Evidence map›Paper›PMID 41386967›Full record

ArticleThe Journal of infectious diseases2026

Uneven Plasmodium falciparum Transmission and Cryptic ovale Transmission From the Asymptomatic Reservoir in Bagamoyo, Tanzania.

Jessica T Lin, Derrick K Mathias, Guozheng Yang, Mwajabu Loya, Meredith S Muller, Christopher Basham, Vincent Nyasembe, Kano Amagai, Isaack Rutha, Claudia Gaither and 9 more

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Jessica T LinInstitute of Global Health and Infectious Diseases, University of North Carolina, Chapel Hill, North Carolina, USA.ORCID 0000-0002-4516-723X
Derrick K MathiasFlorida Medical Entomology Laboratory, Institute of Food and Agricultural Sciences, University of Florida, Vero Beach, Florida, USA.
Guozheng YangInstitute of Global Health and Infectious Diseases, University of North Carolina, Chapel Hill, North Carolina, USA.ORCID 0000-0001-7361-1847
Mwajabu LoyaDepartment of Parasitology and Medical Entomology, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Meredith S MullerInstitute of Global Health and Infectious Diseases, University of North Carolina, Chapel Hill, North Carolina, USA.
Christopher BashamInstitute of Global Health and Infectious Diseases, University of North Carolina, Chapel Hill, North Carolina, USA.
Vincent NyasembeGillings School of Global Public Health, University of North Carolina, Chapel Hill, North Carolina, USA.
Kano AmagaiInstitute of Global Health and Infectious Diseases, University of North Carolina, Chapel Hill, North Carolina, USA.
Isaack RuthaDepartment of Parasitology and Medical Entomology, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Claudia GaitherDepartment of Infectious Diseases and Immunology and Emerging Pathogens Institute, College of Veterinary Medicine, University of Florida, Gainesville, Florida, USA.ORCID 0009-0009-7539-4562
Mwanaidi NyangeDepartment of Parasitology and Medical Entomology, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Hamza SaidDepartment of Parasitology and Medical Entomology, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Srijana B ChhetriInstitute of Global Health and Infectious Diseases, University of North Carolina, Chapel Hill, North Carolina, USA.
Brian SwinehartInstitute of Global Health and Infectious Diseases, University of North Carolina, Chapel Hill, North Carolina, USA.
Feng-Chang LinGillings School of Global Public Health, University of North Carolina, Chapel Hill, North Carolina, USA.ORCID 0000-0002-2638-1775
Rhoel R DinglasanDepartment of Infectious Diseases and Immunology and Emerging Pathogens Institute, College of Veterinary Medicine, University of Florida, Gainesville, Florida, USA.
Jonathan J JulianoInstitute of Global Health and Infectious Diseases, University of North Carolina, Chapel Hill, North Carolina, USA.ORCID 0000-0002-0591-0850
Brian TarimoVector Immunity and Transmission Biology Unit, Department of Environmental Health and Ecological Sciences, Ifakara Health Institute-Bagamoyo Office, Bagamoyo, Tanzania.
Billy NgasalaDepartment of Parasitology and Medical Entomology, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.

Funding

Determinants of malaria transmission by submicroscopic gametocytemiaR01AI137395 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LIN, JESSICA · 2018 to 2022
$3.3M
Mentoring in Translational Malaria GenomicsK24AI134990 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Jonathan J Juliano · 2018 to 2026
$1.6M
Plasmodium ovale hypnozoite development and relapse: a coordinated in vivo in vitro studyR21AI152260 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ADAMS, JOHN H, LIN, JESSICA · 2021 to 2022
$418k
National Institute of Allergy and Infectious DiseasesNIAID NIH HHS K24 AI134990NIAID NIH HHS R01 AI137395NIAID NIH HHS R21 AI152260NIH HHS K24AI134990NIH HHS R01AI137395NIH HHS R21AI152260
6 · The paper itself

Abstract

backgroundAsymptomatic malaria carriers often harbor low parasite densities missed by rapid diagnostic tests (RDTs), yet they contribute to transmission. Direct skin feeding (DSF) assays can sensitively measure their infectiousness to mosquitoes.

methodsTo characterize human-to-mosquito transmission from the asymptomatic reservoir in Bagamoyo, Tanzania, DSFs were performed in persons >5 years of age positive for Plasmodium falciparum by RDT or real-time PCR. Fifty colony-reared Anopheles gambiae were fed on the posterior calves. Successful mosquito infection was defined as ≥1 oocyst-positive mosquito midgut among 25 dissected eight days postskin feeding.

resultsAmong 491 participants with median parasite density of 5.1 parasites/μL who underwent DSF, 22% were infectious to mosquitoes. RDT-positive participants infected roughly twice as many mosquitoes compared to RDT-negative/PCR-positive persons. However, up to 21% of infectious carriers were PCR-negative at the time of skin feeding, after screening PCR-positive a few days earlier. Overall, 9.1% (342/3741) of mosquitoes fed on infectious carriers were parasite-positive at dissection. Half of infectious individuals infected a single mosquito, while the top 16 transmitters (3% of those undergoing DSF) cumulatively infected 57% of infected mosquitoes. RDT-positive school-age children (6-15 years), 27% of the DSF cohort, contributed to 58% of infected mosquitoes. Unexpectedly, mosquito midguts from 39 DSFs (44% of oocyst-positive feeds analyzed) tested positive for Plasmodium ovale.

conclusionsParasites circulating at the limit of PCR detection commonly infect mosquitoes. However, a small proportion of highly infectious carriers contribute disproportionately to transmission, offering potential for targeted interventions. P. ovale was frequently co-transmitted with P. falciparum to mosquitoes.

Indexed as

AnophelesDisease ReservoirsMalariaMalaria, FalciparumPlasmodium falciparumPlasmodium ovaleAdolescentAdultAgedAnimalsAsymptomatic InfectionsCarrier StateChildChild, PreschoolFemaleHumansasymptomatic malariamalaria transmissionmosquito skin feedingPlasmodium falciparumPlasmodium ovale

Identifiers

PMID41386967
PMCPMC12930486

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.