Evidence map›Paper›PMID 21283619›Full record

ArticlePloS one2011

Site-specific integration and expression of an anti-malarial gene in transgenic Anopheles gambiae significantly reduces Plasmodium infections.

Janet M Meredith, Sanjay Basu, Derric D Nimmo, Isabelle Larget-Thiery, Emma L Warr, Ann Underhill, Clare C McArthur, Victoria Carter, Hilary Hurd, Catherine Bourgouin and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

49 citing papers in PubMed, 109 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. ImprovedInternational journal of molecular sciences · 2023
    Article
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  17. Modern Vector Control.Cold Spring Harbor perspectives in medicine · 2018
    Review
  18. Gene Drive for Mosquito Control: Where Did It Come from and Where Are We Headed?International journal of environmental research and public health · 2017
    Review
  19. Article
  20. 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

11 authors at 2 institutions in 3 countries.

Janet M MeredithCentre for Applied Entomology and Parasitology, Keele University, Keele, United Kingdom.
Sanjay Basu
Derric D Nimmo
Isabelle Larget-Thiery
Emma L Warr
Ann Underhill
Clare C McArthur
Victoria Carter
Hilary Hurd
Catherine Bourgouin
Paul Eggleston
Keele University · GBInstitut Pasteur · FR

Funding

Wellcome TrustWellcome Trust 069162Wellcome Trust 077593
6 · The paper itself

Abstract

Diseases transmitted by mosquitoes have a devastating impact on global health and this is worsening due to difficulties with existing control measures and climate change. Genetically modified mosquitoes that are refractory to disease transmission are seen as having great potential in the delivery of novel control strategies. Historically the genetic modification of insects has relied upon transposable elements which have many limitations despite their successful use. To circumvent these limitations the Streptomyces phage phiC31 integrase system has been successfully adapted for site-specific transgene integration in insects. Here, we present the first site-specific transformation of Anopheles gambiae, the principal vector of human malaria. Mosquitoes were initially engineered to incorporate the phiC31 targeting site at a defined genomic location. A second phase of genetic modification then achieved site-specific integration of Vida3, a synthetic anti-malarial gene. Expression of Vida3, specifically in the midgut of bloodfed females, offered consistent and significant protection against Plasmodium yoelii nigeriensis, reducing average parasite intensity by 85%. Similar protection was observed against Plasmodium falciparum in some experiments, although protection was inconsistent. In the fight against malaria, it is imperative to establish a broad repertoire of both anti-malarial effector genes and tissue-specific promoters for their expression, enabling those offering maximum effect with minimum fitness cost to be identified. In the future, this technology will allow effective comparisons and informed choices to be made, potentially leading to complete transmission blockade.

Indexed as

AnimalsAnimals, Genetically ModifiedAnophelesAntimalarialsFemaleGene TargetingHumansInsect VectorsMalariaPlasmodium falciparumPlasmodium yoeliiTransgenesAntimalarials

Identifiers

PMID21283619
PMCPMC3026776
OpenAlexW2085581447

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.