Evidence map›Paper›PMID 28071726›Full record

ArticleScientific reports2017

The PPE2 protein of Mycobacterium tuberculosis translocates to host nucleus and inhibits nitric oxide production.

Khalid Hussain Bhat, Shruti Srivastava, Sandeep Kumar Kotturu, Sudip Ghosh, Sangita Mukhopadhyay

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

32 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. iScience · 2026
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  4. Epigenetic Reprogramming byAntibiotics (Basel, Switzerland) · 2026
    Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. The PE/PPE family proteins ofFrontiers in immunology · 2025
    Review
  11. Biotechnologia · 2025
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Frontiers in tuberculosis · 2024
    Article
  18. Article
  19. Review
  20. Role of MHC class I pathways inFrontiers in cellular and infection microbiology · 2023
    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

5 authors at 3 institutions in 1 country.

Khalid Hussain BhatLaboratory of Molecular Cell Biology, Centre for DNA Fingerprinting and Diagnostics (CDFD), Tuljaguda Complex, Nampally, Hyderabad, India.
Shruti SrivastavaLaboratory of Molecular Cell Biology, Centre for DNA Fingerprinting and Diagnostics (CDFD), Tuljaguda Complex, Nampally, Hyderabad, India.
Sandeep Kumar KotturuMolecular Biology Division, National Institute of Nutrition (ICMR), Jamai-Osmania PO, Hyderabad, India.
Sudip GhoshMolecular Biology Division, National Institute of Nutrition (ICMR), Jamai-Osmania PO, Hyderabad, India.
Sangita MukhopadhyayLaboratory of Molecular Cell Biology, Centre for DNA Fingerprinting and Diagnostics (CDFD), Tuljaguda Complex, Nampally, Hyderabad, India.
Centre for DNA Fingerprinting and Diagnostics · INNational Institute of Nutrition · INManipal Academy of Higher Education · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycobacterium tuberculosis, the bacterium that causes tuberculosis, is one of the most successful pathogens of humans. It has evolved several adaptive skills and evasion mechanisms to hijack the immunologically educated host to suit its intracellular lifestyle. Here, we show that one of the unique PPE family member proteins of M. tuberculosis, PPE2, can limit nitric oxide (NO) production by inhibiting inos gene transcription. PPE2 protein has a leucine zipper DNA-binding motif and a functional nuclear localization signal. PPE2 was translocated into the macrophage nucleus via the classical importin α/β pathway where it interacted with a GATA-binding site overlapping with the TATA box of inos promoter and inhibited NO production. PPE2 prolonged intracellular survival of a surrogate bacterium M. smegmatis in vitro as well as in vivo. This information are likely to improve our knowledge of host-pathogen interactions during M. tuberculosis infection which is crucial for designing effective anti-TB therapeutics.

Indexed as

AnimalsAntigens, BacterialBacterial ProteinsCell NucleusGATA Transcription FactorsHost-Pathogen InteractionsHumansImmune EvasionMacrophagesMiceMycobacterium smegmatisMycobacterium tuberculosisNitric OxideNitric Oxide Synthase Type IIProtein BindingProtein TransportAntigens, BacterialBacterial ProteinsGATA Transcription FactorsNitric OxideNitric Oxide Synthase Type IIPPE2 protein, Mycobacterium tuberculosis

Identifiers

PMID28071726
PMCPMC5223167
OpenAlexW2570877074

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.