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Multiplex Lateral Flow Assay for Rapid Visual Blood Group Genotyping.
Gomez-Martinez, Julien; Silvy, Monique; Chiaroni, Jacques; Fournier-Wirth, Chantal; Roubinet, Francis; Bailly, Pascal; Brès, Jean-Charles.
Afiliación
  • Gomez-Martinez J; Etablissement Français du Sang Occitanie , F-34184 Montpellier , France.
  • Silvy M; Pathogenesis and Control of Chronic Infections , University of Montpellier, INSERM, EFS , F-34184 Montpellier , France.
  • Chiaroni J; Etablissement Français du Sang PACA Corse , Biologie des Groupes Sanguins , F-13385 Marseille , France.
  • Fournier-Wirth C; University of Aix Marseille, CNRS, EFS, ADES , F-13385 Marseille , France.
  • Roubinet F; Etablissement Français du Sang PACA Corse , Biologie des Groupes Sanguins , F-13385 Marseille , France.
  • Bailly P; University of Aix Marseille, CNRS, EFS, ADES , F-13385 Marseille , France.
  • Brès JC; Etablissement Français du Sang Occitanie , F-34184 Montpellier , France.
Anal Chem ; 90(12): 7502-7509, 2018 06 19.
Article en En | MEDLINE | ID: mdl-29842785
Conventional blood group phenotyping by hemagglutination assays, carried out pretransfusion, is unsuitable in certain clinical situations. Molecular typing offers an alternative method, allowing the deduction of blood group phenotype from genotype. However, current methods require a long turnaround time and are not performed on-site, limiting their application in emergency situations. Here, we report the development of a novel, rapid multiplex molecular method to identify seven alleles in three clinically relevant blood group systems (Kidd, Duffy, and MNS). Our test, using a dry-reagent allele-specific lateral flow biosensor, does not require DNA extraction and allows easy visual determination of blood group genotype. Multiplex linear-after-the-exponential (LATE)-PCR and lateral flow parameters were optimized with a total processing time of 1 h from receiving the blood sample. Our assay had a 100% concordance rate between the deduced and the standard serological phenotype in a sample from 108 blood donors, showing the accuracy of the test. Owing to its simple handling, the assay can be operated by nonskilled health-care professionals. The proposed assay offers the potential for the development of other relevant single nucleotide polymorphism (SNP) panels for immunohematology and new applications, such as for infectious diseases, in the near future.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Antígenos de Grupos Sanguíneos / Técnicas de Genotipaje / Reacción en Cadena de la Polimerasa Multiplex Límite: Humans Idioma: En Revista: Anal Chem Año: 2018 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Antígenos de Grupos Sanguíneos / Técnicas de Genotipaje / Reacción en Cadena de la Polimerasa Multiplex Límite: Humans Idioma: En Revista: Anal Chem Año: 2018 Tipo del documento: Article País de afiliación: Francia