Evidence map›Paper›PMID 36241929›Full record

ArticleCellular and molecular life sciences : CMLS2022

Malaria parasites utilize two essential plasma membrane fusogens for gamete fertilization.

Sudhir Kumar, Clari Valansi, Meseret T Haile, Xiaohui Li, Kateryna Flyak, Abhisek Dwivedy, Biley A Abatiyow, Amanda S Leeb, Spencer Y Kennedy, Nelly M Camargo and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.8field-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

17 citing papers in PubMed, 30 citations in OpenAlex.

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  10. FromiScience · 2024
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  16. Host-parasite interactions duringFrontiers in immunology · 2022
    Review
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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

14 authors at 4 institutions in 2 countries.

Sudhir KumarCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-2847-393X
Clari ValansiThe Technion-Israel Institute of Technology, Haifa, Israel.
Meseret T HaileCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, USA.
Xiaohui LiThe Technion-Israel Institute of Technology, Haifa, Israel.
Kateryna FlyakThe Technion-Israel Institute of Technology, Haifa, Israel.
Abhisek DwivedyNucleic Acids Programming Laboratory, University of Illinois Urbana Champaign, Urbana, IL, USA.
Biley A AbatiyowCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, USA.
Amanda S LeebCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, USA.
Spencer Y KennedyCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, USA.
Nelly M CamargoCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, USA.
Ashley M VaughanCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, USA.
Nicolas G BrukmanThe Technion-Israel Institute of Technology, Haifa, Israel.
Benjamin PodbilewiczThe Technion-Israel Institute of Technology, Haifa, Israel.
Stefan H I KappeCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, USA. stefan.kappe@seattlechildrens.org.ORCID http://orcid.org/0000-0003-1540-1731
Infectious Disease Research Institute · USTechnion – Israel Institute of Technology · ILCenter for Infectious Disease Research · USUniversity of Illinois Urbana-Champaign · US

Funding

Systems genetics of artemisinin resistanceP01AI127338 · NIAID · UNIVERSITY OF NOTRE DAME · PI Michael T Ferdig · 2017 to 2026
$21.3M
Israeli Science Foundation F.I.R.S.T No. 2327/19National Institute of Allergy and Infectious Diseases AI127338NIAID NIH HHS P01 AI127338
6 · The paper itself

Abstract

Cell fusion of female and male gametes is the climax of sexual reproduction. In many organisms, the Hapless 2 (HAP2) family of proteins play a critical role in gamete fusion. We find that Plasmodium falciparum, the causative agent of human malaria, expresses two HAP2 proteins: PfHAP2 and PfHAP2p. These proteins are present in stage V gametocytes and localize throughout the flagellum of male gametes. Gene deletion analysis and genetic crosses show that PfHAP2 and PfHAP2p individually are essential for male fertility and thereby, parasite transmission to the mosquito. Using a cell fusion assay, we demonstrate that PfHAP2 and PfHAP2p are both authentic plasma membrane fusogens. Our results establish nonredundant essential roles for PfHAP2 and PfHAP2p in mediating gamete fusion in Plasmodium and suggest avenues in the design of novel strategies to prevent malaria parasite transmission from humans to mosquitoes.

Indexed as

MalariaParasitesAnimalsCell MembraneFemaleFertilizationGerm CellsHumansMalePlasmodium falciparumCell fusionGametocyteMacrogameteMicrogametePlasmodiumTransmission

Identifiers

PMID36241929
PMCPMC9568910
OpenAlexW4306249377

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.