Evidence map›Paper›PMID 26303024›Full record

ArticleScientific reports2015

Selective enrichment of mycobacterial proteins from infected host macrophages.

Ajit G Chande, Zaved Siddiqui, Mukul Kumar Midha, Varsha Sirohi, Srikanth Ravichandran, Kanury V S Rao

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  5. Virulence · 2021
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  9. Review
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  11. Proteomic Profiling ofFrontiers in cellular and infection microbiology · 2018
    Article
  12. Systematic Identification ofMolecular & cellular proteomics : MCP · 2017
    Article
  13. Review
  14. Article
  15. Secretome Prediction of TwoFrontiers in microbiology · 2017
    Article
  16. S2 from equine infectious anemia virus is an infectivity factor which counteracts the retroviral inhibitors SERINC5 and SERINC3.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  17. 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

6 authors at 2 institutions in 1 country.

Ajit G ChandeImmunology Group, International Centre for Genetic Engineering and Biotechnology, New Delhi-India.
Zaved SiddiquiImmunology Group, International Centre for Genetic Engineering and Biotechnology, New Delhi-India.
Mukul Kumar MidhaDrug Discovery Research Centre, Translational Health Science and Technology Institute, Gurgaon, Haryana-India.
Varsha SirohiImmunology Group, International Centre for Genetic Engineering and Biotechnology, New Delhi-India.
Srikanth RavichandranImmunology Group, International Centre for Genetic Engineering and Biotechnology, New Delhi-India.
Kanury V S RaoImmunology Group, International Centre for Genetic Engineering and Biotechnology, New Delhi-India.
International Centre for Genetic Engineering and Biotechnology · INTranslational Health Science and Technology Institute · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Upon infection, Mycobacterium tuberculosis (Mtb) deploys specialized secretion machinery to deliver virulent proteins with the capacity to modulate a variety of host-cellular pathways. Studies on the identification of intra-macrophage Mtb proteins, however, are constricted by an inability to selectively enrich these virulent effectors against overwhelming protein content of the host. Here, we introduce an Mtb-selective protein labeling method based on genetic incorporation of azidonorleucine (Anl) through the expression of a mutant methionyl-tRNA synthetase. Exclusive incorporation of Anl, into native Mtb proteins, provided a click handle to pull out low abundant secretory proteins from the lysates of infected cells. Further, temporal secretome profiling, upon infection with strains of varying degree of virulence, revealed the proficiency of virulent Mtb to secrete chaperones. This ability contributed at least partially to the mycobacterial virulence-specific suppression of ER stress in the host macrophage, representing an important facet of mycobacterial virulence. The Anl labeling approach should facilitate new exciting opportunities for imaging and proteomic investigations of differently virulent Mtb isolates to understand determinants of pathogenicity.

Indexed as

Bacterial ProteinsCell LineGene Expression ProfilingHumansMacrophagesMycobacterium tuberculosisStaining and LabelingVirulence FactorsBacterial ProteinsVirulence Factors

Identifiers

PMID26303024
PMCPMC4548221
OpenAlexW2414727163

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.