Evidence map›Paper›PMID 28837151›Full record

ArticleCell death & disease2017

Mycobacterium abscessus glycopeptidolipids inhibit macrophage apoptosis and bacterial spreading by targeting mitochondrial cyclophilin D.

Jake Whang, Yong Woo Back, Kang-In Lee, Nagatoshi Fujiwara, Seungwha Paik, Chul Hee Choi, Jeong-Kyu Park, Hwa-Jung Kim

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

39 citing papers in PubMed, 58 citations in OpenAlex.

  1. Cells · 2026
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  7. Review
  8. Article
  9. Cell Death Mechanisms inPathogens (Basel, Switzerland) · 2025
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Microorganisms · 2022
    Review
  16. Article
  17. Virulence Mechanisms ofFrontiers in microbiology · 2022
    Review
  18. Review
  19. The Role of NRF2 in Mycobacterial Infection.Antioxidants (Basel, Switzerland) · 2021
    Review
  20. Review
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

8 authors at 2 institutions in 2 countries.

Jake WhangDepartment of Microbiology and Department of Medical Science, College of Medicine, Chungnam National University, Daejeon, South Korea.
Yong Woo BackDepartment of Microbiology and Department of Medical Science, College of Medicine, Chungnam National University, Daejeon, South Korea.
Kang-In LeeDepartment of Microbiology and Department of Medical Science, College of Medicine, Chungnam National University, Daejeon, South Korea.
Nagatoshi FujiwaraDepartment of Food and Nutrition, Tezukayama University, Gakuenminami, Nara, Japan.
Seungwha PaikDepartment of Microbiology and Department of Medical Science, College of Medicine, Chungnam National University, Daejeon, South Korea.
Chul Hee ChoiDepartment of Microbiology and Department of Medical Science, College of Medicine, Chungnam National University, Daejeon, South Korea.
Jeong-Kyu ParkDepartment of Microbiology and Department of Medical Science, College of Medicine, Chungnam National University, Daejeon, South Korea.
Hwa-Jung KimDepartment of Microbiology and Department of Medical Science, College of Medicine, Chungnam National University, Daejeon, South Korea.
Chungnam National University · KRTezukayama University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycobacterium abscessus (MAB) is a species of nontuberculous mycobacteria (NTM) and a major causative pathogen of pulmonary diseases especially in patients with cystic fibrosis. MAB infection is notoriously difficult to treat because of its intrinsic or inducible resistance to most antibiotics. The rough (R) morphotype of MAB, lacking cell surface glycopeptidolipids (GPLs), is associated with more severe and persistent infection than the smooth (S) type; however, the mechanisms underlying the R type's virulence and the relation with GPLs remain unclear. In this study, we found that R-type MAB is much more proapoptotic than the S type, as a result of GPL-mediated inhibition of macrophage apoptosis. Polar GPLs inhibited an apoptotic response (induced by proapoptotic stimuli) by suppressing ROS production and the cytochrome c release and by preserving mitochondrial transmembrane potential. Furthermore, GPLs were found to be targeted to mitochondria and interacted with cyclophilin D; their acetylation was essential for this interaction. Finally, GPLs inhibited the intracellular growth and bacterial spreading of R-type MAB among macrophages via apoptosis inhibition. These findings suggest that GPLs limit MAB virulence by inhibiting apoptosis and the spread of bacteria and therefore provide a novel insight into the mechanism underlying virulence of MAB.

Indexed as

ApoptosisCyclophilinsHumansMacrophagesMitochondriaMycobacterium abscessusNontuberculous MycobacteriaPeptidyl-Prolyl Isomerase FCyclophilinsPeptidyl-Prolyl Isomerase F

Identifiers

PMID28837151
PMCPMC5596598
OpenAlexW2745470821

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.