Background: Malaria transmission depends on the presence of gametocytes in the peripheral blood of infected human hosts. Understanding malaria infectious reservoirs enables transmission-blocking interventions to target the most important hosts for the disease. This study characterized the distribution of gametocyte carriage as a baseline for the clinical evaluation of a Pfs25-based transmission-blocking vaccine candidate in Bagamoyo, Tanzania.
Methods: A malaria survey was conducted in five locations from May to August 2022. A total of 467 participants-192 children (5-12 years), 65 adolescents (13-17 years) and 210 adults (18-45 years)-were enrolled. Malaria was detected using three methods: rapid diagnostic tests, light microscopy and quantitative polymerase chain reaction. The geometric mean of the gametocyte density, and weighted arithmetic mean of the gametocytes sex ratio were estimated.
Results: Overall, 23.5% (110/467) of the participants tested positive for malaria parasites, with the majority of positives (> 92%) being Plasmodium falciparum. The overall gametocytaemia was 5.6%, with a percent positivity of 6.8% (13/192), 6.2% (4/65) and 4.3% (9/210), in children, adolescents, and adults, respectively. The geometric mean gametocyte density (gametocytes/μL) was greater in adults (124.6) than in children (71.7) and adolescents (50.5). Regression analysis revealed that gametocytes were more likely to be present among male participants than among female participants [ORa: 2.79 (95% CI: 1.19 - 6.59) p = 0.019]. The gametocyte sex ratio in children and adult gametocyte carriers was similar but greater than that in adolescents.
Conclusion: The observed gametocyte densities and distribution across age groups suggest the need for malaria transmission-blocking interventions to target all populations in heterogeneous transmission settings. The implication of targeting only children may leave residual malaria transmission and reinfection from the left-out groups.
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http://dx.doi.org/10.1186/s12936-025-05270-4 | DOI Listing |
Trans R Soc Trop Med Hyg
March 2025
Molecular Epidemiology department, ICMR-National Institute of Malaria Research, Sector 8, Dwarka, 110077 New Delhi, India.
Background: Rapid diagnostic tests (RDTs) are vital for malaria diagnosis, especially in resource-limited areas. RDTs targeting histidine-rich protein 2 (PfHRP2) and its structural homologue PfHRP3 are commonly used for detecting Plasmodium falciparum. However, genetic deletions in these proteins can affect test accuracy.
View Article and Find Full Text PDFMalariaworld J
February 2025
Department of Pharmaceutical Microbiology and Biotechnology, Nnamdi Azikiwe University, Awka Nigeria.
Introduction: The genetic diversity of correlates with its pathogenicity, therefore design of evidence-based intervention strategies to eradicate malaria requires genetic diversity surveillance. This study characterised the allelic frequencies and genetic diversity of parasites isolated from Awka, Nigeria.
Materials And Methods: Genomic DNA was extracted from 177 isolates and the polymorphic regions of the and genes were genotyped by nested polymerase chain reaction (PCR).
NPJ Drug Discov
March 2025
Department of Pediatrics, University of California, San Diego, La Jolla, CA USA.
Identification of novel drug targets is a key component of modern drug discovery. While antimalarial targets are often identified through the mechanism of action studies on phenotypically derived inhibitors, this method tends to be time- and resource-consuming. The discoverable target space is also constrained by existing compound libraries and phenotypic assay conditions.
View Article and Find Full Text PDFAnn Afr Med
March 2025
Department of General Medicine, Dr. Pinnamaneni Siddhartha Institute of Medical Sciences and Research Foundation, Krishna, Andhra Pradesh, India.
A 20-year-old male with fever, myalgia, and jaundice developed severe liver dysfunction, progressing to acute liver failure (ALF). Initial treatment for malaria and supportive care did not resolve symptoms, with persistent jaundice and elevated liver enzymes. Laboratory tests confirmed Plasmodium falciparum/Plasmodium vivax infection.
View Article and Find Full Text PDFImmunol Cell Biol
March 2025
Department of Parasitology, Faculty of Medical Laboratory Sciences, Alzaeim Alazhari University, Khartoum, Sudan.
Phagocytosis is a critical immunological process that enables the immune system to recognize and eliminate foreign pathogens and self-derived pathogenic molecules. Improving the overall understanding of this immune mechanism during malarial infection is imperative. The mechanisms by which phagocytosis eradicates malaria parasites, particularly Plasmodium falciparum, remain incompletely understood and warrant further investigation.
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