Evidence map›Paper›PMID 39361039›Full record

ArticlePlanta2024

Butterfly eggs prime anti-herbivore defense in an annual but not perennial Arabidopsis species.

Maryse A P Huve, Norbert Bittner, Reinhard Kunze, Monika Hilker, Mitja N P Remus-Emsermann, Luis R Paniagua Voirol, Vivien Lortzing

Abstract read
In one paragraph

Article in Planta, 2024. 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

7 authors.

Maryse A P Huve *Microbiology, Institute of Biology, Dahlem Centre of Plant Sciences, Freie Universität Berlin, Königin-Luise-Str. 12-16, 14195, Berlin, Germany.
Norbert Bittner *Applied Genetics, Institute of Biology, Dahlem Centre of Plant Sciences, Freie Universität Berlin, Albrecht-Thaer-Weg 6, 14195, Berlin, Germany.
Reinhard KunzeApplied Genetics, Institute of Biology, Dahlem Centre of Plant Sciences, Freie Universität Berlin, Albrecht-Thaer-Weg 6, 14195, Berlin, Germany.
Monika HilkerApplied Zoology/Animal Ecology, Institute of Biology, Dahlem Centre of Plant Sciences, Freie Universität Berlin, Haderslebener Str. 9, 12163, Berlin, Germany.
Mitja N P Remus-EmsermannMicrobiology, Institute of Biology, Dahlem Centre of Plant Sciences, Freie Universität Berlin, Königin-Luise-Str. 12-16, 14195, Berlin, Germany.
Luis R Paniagua VoirolMicrobiology, Institute of Biology, Dahlem Centre of Plant Sciences, Freie Universität Berlin, Königin-Luise-Str. 12-16, 14195, Berlin, Germany. luis.paniagua@fu-berlin.de.ORCID http://orcid.org/0000-0001-9868-1884
Vivien LortzingApplied Zoology/Animal Ecology, Institute of Biology, Dahlem Centre of Plant Sciences, Freie Universität Berlin, Haderslebener Str. 9, 12163, Berlin, Germany. vivien.lortzing@fu-berlin.de.

Funding

Deutsche Forschungsgemeinschaft (DFG) 502563004
6 · The paper itself

Abstract

MAIN

conclusionUnlike Arabidopsis thaliana, defenses of Arabidopsis lyrata against Pieris brassicae larval feeding are not primable by P. brassicae eggs. Thus, egg primability of plant anti-herbivore defenses is not phylogenetically conserved in the genus Arabidopsis. While plant anti-herbivore defenses of the annual species Arabidopsis thaliana were shown to be primable by Pieris brassicae eggs, the primability of the phylogenetically closely related perennial Arabidopsis lyrata has not yet been investigated. Previous studies revealed that closely related wild Brassicaceae plant species, the annual Brassica nigra and the perennial B. oleracea, exhibit an egg-primable defense trait, even though they have different life spans. Here, we tested whether P. brassicae eggs prime anti-herbivore defenses of the perennial A. lyrata. We exposed A. lyrata to P. brassicae eggs and larval feeding and assessed their primability by (i) determining the biomass of P. brassicae larvae after feeding on plants with and without prior P. brassicae egg deposition and (ii) investigating the plant transcriptomic response after egg deposition and/or larval feeding. For comparison, these studies were also conducted with A. thaliana. Consistent with previous findings, A. thaliana's response to prior P. brassicae egg deposition negatively affected conspecific larvae feeding upon A. thaliana. However, this was not observed in A. lyrata. Arabidopsis thaliana responded to P. brassicae eggs with strong transcriptional reprogramming, whereas A. lyrata responses to eggs were negligible. In response to larval feeding, A. lyrata exhibited a greater transcriptome change compared to A. thaliana. Among the strongly feeding-induced A. lyrata genes were those that are egg-primed in feeding-induced A. thaliana, i.e., CAX3, PR1, PR5, and PDF1.4. These results suggest that A. lyrata has evolved a robust feeding response that is independent from prior egg exposure.

Indexed as

ArabidopsisButterfliesHerbivoryLarvaAnimalsGene Expression Regulation, PlantOvumPlant Defense Against HerbivoryTranscriptomeHerbivoryInducible plant defensesInsect ovipositionPieris brassicae

Identifiers

PMID39361039
PMCPMC11450040

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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.