Mur (MNS 10) screening with a novel loop-mediated isothermal amplification assay in Zhongshan, China

ABSTRACT Background The distribution of the Mur blood group antigen is 5–7% in the south of China, and a much higher prevalence is observed in some areas of the region. Anti‐Mur can cause hemolytic disease of the newborn and severe transfusion reactions. Objectives Genetic testing is more ideal than...

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Published inTransfusion medicine (Oxford, England) Vol. 26; no. 3; pp. 215 - 219
Main Authors Wei, S.S., Sun, A.N., Ding, S.H., Meng, Q.L., Wang, H.M., Duan, S.B., Tian, J.J., Chen, Y.Z., Liu, X.M., Li, Y., Liao, Y.T.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.06.2016
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Summary:ABSTRACT Background The distribution of the Mur blood group antigen is 5–7% in the south of China, and a much higher prevalence is observed in some areas of the region. Anti‐Mur can cause hemolytic disease of the newborn and severe transfusion reactions. Objectives Genetic testing is more ideal than conventional serological tests because antibodies for detection are usually not available. Methods In this study, a novel loop‐mediated isothermal amplification (LAMP) assay for the detection of Mur blood group antigen was established. Results Fifteen of 275 (5·5%) samples were confirmed by LAMP as Mur antigen positive. All the Mur antigen‐positive samples were GP.Mur subtype which was confirmed with sequencing. Conclusion The LAMP method has identical results with conventional serology method but more suitable for large‐scale screening.
Bibliography:Medical Instruments and New Medicine Foundation of Suzhou, China - No. ZXY2013017
ArticleID:TME12305
ark:/67375/WNG-VMFCWFDK-N
Natural Science Foundation for Young Scientists of Jiangsu Province, China - No. BK20130343
istex:71E4FBFC4838B716E0BB549C7052309FEDF1A0BD
Postdoctoral Science Foundation of Jiangsu Province, China - No. 1501136B
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0958-7578
1365-3148
DOI:10.1111/tme.12305