Evidence map›Paper›PMID 29460278›Full record

ArticleBiotechnology and bioengineering2018

Structural and metabolic responses of Staphylococcus aureus biofilms to hyperosmotic and antibiotic stress.

Mia M Kiamco, Abdelrhman Mohamed, Patrick N Reardon, Carrie L Marean-Reardon, Wrya M Aframehr, Douglas R Call, Haluk Beyenal, Ryan S Renslow

Open access · greenAbstract read
In one paragraph

Article in Biotechnology and bioengineering, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Mia M KiamcoThe Gene and Linda Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, Washington.
Abdelrhman MohamedThe Gene and Linda Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, Washington.
Patrick N ReardonEnvironmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington.
Carrie L Marean-ReardonEnvironmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington.
Wrya M AframehrThe Gene and Linda Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, Washington.
Douglas R CallPaul G. Allen School for Global Animal Health, Washington State University, Pullman, Washington.
Haluk BeyenalThe Gene and Linda Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, Washington.
Ryan S RenslowThe Gene and Linda Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, Washington.ORCID 0000-0002-3969-5570
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

Biofilms alter their metabolism in response to environmental stress. This study explores the effect of a hyperosmotic agent-antibiotic treatment on the metabolism of Staphylococcus aureus biofilms through the use of nuclear magnetic resonance (NMR) techniques. To determine the metabolic activity of S. aureus, we quantified the concentrations of metabolites in spent medium using high-resolution NMR spectroscopy. Biofilm porosity, thickness, biovolume, and relative diffusion coefficient depth profiles were obtained using NMR microimaging. Dissolved oxygen concentration was measured to determine the availability of oxygen within the biofilm. Under vancomycin-only treatment, the biofilm communities switched to fermentation under anaerobic condition, as evidenced by high concentrations of formate (7.4 ± 2.7 mM), acetate (13.1 ± 0.9 mM), and lactate (3.0 ± 0.8 mM), and there was no detectable dissolved oxygen in the biofilm. In addition, we observed the highest consumption of pyruvate (0.19 mM remaining from an initial 40 mM concentration), the sole carbon source, under the vancomycin-only treatment. On the other hand, relative effective diffusion coefficients increased from 0.73 ± 0.08 to 0.88 ± 0.08 under vancomycin-only treatment but decreased from 0.71 ± 0.04 to 0.60 ± 0.07 under maltodextrin-only and from 0.73 ± 0.06 to 0.56 ± 0.08 under combined treatments. There was an increase in biovolume, from 2.5 ± 1 mm

Indexed as

Anti-Bacterial AgentsBiofilmsMagnetic Resonance SpectroscopyMetabolismMetabolomePolysaccharidesStaphylococcus aureusVancomycinAnti-Bacterial AgentsmaltodextrinPolysaccharidesVancomycinbiofilmdiffusion coefficienthyperosmotic agentmetabolitesporosityStaphylococcus aureus

Identifiers

PMID29460278
PMCPMC5959008
OpenAlexW2793399175

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.