Evidence map›Paper›PMID 31127421›Full record

ArticleJournal of chemical ecology2019

Pathogen-Mediated Tritrophic Interactions: Baculovirus-Challenged Caterpillars Induce Higher Plant Defenses than Healthy Caterpillars.

Qinjian Pan, Ikkei Shikano, Kelli Hoover, Tong-Xian Liu, Gary W Felton

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of chemical ecology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

6 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
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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

5 authors at 2 institutions in 3 countries.

Qinjian PanState Key Laboratory of Crop Stress Biology for Arid Areas, and Key Laboratory of Integrated Pest Management on the Loess Plateau of Ministry of Agriculture, Northwest A&F University, Yangling, Shaanxi, China. panqinjian123@163.com.ORCID http://orcid.org/0000-0001-9045-672X
Ikkei ShikanoDepartment of Entomology and Center for Chemical Ecology, Pennsylvania State University, University Park, PA, 16802, USA.
Kelli HooverDepartment of Entomology and Center for Chemical Ecology, Pennsylvania State University, University Park, PA, 16802, USA.
Tong-Xian LiuState Key Laboratory of Crop Stress Biology for Arid Areas, and Key Laboratory of Integrated Pest Management on the Loess Plateau of Ministry of Agriculture, Northwest A&F University, Yangling, Shaanxi, China. txliu@nwsuaf.edu.cn.
Gary W FeltonDepartment of Entomology and Center for Chemical Ecology, Pennsylvania State University, University Park, PA, 16802, USA.
Pennsylvania State University · USNorth West Agriculture and Forestry University · CN

Funding

China Scholarship Council 201506300111National Science Foundation (US) IOS-1645548Natural Sciences and Engineering Research Council of Canada Postdoctoral Fellowship NSERC PDF-488105-2016
6 · The paper itself

Abstract

Although the tritrophic interactions of plants, insect herbivores and their natural enemies have been intensely studied for several decades, the roles of entomopathogens in their indirect modulation of plant-insect relationships is still unclear. Here, we employed a sublethal dose of a baculovirus with a relatively broad host range (AcMNPV) to explore if feeding by baculovirus-challenged Helicoverpa zea caterpillars induces direct defenses in the tomato plant. We examined induction of plant defenses following feeding by H. zea, including tomato plants fed on by healthy caterpillars, AcMNPV-challenged caterpillars, or undamaged controls, and subsequently compared the transcript levels of defense related proteins (i.e., trypsin proteinase inhibitors, peroxidase and polyphenol oxidase) and other defense genes (i.e., proteinase inhibitor II and cysteine proteinase inhibitor) from these plants, in addition to comparing caterpillar relative growth rates. As a result, AcMNPV-challenged caterpillars induced the highest plant anti-herbivore defenses. We examined several elicitors and effectors in the secretions of these caterpillars (i.e., glucose oxidase, phospholipase C, and ATPase hydrolysis), which surprisingly did not differ between treatments. Hence, we suggest that the greater induction of plant defenses by the virus-challenged caterpillars may be due to differences in the amount of these secretions deposited during feeding or to some other unknown factor(s).

Indexed as

AnimalsBaculoviridaeCatechol OxidaseFeeding BehaviorGene Expression Regulation, PlantHerbivoryHost-Parasite InteractionsLarvaMothsPeroxidasePlant LeavesPlant ProteinsRNA, PlantSalivary GlandsSolanum lycopersicumCatechol OxidasePeroxidasePlant ProteinsRNA, PlantHerbivore perceptionImmune responsesInduce defenseOral secretionsPlant defenseSalivaVentral eversible gland

Identifiers

PMID31127421
OpenAlexW2946090298

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.