Evidence map›Paper›PMID 34036714›Full record

ArticleMolecular plant pathology2021

MoWhi2 regulates appressorium formation and pathogenicity via the MoTor signalling pathway in Magnaporthe oryzae.

Huanbin Shi, Shuai Meng, Jiehua Qiu, Congcong Wang, Yazhou Shu, Chaoxi Luo, Yanjun Kou

Open access · goldAbstract read
In one paragraph

Article in Molecular plant pathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Transcriptional Regulation ofMicrobiology spectrum · 2023
    Article
  9. Article
  10. The Devastating Rice Blast Airborne PathogenPathogens (Basel, Switzerland) · 2023
    Review
  11. Review
  12. Editorial: Virulence of filamentous fungi and its interaction with plants.Frontiers in cellular and infection microbiology · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. MoWhi2 Mediates Mitophagy to Regulate Conidiation and Pathogenesis inInternational journal of molecular sciences · 2022
    Article
  17. Review
  18. Article
  19. 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

7 authors at 2 institutions in 1 country.

Huanbin ShiState Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou, China.
Shuai MengState Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou, China.
Jiehua QiuState Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou, China.
Congcong WangState Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou, China.
Yazhou ShuState Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou, China.
Chaoxi LuoHubei Key Lab of Plant Pathology, and College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, China.ORCID 0000-0002-9385-9898
Yanjun KouState Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou, China.ORCID 0000-0003-4189-0962
China National Rice Research Institute · CNHuazhong Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Magnaporthe oryzae causes rice blast disease, which seriously threatens the safety of food production. Understanding the mechanism of appressorium formation, which is one of the key steps for successful infection by M. oryzae, is helpful to formulate effective control strategies of rice blast. In this study, we identified MoWhi2, the homolog of Saccharomyces cerevisiae Whi2 (Whisky2), as an important regulator that controls appressorium formation in M. oryzae. When MoWHI2 was disrupted, multiple appressoria were formed by one conidium and pathogenicity was significantly reduced. A putative phosphatase, MoPsr1, was identified to interact with MoWhi2 using a yeast two-hybridization screening assay. The knockout mutant ΔMopsr1 displayed similar phenotypes to the ΔMowhi2 strain. Both the ΔMowhi2 and ΔMopsr1 mutants could form appressoria on a hydrophilic surface with cAMP levels increasing in comparison with the wild type (WT). The conidia of ΔMowhi2 and ΔMopsr1 formed a single appressorium per conidium, similar to WT, when the target of rapamycin (TOR) inhibitor rapamycin was present. In addition, compared with WT, the expression levels of MoTOR and the MoTor signalling activation marker gene MoRS3 were increased, suggesting that inappropriate activation of the MoTor signalling pathway is one of the important reasons for the defects in appressorium formation in the ΔMowhi2 and ΔMopsr1 strains. Our results provide insights into MoWhi2 and MoPsr1-mediated appressorium development and pathogenicity by regulating cAMP levels and the activation of MoTor signalling in M. oryzae.

Indexed as

MagnaportheOryzaAscomycotaFungal ProteinsPlant DiseasesVirulenceFungal Proteinsappressorium formationpathogenicityPsr1rice blastTOR signallingWhi2

Identifiers

PMID34036714
PMCPMC8295519
OpenAlexW3163977633

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.