Evidence map›Paper›PMID 39487375›Full record

ArticleArchives of microbiology2024

Ajoene: a natural compound with enhanced antimycobacterial and antibiofilm properties mediated by efflux pump modulation and ROS generation against M. Smegmatis.

Ashirbad Sarangi, Bhabani Shankar Das, Isha Pahuja, Suvendu Ojha, Vishal Singh, Sidhartha Giri, Ashima Bhaskar, Debapriya Bhattacharya

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In one paragraph

Article in Archives of microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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.

Ashirbad Sarangi *Centre for Biotechnology, School of Pharmaceutical Sciences, Siksha 'O' Anusandhan (Deemed to be University), Bhubaneswar, Odisha, 751003, India.
Bhabani Shankar Das *Centre for Biotechnology, School of Pharmaceutical Sciences, Siksha 'O' Anusandhan (Deemed to be University), Bhubaneswar, Odisha, 751003, India.
Isha PahujaImmunobiology Group, International Centre for Genetic Engineering and Biotechnology, New Delhi, India.
Suvendu OjhaDepartment of Infectious Disease Biology, Institute of Life Sciences, Bhubaneswar, India.
Vishal SinghCentre for Biotechnology, School of Pharmaceutical Sciences, Siksha 'O' Anusandhan (Deemed to be University), Bhubaneswar, Odisha, 751003, India.
Sidhartha GiriICMR-Regional Medical Research Centre (RMRC), Bhubaneswar, Odisha, India.
Ashima BhaskarImmunobiology Group, International Centre for Genetic Engineering and Biotechnology, New Delhi, India.
Debapriya BhattacharyaCentre for Biotechnology, School of Pharmaceutical Sciences, Siksha 'O' Anusandhan (Deemed to be University), Bhubaneswar, Odisha, 751003, India. debapriyabhattacharyab@gmail.com.

Funding

Science and Engineering Research Board SRG/2020/001922University Grants Commission FD Diary No. 2183, 01-06-2022 & No. F.30-523/2020(BSR)
6 · The paper itself

Abstract

Tuberculosis (TB) continues to be a primary worldwide health concern due to relatively ineffective treatments. The prolonged duration of conventional antibiotic therapy warrants innovative approaches to shorten treatment courses. In response to challenges, the study explores potential of Ajoene, a naturally occurring garlic extract-derived compound, for potential TB treatment. Mycobacterium smegmatis as a model organism for M. tuberculosis (M. tb) to investigate Ajoene's efficiency. In vitro techniques like antimicrobial susceptibility, antibiofilm, EtBr accumulation assay, and ROS assay evaluate the potency of Ajoene and conventional TB drugs against Mycobacterium smegmatis. An in-silico study also investigated the interaction between Ajoene and quorum-sensing proteins, specifically regX3, MSMEG_5244, and MSMEG_3944, which are involved in biofilm formation and sliding activity. In vitro findings revealed that Ajoene exhibited significant antibacterial activity by inhibiting growth and showing bactericidal effects. It also demonstrated additive interactions with common antibiotics such as Isoniazid and Rifampicin. Furthermore, Ajoene demonstrated a comparative interaction with commonly used antibiotics, such as Isoniazid and Rifampicin, and reduced M. smegmatis motility, both alone and in combination with these antibiotics. In silico analysis shows that Ajoene exhibited a higher binding affinity with regX3, a protein orthologous to the regX3 gene in M.tb. Ajoene also demonstrated consistent antibiofilm effects, particularly when combined synergistically with Isoniazid and Rifampicin. Mechanistic investigations demonstrated Ajoene's potential to inhibit efflux pumps and promote ROS generation in bacteria, suggesting a potential direct killing mechanism. Collectively, the findings emphasize Ajoene's effectiveness as a novel antimycobacterial and antibiofilm molecule for TB treatment.

Indexed as

Antitubercular AgentsBacterial ProteinsBiofilmsMicrobial Sensitivity TestsMycobacterium smegmatisReactive Oxygen SpeciesAnti-Bacterial AgentsDisulfidesDrug SynergismIsoniazidMembrane Transport ProteinsMolecular Docking SimulationMycobacterium tuberculosisQuorum SensingRifampinSulfoxidesajoeneAnti-Bacterial AgentsAntitubercular AgentsBacterial ProteinsDisulfidesIsoniazidMembrane Transport ProteinsReactive Oxygen SpeciesRifampinSulfoxidesAjoeneAnti-biofilmAnti-mycobacterialAnti-sliding motility assayEfflux-pump inhibitorMycobacterium smegmatisTB

Identifiers

PMID39487375

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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.