Evidence map›Paper›PMID 25156390›Full record

ArticleNature communications2014

Unconventionally secreted effectors of two filamentous pathogens target plant salicylate biosynthesis.

Tingli Liu, Tianqiao Song, Xiong Zhang, Hongbo Yuan, Liming Su, Wanlin Li, Jing Xu, Shiheng Liu, Linlin Chen, Tianzi Chen and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Nature communications, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 177 papers.

0numbers the graph read from it
0cells of the map it votes in
177citing papers in PubMed
32.7field-weighted citation impact, top 1% 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

177 citing papers in PubMed, 404 citations in OpenAlex.

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117 more citing papers are in PubMed but not listed here.

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

14 authors at 3 institutions in 1 country.

Tingli Liu1] Department of Plant Pathology, Nanjing Agricultural University, 1 Weigang Road, Nanjing 210095, China [2] Provincial Key Laboratory of Agrobiology, Jiangsu Academy of Agricultural Sciences, Nanjing 210095, China [3].
Tianqiao Song1] Department of Plant Pathology, Nanjing Agricultural University, 1 Weigang Road, Nanjing 210095, China [2].
Xiong ZhangDepartment of Plant Pathology, Nanjing Agricultural University, 1 Weigang Road, Nanjing 210095, China.
Hongbo YuanProvincial Key Laboratory of Agrobiology, Jiangsu Academy of Agricultural Sciences, Nanjing 210095, China.
Liming SuDepartment of Plant Pathology, Nanjing Agricultural University, 1 Weigang Road, Nanjing 210095, China.
Wanlin LiDepartment of Plant Pathology, Nanjing Agricultural University, 1 Weigang Road, Nanjing 210095, China.
Jing XuDepartment of Plant Pathology, Nanjing Agricultural University, 1 Weigang Road, Nanjing 210095, China.
Shiheng LiuState Key Laboratory of Microbial Technology, Shandong University, Jinan 250100, China.
Linlin ChenDepartment of Plant Pathology, Nanjing Agricultural University, 1 Weigang Road, Nanjing 210095, China.
Tianzi ChenProvincial Key Laboratory of Agrobiology, Jiangsu Academy of Agricultural Sciences, Nanjing 210095, China.
Meixiang ZhangDepartment of Plant Pathology, Nanjing Agricultural University, 1 Weigang Road, Nanjing 210095, China.
Lichuan GuState Key Laboratory of Microbial Technology, Shandong University, Jinan 250100, China.
Baolong ZhangProvincial Key Laboratory of Agrobiology, Jiangsu Academy of Agricultural Sciences, Nanjing 210095, China.
Daolong DouDepartment of Plant Pathology, Nanjing Agricultural University, 1 Weigang Road, Nanjing 210095, China.
Nanjing Agricultural University · CNJiangsu Academy of Agricultural Sciences · CNShandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plant diseases caused by fungi and oomycetes pose an increasing threat to food security and ecosystem health worldwide. These filamentous pathogens, while taxonomically distinct, modulate host defense responses by secreting effectors, which are typically identified based on the presence of signal peptides. Here we show that Phytophthora sojae and Verticillium dahliae secrete isochorismatases (PsIsc1 and VdIsc1, respectively) that are required for full pathogenesis. PsIsc1 and VdIsc1 can suppress salicylate-mediated innate immunity in planta and hydrolyse isochorismate in vitro. A conserved triad of catalytic residues is essential for both functions. Thus, the two proteins are isochorismatase effectors that disrupt the plant salicylate metabolism pathway by suppressing its precursor. Furthermore, these proteins lack signal peptides, but exhibit characteristics that lead to unconventional secretion. Therefore, this secretion pathway is a novel mechanism for delivering effectors and might play an important role in host-pathogen interactions.

Indexed as

Host-Pathogen InteractionsCatalytic DomainFungal ProteinsGossypiumHydrolasesOrganisms, Genetically ModifiedPhytophthoraPlant DiseasesProtein TransportSalicylatesVerticilliumVirulence FactorsFungal ProteinsHydrolasesisochorismataseSalicylatesVirulence Factors

Identifiers

PMID25156390
PMCPMC4348438
OpenAlexW2021962147

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.