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Clearance of Circulating Epstein‐Barr Virus DNA in Children with Acute Malaria after Antimalaria Treatment
Author(s) -
Daria Donati,
Eva Espmark,
Fred Kironde,
Edward Mbidde,
Moses R. Kamya,
Åke Lundkvist,
Mats Wahlgren,
Maria Teresa Bejarano,
Kerstin I. Falk
Publication year - 2006
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/500839
Subject(s) - malaria , saliva , virology , virus , epstein–barr virus , immunology , viral load , antibody , medicine , polymerase chain reaction , biology , incidence (geometry) , plasmodium falciparum , biochemistry , physics , optics , gene
Children living in malaria-endemic regions have a high incidence of Burkitt lymphoma (BL), the etiology of which involves Plasmodium falciparum malaria and Epstein-Barr virus (EBV) infections. In the present study, we compared EBV DNA loads in plasma and saliva samples from Ugandan children with acute malaria (M+) at the time of diagnosis and 14 days after antimalaria treatment, children without malaria (M-), and children with BL. EBV DNA was detected, by real-time polymerase chain reaction, in 31% of the plasma and in 79% of the saliva samples from children in the M+ group. Antimalaria treatment led to clearance of plasma viral load in 85% of the cases but did not affect the levels in saliva. There was a significant difference in plasma EBV loads across the groups. The lowest levels were detected in samples from the M- group, increased levels were detected in samples from the M+ group, and levels reached the highest values in samples from children with BL. The same trend was evident in the frequency and levels of anti-BZLF1 antibodies, which is indicative of viral reactivation. In the M+ group, the positive plasma samples clustered around 7-9 years of age, the peak incidence of BL. The clearance of circulating EBV after antimalaria treatment suggests a direct relationship between active malaria infection and viral reactivation.

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