Evidence map›Paper›PMID 42076963›Full record

ArticleMolecular ecology2026

Genetic Variation in Chemical Defence Affects Protection of an Herbivorous Insect Against Predation.

Johannes Körnig, Kris Ortizo, Christian Woehle, Robert Greenhalgh, Holger Schielzeth, Bruno Huettel, David G Heckel, M Denise Dearing, Martin Kaltenpoth, Franziska Beran

Abstract read
In one paragraph

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

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Johannes KörnigDepartment of Insect Symbiosis, Max Planck Institute for Chemical Ecology, Jena, Germany.
Kris OrtizoDepartment of Insect Symbiosis, Max Planck Institute for Chemical Ecology, Jena, Germany.
Christian WoehleMax Planck Genome-Centre Cologne, Max Planck Institute for Plant Breeding Research, Cologne, Germany.
Robert GreenhalghSchool of Biological Sciences, University of Utah, Salt Lake City, Utah, USA.
Holger SchielzethPopulation Ecology Group, Friedrich Schiller University, Jena, Germany.
Bruno HuettelMax Planck Genome-Centre Cologne, Max Planck Institute for Plant Breeding Research, Cologne, Germany.
David G HeckelDepartment of Entomology, Max Planck Institute for Chemical Ecology, Jena, Germany.ORCID https://orcid.org/0000-0001-8991-2150
M Denise DearingSchool of Biological Sciences, University of Utah, Salt Lake City, Utah, USA.ORCID https://orcid.org/0000-0001-7881-4934
Martin KaltenpothDepartment of Insect Symbiosis, Max Planck Institute for Chemical Ecology, Jena, Germany.ORCID https://orcid.org/0000-0001-9450-0345
Franziska BeranDepartment of Insect Symbiosis, Max Planck Institute for Chemical Ecology, Jena, Germany.ORCID https://orcid.org/0000-0003-2213-5347

Funding

Deutsche Forschungsgemeinschaft 501638262Max-Planck-Gesellschaft
6 · The paper itself

Abstract

Genetic variation contributes to intraspecific differences in the chemical defence in many insect species, yet the underlying genetic mechanisms remain poorly understood. The horseradish flea beetle, Phyllotreta armoraciae, sequesters glucosinolates from its horseradish host plant and activates them using endogenous myrosinase enzymes. Of the three known myrosinases in P. armoraciae, PaMyr1 functions primarily in adults, whereas PaMyr2 and PaMyr3 are responsible for myrosinase activity in larvae. Here, we identify natural genetic variation at the myrosinase locus that gives rise to three distinct myrosinase haplotypes, only one of which retains a functional PaMyr3 gene. This variation affected PaMyr gene expression and myrosinase activity in larvae but not in adults. Larvae expressing both PaMyr2 and PaMyr3 showed elevated myrosinase activity toward 2-propenyl glucosinolate, the major glucosinolate in horseradish. Gene expression and biochemical analyses indicate that elevated myrosinase activity results from a subfunctionalization of PaMyr3, which confers greater catalytic efficiency rather than higher total myrosinase abundance. Importantly, PaMyr3-expressing larvae were less susceptible to a model generalist predator in laboratory assays, suggesting a selective advantage under high predation pressure. Consistent with this hypothesis, the PaMyr3-containing haplotype occurred at higher frequency in a natural population than in long-term laboratory populations lacking predators. Together, our results link structural genetic variation to intraspecific differences in insect chemical defence with potential consequences for predator-prey interactions in natural populations.

Indexed as

ColeopteraGenetic VariationGlycoside HydrolasesHerbivoryAnimalsGlucosinolatesHaplotypesLarvaSequence Analysis, DNAGlucosinolatesGlycoside Hydrolasesthioglucosidaseflea beetlegene duplicationglucosinolatemyrosinasePhyllotretasequestration

Identifiers

PMID42076963
PMCPMC13136917

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