Evidence map›Paper›PMID 26205072›Full record

ArticleJournal of insect physiology2016

Pseudomonas syringae enhances herbivory by suppressing the reactive oxygen burst in Arabidopsis.

Simon C Groen, Parris T Humphrey, Daniela Chevasco, Frederick M Ausubel, Naomi E Pierce, Noah K Whiteman

Abstract read
In one paragraph

Article in Journal of insect physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 30 citations in OpenAlex.

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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

6 authors at 3 institutions in 1 country.

Simon C GroenDepartment of Ecology and Evolutionary Biology, University of Arizona, Tucson, AZ 85721, United States; Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138, United States. Electronic address: scgroen@email.arizona.edu.
Parris T HumphreyDepartment of Ecology and Evolutionary Biology, University of Arizona, Tucson, AZ 85721, United States. Electronic address: pth@email.arizona.edu.
Daniela ChevascoDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138, United States. Electronic address: daniela578@gmail.com.
Frederick M AusubelDepartment of Genetics, Harvard Medical School, Boston, MA 02115, United States; Department of Molecular Biology, Massachusetts General Hospital, Boston, MA 02114, United States. Electronic address: ausubel@molbio.mgh.harvard.edu.
Naomi E PierceDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138, United States. Electronic address: npierce@oeb.harvard.edu.
Noah K WhitemanDepartment of Ecology and Evolutionary Biology, University of Arizona, Tucson, AZ 85721, United States; Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138, United States. Electronic address: whiteman@email.arizona.edu.
Harvard University · USUniversity of Arizona · USMassachusetts General Hospital · US

Funding

Genetic Analysis of the Plant Defense ResponseR37GM048707 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI AUSUBEL, FREDERICK M · 2005 to 2014
$5.5M
GENETIC ANALYSIS OF THE PLANT DEFENSE RESPONSER01GM048707 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI AUSUBEL, FREDERICK M · 1993 to 2004
$1.9M
Dissecting Mechanisms of Host Manipulation by PathogensF32AI069732 · NIAID · HARVARD UNIVERSITY · PI WHITEMAN, NOAH K · 2007 to 2009
$143k
NIAID NIH HHS F32 AI069732NIAID NIH HHS F32AI069732NIGMS NIH HHS R01 GM048707NIGMS NIH HHS R37 GM048707NIGMS NIH HHS R37 GM48707
6 · The paper itself

Abstract

Plant-herbivore interactions have evolved in the presence of plant-colonizing microbes. These microbes can have important third-party effects on herbivore ecology, as exemplified by drosophilid flies that evolved from ancestors feeding on plant-associated microbes. Leaf-mining flies in the genus Scaptomyza, which is nested within the paraphyletic genus Drosophila, show strong associations with bacteria in the genus Pseudomonas, including Pseudomonas syringae. Adult females are capable of vectoring these bacteria between plants and larvae show a preference for feeding on P. syringae-infected leaves. Here we show that Scaptomyza flava larvae can also vector P. syringae to and from feeding sites, and that they not only feed more, but also develop faster on plants previously infected with P. syringae. Our genetic and physiological data show that P. syringae enhances S. flava feeding on infected plants at least in part by suppressing anti-herbivore defenses mediated by reactive oxygen species.

Indexed as

HerbivoryAnimalsArabidopsisDrosophilidaeHost-Parasite InteractionsPlant ImmunityPseudomonas syringaeReactive Oxygen SpeciesSymbiosisReactive Oxygen SpeciesArabidopsis thalianaDrosophila melanogasterHerbivorePlant defensePseudomonas syringaeReactive oxygen speciesScaptomyza

Identifiers

PMID26205072
PMCPMC4721946
OpenAlexW1032848452

What OpenQuestion holds

Textmetadata
LicenceTDM
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.