Evidence map›Paper›PMID 27401574›Full record

ArticleAntimicrobial agents and chemotherapy2016

Evaluation of Antibiotics Active against Methicillin-Resistant Staphylococcus aureus Based on Activity in an Established Biofilm.

Daniel G Meeker, Karen E Beenken, Weston B Mills, Allister J Loughran, Horace J Spencer, William B Lynn, Mark S Smeltzer

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 53 citations in OpenAlex.

  1. CRISPR-driven strategies to disrupt methicillin-resistantFrontiers in cellular and infection microbiology · 2026
    Review
  2. Review
  3. Microorganisms · 2025
    Review
  4. Article
  5. Article
  6. Clostridioides difficile Biofilm.Advances in experimental medicine and biology · 2024
    Article
  7. Article
  8. Effect of Antibiotic Exposure onInternational journal of molecular sciences · 2023
    Article
  9. Antimicrobial Treatment ofAntibiotics (Basel, Switzerland) · 2023
    Review
  10. The Medium Composition ImpactsInternational journal of molecular sciences · 2022
    Article
  11. Article
  12. Article
  13. Two Novel Semisynthetic Lipoglycopeptides Active againstPharmaceuticals (Basel, Switzerland) · 2021
    Article
  14. Article
  15. Article
  16. Biofilm Formation in Methicillin-ResistantFrontiers in microbiology · 2021
    Article
  17. Article
  18. Article
  19. Antimicrobial agents and chemotherapy · 2020
    Article
  20. Article
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

7 authors at 1 institution in 1 country.

Daniel G MeekerDepartment of Microbiology & Immunology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Karen E BeenkenDepartment of Microbiology & Immunology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Weston B MillsDepartment of Microbiology & Immunology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Allister J LoughranDepartment of Microbiology & Immunology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Horace J SpencerDepartment of Biostatistics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
William B LynnDepartment of Microbiology & Immunology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Mark S SmeltzerDepartment of Microbiology & Immunology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA smeltzerMarkS@uams.edu.
University of Arkansas for Medical Sciences · US

Funding

Arkansas Center for Clinical and Translational ResearchUL1TR000039 · NCATS · UNIV OF ARKANSAS FOR MED SCIS · PI BECK, CORNELIA MARIE, JAMES, LAURA P · 2012 to 2014
$10.0M
Impact of Staphylococcus aureus in osteomyelitis and bone physiologyR01AI119380 · NIAID · UNIV OF ARKANSAS FOR MED SCIS · PI BEENKEN, KAREN E., SMELTZER, MARK S · 2015 to 2025
$4.1M
Center for Protein Structure and FunctionP30GM103450 · NIGMS · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI MILLETT, FRANCIS S · 2012 to 2014
$3.2M
Systems Pharmacology and Toxicology Training ProgramT32GM106999 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI PRATHER, PAUL L · 2013 to 2022
$1.4M
NCATS NIH HHS UL1 TR000039NIAID NIH HHS R01 AI119380NIGMS NIH HHS P30 GM103450NIGMS NIH HHS T32 GM106999
6 · The paper itself

Abstract

We used in vitro and in vivo models of catheter-associated biofilm formation to compare the relative activity of antibiotics effective against methicillin-resistant Staphylococcus aureus (MRSA) in the specific context of an established biofilm. The results demonstrated that, under in vitro conditions, daptomycin and ceftaroline exhibited comparable activity relative to each other and greater activity than vancomycin, telavancin, oritavancin, dalbavancin, or tigecycline. This was true when assessed using established biofilms formed by the USA300 methicillin-resistant strain LAC and the USA200 methicillin-sensitive strain UAMS-1. Oxacillin exhibited greater activity against UAMS-1 than LAC, as would be expected, since LAC is an MRSA strain. However, the activity of oxacillin was less than that of daptomycin and ceftaroline even against UAMS-1. Among the lipoglycopeptides, telavancin exhibited the greatest overall activity. Specifically, telavancin exhibited greater activity than oritavancin or dalbavancin when tested against biofilms formed by LAC and was the only lipoglycopeptide capable of reducing the number of viable bacteria below the limit of detection. With biofilms formed by UAMS-1, telavancin and dalbavancin exhibited comparable activity relative to each other and greater activity than oritavancin. Importantly, ceftaroline was the only antibiotic that exhibited greater activity than vancomycin when tested in vivo in a murine model of catheter-associated biofilm formation. These results emphasize the need to consider antibiotics other than vancomycin, most notably, ceftaroline, for the treatment of biofilm-associated S. aureus infections, including by the matrix-based antibiotic delivery methods often employed for local antibiotic delivery in the treatment of these infections.

Indexed as

AminoglycosidesAnimalsAnti-Bacterial AgentsBiofilmsCatheter-Related InfectionsDrug Evaluation, PreclinicalDrug Resistance, Multiple, BacterialGlycopeptidesLipoglycopeptidesMethicillin-Resistant Staphylococcus aureusMiceMicrobial Sensitivity TestsTeicoplaninVancomycinAminoglycosidesAnti-Bacterial AgentsdalbavancinGlycopeptidesLipoglycopeptidesoritavancinTeicoplanintelavancinVancomycin

Identifiers

PMID27401574
PMCPMC5038242
OpenAlexW2469403524

What OpenQuestion holds

Textmetadata
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.