Evidence map›Paper›PMID 42380592›Full record

Articlenpj drug discovery2026

Vector venom: venomics of Aedes albopictus reveals a large enzyme repertoire and novel cecropins with activity against E. coli.

Ludwig Dersch, Jonas Krämer, Sabine Hurka, Maik Damm, Ole Bohlken, Alejandra Centurión, Bodunrin Omokungbe, Lennart Schulte, Michael Marner, Kornelia Hardes and 3 more

Abstract read
In one paragraph

Article in npj drug discovery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Ludwig DerschAnimal Venomics Lab, Fraunhofer Institute for Molecular Biology and Applied Ecology, Giessen, Germany. ludwig.dersch@ime.fraunhofer.de.
Jonas KrämerAnimal Venomics Lab, Fraunhofer Institute for Molecular Biology and Applied Ecology, Giessen, Germany.
Sabine HurkaAnimal Venomics Lab, Fraunhofer Institute for Molecular Biology and Applied Ecology, Giessen, Germany.
Maik DammAnimal Venomics Lab, Fraunhofer Institute for Molecular Biology and Applied Ecology, Giessen, Germany.
Ole BohlkenAnimal Venomics Lab, Fraunhofer Institute for Molecular Biology and Applied Ecology, Giessen, Germany.
Alejandra CenturiónLOEWE-Centre for Translational Biodiversity Genomics, Frankfurt a. M., Germany.
Bodunrin OmokungbeLOEWE-Centre for Translational Biodiversity Genomics, Frankfurt a. M., Germany.
Lennart SchulteAnimal Venomics Lab, Fraunhofer Institute for Molecular Biology and Applied Ecology, Giessen, Germany.
Michael MarnerFraunhofer Institute for Molecular Biology and Applied Ecology, Branch for Bioresources, Giessen, Germany.
Kornelia HardesLOEWE-Centre for Translational Biodiversity Genomics, Frankfurt a. M., Germany.
Till F SchäberleInstitute for Insect Biotechnology, Justus-Liebig-University of Giessen, Giessen, Germany.
Andreas VilcinskasLOEWE-Centre for Translational Biodiversity Genomics, Frankfurt a. M., Germany.
Tim LüddeckeAnimal Venomics Lab, Fraunhofer Institute for Molecular Biology and Applied Ecology, Giessen, Germany. tim.lueddecke@ime.fraunhofer.de.

Funding

Bundesministerium für -Forschung, Technologie und Raumfahrt 01KI2024Deutsche Forschungsgemeinschaft 536604070Hessisches Ministerium für Wissenschaft und Kunst LOEWE/1/10/519/03/03.001(0014)/52
6 · The paper itself

Abstract

Mosquitoes are vectors of deadly diseases and pose a global health threat. Particularly, the Asian tiger mosquito Aedes albopictus can transmit several pathogens, and is expanding into temperate regions. During blood feeding, mosquitoes inject chemically complex saliva, here referred to as venom, which modulates hemostasis, inflammation, immune response and pathogen transmission. In-depth knowledge of mosquito venom is crucial for understanding disease biology and enabling biodiscovery. We present a venomics study of Ae. albopictus and identify 119 distinct proteins validated by mass spectrometry and transcriptomics. The venom is rich in enzymes (e.g., hydrolases and Apyrases) and non-enzymatic components (e.g., odorant binding proteins and protease inhibitors). Additionally, we identified six novel cecropin family antimicrobial peptides. Structural analyses indicate an amphipathic N-terminus, hinge region, and hydrophobic C-terminus consistent with type II channel formation. Functional assays revealed that these cecropins exert potent effects on E. coli while leaving mammalian epithelial cells and erythrocytes unaffected. Overall, our study reveals that mosquito venom is a source of diverse biomacromolecules, deepening our understanding of its physiology, vector biology, and biochemical ecology. This opens paths for new mosquito-control strategies and drug discovery.

Identifiers

PMID42380592
PMCPMC13267129

What Socratic 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 Socratic graph.