Evidence map›Paper›PMID 28125719›Full record

ArticlePLoS pathogens2017

Toxoplasma gondii GRA7-Targeted ASC and PLD1 Promote Antibacterial Host Defense via PKCα.

Hyun-Jung Koh, Ye-Ram Kim, Jae-Sung Kim, Jin-Seung Yun, Kiseok Jang, Chul-Su Yang

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Science advances · 2024
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  8. Cells · 2022
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  10. The strategies of NLRP3 inflammasome to combatFrontiers in immunology · 2022
    Review
  11. Article
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  13. International journal of molecular sciences · 2020
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  14. Article
  15. Oncotarget · 2020
    Article
  16. Frontiers in immunology · 2020
    Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Hyun-Jung KohDepartment of Molecular and Life Science, College of Science and Technology, Hanyang University, Ansan, S. Korea.
Ye-Ram KimDepartment of Molecular and Life Science, College of Science and Technology, Hanyang University, Ansan, S. Korea.
Jae-Sung KimDepartment of Molecular and Life Science, College of Science and Technology, Hanyang University, Ansan, S. Korea.
Jin-Seung YunDepartment of Molecular and Life Science, College of Science and Technology, Hanyang University, Ansan, S. Korea.
Kiseok JangDepartment of Pathology, College of Medicine, Hanyang University, Seoul, S. Korea.ORCID 0000-0002-6585-3990
Chul-Su YangDepartment of Molecular and Life Science, College of Science and Technology, Hanyang University, Ansan, S. Korea.ORCID 0000-0003-4918-961X
Hanyang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tuberculosis is a global health problem and at least one-third of the world's population is infected with Mycobacterium tuberculosis (MTB). MTB is a successful pathogen that enhances its own intracellular survival by inhibiting inflammation and arresting phago-lysosomal fusion. We previously demonstrated that Toxoplasma gondii (T. gondii) dense granule antigen (GRA) 7 interacts with TNF receptor-associated factor 6 via Myeloid differentiation primary response gene 88, enabling innate immune responses in macrophages. To extend these studies, we found that GRA7 interacts with host proteins involved in antimicrobial host defense mechanisms as a therapeutic strategy for tuberculosis. Here, we show that protein kinase C (PKC)α-mediated phosphorylation of T. gondii GRA7-I (Ser52) regulates the interaction of GRA7 with PYD domain of apoptosis-associated speck-like protein containing a carboxy-terminal CARD, which is capable of oligomerization and inflammasome activation can lead to antimicrobial defense against MTB. Furthermore, GRA7-III interacted with the PX domain of phospholipase D1, facilitating its enzyme activity, phago-lysosomal maturation, and subsequent antimicrobial activity in a GRA7-III (Ser135) phosphorylation-dependent manner via PKCα. Taken together, these results underscore a previously unrecognized role of GRA7 in modulating antimicrobial host defense mechanism during mycobacterial infection.

Indexed as

AnimalsAntigens, ProtozoanCaspase Activation and Recruitment DomainCell DifferentiationHumansImmunity, InnateInflammasomesMacrophagesMiceMice, Inbred C57BLMycobacteriumMyeloid CellsPhosphorylationProtein Kinase C-alphaProtozoan ProteinsPyrin DomainAntigens, ProtozoanGRA7 protein, Toxoplasma gondiiInflammasomesPRKCA protein, humanProtein Kinase C-alphaProtozoan ProteinsTNF Receptor-Associated Factor 6

Identifiers

PMID28125719
PMCPMC5268361
OpenAlexW2581579460

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.