Evidence map›Paper›PMID 42656854›Full record

ArticleMalariaWorld journal2026

Modified cone bioassay methods for evaluating chlorfenapyr indoor residual spray.

Jordan Benson, Frank S C Tenywa, Saphina Ngonyani, Aidi G Lugenge, Jilly J Mseti, Elingarami Sauli, Luca Facchinelli, Sarah J Moore, Olukayode G Odufuwa

Abstract read
In one paragraph

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

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0citing papers in PubMed
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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

9 authors.

Jordan BensonVector Control Product Testing Unit, Environmental Health and Ecological Science Thematic Group, Ifakara Health Institute, P.O. Box 74, Bagamoyo, Tanzania.
Frank S C TenywaVector Control Product Testing Unit, Environmental Health and Ecological Science Thematic Group, Ifakara Health Institute, P.O. Box 74, Bagamoyo, Tanzania.
Saphina NgonyaniVector Control Product Testing Unit, Environmental Health and Ecological Science Thematic Group, Ifakara Health Institute, P.O. Box 74, Bagamoyo, Tanzania.
Aidi G LugengeVector Control Product Testing Unit, Environmental Health and Ecological Science Thematic Group, Ifakara Health Institute, P.O. Box 74, Bagamoyo, Tanzania.
Jilly J MsetiVector Control Product Testing Unit, Environmental Health and Ecological Science Thematic Group, Ifakara Health Institute, P.O. Box 74, Bagamoyo, Tanzania.
Elingarami SauliSchool of Life Sciences and Bioengineering, The Nelson Mandela African Institution of Science and Technology (NM-AIST), P.O. Box 447, Arusha, Tanzania.
Luca FacchinelliLiverpool School of Tropical Medicine, Pembroke Place, Liverpool, L3 5QA, England, United Kingdom.
Sarah J MooreVector Control Product Testing Unit, Environmental Health and Ecological Science Thematic Group, Ifakara Health Institute, P.O. Box 74, Bagamoyo, Tanzania.
Olukayode G OdufuwaVector Control Product Testing Unit, Environmental Health and Ecological Science Thematic Group, Ifakara Health Institute, P.O. Box 74, Bagamoyo, Tanzania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Chlorfenapyr-based indoor residual spraying (IRS) has been prequalified for malaria control. Residual efficacy (mosquito mortality) of IRS applied to houses is typically assessed using forced-contact cone bioassays. However, chlorfenapyr is a pro-insecticide that requires mosquito metabolic activity for conversion to its toxic metabolite, tralopyril. Cone bioassays consistently underestimate mortality compared to free-flying bioassays. This study evaluated whether increasing mosquito activity during cone bioassays could better capture chlorfenapyr-induced mortality on mud surface using scalable methods. Materials and Methods: The bioefficacy of chlorfenapyr (Sylando® 240 SC) sprayed on mud surfaces was assessed in two experiments using cone bioassays against sugar-fed, laboratory-reared pyrethroid-resistant Results: Mortality remained low across all treatments in experiment 1 (7.8-15.4% at 72 hrs; 14.1-23.1% at 120 hrs), with no consistent improvement from post-exposure activity. In Experiment 2, mortality increased with 12-hrs exposure, particularly in the presence of a host (23.5% at 72 hrs; OR 2.25, 95% CI 1.71-2.97, Conclusions: Prolonged exposure and host presence modestly increased mortality, but did not produce values consistent with expected chlorfenapyr bioefficacy against free-flying mosquitoes. These findings suggest that modified cone bioassays are unlikely to provide reliable estimates of chlorfenapyr-IRS performance. Further validation is required to assess whether overnight cone tests in people's homes can provide a more realistic measure of residual bioefficacy.

Identifiers

PMID42656854
PMCPMC13508122

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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.