Occurrence and Distribution of Nonfalciparum Malaria Parasite Species Among Adolescents and Adults in Malawi

Author:

Gumbo Austin1,Topazian Hillary M2ORCID,Mwanza Alexis2,Mitchell Cedar L2,Puerto-Meredith Sydney2,Njiko Ruth3,Kayange Michael1,Mwalilino David4,Mvula Bernard4,Tegha Gerald3,Mvalo Tisungane35,Hoffman Irving36,Juliano Jonathan J7

Affiliation:

1. National Malaria Control Programme, Malawi Ministry of Health, Lilongwe, Malawi

2. Department of Epidemiology, University of North Carolina, Chapel Hill, North Carolina, USA

3. University of North Carolina Project-Malawi, Lilongwe, Malawi

4. National HIV Reference Laboratory, Malawi Ministry of Health, Lilongwe, Malawi

5. Department of Pediatrics, School of Medicine, University of North Carolina, Chapel Hill, North Carolina, USA

6. Institute for Global Health and Infectious Diseases, University of North Carolina, Chapel Hill, North Carolina, USA

7. Division of Infectious Diseases, School of Medicine, University of North Carolina, Chapel Hill, North Carolina, USA

Abstract

Abstract Background Plasmodium falciparum malaria dominates throughout sub-Saharan Africa, but the prevalence of Plasmodium malariae, Plasmodium ovale spp., and Plasmodium vivax increasingly contribute to infection in countries that control malaria using P. falciparum-specific diagnostic and treatment strategies. Methods We performed quantitative polymerase chain reaction (qPCR) on 2987 dried blood spots from the 2015–2016 Malawi Demographic and Health Survey to identify presence and distribution of nonfalciparum infection. Bivariate models were used to determine species-specific associations with demographic and environmental risk factors. Results Nonfalciparum infections had broad spatial distributions. Weighted prevalence was 0.025 (SE, 0.004) for P. malariae, 0.097 (SE, 0.008) for P. ovale spp., and 0.001 (SE, 0.0005) for P. vivax. Most infections (85.6%) had low-density parasitemias ≤ 10 parasites/µL, and 66.7% of P. malariae, 34.6% of P. ovale spp., and 40.0% of P. vivax infections were coinfected with P. falciparum. Risk factors for P. malariae were like those known for P. falciparum; however, there were few risk factors recognized for P. ovale spp. and P. vivax, perhaps due to the potential for relapsing episodes. Conclusions The prevalence of any nonfalciparum infection was 11.7%, with infections distributed across Malawi. Continued monitoring of Plasmodium spp. becomes critical as nonfalciparum infections become important sources of ongoing transmission.

Funder

University of North Carolina Institute for Global Health and Infectious Disease

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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