Evidence map›Paper›PMID 34989880›Full record

ArticleWorld journal of microbiology & biotechnology2022

Oxidative stress, DNA, and membranes targets as modes of antibacterial and antibiofilm activity of facile synthesized biocompatible keratin-copper nanoparticles against multidrug resistant uro-pathogens.

Satarupa Banerjee, Kumari Vishakha, Shatabdi Das, Priyanka D Sangma, Sandhimita Mondal, Arnab Ganguli

Abstract read
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In one paragraph

Article in World journal of microbiology & biotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.6field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
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  6. Ni-Fe Nanoparticles fromCurrent pharmaceutical design · 2026
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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

6 authors at 1 institution in 1 country.

Satarupa BanerjeeDepartment of Microbiology, Techno India University, EM-4 Sector-V, Saltlake City, Calcutta, West Bengal, 700091, India.
Kumari VishakhaDepartment of Microbiology, Techno India University, EM-4 Sector-V, Saltlake City, Calcutta, West Bengal, 700091, India.
Shatabdi DasDepartment of Microbiology, Techno India University, EM-4 Sector-V, Saltlake City, Calcutta, West Bengal, 700091, India.
Priyanka D SangmaDepartment of Microbiology, Techno India University, EM-4 Sector-V, Saltlake City, Calcutta, West Bengal, 700091, India.
Sandhimita MondalDepartment of Microbiology, Techno India University, EM-4 Sector-V, Saltlake City, Calcutta, West Bengal, 700091, India.
Arnab GanguliDepartment of Microbiology, Techno India University, EM-4 Sector-V, Saltlake City, Calcutta, West Bengal, 700091, India. ganguli.arnab009@gmail.com.ORCID http://orcid.org/0000-0001-9939-027X
Techno India University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Escherichia coli and Enterococcus faecalis are two of the most prevalent uro-pathogens and are difficult to treat as they acquire multidrug-resistant traits. In this study, the main objective was to develop biocompatible copper nanoparticles using chicken feather keratin protein (CuNPs-K) and to investigate their impact on multidrug-resistant (MDR) uro-pathogens, E. coli and E. faecalis, under both single and mixed culture conditions. CuNPs-K were characterised by UV-Vis spectroscopy, dynamic light scattering, X-ray diffraction, Fourier transform infrared spectroscopy, and docking experiments. The MIC values of CuNPs-K against single and mixed planktonic cultures were 50 μg/ml and 75 μg/ml, respectively. CuNPs-K efficiently disrupted the biofilm of single and mixed uro-pathogen cultures by eliminating sessile cells. This biofilm disruption may be attributed to a decline in the production of extracellular polymeric substances in both single and mixed bacterial cultures treated with CuNPs-K. Moreover, selective antimicrobial activity was determined by selectivity assays using T24 cells. CuNPs-K targets both the bacterial membrane and DNA with elevated reactive oxygen species (ROS) as their bactericidal mode of action. This comprehensive antimicrobial activity of CuNPs-K was further confirmed in vivo by using the zebra fish model. In this study, CuNPs-K effectively reduced bacterial load with increased survivability of infected zebrafish. All these results suggest that CuNPs-K can be explored as an exceptional antibacterial agent against MDR uro-pathogenic E. coli and E. faecalis.

Indexed as

AnimalsAnti-Bacterial AgentsBiofilmsCell MembraneCopperDisease Models, AnimalDNADrug Resistance, Multiple, BacterialEscherichia coliEscherichia coli InfectionsKeratinsMetal NanoparticlesMicrobial Sensitivity TestsOxidative StressReactive Oxygen SpeciesSpectroscopy, Fourier Transform InfraredAnti-Bacterial AgentsCopperDNAKeratinsReactive Oxygen SpeciesDNA bindingKeratin-copper-nanoparticlesMultidrug-resistance-uro-pathogensReactive oxygen speciesSelective-antibacterial propertiesZebrafish model

Identifiers

PMID34989880
OpenAlexW4205485921

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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.