Evidence map›Paper›PMID 26084588›Full record

ArticleBiotechnology and bioengineering2015

Vancomycin and maltodextrin affect structure and activity of Staphylococcus aureus biofilms.

Mia Mae Kiamco, Erhan Atci, Qaiser Farid Khan, Abdelrhman Mohamed, Ryan S Renslow, Nehal Abu-Lail, Boel A Fransson, Douglas R Call, Haluk Beyenal

Open access · greenAbstract read
In one paragraph

Article in Biotechnology and bioengineering, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Bacterial Hybrid Light-Emitting Diodes.Advanced materials (Deerfield Beach, Fla.) · 2024
    Article
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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

9 authors at 2 institutions in 1 country.

Mia Mae KiamcoThe Gene and Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, Washington.
Erhan AtciThe Gene and Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, Washington.
Qaiser Farid KhanThe Gene and Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, Washington.
Abdelrhman MohamedThe Gene and Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, Washington.
Ryan S RenslowEnvironmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington.
Nehal Abu-LailThe Gene and Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, Washington.
Boel A FranssonDepartment of Veterinary Clinical Sciences, Washington State University, Pullman, Washington.
Douglas R CallPaul G. Allen School for Global Animal Health, Washington State University, Pullman, Washington.
Haluk BeyenalThe Gene and Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, Washington. beyenal@wsu.edu.
Washington State University · USPacific Northwest National Laboratory · US

Funding

TRAINING IN BIOTECHNOLOGY: EMPHASIS ON PROTEIN CHEMISTRYT32GM008336 · NIGMS · WASHINGTON STATE UNIVERSITY · PI CALL, DOUGLAS R. · 1989 to 2023
$8.9M
NIGMS NIH HHS T32 GM008336
6 · The paper itself

Abstract

Hyperosmotic agents such as maltodextrin negatively impact bacterial growth through osmotic stress without contributing to drug resistance. We hypothesized that a combination of maltodextrin (osmotic agent) and vancomycin (antibiotic) would be more effective against Staphylococcus aureus biofilms than either alone. To test our hypothesis, S. aureus was grown in a flat plate flow cell reactor. Confocal laser scanning microscopy images were analyzed to quantify changes in biofilm structure. We used dissolved oxygen microelectrodes to quantify how vancomycin and maltodextrin affected the respiration rate and oxygen penetration into the biofilm. We found that treatment with vancomycin or maltodextrin altered biofilm structure. The effect on the structure was significant when they were used simultaneously to treat S. aureus biofilms. In addition, vancomycin treatment increased the oxygen respiration rate, while maltodextrin treatment caused an increase and then a decrease. An increased maltodextrin concentration decreased the diffusivity of the antibiotic. Overall, we conclude that (1) an increased maltodextrin concentration decreases vancomycin diffusion but increases the osmotic effect, leading to the optimum treatment condition, and (2) the combination of vancomycin and maltodextrin is more effective against S. aureus biofilms than either alone. Vancomycin and maltodextrin act together to increase the effectiveness of treatment against S. aureus biofilm growth.

Indexed as

Anti-Bacterial AgentsBiofilmsBioreactorsDrug InteractionsOsmotic PressureOxygenPolysaccharidesStaphylococcus aureusVancomycinAnti-Bacterial AgentsmaltodextrinOxygenPolysaccharidesVancomycinbiofilmmaltodextrinoxygenStaphylococcus aureusstructurevancomycin

Identifiers

PMID26084588
PMCPMC5096838
OpenAlexW2105847762

What OpenQuestion holds

Textmetadata
LicenceTDM
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.