Evidence map›Paper›PMID 41849041›Full record

ArticleWorld journal of microbiology & biotechnology2026

Deciphering the potentiality of Andrographolide derivatives against Pseudomonas aeruginosa: in vitro analysis and mechanistic insights.

Tashi Palmo, Bhupesh K Sharma, Meenakshi Sharma, Shazia Choudhary, Ravi Shankar, Kuljit Singh

Abstract read
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In one paragraph

Article in World journal of microbiology & biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Discovery of new bioactive secondary metabolites from the stem bark of oroxylum indicum: isolation, structural identification, antimicrobial and cytotoxicity assessment.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2026
    Article
  3. 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.

Tashi PalmoInfectious Diseases Division, CSIR- Indian Institute of Integrative Medicine, Jammu, 180001, India.
Bhupesh K SharmaNatural Products & Medicinal Chemistry Division, CSIR- Indian Institute of Integrative Medicine, Jammu, 180001, India.
Meenakshi SharmaInfectious Diseases Division, CSIR- Indian Institute of Integrative Medicine, Jammu, 180001, India.
Shazia ChoudharyNatural Products & Medicinal Chemistry Division, CSIR- Indian Institute of Integrative Medicine, Jammu, 180001, India.
Ravi ShankarNatural Products & Medicinal Chemistry Division, CSIR- Indian Institute of Integrative Medicine, Jammu, 180001, India. rshankar.iiim@csir.res.in.
Kuljit SinghInfectious Diseases Division, CSIR- Indian Institute of Integrative Medicine, Jammu, 180001, India. singhkuljit.iiim@csir.res.in.

Funding

CSIR CSPS24/RDSF/IIIM/IHP24/03
6 · The paper itself

Abstract

Antimicrobial resistance (AMR) has become a global challenge in the treatment of infectious diseases. In 2024, the WHO updated the bacterial priority pathogens list, underscoring several high-priority resistant bacteria of major public health concern. Among these, Gram-negative bacteria are particularly prone to antibiotic resistance due to their complex outer membrane architecture. The reduced effectiveness of current therapies has resulted in an increasing global disease burden and mortality rates. Pseudomonas aeruginosa colonizes the upper respiratory tract and is frequently associated with secondary infections during viral pneumonia, contributing to increased complications. In the present study, we investigated the potentiality of plant-based Andrographolide and its derivatives. Initial screening identified four compounds along with the parent molecule (Andrographolide) that exhibited promising antipseudomonal activity, and among them, IIIM(ND)-RS03 demonstrated greater inhibitory activity, which was further supported by Minimum Bactericidal Concentration (MBC) profiling, which shows a markedly lower bacterial colony count compared with the remaining molecules. Time-kill kinetics analysis revealed the bactericidal nature of the potent molecule, along with noteworthy biofilm inhibition and disruption potential with respect to the untreated control. Mechanistic studies revealed pronounced morphological alterations in bacterial cells, as confirmed by scanning electron microscopy analysis. Moreover, it can trigger multiple pathways that lead to cell death, including membrane disruption, increased permeability, reduction in intracellular ATP levels, and enhanced ROS generation. Taken together, the antibacterial activity as well as mechanistic insights, the present study underlines the potential of the selected molecule as a promising lead for the development of next-generation antimicrobial agents.

Indexed as

Anti-Bacterial AgentsDiterpenesPseudomonas aeruginosaBiofilmsMicrobial Sensitivity TestsReactive Oxygen SpeciesandrographolideAnti-Bacterial AgentsDiterpenesReactive Oxygen SpeciesAntibiofilmAntimicrobial resistance (AMR)ATP quantificationMembrane permeabilityReactive oxygen speciesScanning electron microscopy

Identifiers

What OpenQuestion holds

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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.