Evidence map›Paper›PMID 39724074›Full record

ArticlePLoS pathogens2024

A Ralstonia solanacearum type III effector alters the actin and microtubule cytoskeleton to promote bacterial virulence in plants.

Rachel Hiles, Abigail Rogers, Namrata Jaiswal, Weiwei Zhang, Jules Butchacas, Marcus V Merfa, Taylor Klass, Pragya Barua, Venkatesh P Thirumalaikumar, Jonathan M Jacobs and 3 more

Abstract read
In one paragraph

Article in PLoS pathogens, 2024. 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
–field-weighted citation impact
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.

  1. Review
  2. 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.

Rachel HilesDepartment of Botany and Plant Pathology, and Center for Plant Biology, Purdue University, West Lafayette, Indiana, United States of America.
Abigail RogersDepartment of Botany and Plant Pathology, and Center for Plant Biology, Purdue University, West Lafayette, Indiana, United States of America.
Namrata JaiswalCrop Production and Pest Control Research Unit, USDA-ARS: USDA Agricultural Research Service, West Lafayette, Indiana, United States of America.
Weiwei ZhangDepartment of Botany and Plant Pathology, and Center for Plant Biology, Purdue University, West Lafayette, Indiana, United States of America.
Jules ButchacasDepartment of Plant Pathology, The Ohio State University, Columbus, Ohio, United States of America.
Marcus V MerfaDepartment of Plant Pathology, The Ohio State University, Columbus, Ohio, United States of America.
Taylor KlassDepartment of Plant Pathology, The Ohio State University, Columbus, Ohio, United States of America.
Pragya BaruaDepartment of Botany and Plant Pathology, and Center for Plant Biology, Purdue University, West Lafayette, Indiana, United States of America.
Venkatesh P ThirumalaikumarDepartment of Botany and Plant Pathology, and Center for Plant Biology, Purdue University, West Lafayette, Indiana, United States of America.
Jonathan M JacobsDepartment of Plant Pathology, The Ohio State University, Columbus, Ohio, United States of America.
Christopher J StaigerDepartment of Botany and Plant Pathology, and Center for Plant Biology, Purdue University, West Lafayette, Indiana, United States of America.
Matthew HelmCrop Production and Pest Control Research Unit, USDA-ARS: USDA Agricultural Research Service, West Lafayette, Indiana, United States of America.
Anjali S Iyer-PascuzziDepartment of Botany and Plant Pathology, and Center for Plant Biology, Purdue University, West Lafayette, Indiana, United States of America.ORCID 0000-0001-5356-4350

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cellular responses to biotic stress frequently involve signaling pathways that are conserved across eukaryotes. These pathways include the cytoskeleton, a proteinaceous network that senses external cues at the cell surface and signals to interior cellular components. During biotic stress, dynamic cytoskeletal rearrangements serve as a platform from which early immune-associated processes are organized and activated. Bacterial pathogens of plants and animals use proteins called type III effectors (T3Es) to interfere with host immune signaling, thereby promoting virulence. We previously found that RipU, a T3E from the soilborne phytobacterial pathogen Ralstonia solanacearum, co-localizes with the plant cytoskeleton. Here, we show that RipU from R. solanacearum K60 (RipUK60) associated with and altered the organization of both the actin and microtubule cytoskeleton. We found that pharmacological disruption of the tomato (Solanum lycopersicum) cytoskeleton promoted R. solanacearum K60 colonization. Importantly, tomato plants inoculated with R. solanacearum K60 lacking RipUK60 (ΔripUK60) had reduced wilting symptoms and significantly reduced root colonization when compared to plants inoculated with wild-type R. solanacearum K60. Collectively, our data suggest that R. solanacearum K60 uses the type III effector RipUK60 to remodel cytoskeletal organization, thereby promoting pathogen virulence.

Indexed as

Bacterial ProteinsMicrotubulesPlant DiseasesRalstonia solanacearumSolanum lycopersicumActin CytoskeletonActinsCytoskeletonType III Secretion SystemsVirulenceActinsBacterial ProteinsType III Secretion Systems

Identifiers

PMID39724074
PMCPMC11723619

What Socratic holds

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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 Socratic graph.