Evidence map›Paper›PMID 32989301›Full record

ArticleNature chemical biology2020

Glucosylation prevents plant defense activation in phloem-feeding insects.

Osnat Malka, Michael L A E Easson, Christian Paetz, Monika Götz, Michael Reichelt, Beate Stein, Katrin Luck, Aleksa Stanišić, Ksenia Juravel, Diego Santos-Garcia and 7 more

Abstract read
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In one paragraph

Article in Nature chemical biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
7.0field-weighted citation impact, top 3% 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

20 citing papers in PubMed, 45 citations in OpenAlex.

  1. Two-component plant defenses are better than one.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  13. The downside of metabolic diversity: Postingestive rearrangements by specialized insects.Proceedings of the National Academy of Sciences of the United States of America · 2022
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  20. Making use of surplus sugar.Nature chemical biology · 2020
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 5 institutions in 3 countries.

Osnat Malka *The Hebrew University of Jerusalem, Rehovot, Israel. osnat226@gmail.com.ORCID http://orcid.org/0000-0003-0193-377X
Michael L A E Easson *Max Planck Institute for Chemical Ecology, Jena, Germany.ORCID http://orcid.org/0000-0002-9601-8410
Christian PaetzMax Planck Institute for Chemical Ecology, Jena, Germany.ORCID http://orcid.org/0000-0002-5776-7574
Monika GötzLeibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.
Michael ReicheltMax Planck Institute for Chemical Ecology, Jena, Germany.ORCID http://orcid.org/0000-0002-6691-6500
Beate SteinLeibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.
Katrin LuckMax Planck Institute for Chemical Ecology, Jena, Germany.
Aleksa StanišićMax Planck Institute for Chemical Ecology, Jena, Germany.
Ksenia JuravelThe Hebrew University of Jerusalem, Rehovot, Israel.ORCID http://orcid.org/0000-0002-3493-4907
Diego Santos-GarciaThe Hebrew University of Jerusalem, Rehovot, Israel.ORCID http://orcid.org/0000-0002-3401-2662
Lilach L MondacaSapir Academic Collage, D.N. Hof, Askelon, Israel.
Simon SpringateNatural Resources Institute, University of Greenwich, Chatham Maritime, Kent, UK.
John ColvinNatural Resources Institute, University of Greenwich, Chatham Maritime, Kent, UK.
Stephan WinterLeibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.
Jonathan GershenzonMax Planck Institute for Chemical Ecology, Jena, Germany.ORCID http://orcid.org/0000-0002-1812-1551
Shai MorinThe Hebrew University of Jerusalem, Rehovot, Israel.
Daniel G VassãoMax Planck Institute for Chemical Ecology, Jena, Germany. vassao@ice.mpg.de.ORCID http://orcid.org/0000-0001-8455-9298
Max Planck Institute for Chemical Ecology · DEHebrew University of Jerusalem · ILLeibniz Institute DSMZ – German Collection of Microorganisms and Cell Cultures · DENatural Resources Institute · GBSapir College · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The metabolic adaptations by which phloem-feeding insects counteract plant defense compounds are poorly known. Two-component plant defenses, such as glucosinolates, consist of a glucosylated protoxin that is activated by a glycoside hydrolase upon plant damage. Phloem-feeding herbivores are not generally believed to be negatively impacted by two-component defenses due to their slender piercing-sucking mouthparts, which minimize plant damage. However, here we document that glucosinolates are indeed activated during feeding by the whitefly Bemisia tabaci. This phloem feeder was also found to detoxify the majority of the glucosinolates it ingests by the stereoselective addition of glucose moieties, which prevents hydrolytic activation of these defense compounds. Glucosylation of glucosinolates in B. tabaci was accomplished via a transglucosidation mechanism, and two glycoside hydrolase family 13 (GH13) enzymes were shown to catalyze these reactions. This detoxification reaction was also found in a range of other phloem-feeding herbivores.

Indexed as

AnimalsArabidopsisFeeding BehaviorGene ExpressionGlucosinolatesGlycoside HydrolasesGlycosylationHemipteraHost-Parasite InteractionsInsect ProteinsPhloemPhylogenyPlant ImmunityGlucosinolatesGlycoside HydrolasesInsect Proteins

Identifiers

PMID32989301
OpenAlexW3089941662

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.