{"title":"间日疟原虫Duffy结合蛋白拷贝数变异和Duffy基因型的空间分布及其与埃塞俄比亚寄生虫病的关系","authors":"Yasin Nasir, Eshetu Molla, Getnet Habtamu, Solomon Sisay, Legesse Alamerie Ejigu, Fikregabrail Aberra Kassa, Mulugeta Demisse, Wakweya Chali, Melat Abdo, Dawit Hailu Alemayehu, Lina Alemayehu, Alemayehu Letebo, Tadele Emiru, Jimma Dinsa Deressa, Tajudin Abdurhaman Hamza, Abel Beliyu Tamirat, Tadesse Misganaw, Alayu Bogale, Zufan Yiheyis Abriham, Sisay Dugassa, Migbaru Keffale, Fekadu Massebo, Hassen Mamo, Endalamaw Gadisa, Chris Drakeley, Alemayehu Godana Birhanu, Cristian Koepfli, Fitsum G Tadesse","doi":"10.1371/journal.pntd.0012837","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Duffy Binding Protein (PvDBP) binding to the Duffy antigen receptor for chemokine (DARC) is essential for Plasmodium vivax invasion of human reticulocytes. PvDBP copy number variation (CNV) might increase parasite invasion and thus parasitemia. We examined the spatial distribution of PvDBP CNVs and DARC genotypes and their association with parasitemia in P. vivax endemic settings in Ethiopia.</p><p><strong>Methodology/principal findings: </strong>P. vivax isolates (n = 435) collected from five P. vivax endemic settings in Ethiopia were genotyped by amplifying the GATA1 transcription factor-binding site of the Duffy blood group and the CNV of PvDBP was quantified. Parasitemia was determined using 18S-based qPCR. The majority of participants were Duffy positive (96.8%, 421/435). Of the few Duffy negative individuals, most (n = 8) were detected from one site (Gondar). Multiple copies of PvDBP were detected in 83% (363/435) isolates with significant differences between sites (range 60%-94%). Both heterozygous (p = 0.005) and homozygous (p = 0.006) patients were more likely to have been infected by parasites with multiple PvDBP copies than Duffy negatives. Parasitemia was higher among the Duffy positives (median 17,218 parasites/µL; interquartile range [IQR] 2,895-104,489) than Duffy negatives (170; 78-24,132, p = 0.004) as well as in infections with 2 to 3 PvDBP copies (20,468; 3,649-110,632, p = 0.001) and more than 3 PvDBP copies (17,139; 2,831-95,946, p = 0.004) than single copy (5,673; 249-76,605).</p><p><strong>Conclusions/significance: </strong>A high proportion of P. vivax infection was observed in Duffy positives in this study, yet few Duffy negatives were found infected with P. vivax. The significant prevalence of multi-copy PvDBP observed among Ethiopian P. vivax isolates explains the high prevalence and parasitemia observed in clinical cases. This suggests that vivax malaria is a public health concern in the country where the Duffy positive population predominates. Investigating the relative contribution to the maintenance of the infectious reservoir of infections with different genotyping backgrounds (both host and parasite) might be required.</p>","PeriodicalId":49000,"journal":{"name":"PLoS Neglected Tropical Diseases","volume":"19 2","pages":"e0012837"},"PeriodicalIF":3.4000,"publicationDate":"2025-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11870341/pdf/","citationCount":"0","resultStr":"{\"title\":\"Spatial distribution of Plasmodium vivax Duffy Binding Protein copy number variation and Duffy genotype, and their association with parasitemia in Ethiopia.\",\"authors\":\"Yasin Nasir, Eshetu Molla, Getnet Habtamu, Solomon Sisay, Legesse Alamerie Ejigu, Fikregabrail Aberra Kassa, Mulugeta Demisse, Wakweya Chali, Melat Abdo, Dawit Hailu Alemayehu, Lina Alemayehu, Alemayehu Letebo, Tadele Emiru, Jimma Dinsa Deressa, Tajudin Abdurhaman Hamza, Abel Beliyu Tamirat, Tadesse Misganaw, Alayu Bogale, Zufan Yiheyis Abriham, Sisay Dugassa, Migbaru Keffale, Fekadu Massebo, Hassen Mamo, Endalamaw Gadisa, Chris Drakeley, Alemayehu Godana Birhanu, Cristian Koepfli, Fitsum G Tadesse\",\"doi\":\"10.1371/journal.pntd.0012837\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Duffy Binding Protein (PvDBP) binding to the Duffy antigen receptor for chemokine (DARC) is essential for Plasmodium vivax invasion of human reticulocytes. PvDBP copy number variation (CNV) might increase parasite invasion and thus parasitemia. We examined the spatial distribution of PvDBP CNVs and DARC genotypes and their association with parasitemia in P. vivax endemic settings in Ethiopia.</p><p><strong>Methodology/principal findings: </strong>P. vivax isolates (n = 435) collected from five P. vivax endemic settings in Ethiopia were genotyped by amplifying the GATA1 transcription factor-binding site of the Duffy blood group and the CNV of PvDBP was quantified. Parasitemia was determined using 18S-based qPCR. The majority of participants were Duffy positive (96.8%, 421/435). Of the few Duffy negative individuals, most (n = 8) were detected from one site (Gondar). Multiple copies of PvDBP were detected in 83% (363/435) isolates with significant differences between sites (range 60%-94%). Both heterozygous (p = 0.005) and homozygous (p = 0.006) patients were more likely to have been infected by parasites with multiple PvDBP copies than Duffy negatives. Parasitemia was higher among the Duffy positives (median 17,218 parasites/µL; interquartile range [IQR] 2,895-104,489) than Duffy negatives (170; 78-24,132, p = 0.004) as well as in infections with 2 to 3 PvDBP copies (20,468; 3,649-110,632, p = 0.001) and more than 3 PvDBP copies (17,139; 2,831-95,946, p = 0.004) than single copy (5,673; 249-76,605).</p><p><strong>Conclusions/significance: </strong>A high proportion of P. vivax infection was observed in Duffy positives in this study, yet few Duffy negatives were found infected with P. vivax. The significant prevalence of multi-copy PvDBP observed among Ethiopian P. vivax isolates explains the high prevalence and parasitemia observed in clinical cases. This suggests that vivax malaria is a public health concern in the country where the Duffy positive population predominates. Investigating the relative contribution to the maintenance of the infectious reservoir of infections with different genotyping backgrounds (both host and parasite) might be required.</p>\",\"PeriodicalId\":49000,\"journal\":{\"name\":\"PLoS Neglected Tropical Diseases\",\"volume\":\"19 2\",\"pages\":\"e0012837\"},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2025-02-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11870341/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"PLoS Neglected Tropical Diseases\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1371/journal.pntd.0012837\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/2/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"PARASITOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"PLoS Neglected Tropical Diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1371/journal.pntd.0012837","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"PARASITOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
背景:Duffy结合蛋白(PvDBP)与Duffy抗原趋化因子受体(DARC)结合是间日疟原虫侵袭人网织细胞的必要条件。PvDBP拷贝数变异(CNV)可能增加寄生虫的入侵,从而增加寄生虫血症。我们研究了埃塞俄比亚间日疟原虫流行环境中PvDBP CNVs和DARC基因型的空间分布及其与寄生虫病的关系。方法/主要发现:通过扩增Duffy血型GATA1转录因子结合位点,从埃塞俄比亚5个间日疟原虫流行区收集的435株间日疟原虫分离株进行基因分型,并定量PvDBP的CNV。采用基于18 - s的qPCR检测寄生虫血症。大多数受试者为Duffy阳性(96.8%,421/435)。在少数Duffy阴性个体中,大多数(n = 8)来自一个位点(Gondar)。在83%(363/435)分离株中检测到PvDBP多拷贝,位点间差异显著(60% ~ 94%)。杂合子(p = 0.005)和纯合子(p = 0.006)患者都比Duffy阴性患者更容易感染具有多个PvDBP拷贝的寄生虫。Duffy阳性患者的寄生率较高(中位数为17,218只/µL;四分位间距[IQR] 2,895-104,489)比Duffy阴性(170;78-24,132, p = 0.004),以及2至3个PvDBP拷贝的感染(20,468;3,649-110,632, p = 0.001)和超过3个PvDBP拷贝(17,139;2,831-95,946, p = 0.004)比单份(5,673;249 - 76605)。结论/意义:本研究中Duffy阳性人群感染间日疟原虫的比例较高,而Duffy阴性人群感染间日疟原虫的比例较低。在埃塞俄比亚间日疟原虫分离株中观察到的多拷贝PvDBP的显著流行解释了临床病例中观察到的高流行率和寄生虫血症。这表明间日疟疾在达菲阳性人口占多数的国家是一个公共卫生问题。可能需要调查不同基因分型背景(宿主和寄生虫)对传染病库维持的相对贡献。
Spatial distribution of Plasmodium vivax Duffy Binding Protein copy number variation and Duffy genotype, and their association with parasitemia in Ethiopia.
Background: Duffy Binding Protein (PvDBP) binding to the Duffy antigen receptor for chemokine (DARC) is essential for Plasmodium vivax invasion of human reticulocytes. PvDBP copy number variation (CNV) might increase parasite invasion and thus parasitemia. We examined the spatial distribution of PvDBP CNVs and DARC genotypes and their association with parasitemia in P. vivax endemic settings in Ethiopia.
Methodology/principal findings: P. vivax isolates (n = 435) collected from five P. vivax endemic settings in Ethiopia were genotyped by amplifying the GATA1 transcription factor-binding site of the Duffy blood group and the CNV of PvDBP was quantified. Parasitemia was determined using 18S-based qPCR. The majority of participants were Duffy positive (96.8%, 421/435). Of the few Duffy negative individuals, most (n = 8) were detected from one site (Gondar). Multiple copies of PvDBP were detected in 83% (363/435) isolates with significant differences between sites (range 60%-94%). Both heterozygous (p = 0.005) and homozygous (p = 0.006) patients were more likely to have been infected by parasites with multiple PvDBP copies than Duffy negatives. Parasitemia was higher among the Duffy positives (median 17,218 parasites/µL; interquartile range [IQR] 2,895-104,489) than Duffy negatives (170; 78-24,132, p = 0.004) as well as in infections with 2 to 3 PvDBP copies (20,468; 3,649-110,632, p = 0.001) and more than 3 PvDBP copies (17,139; 2,831-95,946, p = 0.004) than single copy (5,673; 249-76,605).
Conclusions/significance: A high proportion of P. vivax infection was observed in Duffy positives in this study, yet few Duffy negatives were found infected with P. vivax. The significant prevalence of multi-copy PvDBP observed among Ethiopian P. vivax isolates explains the high prevalence and parasitemia observed in clinical cases. This suggests that vivax malaria is a public health concern in the country where the Duffy positive population predominates. Investigating the relative contribution to the maintenance of the infectious reservoir of infections with different genotyping backgrounds (both host and parasite) might be required.
期刊介绍:
PLOS Neglected Tropical Diseases publishes research devoted to the pathology, epidemiology, prevention, treatment and control of the neglected tropical diseases (NTDs), as well as relevant public policy.
The NTDs are defined as a group of poverty-promoting chronic infectious diseases, which primarily occur in rural areas and poor urban areas of low-income and middle-income countries. Their impact on child health and development, pregnancy, and worker productivity, as well as their stigmatizing features limit economic stability.
All aspects of these diseases are considered, including:
Pathogenesis
Clinical features
Pharmacology and treatment
Diagnosis
Epidemiology
Vector biology
Vaccinology and prevention
Demographic, ecological and social determinants
Public health and policy aspects (including cost-effectiveness analyses).