Evidence map›Paper›PMID 34538247›Full record

ArticleMalaria journal2021

Population genetic analysis of the Plasmodium falciparum erythrocyte binding antigen-175 (EBA-175) gene in Equatorial Guinea.

Pei-Kui Yang, Xue-Yan Liang, Min Lin, Jiang-Tao Chen, Hui-Ying Huang, Li-Yun Lin, Carlos Salas Ehapo, Urbano Monsuy Eyi, Yu-Zhong Zheng, Dong-De Xie and 5 more

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 7 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

15 authors at 5 institutions in 2 countries.

Pei-Kui Yang *Department of Medical Laboratory, Chaozhou People's Hospital Affiliated to Shantou University Medical College, Chaozhou, Guangdong Province, People's Republic of China.
Xue-Yan Liang *Department of Clinical Laboratory, Huizhou Municipal Central Hospital, Huizhou, People's Republic of China.
Min LinSchool of Life Science and Food Engineering, Hanshan Normal University, Chaozhou, People's Republic of China.
Jiang-Tao ChenDepartment of Clinical Laboratory, Huizhou Municipal Central Hospital, Huizhou, People's Republic of China.
Hui-Ying HuangDepartment of Medical Laboratory, Chaozhou People's Hospital Affiliated to Shantou University Medical College, Chaozhou, Guangdong Province, People's Republic of China.
Li-Yun LinSchool of Life Science and Food Engineering, Hanshan Normal University, Chaozhou, People's Republic of China.
Carlos Salas EhapoDepartment of Medical Laboratory, Malabo Regional Hospital, Malabo, Equatorial Guinea.
Urbano Monsuy EyiDepartment of Medical Laboratory, Malabo Regional Hospital, Malabo, Equatorial Guinea.
Yu-Zhong ZhengSchool of Life Science and Food Engineering, Hanshan Normal University, Chaozhou, People's Republic of China.
Dong-De XieThe Chinese Medical Aid Team to the Republic of Equatorial Guinea, Guangzhou, Guangdong Province, People's Republic of China.
Jin-Quan HeThe Chinese Medical Aid Team to the Republic of Equatorial Guinea, Guangzhou, Guangdong Province, People's Republic of China.
Huan-Tong MoDepartment of Medical Laboratory, Chaozhou People's Hospital Affiliated to Shantou University Medical College, Chaozhou, Guangdong Province, People's Republic of China.
Xin-Yao ChenDepartment of Medical Laboratory, Chaozhou People's Hospital Affiliated to Shantou University Medical College, Chaozhou, Guangdong Province, People's Republic of China.
Xiang-Zhi LiuDepartment of Medical Laboratory, Chaozhou People's Hospital Affiliated to Shantou University Medical College, Chaozhou, Guangdong Province, People's Republic of China. Liu2262218@163.com.
Ying-E WuDepartment of Medical Laboratory, First Affiliated Hospital of Shantou University Medical College, Shantou, Guangdong Province, People's Republic of China. yinge_wu@126.com.
Shantou University · CNHanshan Normal University · CNHuizhou Central People's Hospital · CNNational University of Equatorial Guinea · GQShantou University Medical College · CN

Funding

Applied Basic Research Foundation of Yunnan Province (CN) 2019A1515110981Guangxi Key Research and Development Foundation 2019JJD140052Guangxi Key Research and Development Foundation 2020JJA140656Key scientific research projects of Guangdong Provincial Department of Education 2019GDXK0031Key scientific research projects of Guangdong Provincial Department of Education 2019KTSCX101
6 · The paper itself

Abstract

backgroundPlasmodium falciparum erythrocyte binding antigen-175 (PfEBA-175) is a candidate antigen for a blood-stage malaria vaccine, while various polymorphisms and dimorphism have prevented to development of effective vaccines based on this gene. This study aimed to investigate the dimorphism of PfEBA-175 on both the Bioko Island and continent of Equatorial Guinea, as well as the genetic polymorphism and natural selection of global PfEBA-175.

methodsThe allelic dimorphism of PfEBA-175 region II of 297 bloods samples from Equatorial Guinea in 2018 and 2019 were investigated by nested polymerase chain reaction and sequencing. Polymorphic characteristics and the effect of natural selection were analyzed using MEGA 7.0, DnaSP 6.0 and PopART programs. Protein function prediction of new amino acid mutation sites was performed using PolyPhen-2 and Foldx program.

resultsBoth Bioko Island and Bata district populations, the frequency of the F-fragment was higher than that of the C-fragment of PfEBA-175 gene. The PfEBA-175 of Bioko Island and Bata district isolates showed a high degree of genetic variability and heterogeneity, with π values of 0.00407 & 0.00411 and Hd values of 0.958 & 0.976 for nucleotide diversity, respectively. The values of Tajima's D of PfEBA-175 on Bata district and Bioko Island were 0.56395 and - 0.27018, respectively. Globally, PfEBA-175 isolates from Asia were more diverse than those from Africa and South America, and genetic differentiation quantified by the fixation index between Asian and South American countries populations was significant (FST > 0.15, P < 0.05). A total of 310 global isolates clustered in 92 haplotypes, and only one cluster contained isolates from three continents. The mutations A34T, K109E, D278Y, K301N, L305V and D329N were predicted as probably damaging.

conclusionsThis study demonstrated that the dimorphism of F-fragment PfEBA-175 was remarkably predominant in the study area. The distribution patterns and genetic diversity of PfEBA-175 in Equatorial Guinea isolates were similar another region isolates. And the levels of recombination events suggested that natural selection and intragenic recombination might be the main drivers of genetic diversity in global PfEBA-175. These results have important reference value for the development of blood-stage malaria vaccine based on this antigen.

Indexed as

Polymorphism, GeneticSelection, GeneticAdolescentAdultAgedAntigens, ProtozoanChildChild, PreschoolEquatorial GuineaHumansInfantMalaria, FalciparumMiddle AgedPlasmodium falciparumProtozoan ProteinsYoung AdultAntigens, Protozoanerythrocyte-binding antigen 175, PlasmodiumProtozoan ProteinsBata districtBioko IslandGenetic diversityNatural selectionPfEBA-175Plasmodium falciparum

Identifiers

PMID34538247
PMCPMC8451130
OpenAlexW3157705073

What OpenQuestion holds

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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.