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We report a proof-of-concept surveillance strategy that combines simplicity with modest cost to achieve high analytical performance for the detection of asymptomatic malaria infection. We developed a microfluidic paper-based analytical device (μPAD) that automates immunoassay using 30 μL of whole blood. A novel dendrimer-based signal transduction method was introduced to amplify the mass spectrometry (MS) signal. Our ability to detect an immunoassay signal with MS was achieved using cleavable ionic probes that were attached to monoclonal antibodies via dendrimer bioconjugation. The limit of detection of this MS-based immunoassay was determined to be 4.5 pM in serum for histidine-rich protein 2. The high stability of the ionic probes allowed storage of the paper device at room temperature, facilitating field sampling of whole blood from 266 asymptomatic volunteers in Ghana. The performance of the μPAD platform was compared with polymerase chain reaction (PCR), light microscopy, and rapid diagnostic test (RDT). Using PCR as the reference, we observed 96.5% sensitivity for our μPAD platform, as opposed to 43% for RDT and 16.9% for microscopy. Cohen's Kappa statistical analysis confirmed almost perfect agreement between μPAD and PCR (%agree = 81% in Kappa's categorical terms). False-negative rate in μPAD was calculated to be 3.5%. These results highlight the need for a more sensitive tool for asymptomatic malaria screening. Our method is highly sensitive yet deliverable, making sustainable implementation possible in underserved communities.
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http://dx.doi.org/10.1021/acs.analchem.5c01324 | DOI Listing |
Commun Med (Lond)
September 2025
Department of Microbiology and Immunology, Bio21 Institute and The Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, VIC, Australia.
Background: Mixed-species, mixed-strain plasmodia infections are known to occur in humans in malaria endemic areas. It may be surprising that to date, the extent of this complexity has not been systematically explored in high-burden countries of sub-Saharan Africa, especially in the reservoir of asymptomatic infections in all ages, which sustains transmission.
Methods: Here we take a metagenomic lens to these infections by sampling variable blood volumes from 188 afebrile residents living in high, seasonal transmission in Northern Sahelian Ghana.
Biomed Res Int
September 2025
Department of Biostatistics and Medical Informatics, Faculty of Medicine, Kahramanmaraş Sütçü Imam University, Kahramanmaraş, Türkiye.
In countries like Somalia, where health infrastructure is inadequate and malaria is endemic, immunosuppression during pregnancy increases the risk of placental malaria; this, in turn, leads to anemia, low birth weight, preterm delivery, and stillbirth, causing severe complications that pose a life-threatening risk to both the mother and fetus. The aim of this study was to investigate the prevalence and associated factors of malaria parasitemia among pregnant women attending the obstetric clinic of a tertiary hospital in Somalia. This cross-sectional study, conducted from November 2022 to January 2023 at a tertiary hospital in Mogadishu, involved 398 pregnant women.
View Article and Find Full Text PDFMath Biosci Eng
July 2025
Department of Mathematics and Applied Mathematics, NorthWest University, Mahikeng, South Africa.
We consider a two-Patch malaria model, where the individuals can freely move between the patches. We assume that one site has better resources to fight the disease, such as screening facilities and the availability of transmission-blocking drugs (TBDs) that offer full, though waning, immunity and non-infectivity. Moreover, individuals moving to this site are screened at the entry points, and the authorities can either refuse entry to infected individuals or allow them in but immediately administer a TBD.
View Article and Find Full Text PDFMath Biosci Eng
June 2025
MIVEGEC, Univ. Montpellier, CNRS, IRD, Montpellier, France.
Antimalarial drugs are critical for controlling malaria, but the emergence of drug resistance poses a significant challenge to global eradication efforts. This study explores strategies to minimize resistance prevalence and improve malaria control, particularly through the use of mass drug administration (MDA) in combination with antimalarial drugs. We develop a compartmental mathematical model that incorporates asymptomatic, paucisymptomatic, and clinical states of infection and evaluates the impact of resistance mutations on transmission dynamics.
View Article and Find Full Text PDFmedRxiv
August 2025
Department of Microbiology and Immunology, Bio21 Institute and Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, VIC, Australia.
Current interventions targeting malaria control in sub-Saharan Africa (SSA) are focused on , the most prevalent species infecting humans. Despite renewed efforts for malaria elimination in SSA, little attention has been paid to the neglected parasites and spp. and the impact of interventions like long-lasting insecticidal nets (LLINs), indoor residual spraying (IRS) with non-pyrethroid insecticides, and/or seasonal malaria chemoprevention (SMC) on these minor spp.
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