Evidence map›Paper›PMID 37310613›Full record

ArticleMolecular plant pathology2023

The Ralstonia pseudosolanacearum effector RipE1 is recognized at the plasma membrane by NbPtr1, the Nicotiana benthamiana homologue of Pseudomonas tomato race 1.

Boyoung Kim, Injae Kim, Wenjia Yu, Meng Li, Haseong Kim, Ye Jin Ahn, Kee Hoon Sohn, Alberto P Macho, Cécile Segonzac

Open access · goldAbstract read
In one paragraph

Article in Molecular plant pathology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
7.5field-weighted citation impact, top 3% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. ThePlants (Basel, Switzerland) · 2026
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  9. TheInternational journal of molecular sciences · 2023
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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

9 authors at 3 institutions in 2 countries.

Boyoung KimDepartment of Agriculture, Forestry and Bioresources, Seoul National University, Seoul, Republic of Korea.
Injae KimDepartment of Agriculture, Forestry and Bioresources, Seoul National University, Seoul, Republic of Korea.
Wenjia YuShanghai Center for Plant Stress Biology, CAS Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai, China.
Meng LiShanghai Center for Plant Stress Biology, CAS Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai, China.
Haseong KimPlant Immunity Research Center, Seoul National University, Seoul, Republic of Korea.
Ye Jin AhnDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea.
Kee Hoon SohnPlant Immunity Research Center, Seoul National University, Seoul, Republic of Korea.
Alberto P MachoShanghai Center for Plant Stress Biology, CAS Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai, China.ORCID 0000-0001-9935-8026
Cécile SegonzacDepartment of Agriculture, Forestry and Bioresources, Seoul National University, Seoul, Republic of Korea.ORCID 0000-0002-5537-7556
Seoul National University · KRChinese Academy of Sciences · CNPohang University of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The bacterial wilt disease caused by soilborne bacteria of the Ralstonia solanacearum species complex (RSSC) threatens important crops worldwide. Only a few immune receptors conferring resistance to this devastating disease are known so far. Individual RSSC strains deliver around 70 different type III secretion system effectors into host cells to manipulate the plant physiology. RipE1 is an effector conserved across the RSSC and triggers immune responses in the model solanaceous plant Nicotiana benthamiana. Here, we used multiplexed virus-induced gene silencing of the nucleotide-binding and leucine-rich repeat receptor family to identify the genetic basis of RipE1 recognition. Specific silencing of the N. benthamiana homologue of Solanum lycopersicoides Ptr1 (confers resistance to Pseudomonas syringae pv. tomato race 1) gene (NbPtr1) completely abolished RipE1-induced hypersensitive response and immunity to Ralstonia pseudosolanacearum. The expression of the native NbPtr1 coding sequence was sufficient to restore RipE1 recognition in Nb-ptr1 knockout plants. Interestingly, RipE1 association with the host cell plasma membrane was necessary for NbPtr1-dependent recognition. Furthermore, NbPtr1-dependent recognition of RipE1 natural variants is polymorphic, providing additional evidence for the indirect mode of activation of NbPtr1. Altogether, this work supports NbPtr1 relevance for resistance to bacterial wilt disease in Solanaceae.

Indexed as

Ralstonia solanacearumSolanum lycopersicumBacterial ProteinsCell MembraneNicotianaPlant DiseasesPseudomonas syringaeRalstoniaBacterial Proteinsnucleotide-binding leucine-rich repeat receptorplant immune systemsubcellular localizationtype III secreted effectorsvirus-induced gene silencing

Identifiers

PMID37310613
PMCPMC10502825
OpenAlexW4380422220

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.