Evidence map›Paper›PMID 25991725›Full record

ArticleThe Journal of biological chemistry2015

Anopheles Midgut FREP1 Mediates Plasmodium Invasion.

Genwei Zhang, Guodong Niu, Caio M Franca, Yuemei Dong, Xiaohong Wang, Noah S Butler, George Dimopoulos, Jun Li

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

55 citing papers in PubMed, 100 citations in OpenAlex.

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  15. Applications of CRISPR in Parasitology.Current pharmaceutical biotechnology · 2025
    Review
  16. Article
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  20. Review
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 at 3 institutions in 1 country.

Genwei ZhangFrom the Department of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma 73019.
Guodong NiuFrom the Department of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma 73019.
Caio M FrancaFrom the Department of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma 73019.
Yuemei Dongthe W. Harry Feinstone Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205, and.
Xiaohong WangFrom the Department of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma 73019.
Noah S Butlerthe Department of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104.
George Dimopoulosthe W. Harry Feinstone Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205, and.
Jun LiFrom the Department of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma 73019, junli@ou.edu.
University of Oklahoma · USJohns Hopkins University · USUniversity of Oklahoma Health Sciences Center · US

Funding

Proteomics CoreP20GM103447 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI DARRIN R. AKINS · 2012 to 2026
$60.2M
Targeting Mosquito FREP1 Protein for Malaria ControlR21AI115178 · NIAID · UNIVERSITY OF OKLAHOMA · PI LI, JUN · 2015 to 2016
$421k
NIAID NIH HHS 1R21AI115178-01A1NIAID NIH HHS R21 AI115178NIGMS NIH HHS GM103447NIGMS NIH HHS P20 GM103447
6 · The paper itself

Abstract

Malaria transmission depends on sexual stage Plasmodium parasites successfully invading Anopheline mosquito midguts following a blood meal. However, the molecular mechanisms of Plasmodium invasion of mosquito midguts have not been fully elucidated. Previously, we showed that genetic polymorphisms in the fibrinogen-related protein 1 (FREP1) gene are significantly associated with Plasmodium falciparum infection in Anopheles gambiae, and FREP1 is important for Plasmodium berghei infection of mosquitoes. Here we identify that the FREP1 protein is secreted from the mosquito midgut epithelium and integrated as tetramers into the peritrophic matrix, a chitinous matrix formed inside the midgut lumen after a blood meal feeding. Moreover, we show that the FREP1 can directly bind Plasmodia sexual stage gametocytes and ookinetes. Notably, ablating FREP1 expression or targeting FREP1 with antibodies significantly decreases P. falciparum infection in mosquito midguts. Our data support that the mosquito-expressed FREP1 mediates mosquito midgut invasion by multiple species of Plasmodium parasites via anchoring ookinetes to the peritrophic matrix and enabling parasites to penetrate the peritrophic matrix and the epithelium. Thus, targeting FREP1 can limit malaria transmission.

Indexed as

AnimalsAnophelesDigestive SystemFemaleFibrinogenHost-Parasite InteractionsInsect ProteinsInsect VectorsMalePlasmodium falciparumFibrinogenInsect Proteinsfibrinogenhost-pathogen interactioninsectinvasionmalariavaccine

Identifiers

PMID25991725
PMCPMC4505404
OpenAlexW2212653570

What OpenQuestion holds

Textmetadata
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.