Evidence map›Paper›PMID 40841612›Full record

ArticleBMC infectious diseases2025

Urban malaria in Accra, Ghana: transmission risk and influence of irrigated vegetable farms.

Abdul Rahim Mohammed Sabtiu, Isaac Kwame Sraku, Christopher Mfum Owusu-Asenso, Yaw Akuamoah-Boateng, Richard Tettey Doe, Emmanuel Nana Boadu, Judith Dzifa Azumah, Nana Aba Setorwu Eyeson, Anisa Abdulai, Godfred Amoateng and 3 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Spatial temporal distribution ofGigaByte (Hong Kong, China) · 2026
    Article
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

13 authors.

Abdul Rahim Mohammed SabtiuCentre for Vector-Borne Disease Research, Department of Medical Microbiology, University of Ghana Medical School, Accra, Ghana. abdulrahimmoh16@gmail.com.
Isaac Kwame SrakuCentre for Vector-Borne Disease Research, Department of Medical Microbiology, University of Ghana Medical School, Accra, Ghana.
Christopher Mfum Owusu-AsensoCentre for Vector-Borne Disease Research, Department of Medical Microbiology, University of Ghana Medical School, Accra, Ghana.
Yaw Akuamoah-BoatengCentre for Vector-Borne Disease Research, Department of Medical Microbiology, University of Ghana Medical School, Accra, Ghana.
Richard Tettey DoeCentre for Vector-Borne Disease Research, Department of Medical Microbiology, University of Ghana Medical School, Accra, Ghana.
Emmanuel Nana BoaduCentre for Vector-Borne Disease Research, Department of Medical Microbiology, University of Ghana Medical School, Accra, Ghana.
Judith Dzifa AzumahCentre for Vector-Borne Disease Research, Department of Medical Microbiology, University of Ghana Medical School, Accra, Ghana.
Nana Aba Setorwu EyesonCentre for Vector-Borne Disease Research, Department of Medical Microbiology, University of Ghana Medical School, Accra, Ghana.
Anisa AbdulaiCentre for Vector-Borne Disease Research, Department of Medical Microbiology, University of Ghana Medical School, Accra, Ghana.
Godfred AmoatengCentre for Vector-Borne Disease Research, Department of Medical Microbiology, University of Ghana Medical School, Accra, Ghana.
Simon Kwaku AttahCentre for Vector-Borne Disease Research, Department of Medical Microbiology, University of Ghana Medical School, Accra, Ghana.
Fred Aboagye-AntwiAfrican Regional Postgraduate Programme in Insect Sciences (ARPPIS), Department of Animal Biology and Conservation Science, College of Basic and Applied Sciences, University of Ghana, Accra, Ghana. faboagye-antwi@ug.edu.gh.
Yaw Asare AfraneCentre for Vector-Borne Disease Research, Department of Medical Microbiology, University of Ghana Medical School, Accra, Ghana.

Funding

Regional Centre for Vector Borne Diseases in West Africa (RCVBD)D43TW011513 · FIC · UNIVERSITY OF GHANA · PI YAW ASARE AFRANE, Guiyun Yan · 2021 to 2026
$1.5M
Impact of insecticide resistance on the behavior and fitness of malaria vectorsR01AI123074 · NIAID · UNIVERSITY OF GHANA · PI YAW ASARE AFRANE · 2016 to 2026
$1.2M
Invasive Anopheles stephensi in Ghana: Sampling Tools and Vector Population DynamicsR03AI186018 · NIAID · COLLEGE OF HEALTH SCIENCES, UNIVERSITY OF GHANA · PI AFRANE, YAW ASARE · 2024 to 2025
$108k
FIC NIH HHS D43 TW011513NIAID NIH HHS R01 AI123074NIAID NIH HHS R03 AI186018
6 · The paper itself

Abstract

Urban malaria transmission in sub-Saharan Africa is often underestimated, emphasizing the need for research on vector distribution, abundance, behavior, and infectivity in cities. Urban malaria transmission has been on the rise across sub-Saharan Africa since 2003. Also, monitoring Anopheles populations is crucial for developing effective interventions. This study examined the biting and resting habits, distribution, abundance, and Plasmodium infection of malaria vectors in Accra. Adult malaria vectors were collected using human landing catch (HLC) and Prokopack aspiration (PPK) at ten sites in Accra, categorized into five groups: sites with Irrigated Urban Farming (IUF), Lower Socioeconomic Status (LS), Middle Socioeconomic Status (MS), High Socioeconomic Status (HS), and Peri-urban (PU) areas. Biting patterns and entomological transmission indices of malaria vectors were assessed. Molecular methods were used to detect sporozoite infection, bloodmeal sources, vector species, and insecticide resistant mutation genes. A total of 41,747 mosquitoes were collected. Of these, 95.49% (39,863/41,747) were host-seeking collected through human landing catch (HLC), consisting of Anopheles (52.54%, 20,945/39,863), Culex (42.00%, 16,742/39,863), Aedes (3.74%, 1,491/39,863), and Mansonia (1.72%, 685/39,863). The remaining 4.51% (1,884/41,747) were resting mosquitoes collected using a Procopack aspirator, comprising Anopheles (31.26%, 589/1,884), Culex (57.21%, 1,078/1,884), and Aedes (11.52%, 217/1,884). Overall, the IUF site category had the highest abundance of An. gambiae s.l. (48.63%, 10,466/21,520), followed by the PU (18.06%, 3,887/21,520), HS (16.42%, 3,533/21,520), MS (13.74%, 2,956/21,520) and LS (3.15%, 678/21,520) in both HLC and Procopack collections. Indoor An. gambiae s.l. had higher sporozoite infectivity (4.56%, 16/351) than outdoor (3.78%, 9/238) (χ

Indexed as

AnophelesMalariaMosquito VectorsAgricultural IrrigationAnimalsCitiesFarmsFeeding BehaviorFemaleGhanaHumansPlasmodiumUrban PopulationVegetablesAnophelesBloodmealEntomological inoculation rateSporozoite rateUrban agricultureUrban malaria

Identifiers

PMID40841612
PMCPMC12369028

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.