Evidence map›Paper›PMID 33243237›Full record

ArticleMalaria journal2020

Efficacy of extended release formulations of Natular™ (spinosad) against larvae and adults of Anopheles mosquitoes in western Kenya.

John E Gimnig, Maurice Ombok, Nabie Bayoh, Derrick Mathias, Eric Ochomo, William Jany, Edward D Walker

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 22% of its field
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

5 citing papers in PubMed, 10 citations in OpenAlex.

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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

7 authors at 4 institutions in 2 countries.

John E GimnigCenters for Disease Control and Prevention, Division of Parasitic Diseases and Malaria, Atlanta, GA, USA. hzg1@cdc.gov.ORCID http://orcid.org/0000-0003-4218-447X
Maurice OmbokKenya Medical Research Institute, Centre for Global Health Research, Kisumu, Kenya.
Nabie BayohKenya Medical Research Institute, Centre for Global Health Research, Kisumu, Kenya.
Derrick MathiasCenters for Disease Control and Prevention, Division of Parasitic Diseases and Malaria, Atlanta, GA, USA.
Eric OchomoKenya Medical Research Institute, Centre for Global Health Research, Kisumu, Kenya.
William JanyClarke International, St. Charles, IL, USA.
Edward D WalkerDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI, USA.
Kenya Medical Research Institute · KECenters for Disease Control and Prevention · USClarke (United States) · USMichigan State University · US

Funding

Microbial Mediation of Habitat Selection and ProductionR01AI050703 · NIAID · MICHIGAN STATE UNIVERSITY · PI WALKER, EDWARD D · 2002 to 2006
$1.6M
NIAID NIH HHS R01 AI050703NIH HHS R01AI50703NIH HHS U01AI0508542
6 · The paper itself

Abstract

backgroundLarval source management is recommended as a supplementary vector control measure for the prevention of malaria. Among the concerns related to larviciding is the feasibility of implementation in tropical areas with large numbers of habitats and the need for frequent application. Formulated products of spinosad that are designed to be effective for several weeks may mitigate some of these concerns.

methodsIn a semi-field study, three formulations of spinosad (emulsifiable concentrate, extended release granules and tablet formulations) were tested in naturalistic habitats in comparison to an untreated control. Cohorts of third instar Anopheles gambiae (Diptera: Culicidae) were introduced into the habitats in screened cages every week up to four weeks after application and monitored for survivorship over three days. A small-scale field trial was then conducted in two villages. Two of the spinosad formulations were applied in one village over the course of 18 months. Immature mosquito populations were monitored with standard dippers in sentinel sites and adult populations were monitored by pyrethrum spray catches.

resultsIn the semi-field study, the efficacy of the emulsifiable concentrate of spinosad waned 1 week after treatment. Mortality in habitats treated with the extended release granular formulation of spinosad was initially high but declined gradually over 4 weeks while mortality in habitats treated with the dispersable tablet formulation was low immediately after treatment but rose to 100% through four weeks. In the field study, immature and adult Anopheles mosquito populations were significantly lower in the intervention village compared to the control village during the larviciding period. Numbers of collected mosquitoes were lower in the intervention village compared to the control village during the post-intervention period but the difference was not statistically significant.

conclusionsThe extended release granular formulation and the dispersible tablet formulations of spinosad are effective against larval Anopheles mosquitoes for up to four weeks and may be an effective tool as part of larval source management programmes for reducing adult mosquito density and malaria transmission.

Indexed as

AnophelesInsecticidesMacrolidesMosquito ControlMosquito VectorsAnimalsDelayed-Action PreparationsDrug CombinationsKenyaLarvaMalariaDelayed-Action PreparationsDrug CombinationsInsecticidesMacrolidesspinosadLarval source managementMalariaMosquitoesSpinosad

Identifiers

PMID33243237
PMCPMC7691113
OpenAlexW3108882639

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.