Evidence map›Paper›PMID 29124568›Full record

ArticleMolecular and cellular biochemistry2018

PknG supports mycobacterial adaptation in acidic environment.

Ruchi Paroha, Rashmi Chourasia, Rajesh Mondal, Shivendra K Chaurasiya

Abstract read
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In one paragraph

Article in Molecular and cellular biochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Structural insights into multitargetingMicrobiology spectrum · 2026
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  4. CRISPRi-mediated silencing of the ABC transporterFrontiers in microbiology · 2026
    Article
  5. Cloning, expression, purification, and characterization of glutamate decarboxylase (Rv3432c) from Mycobacterium tuberculosis.International microbiology : the official journal of the Spanish Society for Microbiology · 2025
    Article
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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

4 authors at 1 institution in 1 country.

Ruchi ParohaHost-Pathogen Interaction and Signal Transduction Laboratory, Department of Microbiology, School of Biological Sciences, Dr. Hari Singh Gour University, Sagar, MP, 470003, India.
Rashmi ChourasiaDepartment of Chemistry, School of Chemical Sciences, Dr. Hari Singh Gour University, Sagar, MP, 470003, India.
Rajesh MondalHost-Pathogen Interaction and Signal Transduction Laboratory, Department of Microbiology, School of Biological Sciences, Dr. Hari Singh Gour University, Sagar, MP, 470003, India.
Shivendra K ChaurasiyaHost-Pathogen Interaction and Signal Transduction Laboratory, Department of Microbiology, School of Biological Sciences, Dr. Hari Singh Gour University, Sagar, MP, 470003, India. shivendrachaurasiya@gmail.com.
Dr. Hari Singh Gour University · IN

Funding

Department of Biotechnology , Ministry of Science and Technology BT/PR8640/AGR/36/785/2013Science and Engineering Research Board SB/Y/LS-143/2013University Grants Commission 30-12/2014(BSR)
6 · The paper itself

Abstract

Mycobacterium tuberculosis (Mtb), causative agent of human tuberculosis (TB), has the remarkable ability to adapt to the hostile environment inside host cells. Eleven eukaryotic like serine-threonine protein kinases (STPKs) are present in Mtb. Protein kinase G (PknG) has been shown to promote mycobacterial survival inside host cells. A homolog of PknG is also present in Mycobacterium smegmatis (MS), a fast grower, non-pathogenic mycobacterium. In the present study, we have analyzed the role of PknG in mycobacteria during exposure to acidic environment. Expression of pknG in MS was decreased in acidic medium. Recombinant MS ectopically expressing pknG (MS-G) showed higher growth in acidic medium compared to wild type counterpart. MS-G also showed higher resistance upon exposure to 3.0 pH and better adaptability to acidic pH. Western blot analysis showed differential threonine but not serine phosphorylation of cellular proteins in MS at acidic pH which was restored by ectopic expression of pknG in MS. In Mtb H37Ra (Mtb-Ra), expression of pknG was increased at acidic pH. We also observed decreased expression of pknG in MS during infection in macrophages while the expression of pknG in Mtb-Ra was increased in similar conditions. Taken together, our data strongly suggests that pknG regulates growth of mycobacteria in acidic environment and is differentially transcribed in MS and Mtb under these conditions.

Indexed as

Adaptation, PhysiologicalBacterial ProteinsHumansHydrogen-Ion ConcentrationMycobacterium smegmatisMycobacterium tuberculosisProtein Serine-Threonine KinasesTHP-1 CellsBacterial Proteinsprotein kinase G, Mycobacterium tuberculosisProtein Serine-Threonine KinasesAcidic stressMycobacterium smegmatisPhosphorylationProtein kinase G

Identifiers

PMID29124568
OpenAlexW2767731303

What OpenQuestion holds

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Registered trials

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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.