Evidence map›Paper›PMID 38871839›Full record

ArticleScientific reports2024

Vectorial drivers of malaria transmission in Jabi Tehnan district, Amhara Regional State, Ethiopia.

Aklilu K Belay, Abebe Asale, Catherine L Sole, Fiona Kinya, Abdullahi A Yusuf, Baldwyn Torto, Clifford M Mutero, David P Tchouassi

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Trial
  2. Article
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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

8 authors.

Aklilu K BelayInternational Centre of Insect Physiology and Ecology, P.O. Box 30772-00100, Nairobi, Kenya.
Abebe AsaleInternational Centre of Insect Physiology and Ecology, P.O. Box 5689, Addis Ababa, Ethiopia.
Catherine L SoleDepartment of Zoology and Entomology, University of Pretoria, Private Bag X0028, Pretoria, South Africa.
Fiona KinyaInternational Centre of Insect Physiology and Ecology, P.O. Box 30772-00100, Nairobi, Kenya.
Abdullahi A YusufDepartment of Zoology and Entomology, University of Pretoria, Private Bag X0028, Pretoria, South Africa.
Baldwyn TortoInternational Centre of Insect Physiology and Ecology, P.O. Box 30772-00100, Nairobi, Kenya.
Clifford M MuteroInternational Centre of Insect Physiology and Ecology, P.O. Box 30772-00100, Nairobi, Kenya.
David P TchouassiInternational Centre of Insect Physiology and Ecology, P.O. Box 30772-00100, Nairobi, Kenya. dtchouassi@icipe.org.

Funding

Norwegian Agency for Development Cooperation (Norad) RAF-3058 KEN-18/0005Wellcome Trust 222005Wellcome Trust 222005/Z/20/Z
6 · The paper itself

Abstract

Among the factors affecting the effectiveness of malaria control is poor knowledge of the entomologic drivers of the disease. We investigated anopheline populations as part of a baseline study to implement house screening of windows and doors as a supplementary malaria control tool towards elimination in Jabi Tehnan district, Amhara Regional State of Ethiopia. The samples were surveyed monthly using CDC light traps between June 2020 and May 2021. Mosquito trap density (< 3 mosquitoes/trap) was low, however, with a high overall Plasmodium sporozoite rate (9%; indoor = 4.3%, outdoor = 13.1%) comprising P. falciparum (88.9%) and P. vivax (11.1%). Anopheles gambiae s.l., mostly An. arabiensis, comprised > 80% of total anopheline captures and contributed ~ 42% of Plasmodium-infected mosquitoes. On the other hand, morphologically scored Anopheles funestus s.l., constituting about 6% of anopheline collections, accounted for 50% of sporozoite-infected mosquitoes. Most of the infected An. funestus s.l. specimens (86.7%) were grouped with previously unknown or undescribed Anopheles species previously implicated as a cryptic malaria vector in the western Kenyan highlands, confirming its wider geographic distribution in eastern Africa. Other species with Plasmodium infection included An. longipalpis C, An. theileri, An. demillioni, and An. nili. Cumulatively, 77.8% of the infected mosquitoes occurred outdoors. These results suggest efficient malaria parasite transmission despite the low vector densities, which has implications for effective endpoint indicators to monitor malaria control progress. Additionally, the largely outdoor infection and discovery of previously unknown and cryptic vectors suggest an increased risk of residual malaria transmission and, thus, a constraint on effective malaria prevention and control.

Indexed as

AnophelesMosquito VectorsAnimalsEthiopiaFemaleHumansMalariaMalaria, FalciparumMalaria, VivaxMosquito ControlPlasmodium falciparumPlasmodium vivaxSporozoitesCryptic vectorsHighland areasMalaria surveillanceOutdoor bitingResidual malaria transmission

Identifiers

PMID38871839
PMCPMC11176308

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Registered trials

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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.