Evidence map›Paper›PMID 39626640›Full record

ArticleJournal of innate immunity2025

Pore-Forming Toxin-Like Proteins in the Anti-Parasitoid Immune Response of Drosophila.

Lilla B Magyar, Edit Ábrahám, Zoltán Lipinszki, Rebecca L Tarnopol, Noah K Whiteman, Viktória Varga, Dan Hultmark, István Andó, Gyöngyi Cinege

Abstract read
In one paragraph

Article in Journal of innate immunity, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
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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

9 authors.

Lilla B MagyarInnate Immunity Group, Institute of Genetics, HUN-REN Biological Research Centre, Szeged, Hungary.
Edit ÁbrahámSynthetic and Systems Biology Unit, Institute of Biochemistry, HUN-REN Biological Research Centre, Szeged, Hungary.
Zoltán LipinszkiSynthetic and Systems Biology Unit, Institute of Biochemistry, HUN-REN Biological Research Centre, Szeged, Hungary.
Rebecca L TarnopolDepartment of Plant and Microbial Biology, University of California, Berkeley, California, USA.
Noah K WhitemanDepartment of Integrative Biology, University of California, Berkeley, California, USA.
Viktória VargaInnate Immunity Group, Institute of Genetics, HUN-REN Biological Research Centre, Szeged, Hungary.
Dan HultmarkDepartment of Molecular Biology, Umea University, Umea, Sweden.
István AndóInnate Immunity Group, Institute of Genetics, HUN-REN Biological Research Centre, Szeged, Hungary.
Gyöngyi CinegeInnate Immunity Group, Institute of Genetics, HUN-REN Biological Research Centre, Szeged, Hungary.

Funding

Co-evolutionary Genetics of Host-Parasite InteractionsR35GM119816 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI NOAH K WHITEMAN · 2016 to 2026
$4.7M
NIGMS NIH HHS R35 GM119816
6 · The paper itself

Abstract

introductionSpecies of the ananassae subgroup of Drosophilidae are highly resistant to parasitoid wasp infections. We have previously shown that the genes encoding cytolethal distending toxin B (CdtB) and the apoptosis inducing protein of 56 kDa (AIP56) were horizontally transferred to these fly species from prokaryotes and are now instrumental in the anti-parasitoid immune defense of Drosophila ananassae. Here we describe a new family of genes, which encode proteins with hemolysin E domains, heretofore only identified in prokaryotes. Hemolysin E proteins are pore-forming toxins, important virulence factors of bacteria.

methodsBioinformatical, transcriptional, and protein expressional studies were used.

resultsThe hemolysin E-like genes have a scattered distribution among the genomes of species belonging to several different monophyletic lineages in the family Drosophilidae. We detected structural homology with the bacterial Hemolysin E toxins and showed that the origin of the D. ananassae hemolysin E-like genes (hl1-38) is consistent with prokaryotic horizontal gene transfer. These genes encode humoral factors, secreted into the hemolymph by the fat body and hemocytes. Their expression is induced solely by parasitoid infection and the proteins bind to the developing parasitoids.

conclusionsHemolysin E-like proteins acquired by horizontal gene transfer and expressed by the primary immune organs may contribute to the elimination of parasitoids, as novel humoral factors in Drosophila innate immunity.

Indexed as

DrosophilaDrosophila ProteinsHemolysin ProteinsPore Forming Cytotoxic ProteinsWaspsAnimalsBacterial ToxinsGene Transfer, HorizontalHemocytesHemolymphImmunity, InnatePhylogenyBacterial ToxinsDrosophila ProteinsHemolysin ProteinsPore Forming Cytotoxic ProteinsDrosophilaHemolysinHorizontal gene transferParasitoidPore-forming toxin

Identifiers

PMID39626640
PMCPMC11731912

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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.