OBJECTIVES: Plasmodium vivax malaria was thought to be rare in Africans who lack the Duffy blood group antigen expression. However, recent studies indicate that P. vivax can infect Duffy-negative individuals and has penetrated into areas of high Duffy-negativity across Africa. This study compares epidemiological and genetic features of P. vivax between African regions.METHODS: We utilized a standardized approach to identify and quantify P. vivax from Botswana, Ethiopia, and Sudan, where Duffy-positive and Duffy-negative individuals coexist. We sequenced Duffy Binding Protein (DBP) gene and inferred genetic relationships among all Africa P. vivax.RESULTS: Among 1,215 febrile patients, the proportions of Duffy negativity range from 20-36% in East Africa to 84% in Southern Africa. P. vivax prevalence among Duffy-negative populations ranging from averaged 9.2% in Sudan to 86% in Botswana. Parasite density in Duffy-negative is significantly lower than in Duffy-positive infections. P. vivax in Duffy-negative populations were not monophyletic. Duffy-negative and Duffy-positive P. vivax shared similar DBP haplotypes and occurred in multiple well-supported clades.CONCLUSIONS: Duffy-negative Africans are not resistant to P. vivax and the public health significance should not be neglected. This study highlights need for standardized approach and more resources/training to diagnosis of vivax malaria in Africa.

Contrasting epidemiology and genetic variation of Plasmodium vivax infecting Duffy negatives across Africa / Lo, Eugenia; Russo, Gianluca; Pestana, Kareen; Kepple, Daniel; Abargero, Beka Raya; Dongho, Ghyslaine Bruna Djeunang; Gunalan, Karthigayan; Miller, Louis H; Hamid, Muzamil Mahdi Abdel; Yewhalaw, Delenasaw; Paganotti, Giacomo Maria. - In: INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES. - ISSN 1201-9712. - 108:(2021), pp. 63-71. [10.1016/j.ijid.2021.05.009]

Contrasting epidemiology and genetic variation of Plasmodium vivax infecting Duffy negatives across Africa

Russo, Gianluca
Secondo
;
2021

Abstract

OBJECTIVES: Plasmodium vivax malaria was thought to be rare in Africans who lack the Duffy blood group antigen expression. However, recent studies indicate that P. vivax can infect Duffy-negative individuals and has penetrated into areas of high Duffy-negativity across Africa. This study compares epidemiological and genetic features of P. vivax between African regions.METHODS: We utilized a standardized approach to identify and quantify P. vivax from Botswana, Ethiopia, and Sudan, where Duffy-positive and Duffy-negative individuals coexist. We sequenced Duffy Binding Protein (DBP) gene and inferred genetic relationships among all Africa P. vivax.RESULTS: Among 1,215 febrile patients, the proportions of Duffy negativity range from 20-36% in East Africa to 84% in Southern Africa. P. vivax prevalence among Duffy-negative populations ranging from averaged 9.2% in Sudan to 86% in Botswana. Parasite density in Duffy-negative is significantly lower than in Duffy-positive infections. P. vivax in Duffy-negative populations were not monophyletic. Duffy-negative and Duffy-positive P. vivax shared similar DBP haplotypes and occurred in multiple well-supported clades.CONCLUSIONS: Duffy-negative Africans are not resistant to P. vivax and the public health significance should not be neglected. This study highlights need for standardized approach and more resources/training to diagnosis of vivax malaria in Africa.
2021
duffy negatives; genetic relationships; malaria; molecular epidemiology; pasmodium vivax; sub-saharan africa
01 Pubblicazione su rivista::01a Articolo in rivista
Contrasting epidemiology and genetic variation of Plasmodium vivax infecting Duffy negatives across Africa / Lo, Eugenia; Russo, Gianluca; Pestana, Kareen; Kepple, Daniel; Abargero, Beka Raya; Dongho, Ghyslaine Bruna Djeunang; Gunalan, Karthigayan; Miller, Louis H; Hamid, Muzamil Mahdi Abdel; Yewhalaw, Delenasaw; Paganotti, Giacomo Maria. - In: INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES. - ISSN 1201-9712. - 108:(2021), pp. 63-71. [10.1016/j.ijid.2021.05.009]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1548117
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