Evidence map›Paper›PMID 26991784›Full record

ArticlePlant, cell & environment2016

Oral secretions from Mythimna separata insects specifically induce defence responses in maize as revealed by high-dimensional biological data.

Jinfeng Qi, Guiling Sun, Lei Wang, Chunxia Zhao, Christian Hettenhausen, Meredith C Schuman, Ian T Baldwin, Jing Li, Juan Song, Zhudong Liu and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Plant, cell & environment, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
7.1field-weighted citation impact, top 4% 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

31 citing papers in PubMed, 77 citations in OpenAlex.

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  13. AxenicFrontiers in plant science · 2023
    Article
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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

13 authors at 5 institutions in 3 countries.

Jinfeng Qi *Department of Economic Plants and Biotechnology, Yunnan Key Laboratory for Wild Plant Resources, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.
Guiling Sun *Department of Economic Plants and Biotechnology, Yunnan Key Laboratory for Wild Plant Resources, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.
Lei Wang *Department of Economic Plants and Biotechnology, Yunnan Key Laboratory for Wild Plant Resources, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.
Chunxia Zhao *Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Christian HettenhausenDepartment of Economic Plants and Biotechnology, Yunnan Key Laboratory for Wild Plant Resources, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.
Meredith C SchumanDepartment of Molecular Ecology, Max Planck Institute for Chemical Ecology, Jena 07745, Germany.
Ian T BaldwinDepartment of Molecular Ecology, Max Planck Institute for Chemical Ecology, Jena 07745, Germany.
Jing LiDepartment of Economic Plants and Biotechnology, Yunnan Key Laboratory for Wild Plant Resources, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.
Juan SongDepartment of Economic Plants and Biotechnology, Yunnan Key Laboratory for Wild Plant Resources, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.
Zhudong LiuState Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing 100080, China.
Guowang XuDalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Xin LuDalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Jianqiang WuDepartment of Economic Plants and Biotechnology, Yunnan Key Laboratory for Wild Plant Resources, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.
Kunming Institute of Botany · CNDalian Institute of Chemical Physics · CNMax Planck Institute for Chemical Ecology · DEChinese Academy of Sciences · CNInstitute of Zoology · CN

Funding

European Research Council 293926
6 · The paper itself

Abstract

Attack from insect herbivores poses a major threat to plant survival, and accordingly, plants have evolved sophisticated defence systems. Maize is cultivated as a staple crop worldwide, and insect feeding causes large production losses. Despite its importance in agriculture, little is known about how maize reacts to insect herbivory. Taking advantage of advances in sequencing and mass spectrometry technology, we studied the response of maize to mechanical wounding and simulated Mythimna separata (a specialist insect) herbivory by applying its oral secretions (OS) to wounds. In comparison to the responses induced by mechanical wounding, OS elicited larger and longer-lasting changes in the maize transcriptome, proteome, metabolome and phytohormones. Specifically, many genes, proteins and metabolites were uniquely induced or repressed by OS. Nearly 290 transcription factor genes from 39 families were involved in OS-induced responses, and among these, more transcription factor genes were specifically regulated by OS than by wounding. This study provides a large-scale omics dataset for understanding maize response to chewing insects and highlights the essential role of OS in plant-insect interactions.

Indexed as

HerbivoryProteomeTranscriptomeAnimalsGene Expression ProfilingMothsPlant Growth RegulatorsTranscription FactorsZea maysPlant Growth RegulatorsProteomeTranscription Factorsmetabolomephytohormonesproteometranscriptome

Identifiers

PMID26991784
PMCPMC5295635
OpenAlexW2297933436

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.