Evidence map›Paper›PMID 40890562›Full record

ReviewFolia microbiologica2025

Colistin resistance in the era of antimicrobial resistance: challenges and strategic countermeasures.

Debasrita RoyChowdhury, Arnima Manna, Sukhendu Mandal, Poulami Mukherjee, Arnab Basu

Abstract readReview
PubMed Publisher
In one paragraph

Review in Folia microbiologica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Antibiotic resistance inFrontiers in microbiology · 2026
    Review
  4. α-Terpineol reversesFrontiers in cellular and infection microbiology · 2026
    Article
  5. 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

5 authors.

Debasrita RoyChowdhury *Department of Biomedical Science and Technology, The School of Biological Sciences, Ramakrishna Mission Vivekananda Educational and Research Institute, Howrah, West Bengal, 711202, India.
Arnima Manna *Department of Biomedical Science and Technology, The School of Biological Sciences, Ramakrishna Mission Vivekananda Educational and Research Institute, Howrah, West Bengal, 711202, India.
Sukhendu MandalDepartment of Microbiology, University of Calcutta, 35, Ballygunge Circular Road, Ballygunge, Kolkata, 700019, India.
Poulami MukherjeeDepartment of Microbiology, Ramakrishna Mission Seva Pratishthan, 99 Sarat Bose Road, Kolkata, West Bengal, 700026, India.
Arnab BasuDepartment of Biomedical Science and Technology, The School of Biological Sciences, Ramakrishna Mission Vivekananda Educational and Research Institute, Howrah, West Bengal, 711202, India. arnab.basu@gm.rkmvu.ac.in.ORCID http://orcid.org/0000-0002-8048-8733

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colistin resistance represents a mounting global health concern, particularly alarming in the face of multidrug-resistant (MDR) and extensively drug-resistant (XDR) bacterial infections. As a polymyxin-class antibiotic, colistin has long served as a critical last-line defence against severe Gram-negative infections caused by pathogens such as Pseudomonas aeruginosa, Acinetobacter baumannii, and Klebsiella pneumoniae. However, its increasing and, at times, indiscriminate use has driven the emergence of resistant strains, thereby compromising its clinical utility.Mechanistically, colistin resistance arises from diverse genetic adaptations that alter the bacterial outer membrane, diminishing the drug's binding affinity. Prominent among these are modifications to lipopolysaccharides (LPS), including the incorporation of cationic groups that neutralise the membrane's negative charge, effectively impeding colistin interaction. In addition to chromosomal mutations, resistance is often mediated through horizontal gene transfer-most notably via mobile colistin resistance (mcr) genes-which facilitates rapid dissemination among bacterial populations.To counter this growing threat, innovative therapeutic strategies are urgently needed. These include the development of novel antibiotics with distinct mechanisms of action, synergistic combination regimens (e.g., colistin paired with potentiating agents), and the exploration of alternative modalities such as bacteriophage therapy. Gene-editing technologies like CRISPR-Cas9 also offer a promising frontier for targeting resistance determinants directly at the genetic level.Equally important are robust antimicrobial stewardship programmes and comprehensive surveillance systems to monitor resistance trends and guide rational antibiotic use. Ultimately, overcoming colistin resistance demands a multifaceted and integrative approach-one that merges scientific innovation with global public health initiatives.

Indexed as

Anti-Bacterial AgentsBacteriaColistinDrug Resistance, BacterialGram-Negative BacteriaDrug Resistance, Multiple, BacterialGene Transfer, HorizontalGram-Negative Bacterial InfectionsHumansAnti-Bacterial AgentsColistinAMRColistinEfflux pumpMcr

Identifiers

What OpenQuestion holds

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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.