Evidence map›Paper›PMID 30921464›Full record

ArticleJournal of experimental botany2019

Rice aquaporin PIP1;3 and harpin Hpa1 of bacterial blight pathogen cooperate in a type III effector translocation.

Ping Li, Liyuan Zhang, Xuyan Mo, Hongtao Ji, Huijie Bian, Yiqun Hu, Taha Majid, Juying Long, Hao Pang, Yuan Tao and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of experimental botany, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
11.3field-weighted citation impact, top 2% 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

25 citing papers in PubMed, 63 citations in OpenAlex.

  1. Overexpression ofPlant signaling & behavior · 2025
    Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Membrane Dynamics Regulated by Cytoskeleton in Plant Immunity.International journal of molecular sciences · 2023
    Review
  9. Article
  10. Article
  11. Identification of Genes inPlants (Basel, Switzerland) · 2022
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Roles of Aquaporins in Plant-Pathogen Interaction.Plants (Basel, Switzerland) · 2020
    Review
  17. Review
  18. Review
  19. Article
  20. 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

12 authors at 2 institutions in 1 country.

Ping LiDepartment of Plant Pathology, Nanjing Agricultural University, Nanjing, Jiangsu Province, China.
Liyuan ZhangDepartment of Plant Pathology, Nanjing Agricultural University, Nanjing, Jiangsu Province, China.
Xuyan MoDepartment of Plant Pathology, Nanjing Agricultural University, Nanjing, Jiangsu Province, China.
Hongtao JiDepartment of Plant Pathology, Nanjing Agricultural University, Nanjing, Jiangsu Province, China.
Huijie BianDepartment of Plant Pathology, Nanjing Agricultural University, Nanjing, Jiangsu Province, China.
Yiqun HuDepartment of Plant Pathology, Nanjing Agricultural University, Nanjing, Jiangsu Province, China.
Taha MajidDepartment of Plant Pathology, Nanjing Agricultural University, Nanjing, Jiangsu Province, China.
Juying LongDepartment of Plant Pathology, Nanjing Agricultural University, Nanjing, Jiangsu Province, China.
Hao PangDepartment of Plant Pathology, Nanjing Agricultural University, Nanjing, Jiangsu Province, China.
Yuan TaoDepartment of Plant Pathology, Nanjing Agricultural University, Nanjing, Jiangsu Province, China.
Jinbiao MaDepartment of Plant Pathology, Nanjing Agricultural University, Nanjing, Jiangsu Province, China.
Hansong DongDepartment of Plant Pathology, Nanjing Agricultural University, Nanjing, Jiangsu Province, China.
Nanjing Agricultural University · CNJiangsu Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Varieties of Gram-negative bacterial pathogens infect their eukaryotic hosts by deploying the type III translocon to deliver effector proteins into the cytosol of eukaryotic cells in which effectors execute their pathological functions. The translocon is hypothetically assembled by bacterial translocators in association with the assumed receptors situated on eukaryotic plasma membranes. This hypothesis is partially verified in the present study with genetic, biochemical, and pathological evidence for the role of a rice aquaporin, plasma membrane intrinsic protein PIP1;3, in the cytosolic import of the transcription activator-like effector PthXo1 from the bacterial blight pathogen. PIP1;3 interacts with the bacterial translocator Hpa1 at rice plasma membranes to control PthXo1 translocation from cells of a well-characterized strain of the bacterial blight pathogen into the cytosol of cells of a susceptible rice variety. An extracellular loop sequence of PIP1;3 and the α-helix motif of Hpa1 determine both the molecular interaction and its consequences with respect to the effector translocation and the bacterial virulence on the susceptible rice variety. Overall, these results provide multiple experimental avenues to support the hypothesis that interactions between bacterial translocators and their interactors at the target membrane are essential for bacterial effector translocation.

Indexed as

Host-Pathogen InteractionsAquaporinsBacterial ProteinsGlycosyltransferasesOryzaPlant DiseasesPlant ProteinsXanthomonasAquaporinsBacterial ProteinsGlycosyltransferasesHpa2 protein, Xanthomonas oryzaePlant ProteinsAquaporinbacterial pathogenPIP1ricetranslocationtype III effector

Identifiers

PMID30921464
PMCPMC6598099
OpenAlexW2929531550

What Socratic 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 Socratic graph.