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dc.contributor.authorMotshoge, Thato
dc.contributor.authorAbabio, Grace K.
dc.contributor.authorAleksenko, Larysa
dc.contributor.authorRead, John
dc.contributor.authorPeloewetse, Elias
dc.contributor.authorLoeto, Mazhani
dc.contributor.authorMosweunyane, Tjantilili
dc.contributor.authorMoakofhi, Kentse
dc.contributor.authorNtebele, Davies S.
dc.contributor.authorChihanga, Simon
dc.contributor.authorMotlaleng, Mpho
dc.contributor.authorChinorumba, Anderson
dc.contributor.authorVurayai, Moses
dc.contributor.authorPernica, Jeffrey M.
dc.contributor.authorPaganotti, Giacomo M.
dc.contributor.authorQuaye, Isaac K.
dc.date.accessioned2016-11-10T12:10:40Z
dc.date.available2016-11-10T12:10:40Z
dc.date.issued2016
dc.identifier.citationMotshoge, T. et al. (2016) Molecular evidence of high rates of asymptomatic P. vivax infection and very low P. falciparum malaria in Botswana. BMC Infectious Diseases, 16:520en_US
dc.identifier.issn1471-2334
dc.identifier.urihttp://hdl.handle.net/10311/1548
dc.description.abstractBackground: Botswana is one of eight SADC countries targeting malaria elimination by 2018. Through spirited upscaling of control activities and passive surveillance, significant reductions in case incidence of Plasmodium falciparum (0.96 – 0.01) was achieved between 2008 and 2012. As part of the elimination campaign, active detection of asymptomatic Plasmodium species by a highly sensitive method was deemed necessary. This study was carried out to determine asymptomatic Plasmodium species carriage by nested PCR in the country, in 2012. Method: A cross-sectional study involving 3924 apparently healthy participants were screened for Plasmodium species in 14 districts (5 endemic: Okavango, Ngami, Tutume, Boteti and Bobirwa; and 9 epidemic: North East, Francistown, Serowe-Palapye, Ghanzi, Kweneng West, Kweneng East, Kgatleng, South East, and Good Hope). Venous blood was taken from each participant for a nested PCR detection of Plasmodium species. Results: The parasite rates of asymptomatic Plasmodium species detected were as follows: Plasmodium falciparum, 0.16 %; Plasmodium vivax, 4.66 %; Plasmodium malariae, (Pm) 0.16 %; Plasmodium ovale, 0 %, mixed infections (P. falciparum and P. vivax), 0.055 %; and (P. vivax and P. malariae), 0.027 %, (total: 5.062 %). The high proportion of asymptomatic reservoir of P. vivax was clustered in the East, South Eastern and Central districts of the country. There appeared to be a correlation between the occurrence of P. malariae infection with P. vivax infection, with the former only occurring in districts that had substantial P. vivax circulation. The median age among 2–12 year olds for P. vivax infection was 5 years (Mean 5.13 years, interquartile range 3–7 years). The odds of being infected with P. vivax decreased by 7 % for each year increase in age (OR 0.93, 95 % CI 0.87–1.00, p = 0.056). Conclusion: We have confirmed low parasite rate of asymptomatic Plasmodium species in Botswana, with the exception of P.vivax which was unexpectedly high. This has implication for the elimination campaign so a follow up study is warranted to inform decisions on new strategies that take this evidence into account in the elimination campaign.en_US
dc.language.isoenen_US
dc.publisherBioMed Central, https://bmcinfectdis.biomedcentral.com/en_US
dc.subjectAsymptomatic Plasmodium vivaxen_US
dc.subjectBotswanaen_US
dc.titleMolecular evidence of high rates of asymptomatic P. vivax infection and very low P. falciparum malaria in Botswanaen_US
dc.typePublished Articleen_US
dc.linkhttps://bmcinfectdis.biomedcentral.com/articles/10.1186/s12879-016-1857-8en_US


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