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High frequency of the Duffy-negative genotype and absence of Plasmodium vivax infections in Ghana

BACKGROUND: Recent studies from different malaria-endemic regions including western Africa have now shown that Plasmodium vivax can infect red blood cells (RBCs) and cause clinical disease in Duffy-negative people, though the Duffy-negative phenotype was thought to confer complete refractoriness aga...

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Autores principales: Brown, Charles A., Pappoe-Ashong, Prince J., Duah, Nancy, Ghansah, Anita, Asmah, Harry, Afari, Edwin, Koram, Kwadwo A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7888148/
https://www.ncbi.nlm.nih.gov/pubmed/33596926
http://dx.doi.org/10.1186/s12936-021-03618-0
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author Brown, Charles A.
Pappoe-Ashong, Prince J.
Duah, Nancy
Ghansah, Anita
Asmah, Harry
Afari, Edwin
Koram, Kwadwo A.
author_facet Brown, Charles A.
Pappoe-Ashong, Prince J.
Duah, Nancy
Ghansah, Anita
Asmah, Harry
Afari, Edwin
Koram, Kwadwo A.
author_sort Brown, Charles A.
collection PubMed
description BACKGROUND: Recent studies from different malaria-endemic regions including western Africa have now shown that Plasmodium vivax can infect red blood cells (RBCs) and cause clinical disease in Duffy-negative people, though the Duffy-negative phenotype was thought to confer complete refractoriness against blood invasion with P. vivax. The actual prevalence of P. vivax in local populations in Ghana is unknown and little information is available about the distribution of Duffy genotypes. The aim of this study was to assess the prevalence of P. vivax in both asymptomatic and symptomatic outpatients and the distribution of Duffy genotypes in Ghana. METHODS: DNA was extracted from dried blood spots (DBS) collected from 952 subjects (845 malaria patients and 107 asymptomatic persons) from nine locations in Ghana. Plasmodium species identification was carried out by nested polymerase chain reaction (PCR) amplification of the small-subunit (SSU) rRNA genes. For P. vivax detection, a second PCR of the central region of the Pvcsp gene was carried out. Duffy blood group genotyping was performed by allele-specific PCR to detect the presence of the FY(ES) allele. RESULTS: No cases of P. vivax were detected in any of the samples by both PCR methods used. Majority of infections (542, 94.8%) in the malaria patient samples were due to P. falciparum with only 1 infection (0.0017%) due to Plasmodium malariae, and 2 infections (0.0034%) due to Plasmodium ovale. No case of mixed infection was identified. Of the samples tested for the FY(ES) allele from all the sites, 90.5% (862/952) had the FY(ES) allele. All positive samples were genotyped as FY*B-33/FY*B-33 (Duffy-negative homozygous) and therefore classified as Fy(a−b−). CONCLUSIONS: No cases of P. vivax were detected by both PCRs and majority of the subjects tested carried the FY(ES) allele. The lack of P. vivax infections observed can be attributed to the high frequency of the FY(ES) allele that silences erythroid expression of the Duffy. These results provide insights on the host susceptibility for P. vivax infections that had not been investigated in Ghana before.
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spelling pubmed-78881482021-02-22 High frequency of the Duffy-negative genotype and absence of Plasmodium vivax infections in Ghana Brown, Charles A. Pappoe-Ashong, Prince J. Duah, Nancy Ghansah, Anita Asmah, Harry Afari, Edwin Koram, Kwadwo A. Malar J Research BACKGROUND: Recent studies from different malaria-endemic regions including western Africa have now shown that Plasmodium vivax can infect red blood cells (RBCs) and cause clinical disease in Duffy-negative people, though the Duffy-negative phenotype was thought to confer complete refractoriness against blood invasion with P. vivax. The actual prevalence of P. vivax in local populations in Ghana is unknown and little information is available about the distribution of Duffy genotypes. The aim of this study was to assess the prevalence of P. vivax in both asymptomatic and symptomatic outpatients and the distribution of Duffy genotypes in Ghana. METHODS: DNA was extracted from dried blood spots (DBS) collected from 952 subjects (845 malaria patients and 107 asymptomatic persons) from nine locations in Ghana. Plasmodium species identification was carried out by nested polymerase chain reaction (PCR) amplification of the small-subunit (SSU) rRNA genes. For P. vivax detection, a second PCR of the central region of the Pvcsp gene was carried out. Duffy blood group genotyping was performed by allele-specific PCR to detect the presence of the FY(ES) allele. RESULTS: No cases of P. vivax were detected in any of the samples by both PCR methods used. Majority of infections (542, 94.8%) in the malaria patient samples were due to P. falciparum with only 1 infection (0.0017%) due to Plasmodium malariae, and 2 infections (0.0034%) due to Plasmodium ovale. No case of mixed infection was identified. Of the samples tested for the FY(ES) allele from all the sites, 90.5% (862/952) had the FY(ES) allele. All positive samples were genotyped as FY*B-33/FY*B-33 (Duffy-negative homozygous) and therefore classified as Fy(a−b−). CONCLUSIONS: No cases of P. vivax were detected by both PCRs and majority of the subjects tested carried the FY(ES) allele. The lack of P. vivax infections observed can be attributed to the high frequency of the FY(ES) allele that silences erythroid expression of the Duffy. These results provide insights on the host susceptibility for P. vivax infections that had not been investigated in Ghana before. BioMed Central 2021-02-17 /pmc/articles/PMC7888148/ /pubmed/33596926 http://dx.doi.org/10.1186/s12936-021-03618-0 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research
Brown, Charles A.
Pappoe-Ashong, Prince J.
Duah, Nancy
Ghansah, Anita
Asmah, Harry
Afari, Edwin
Koram, Kwadwo A.
High frequency of the Duffy-negative genotype and absence of Plasmodium vivax infections in Ghana
title High frequency of the Duffy-negative genotype and absence of Plasmodium vivax infections in Ghana
title_full High frequency of the Duffy-negative genotype and absence of Plasmodium vivax infections in Ghana
title_fullStr High frequency of the Duffy-negative genotype and absence of Plasmodium vivax infections in Ghana
title_full_unstemmed High frequency of the Duffy-negative genotype and absence of Plasmodium vivax infections in Ghana
title_short High frequency of the Duffy-negative genotype and absence of Plasmodium vivax infections in Ghana
title_sort high frequency of the duffy-negative genotype and absence of plasmodium vivax infections in ghana
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7888148/
https://www.ncbi.nlm.nih.gov/pubmed/33596926
http://dx.doi.org/10.1186/s12936-021-03618-0
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