polymorphism with diseases, and therefore has its clinical significance. In order to improve the existing methods for genotyping of Duffy blood group, which normally require post-PCR manipulation, a new method was developed by using 5'-nuclease assay (NA) with TaqMan minor groove binding (MGB) probes. METHODS: Primers and TaqMan-MGB probes were designed and synthesized to genotype FY*A and FY*B alleles at Duffy blood group locus on a real-time PCR platform. A total of 120 samples were genotyped by using the new 5'-NA and conventional polymerase chain reaction with allele-specific primers (PCR-ASP). The results obtained by the two methods were compared. RESULTS: There was a complete concordance of results for all samples genotyped by 5'-NA and PCR-ASP. The retesting results of 5'-NA were consistent with those of the initial testing. The detection limit of 5'-NA was determined as 100 pg per reaction. The FY*A and FY*B allelic frequencies were 93.3% and 6.7% respectively in the Chinese Han population in Dalian. CONCLUSIONS: The 5'-NA for genotyping of Duffy blood group is simple, rapid, reliable, reproducible, sensitive, and high-throughput and is superior to PCR-ASP used in routine genotyping.
Authors: Poonsub Palacajornsuk; Christine Halter; Victoria Isakova; Michal Tarnawski; James Farmar; Marion E Reid; Asok Chaudhuri Journal: Transfusion Date: 2009-01-02 Impact factor: 3.157
Authors: Rosalind E Howes; Anand P Patil; Frédéric B Piel; Oscar A Nyangiri; Caroline W Kabaria; Peter W Gething; Peter A Zimmerman; Céline Barnadas; Cynthia M Beall; Amha Gebremedhin; Didier Ménard; Thomas N Williams; David J Weatherall; Simon I Hay Journal: Nat Commun Date: 2011 Impact factor: 14.919