Evidence map›Paper›PMID 36287008›Full record

ArticleMicrobiology spectrum2022

Plant Signals Anticipate the Induction of the Type III Secretion System in Pseudomonas syringae pv.

Maria Rita Puttilli, Davide Danzi, Cristiana Correia, Jessica Brandi, Daniela Cecconi, Marcello Manfredi, Emilio Marengo, Conceição Santos, Francesco Spinelli, Annalisa Polverari and 1 more

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.1field-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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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

11 authors at 4 institutions in 2 countries.

Maria Rita Puttilli *Department of Biotechnology, University of Veronagrid.5611.3, Verona, Italy.
Davide Danzi *Department of Biotechnology, University of Veronagrid.5611.3, Verona, Italy.
Cristiana CorreiaDepartment of Biotechnology, University of Veronagrid.5611.3, Verona, Italy.
Jessica BrandiDepartment of Biotechnology, University of Veronagrid.5611.3, Verona, Italy.
Daniela CecconiDepartment of Biotechnology, University of Veronagrid.5611.3, Verona, Italy.
Marcello ManfrediDepartment of Translational Medicine, Center for Translational Research on Autoimmune & Allergic Diseases (CAAD), University of Piemonte Orientale, Novara, Italy.
Emilio MarengoDepartment of Science and Technological Innovation, University of Piemonte Orientale, Alessandria, Italy.
Conceição SantosDepartment of Biology, LAQV-REQUIMTE, Faculty of Sciences, University of Portogrid.5808.5, Porto, Portugal.
Francesco SpinelliDepartment of Agricultural Sciences, Alma Mater Studiorum University of Bolognagrid.6292.f, Bologna, Italy.
Annalisa PolverariDepartment of Biotechnology, University of Veronagrid.5611.3, Verona, Italy.
Elodie VandelleDepartment of Biotechnology, University of Veronagrid.5611.3, Verona, Italy.ORCID 0000-0002-4205-6331
University of Verona · ITUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITUniversidade do Porto · PTUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disease resistance in plants depends on a molecular dialogue with microbes that involves many known chemical effectors, but the time course of the interaction and the influence of the environment are largely unknown. The outcome of host-pathogen interactions is thought to reflect the offensive and defensive capabilities of both players. When plants interact with Pseudomonas syringae, several well-characterized virulence factors contribute to early bacterial pathogenicity, including the type III secretion system (T3SS), which must be activated by signals from the plant and environment to allow the secretion of virulence effectors. The manner in which these signals regulate T3SS activity is still unclear. Here, we strengthen the paradigm of the plant-pathogen molecular dialogue by addressing overlooked details concerning the timing of interactions, specifically the role of plant signals and temperature on the regulation of bacterial virulence during the first few hours of the interaction. Whole-genome expression profiling after 1 h revealed that the perception of plant signals from kiwifruit or tomato extracts anticipated T3SS expression in P. syringae pv.

Indexed as

Pseudomonas syringaeType III Secretion SystemsBacterial ProteinsPlant DiseasesTemperatureVirulenceBacterial ProteinsType III Secretion Systemsbacterial virulenceenvironmental signalsplant-bacteria communicationplant-pathogen interactionssignalingvirulence regulationvirulence timing

Identifiers

PMID36287008
PMCPMC9770001
OpenAlexW4307301974

What OpenQuestion holds

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LicenceCC BY
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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.