Evidence map›Paper›PMID 30558627›Full record

ArticleMalaria journal2018

Characterization of Plasmodium falciparum structure in Nigeria with malaria SNPs barcode.

Bolajoko E Bankole, Adeyemi T Kayode, Iguosadolo O Nosamiefan, Philomena Eromon, Mary L Baniecki, Rachel F Daniels, Elizabeth J Hamilton, Katelyn Durfee, Bronwyn MacInnis, Henrietta Okafor and 6 more

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 22 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 6 institutions in 2 countries.

Bolajoko E BankoleAfrican Centre of Excellence for Genomics of Infectious Diseases, Redeemer's University, Ede, Osun State, Nigeria.
Adeyemi T KayodeAfrican Centre of Excellence for Genomics of Infectious Diseases, Redeemer's University, Ede, Osun State, Nigeria.
Iguosadolo O NosamiefanAfrican Centre of Excellence for Genomics of Infectious Diseases, Redeemer's University, Ede, Osun State, Nigeria.
Philomena EromonAfrican Centre of Excellence for Genomics of Infectious Diseases, Redeemer's University, Ede, Osun State, Nigeria.
Mary L BanieckiBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Rachel F DanielsHarvard T.H. Chan School of Public Health, Boston, MA, USA.
Elizabeth J HamiltonHarvard T.H. Chan School of Public Health, Boston, MA, USA.
Katelyn DurfeeHarvard T.H. Chan School of Public Health, Boston, MA, USA.
Bronwyn MacInnisBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Henrietta OkaforDepartment of Paediatrics, Institute of Child Health, University of Nigeria Teaching Hospital, Enugu, Enugu State, Nigeria.
Akintunde SowunmiDepartment of Pharmacology and Therapeutics, College of Basic Medical Sciences, University of Ibadan, Ibadan, Oyo State, Nigeria.
Sarah K VolkmanBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Pardis SabetiBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Dyann WirthBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Christian T HappiAfrican Centre of Excellence for Genomics of Infectious Diseases, Redeemer's University, Ede, Osun State, Nigeria.
Onikepe A FolarinAfrican Centre of Excellence for Genomics of Infectious Diseases, Redeemer's University, Ede, Osun State, Nigeria. folarino@run.edu.ng.
Redeemer's University · NGHarvard University · USBroad Institute · USSimmons University · USUniversity of Ibadan · NGUniversity of Nigeria Teaching Hospital · NG

Funding

Host and Microbial Genetic Determinants of Febrile Illness in West AfricaU01HG007480 · NHGRI · REDEEMER'S UNIVERSITY · PI HAPPI, CHRISTIAN T. · 2013 to 2016
$1.6M
National Institutes of Health 5U01HG007480-03NHGRI NIH HHS U01 HG007480World Bank Group ACE019
6 · The paper itself

Abstract

backgroundPlasmodium falciparum malaria remains a major health challenge in Nigeria despite the global decline of its incidence and mortality rates. Although significant progress has been made in preventing the transmission of P. falciparum and controlling the spread of the infection, there is much to be done in the area of proper monitoring, surveillance of the parasite, investigating the population dynamics and drug resistance profiling of the parasite as these are important to its eventual eradication. Polymorphic loci of msp1, msp2 and/or glurp genes or microsatellites have been traditionally used to characterize P. falciparum population structure in various parts of Nigeria. The lack of standardization in the interpretation of results, as well as the inability of these methods to distinguish closely related parasites, remains a limitation of these techniques. Conversely, the recently developed 24 single nucleotide polymorphism (SNP)-based molecular barcode assay has the possibility of differentiating between closely related parasites and offer additional information in determining the population diversity of P. falciparum within and between parasite populations. This study is therefore aimed at defining the population diversity of P. falciparum in and between two localities in Nigeria using the SNPs barcode technique.

methodsThe 24-SNP high-resolution melt (HRM) barcode assay and msp2 genotyping was used to investigate both intra and inter population diversity of the parasite population in two urban cities of Nigeria.

resultsBased on SNP barcode analysis, polygenomic malaria infections were observed in 17.9% and 13.5% of population from Enugu and Ibadan, respectively, while msp2 analyses showed 21% and 19.4% polygenomic infections in Enugu and Ibadan, respectively. Low levels of genetic diversity (π) of 0.328 and 0.318 were observed in Enugu and Ibadan parasite populations, respectively, while the F

conclusionsThe 24-SNP barcode assay was effective in analysing P. falciparum population diversity. This study also showed that P. falciparum populations in Enugu and Ibadan had a degree of intra-population diversity, but very low divergence between the population. A low degree of polygenomic infections were also observed in the two parasite populations unlike previous years. This maybe as a result of the effect of artemisinin-based combination therapy (ACT), long-lasting insecticide-treated nets (LLITNs) and intermittent preventive treatments in the study populations.

Indexed as

Polymorphism, Single NucleotideAmino Acid SequenceDNA Barcoding, TaxonomicGenetic VariationNigeriaPlasmodium falciparumPopulation DynamicsBarcodeGenotypeHRMMalariaNigeriaPlasmodium falciparumSNPWest Africa

Identifiers

PMID30558627
PMCPMC6296064
OpenAlexW2905089101

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.