Evidence map›Paper›PMID 41171349›Full record

ArticleCurrent microbiology2025

Nitroxoline Shows Synergy with Colistin Potentiating its Bactericidal Efficacy in Opportunist Pathogen Pseudomonas aeruginosa.

Debasrita RoyChowdhury, Soumyananda Chakraborti, Sukhendu Mandal, Ali Hossain Khan, Kunal Sikder, Dipak Manna, Abhrajyoti Ghosh, Subhash Haldar, Poulami Mukherjee, Arnab Basu

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Article in Current microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Debasrita RoyChowdhuryDepartment of Biomedical Science and Technology, The School of Biological Sciences, Ramakrishna Mission Vivekananda Educational and Research Institute, Howrah, 711202, West Bengal, India.
Soumyananda ChakrabortiDepartment of Biological Sciences, Birla Institute of Technology & Science, Pilani, Hyderabad Campus Jawahar Nagar, Kapra Mandal Dist.-Medchal-500 078, Hyderabad, Telengana, India.
Sukhendu MandalDepartment of Microbiology, University of Calcutta, Kolkata, West Bengal, India.
Ali Hossain KhanS. N. Bose National Centre for Basic Sciences, Kolkata, 700106, West Bengal, India.
Kunal SikderDepartment of Biomedical Science and Technology, The School of Biological Sciences, Ramakrishna Mission Vivekananda Educational and Research Institute, Howrah, 711202, West Bengal, India.
Dipak MannaDepartment of Biomedical Science and Technology, The School of Biological Sciences, Ramakrishna Mission Vivekananda Educational and Research Institute, Howrah, 711202, West Bengal, India.
Abhrajyoti GhoshBiological Sciences Unified Academic Campus Bose Institute EN-80, Sector V Bidhan Nagar, Kolkata, 700 091, India.
Subhash HaldarBiological Sciences Unified Academic Campus Bose Institute EN-80, Sector V Bidhan Nagar, Kolkata, 700 091, India.
Poulami MukherjeeRamkrishna Mission Seva Pratishthan, Kolkata, 700026, West Bengal, India.
Arnab BasuDepartment of Biomedical Science and Technology, The School of Biological Sciences, Ramakrishna Mission Vivekananda Educational and Research Institute, Howrah, 711202, West Bengal, India. arnab.basu@gm.rkmvu.ac.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pseudomonas aeruginosa is a highly virulent Gram-negative pathogen that exhibits multiple mechanisms of antibiotic resistance, including resistance to colistin, a last-resort therapeutic agent, posing a significant clinical challenge. Recently designated by the World Health Organization (WHO) as a high-priority pathogen, P. aeruginosa underscores the urgent need for novel therapeutic strategies. In this study, we explored the potential of combination therapy, specifically investigating the synergistic interaction between colistin and nitroxoline, a hydroxyquinoline derivative, against a highly colistin-resistant P. aeruginosa strain.Bacterial viability was assessed through growth curve analysis, and the mechanistic basis of the observed synergy was examined using membrane permeability assays, intracellular reactive oxygen species (ROS) quantification, and gene expression profiling via quantitative real-time PCR (qRT-PCR). Additionally, the impact of this combination on bacterial survival was evaluated by analyzing its effects on biofilm formation and persister cell development under antimicrobial stress, both critical contributors to chronic and treatment-refractory infections in humans.Our results demonstrate that nitroxoline potentiates the bactericidal activity of colistin by enhancing membrane permeability, leading to significant inhibition of planktonic growth and pronounced efficacy against structured microbial communities such as biofilms and persister cells. Furthermore, the combination therapy completely suppressed bacterial motility, a critical virulence trait that facilitates immune evasion.These findings present a compelling therapeutic strategy to combat antibiotic resistance in Gram-negative pathogens, including both wild-type and drug-resistant clinical isolates of P. aeruginosa and Acinetobacter baumannii. The study highlights the significant potential of the colistin-nitroxoline combination to mitigate colistin resistance and reduce the global burden of multidrug-resistant infections.

Indexed as

Anti-Bacterial AgentsColistinNitroquinolinesPseudomonas aeruginosaBiofilmsDrug Resistance, BacterialDrug SynergismHumansMicrobial Sensitivity TestsMicrobial ViabilityPseudomonas InfectionsReactive Oxygen SpeciesAnti-Bacterial AgentsColistinNitroquinolinesnitroxolineReactive Oxygen Species

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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.