Evidence map›Paper›PMID 29518156›Full record

ArticlePLoS pathogens2018

CRISPR/Cas9 -mediated gene knockout of Anopheles gambiae FREP1 suppresses malaria parasite infection.

Yuemei Dong, Maria L Simões, Eric Marois, George Dimopoulos

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed, 1 pooled it
19.5field-weighted citation impact, top 1% 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

76 citing papers in PubMed, 1 synthesis or guideline pooled it, 164 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
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  7. Article
  8. Article
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  10. Review
  11. Article
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  13. Article
  14. Article
  15. Review
  16. Applications of CRISPR in Parasitology.Current pharmaceutical biotechnology · 2025
    Review
  17. Review
  18. Article
  19. Article
  20. Genes drive organisms and slippery slopes.Pathogens and global health · 2024
    Review

16 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 2 countries.

Yuemei DongW. Harry Feinstone Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Malaria Research Institute, Johns Hopkins University, Baltimore, Maryland, United States of America.
Maria L SimõesW. Harry Feinstone Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Malaria Research Institute, Johns Hopkins University, Baltimore, Maryland, United States of America.
Eric MaroisInserm, CNRS, Université de Strasbourg, Strasbourg, France.ORCID 0000-0003-4147-3747
George DimopoulosW. Harry Feinstone Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Malaria Research Institute, Johns Hopkins University, Baltimore, Maryland, United States of America.ORCID 0000-0001-6755-8111
Johns Hopkins University · USCentre National de la Recherche Scientifique · FR

Funding

MicroRNA regulation of Anopheles immunity to PlasmodiumR01AI122743 · NIAID · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI DIMOPOULOS, GEORGE, ZHU, JINSONG · 2016 to 2020
$3.3M
Plasmodium agonists for transmission-blockingR21AI131574 · NIAID · JOHNS HOPKINS UNIVERSITY · PI DIMOPOULOS, GEORGE · 2017 to 2018
$450k
NIAID NIH HHS R01 AI122743NIAID NIH HHS R21 AI131574NIH HHS R21AI131574NIH HHS RO1AI122743
6 · The paper itself

Abstract

Plasmodium relies on numerous agonists during its journey through the mosquito vector, and these agonists represent potent targets for transmission-blocking by either inhibiting or interfering with them pre- or post-transcriptionally. The recently developed CRISPR/Cas9-based genome editing tools for Anopheles mosquitoes provide new and promising opportunities for the study of agonist function and for developing malaria control strategies through gene deletion to achieve complete agonist inactivation. Here we have established a modified CRISPR/Cas9 gene editing procedure for the malaria vector Anopheles gambiae, and studied the effect of inactivating the fibrinogen-related protein 1 (FREP1) gene on the mosquito's susceptibility to Plasmodium and on mosquito fitness. FREP1 knockout mutants developed into adult mosquitoes that showed profound suppression of infection with both human and rodent malaria parasites at the oocyst and sporozoite stages. FREP1 inactivation, however, resulted in fitness costs including a significantly lower blood-feeding propensity, fecundity and egg hatching rate, a retarded pupation time, and reduced longevity after a blood meal.

Indexed as

CRISPR-Cas SystemsAnimalsAnophelesGene Knockout TechniquesHumansInsect ProteinsMalaria, FalciparumMiceOocystsPlasmodium falciparumSporozoitesInsect Proteins

Identifiers

PMID29518156
PMCPMC5843335
OpenAlexW2793956832

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.