{"title":"<i>Plasmodium vivax</i> Infections in Duffy-Negative Individuals: A Paradigm Shift in Indian Malaria Epidemiology.","authors":"Roshan Shaikh, Kanjaksha Ghosh, Ajit Gorakshakar","doi":"10.4084/MJHID.2025.044","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>To investigate the occurrence of <i>Plasmodium vivax</i> infections in Duffy-negative individuals, challenging the long-held belief that <i>P. vivax</i> requires the Duffy antigen receptor for chemokines to infect human erythrocytes.</p><p><strong>Materials and methods: </strong>In the present study, 365 samples were screened using serological techniques, PCR-RFLP analysis, and DNA sequencing of the <i>ACKR1</i> gene promoter region mutation to identify Duffy-negative individuals. <i>P. vivax</i> infection was detected using PCR targeting the <i>18S rRNA</i> gene and microscopic examination of Giemsa-stained blood smears.</p><p><strong>Results: </strong>Five individuals (1.36%) were confirmed Duffy-negative (Fy<sup>(a-b-)</sup>). Surprisingly, 3 out of these 5 Duffy-negative subjects (60%) were infected with <i>P. vivax</i>, as confirmed by both microscopy and PCR. Various parasite stages were observed in infected Duffy-negative samples, with parasitaemia ranging from 0.01% to 0.5%.</p><p><strong>Discussion: </strong>Our findings provide compelling evidence that <i>P. vivax</i> can infect Duffy-negative individuals, suggesting the existence of alternative invasion pathways or adaptations. This has profound implications for <i>P. vivax</i> biology, evolution, and global distribution. The burden of vivax malaria may be underestimated, particularly in regions with a high prevalence of Duffy negativity. This study highlights the need to reevaluate <i>P. vivax</i> epidemiology, diagnostic approaches, and control strategies, especially in areas previously considered at low risk. Further research is needed to elucidate the mechanisms enabling <i>P. vivax</i> invasion of Duffy-negative erythrocytes and to assess the clinical and epidemiological consequences of these infections.</p>","PeriodicalId":18498,"journal":{"name":"Mediterranean Journal of Hematology and Infectious Diseases","volume":"17 1","pages":"e2025044"},"PeriodicalIF":2.0000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12081053/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mediterranean Journal of Hematology and Infectious Diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.4084/MJHID.2025.044","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: To investigate the occurrence of Plasmodium vivax infections in Duffy-negative individuals, challenging the long-held belief that P. vivax requires the Duffy antigen receptor for chemokines to infect human erythrocytes.
Materials and methods: In the present study, 365 samples were screened using serological techniques, PCR-RFLP analysis, and DNA sequencing of the ACKR1 gene promoter region mutation to identify Duffy-negative individuals. P. vivax infection was detected using PCR targeting the 18S rRNA gene and microscopic examination of Giemsa-stained blood smears.
Results: Five individuals (1.36%) were confirmed Duffy-negative (Fy(a-b-)). Surprisingly, 3 out of these 5 Duffy-negative subjects (60%) were infected with P. vivax, as confirmed by both microscopy and PCR. Various parasite stages were observed in infected Duffy-negative samples, with parasitaemia ranging from 0.01% to 0.5%.
Discussion: Our findings provide compelling evidence that P. vivax can infect Duffy-negative individuals, suggesting the existence of alternative invasion pathways or adaptations. This has profound implications for P. vivax biology, evolution, and global distribution. The burden of vivax malaria may be underestimated, particularly in regions with a high prevalence of Duffy negativity. This study highlights the need to reevaluate P. vivax epidemiology, diagnostic approaches, and control strategies, especially in areas previously considered at low risk. Further research is needed to elucidate the mechanisms enabling P. vivax invasion of Duffy-negative erythrocytes and to assess the clinical and epidemiological consequences of these infections.
期刊介绍:
Reciprocal interdependence between infectious and hematologic diseases (malignant and non-malignant) is well known. This relationship is particularly evident in Mediterranean countries. Parasitosis as Malaria, Leishmaniosis, B Hookworms, Teniasis, very common in the southeast Mediterranean area, infect about a billion people and manifest prevalently with anemia so that they are usually diagnosed mostly by experienced hematologist on blood or bone marrow smear. On the other hand, infections are also a significant problem in patients affected by hematological malignancies. The blood is the primary vector of HIV infection, which otherwise manifest with symptoms related to a reduction in T lymphocytes. In turn, infections can favor the insurgency of hematological malignancies. The causative relationship between Epstein-Barr virus infection, Helicobacter pylori, hepatitis C virus, HIV and lymphoproliferative diseases is well known.