Evidence map›Paper›PMID 25482800›Full record

ArticlePlant signaling & behavior2015

Molecular chaperons and co-chaperons, Hsp90, RAR1, and SGT1 negatively regulate bacterial wilt disease caused by Ralstonia solanacearum in Nicotiana benthamiana.

Makoto Ito, Kouhei Ohnishi, Yasufumi Hikichi, Akinori Kiba

Open access · bronzeAbstract read
In one paragraph

Article in Plant signaling & behavior, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Functional characterization of HbRAR1 inFrontiers in plant science · 2026
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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

4 authors at 1 institution in 1 country.

Makoto Itoa Laboratory of Plant Pathology and Biotechnology ; Faculty of Agriculture; Kochi University ; Nankoku , Japan.
Kouhei Ohnishi
Yasufumi Hikichi
Akinori Kiba
Kōchi University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ralstonia solanacearum is the causal agent of bacterial wilt disease. To better understand the molecular mechanisms involved in interaction between Nicotiana benthamiana and R. solanacearum, we focused on Hsp90, RAR1 and SGT1. Appearances of wilt symptom were significantly suppressed in Hsp90, RAR1 and SGT1-silenced plants compared with control plants. In RAR1-silenced plants, population of R. solanacearum increased in a similar manner to control plants. In contrast, multiplication of R. solanacearum was significantly suppressed in Hsp90 and SGT1-silenced plants. In addition, expression of PR genes were increased in Hsp90 and SGT1-silenced plants challenged with R. solanacearum. Therefore, RAR1 might be required for disease development or suppression of disease tolerance. These results also suggested that Hsp90 and/or SGT1 might play an important role in suppression of plant defenses leading to disease susceptibility and disease development.

Indexed as

Gene Expression Regulation, PlantGene SilencingHSP90 Heat-Shock ProteinsNicotianaPlant DiseasesPlant ProteinsRalstonia solanacearumHSP90 Heat-Shock ProteinsPlant ProteinsHR, hypersensitive responseHsp90Hsp, heat shock proteinNicotiana benthamianaPCR, polymerase chain reactionplant immunityqRT-PCR, quantitative real time polymerase chain reactionRAR1, required for Mla12 resistance 1required for Mla12 resistance 1RT-PCR, reverse transcription-polymerase chain reactionSGT1 suppressor-of-G2-allele-of-skp1suppressor-of-G2-allele-of-skp1TTSS, type III secretion systemVIGS, virus-induced gene silencing.virus-induced gene silencing

Identifiers

PMID25482800
PMCPMC4622423
OpenAlexW2068032653

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.