Evidence map›Paper›PMID 40796787›Full record

ArticleScientific reports2025

Quaternized chitosan derivatives inhibit growth and affect biofilm formation of Staphylococcus aureus.

Alex Miranda, Nichole D Brandquist, Kristen Johnson, Elena Muldiiarova, Aleksandr Fadeev, Mahboubeh Ghanbari, Jennifer L Endres, Kenneth W Bayles, Jason MacTaggart, Denis Svechkarev and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
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  6. 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

12 authors.

Alex MirandaDepartment of Chemistry, University of Nebraska at Omaha, Omaha, NE, USA.
Nichole D BrandquistDepartment of Pathology, Microbiology and Immunology, University of Nebraska Medical Center, Omaha, NE, 68198-6858, USA.
Kristen JohnsonDepartment of Biology, University of Nebraska at Omaha, Omaha, NE, USA.
Elena MuldiiarovaDepartment of Pathology, Microbiology and Immunology, University of Nebraska Medical Center, Omaha, NE, 68198-6858, USA.
Aleksandr FadeevDepartment of Biomechanics, University of Nebraska at Omaha, Omaha, NE, USA.
Mahboubeh GhanbariDepartment of Biomechanics, University of Nebraska at Omaha, Omaha, NE, USA.
Jennifer L EndresDepartment of Pathology, Microbiology and Immunology, University of Nebraska Medical Center, Omaha, NE, 68198-6858, USA.
Kenneth W BaylesDepartment of Pathology, Microbiology and Immunology, University of Nebraska Medical Center, Omaha, NE, 68198-6858, USA.
Jason MacTaggartDepartment of Surgery, University of Nebraska Medical Center, Omaha, NE, USA.
Denis SvechkarevDepartment of Chemistry, University of Nebraska at Omaha, Omaha, NE, USA. dsvechkarev@unomaha.edu.
Marat R SadykovDepartment of Pathology, Microbiology and Immunology, University of Nebraska Medical Center, Omaha, NE, 68198-6858, USA. msadykov@unmc.edu.
Yury SalkovskiyDepartment of Biomechanics, University of Nebraska at Omaha, Omaha, NE, USA. ysalkovskiy@unomaha.edu.

Funding

The S. aureus biofilm lifecycleP01AI083211 · NIAID · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI KIELIAN, TAMMY L · 2009 to 2023
$32.1M
Visual control of locomotion in people with Parkinsons diseaseP20GM109090 · NIGMS · UNIVERSITY OF NEBRASKA OMAHA · PI KNARR, BRIAN ANDREW · 2014 to 2023
$20.5M
Tissue Analysis Core (TAC)P20GM152301 · NIGMS · UNIVERSITY OF NEBRASKA OMAHA · PI Yury Salkovskiy · 2024 to 2026
$8.8M
Nebraska Research Initiative 51233NIAID NIH HHS P01 AI083211NIGMS NIH HHS P20 GM109090NIGMS NIH HHS P20 GM152301NIH HHS P01-AI83211NIH HHS P20GM152301
6 · The paper itself

Abstract

Antimicrobial resistance (AMR) poses a global health threat, severely impeding the effective treatment of bacterial infections and jeopardizing the safety of routine medical procedures. Methicillin-resistant Staphylococcus aureus (MRSA) is particularly problematic because of its resistance to beta-lactams and the ability to form resilient biofilms. Conventional antibiotics, including last-resort options, have serious side effects and may contribute to further resistance. Chitosan, a natural biopolymer, offers a promising alternative due to its biocompatibility and antimicrobial properties, though its effectiveness against biofilms is limited. Recent studies suggest that increasing the positive charge density and adding hydrophobic moieties to chitosan, can enhance its antimicrobial properties. In this work, the antibacterial activity of quaternized chitosan derivatives against AMR S. aureus strains was assessed. Quaternization of chitosan's amino group and introduction of hydrophobic side chains was found to significantly inhibit bacterial growth in both methicillin-sensitive (MSSA) and MRSA strains. Notably, nanofibrous materials composed of polyethylene oxide and hexyl-modified chitosan demonstrate alterations in S. aureus biofilm development, leading to significant accumulation of dead cells. Combined, these results highlight the potential of modified chitosan derivatives as effective antimicrobial agents for surface treatments and medical device coatings, particularly in applications where antibiotics are traditionally used, such as biofilm-prone environments.

Indexed as

Anti-Bacterial AgentsBiofilmsChitosanMethicillin-Resistant Staphylococcus aureusStaphylococcus aureusMicrobial Sensitivity TestsAnti-Bacterial AgentsChitosanAMR bacteriaAntimicrobial polymersBacterial biofilmsGrowth inhibitionS. aureus

Identifiers

PMID40796787
PMCPMC12343826

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.