Evidence map›Paper›PMID 35972714›Full record

ArticleJournal of chemical ecology2022

What Goes in Must Come Out? The Metabolic Profile of Plants and Caterpillars, Frass, And Adults of Asota (Erebidae: Aganainae) Feeding on Ficus (Moraceae) in New Guinea.

Alyssa M Fontanilla, Gibson Aubona, Mentap Sisol, Ilari Kuukkanen, Juha-Pekka Salminen, Scott E Miller, Jeremy D Holloway, Vojtech Novotny, Martin Volf, Simon T Segar

Abstract read
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In one paragraph

Article in Journal of chemical ecology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
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

10 authors at 6 institutions in 5 countries.

Alyssa M FontanillaBiology Centre, Institute of Entomology, the Czech Academy of Sciences, České Budějovice, Czech Republic.ORCID http://orcid.org/0000-0002-4707-4918
Gibson AubonaNew Guinea Binatang Research Center, Madang, Papua New Guinea.
Mentap SisolNew Guinea Binatang Research Center, Madang, Papua New Guinea.
Ilari KuukkanenNatural Chemistry Research Group, Department of Chemistry, University of Turku, Turku, Finland.
Juha-Pekka SalminenNatural Chemistry Research Group, Department of Chemistry, University of Turku, Turku, Finland.ORCID http://orcid.org/0000-0002-2912-7094
Scott E MillerNational Museum of Natural History, Smithsonian Institution, Washington, DC, USA.ORCID http://orcid.org/0000-0002-4138-1378
Jeremy D HollowayDepartment of Life Sciences, The Natural History Museum, London, UK.
Vojtech NovotnyBiology Centre, Institute of Entomology, the Czech Academy of Sciences, České Budějovice, Czech Republic.ORCID http://orcid.org/0000-0001-7918-8023
Martin VolfBiology Centre, Institute of Entomology, the Czech Academy of Sciences, České Budějovice, Czech Republic.ORCID http://orcid.org/0000-0003-4126-3897
Simon T SegarAgriculture and Environment Department, Harper Adams University, Newport, UK. ssegar@harper-adams.ac.uk.ORCID http://orcid.org/0000-0001-6621-9409
Czech Academy of Sciences · CZNew Guinea Binatang Research Center · PGUniversity of Turku · FIHarper Adams University · GBNatural History Museum · GBSmithsonian Institution · US

Funding

Grantová Agentura České Republiky 19-28126XH2020 European Research Council 669609
6 · The paper itself

Abstract

Insect herbivores have evolved a broad spectrum of adaptations in response to the diversity of chemical defences employed by plants. Here we focus on two species of New Guinean Asota and determine how these specialist moths deal with the leaf alkaloids of their fig (Ficus) hosts. As each focal Asota species is restricted to one of three chemically distinct species of Ficus, we also test whether these specialized interactions lead to similar alkaloid profiles in both Asota species. We reared Asota caterpillars on their respective Ficus hosts in natural conditions and analyzed the alkaloid profiles of leaf, frass, caterpillar, and adult moth samples using UHPLC-MS/MS analyses. We identified 43 alkaloids in our samples. Leaf alkaloids showed various fates. Some were excreted in frass or found in caterpillars and adult moths. We also found two apparently novel indole alkaloids-likely synthesized de novo by the moths or their microbiota-in both caterpillar and adult tissue but not in leaves or frass. Overall, alkaloids unique or largely restricted to insect tissue were shared across moth species despite feeding on different hosts. This indicates that a limited number of plant compounds have a direct ecological function that is conserved among the studied species. Our results provide evidence for the importance of phytochemistry and metabolic strategies in the formation of plant-insect interactions and food webs in general. Furthermore, we provide a new potential example of insects acquiring chemicals for their benefit in an ecologically relevant insect genus.

Indexed as

AlkaloidsFicusMothsAnimalsHerbivoryInsectaLarvaMetabolomeNew GuineaPlantsTandem Mass SpectrometryAlkaloidsAlkaloidsBiodiversityFood-websHerbivoresHost-specificityPlant–insect interactions

Identifiers

PMID35972714
OpenAlexW4291940556

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.