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Bead-based assays to simultaneously detect multiple human inherited blood disorders associated with malaria

BACKGROUND: Glucose-6-phosphate dehydrogenase deficiency (G6PDd), haemoglobin C (HbC) and S (HbS) are inherited blood disorders (IBD) common in populations in malaria endemic areas. All are associated to some degree with protection against clinical malaria whilst additionally G6PDd is associated wit...

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Autores principales: Grignard, Lynn, Mair, Catherine, Curry, Jonathan, Mahey, Laleta, Bastiaens, Guide J. H., Tiono, Alfred B., Okebe, Joseph, Coulibaly, Sam A., Gonçalves, Bronner P., Affara, Muna, Ouédraogo, Alphonse, Bougouma, Edith C., Sanou, Guillaume S., Nébié, Issa, Lanke, Kjerstin H. W., Sirima, Sodiomon B., d’Alessandro, Umberto, Clark, Taane G., Campino, Susana, Bousema, Teun, Drakeley, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341711/
https://www.ncbi.nlm.nih.gov/pubmed/30665411
http://dx.doi.org/10.1186/s12936-019-2648-7
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author Grignard, Lynn
Mair, Catherine
Curry, Jonathan
Mahey, Laleta
Bastiaens, Guide J. H.
Tiono, Alfred B.
Okebe, Joseph
Coulibaly, Sam A.
Gonçalves, Bronner P.
Affara, Muna
Ouédraogo, Alphonse
Bougouma, Edith C.
Sanou, Guillaume S.
Nébié, Issa
Lanke, Kjerstin H. W.
Sirima, Sodiomon B.
d’Alessandro, Umberto
Clark, Taane G.
Campino, Susana
Bousema, Teun
Drakeley, Chris
author_facet Grignard, Lynn
Mair, Catherine
Curry, Jonathan
Mahey, Laleta
Bastiaens, Guide J. H.
Tiono, Alfred B.
Okebe, Joseph
Coulibaly, Sam A.
Gonçalves, Bronner P.
Affara, Muna
Ouédraogo, Alphonse
Bougouma, Edith C.
Sanou, Guillaume S.
Nébié, Issa
Lanke, Kjerstin H. W.
Sirima, Sodiomon B.
d’Alessandro, Umberto
Clark, Taane G.
Campino, Susana
Bousema, Teun
Drakeley, Chris
author_sort Grignard, Lynn
collection PubMed
description BACKGROUND: Glucose-6-phosphate dehydrogenase deficiency (G6PDd), haemoglobin C (HbC) and S (HbS) are inherited blood disorders (IBD) common in populations in malaria endemic areas. All are associated to some degree with protection against clinical malaria whilst additionally G6PDd is associated with haemolysis following treatment with 8-aminoquinolines. Measuring the prevalence of these inherited blood disorders in affected populations can improve understanding of disease epidemiology. Current methodologies in epidemiological studies commonly rely on individual target amplification and visualization; here a method is presented to simultaneously detect the polymorphisms and that can be expanded to include other single nucleotide polymorphisms (SNPs) of interest. METHODS: Human DNA from whole blood samples was amplified in a novel, multiplex PCR reaction and extended with SNP-specific probes in an allele specific primer extension (ASPE) to simultaneously detect four epidemiologically important human markers including G6PD SNPs (G202A and A376G) and common haemoglobin mutations (HbS and HbC). The products were hybridized to magnetic beads and the median fluorescence intensity (MFI) was read on MAGPIX(®) (Luminex corp.). Genotyping data was compared to phenotypical data generated by flow cytometry and to established genotyping methods. RESULTS: Seventy-five samples from Burkina Faso (n = 75/78, 96.2%) and 58 samples from The Gambia (n = 58/61, 95.1%) had a G6PD and a HBB genotype successfully assigned by the bead-based assay. Flow cytometry data available for n = 61 samples further supported the concordance between % G6PD normal/deficient cells and genotype. CONCLUSIONS: The bead based assay compares well to alternative measures of genotyping and phenotyping for G6PD. The screening is high throughput, adaptable to inclusion of multiple targets of interest and easily standardized. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-019-2648-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-63417112019-01-24 Bead-based assays to simultaneously detect multiple human inherited blood disorders associated with malaria Grignard, Lynn Mair, Catherine Curry, Jonathan Mahey, Laleta Bastiaens, Guide J. H. Tiono, Alfred B. Okebe, Joseph Coulibaly, Sam A. Gonçalves, Bronner P. Affara, Muna Ouédraogo, Alphonse Bougouma, Edith C. Sanou, Guillaume S. Nébié, Issa Lanke, Kjerstin H. W. Sirima, Sodiomon B. d’Alessandro, Umberto Clark, Taane G. Campino, Susana Bousema, Teun Drakeley, Chris Malar J Research BACKGROUND: Glucose-6-phosphate dehydrogenase deficiency (G6PDd), haemoglobin C (HbC) and S (HbS) are inherited blood disorders (IBD) common in populations in malaria endemic areas. All are associated to some degree with protection against clinical malaria whilst additionally G6PDd is associated with haemolysis following treatment with 8-aminoquinolines. Measuring the prevalence of these inherited blood disorders in affected populations can improve understanding of disease epidemiology. Current methodologies in epidemiological studies commonly rely on individual target amplification and visualization; here a method is presented to simultaneously detect the polymorphisms and that can be expanded to include other single nucleotide polymorphisms (SNPs) of interest. METHODS: Human DNA from whole blood samples was amplified in a novel, multiplex PCR reaction and extended with SNP-specific probes in an allele specific primer extension (ASPE) to simultaneously detect four epidemiologically important human markers including G6PD SNPs (G202A and A376G) and common haemoglobin mutations (HbS and HbC). The products were hybridized to magnetic beads and the median fluorescence intensity (MFI) was read on MAGPIX(®) (Luminex corp.). Genotyping data was compared to phenotypical data generated by flow cytometry and to established genotyping methods. RESULTS: Seventy-five samples from Burkina Faso (n = 75/78, 96.2%) and 58 samples from The Gambia (n = 58/61, 95.1%) had a G6PD and a HBB genotype successfully assigned by the bead-based assay. Flow cytometry data available for n = 61 samples further supported the concordance between % G6PD normal/deficient cells and genotype. CONCLUSIONS: The bead based assay compares well to alternative measures of genotyping and phenotyping for G6PD. The screening is high throughput, adaptable to inclusion of multiple targets of interest and easily standardized. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-019-2648-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-21 /pmc/articles/PMC6341711/ /pubmed/30665411 http://dx.doi.org/10.1186/s12936-019-2648-7 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Grignard, Lynn
Mair, Catherine
Curry, Jonathan
Mahey, Laleta
Bastiaens, Guide J. H.
Tiono, Alfred B.
Okebe, Joseph
Coulibaly, Sam A.
Gonçalves, Bronner P.
Affara, Muna
Ouédraogo, Alphonse
Bougouma, Edith C.
Sanou, Guillaume S.
Nébié, Issa
Lanke, Kjerstin H. W.
Sirima, Sodiomon B.
d’Alessandro, Umberto
Clark, Taane G.
Campino, Susana
Bousema, Teun
Drakeley, Chris
Bead-based assays to simultaneously detect multiple human inherited blood disorders associated with malaria
title Bead-based assays to simultaneously detect multiple human inherited blood disorders associated with malaria
title_full Bead-based assays to simultaneously detect multiple human inherited blood disorders associated with malaria
title_fullStr Bead-based assays to simultaneously detect multiple human inherited blood disorders associated with malaria
title_full_unstemmed Bead-based assays to simultaneously detect multiple human inherited blood disorders associated with malaria
title_short Bead-based assays to simultaneously detect multiple human inherited blood disorders associated with malaria
title_sort bead-based assays to simultaneously detect multiple human inherited blood disorders associated with malaria
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341711/
https://www.ncbi.nlm.nih.gov/pubmed/30665411
http://dx.doi.org/10.1186/s12936-019-2648-7
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