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      Malaria Species Positivity Rates Among Symptomatic Individuals Across Regions of Differing Transmission Intensities in Mainland Tanzania

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          Abstract

          Background

          Recent data indicate that non- Plasmodium falciparum species may be more prevalent than thought in sub-Saharan Africa. Although Plasmodium malariae, Plasmodium ovale spp., and Plasmodium vivax are less severe than P. falciparum, treatment and control are more challenging, and their geographic distributions are not well characterized.

          Methods

          We randomly selected 3284 of 12 845 samples collected from cross-sectional surveys in 100 health facilities across 10 regions of Mainland Tanzania and performed quantitative real-time PCR to determine presence and parasitemia of each malaria species.

          Results

          P. falciparum was most prevalent, but P. malariae and P. ovale were found in all but 1 region, with high levels (>5%) of P. ovale in 7 regions. The highest P. malariae positivity rate was 4.5% in Mara and 8 regions had positivity rates ≥1%. We only detected 3 P. vivax infections, all in Kilimanjaro. While most nonfalciparum malaria-positive samples were coinfected with P. falciparum, 23.6% (n = 13 of 55) of P. malariae and 14.7% (n = 24 of 163) of P. ovale spp. were monoinfections.

          Conclusions

          P. falciparum remains by far the largest threat, but our data indicate that malaria elimination efforts in Tanzania will require increased surveillance and improved understanding of the biology of nonfalciparum species.

          Abstract

          A molecular analysis of 3284 dried blood spots collected from cross-sectional surveys in 100 health facilities across 10 regions of Mainland Tanzania found that P. ovale spp. and P. malariae are present nationwide and must be considered in surveillance activities.

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          Most cited references47

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          Epidemiology and infectivity of Plasmodium falciparum and Plasmodium vivax gametocytes in relation to malaria control and elimination.

          Malaria remains a major cause of morbidity and mortality in the tropics, with Plasmodium falciparum responsible for the majority of the disease burden and P. vivax being the geographically most widely distributed cause of malaria. Gametocytes are the sexual-stage parasites that infect Anopheles mosquitoes and mediate the onward transmission of the disease. Gametocytes are poorly studied despite this crucial role, but with a recent resurgence of interest in malaria elimination, the study of gametocytes is in vogue. This review highlights the current state of knowledge with regard to the development and longevity of P. falciparum and P. vivax gametocytes in the human host and the factors influencing their distribution within endemic populations. The evidence for immune responses, antimalarial drugs, and drug resistance influencing infectiousness to mosquitoes is reviewed. We discuss how the application of molecular techniques has led to the identification of submicroscopic gametocyte carriage and to a reassessment of the human infectious reservoir. These components are drawn together to show how control measures that aim to reduce malaria transmission, such as mass drug administration and a transmission-blocking vaccine, might better be deployed.
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            School-Age Children Are a Reservoir of Malaria Infection in Malawi

            Malaria surveillance and interventions in endemic countries often target young children at highest risk of malaria morbidity and mortality. We aimed to determine whether school-age children and adults not captured in surveillance serve as a reservoir for malaria infection and may contribute to malaria transmission. Cross-sectional surveys were conducted in one rainy and one dry season in southern Malawi. Demographic and health information was collected for all household members. Blood samples were obtained for microscopic and PCR identification of Plasmodium falciparum. Among 5796 individuals aged greater than six months, PCR prevalence of malaria infection was 5%, 10%, and 20% in dry, and 9%, 15%, and 32% in rainy seasons in Blantyre, Thyolo, and Chikhwawa, respectively. Over 88% of those infected were asymptomatic. Participants aged 6–15 years were at higher risk of infection (OR=4.8; 95%CI, 4.0–5.8) and asymptomatic infection (OR=4.2; 95%CI, 2.7–6.6) than younger children in all settings. School-age children used bednets less frequently than other age groups. Compared to young children, school-age children were brought less often for treatment and more often to unreliable treatment sources. Conclusion: School-age children represent an underappreciated reservoir of malaria infection and have less exposure to antimalarial interventions. Malaria control and elimination strategies may need to expand to include this age group.
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              World malaria report 2022

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                Author and article information

                Contributors
                Journal
                J Infect Dis
                J Infect Dis
                jid
                The Journal of Infectious Diseases
                Oxford University Press (US )
                0022-1899
                1537-6613
                15 April 2024
                22 November 2023
                22 November 2023
                : 229
                : 4
                : 959-968
                Affiliations
                Institute for Global Health and Infectious Diseases, University of North Carolina , Chapel Hill, North Carolina, USA
                National Institute for Medical Research , Dar es Salaam, Tanzania
                National Institute for Medical Research , Dar es Salaam, Tanzania
                National Institute for Medical Research , Dar es Salaam, Tanzania
                National Institute for Medical Research , Dar es Salaam, Tanzania
                National Institute for Medical Research, Tanga Center , Tanga, Tanzania
                National Institute for Medical Research , Dar es Salaam, Tanzania
                Department of Entomology, The Connecticut Agricultural Experiment Station , New Haven, Connecticut, USA
                National Institute for Medical Research , Dar es Salaam, Tanzania
                National Malaria Control Programme , Dodoma, Tanzania
                National Malaria Control Programme , Dodoma, Tanzania
                National Malaria Control Programme , Dodoma, Tanzania
                National Malaria Control Programme , Dodoma, Tanzania
                Department of Pathology and Laboratory Medicine, Warren Alpert Medical School, Brown University , Providence, Rhode Island, USA
                Center for Computational Molecular Biology, Brown University , Providence, Rhode Island, USA
                Institute for Global Health and Infectious Diseases, University of North Carolina , Chapel Hill, North Carolina, USA
                National Institute for Medical Research , Dar es Salaam, Tanzania
                Department of Immunology and Infectious Diseases, Harvard T. H. Chan School of Public Health , Boston, Massachusetts, USA
                Faculty of Pharmaceutical Sciences, Monash University , Melbourne, Victoria, Australia
                Author notes

                Presented in part: American Society of Tropical Medicine and Hygiene Annual Meeting, Seattle, WA, 1 November 2022.

                J. A. B., J. J. J., and D. S. I are cosenior authors.

                Correspondence: Zachary R. Popkin-Hall, PhD, Institute for Global Health and Infectious Diseases, University of North Carolina, 2336 Medical Biomolecular Research Building, 111 Mason Farm Road, Chapel Hill, NC 27599 ( zach_popkin-hall@ 123456med.unc.edu )
                Correspondence: Deus S. Ishengoma, PhD, National Institute for Medical Research, 3 Baracka Obama Drive, PO Box 9653, 11101 Dar es Salaam, Tanzania ( deusishe@ 123456yahoo.com ).

                Potential conflicts of interest. All authors: No reported conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

                Author information
                https://orcid.org/0000-0002-8308-5294
                https://orcid.org/0000-0002-6743-4108
                https://orcid.org/0000-0003-0297-9219
                https://orcid.org/0000-0002-8710-1765
                https://orcid.org/0000-0003-1000-4729
                https://orcid.org/0000-0003-2813-1312
                https://orcid.org/0000-0003-2498-4705
                https://orcid.org/0000-0003-4317-4425
                https://orcid.org/0000-0002-6899-8204
                https://orcid.org/0000-0002-0591-0850
                https://orcid.org/0000-0003-2040-3416
                Article
                jiad522
                10.1093/infdis/jiad522
                11011190
                37992117
                301a79bd-6bb4-4f30-95f2-a67e6d327176
                © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence ( https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 20 September 2023
                : 17 November 2023
                : 20 November 2023
                : 22 December 2023
                Page count
                Pages: 10
                Funding
                Funded by: Bill and Melinda Gates Foundation, DOI 10.13039/100000865;
                Award ID: 002202
                Funded by: National Institutes of Health, DOI 10.13039/100000002;
                Award ID: K24AI134990
                Categories
                Major Article
                Parasites
                AcademicSubjects/MED00290

                Infectious disease & Microbiology
                malaria,tanzania,plasmodium falciparum,plasmodium malariae,plasmodium ovale,plasmodium vivax,nonfalciparum species

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