Evidence map›Paper›PMID 23246911›Full record

ArticleJournal of microbiological methods2013

A mucosal model to study microbial biofilm development and anti-biofilm therapeutics.

Michele J Anderson, Patrick J Parks, Marnie L Peterson

Open access · bronzeAbstract read
In one paragraph

Article in Journal of microbiological methods, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 34 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

3 authors at 2 institutions in 2 countries.

Michele J AndersonDepartment of Experimental and Clinical Pharmacology, University of Minnesota, Minneapolis, MN 55455, USA.
Patrick J Parks
Marnie L Peterson
University of Minnesota · USSKiN Health · CA

Funding

Staphylococcal Superantigen Interactions With Vaginal EpitheliumR01AI073366 · NIAID · UNIVERSITY OF MINNESOTA · PI PETERSON, MARNIE L · 2009 to 2012
$1.2M
NIAID NIH HHS AI-73366NIAID NIH HHS R01 AI073366
6 · The paper itself

Abstract

Biofilms are a sessile colony of bacteria which adhere to and persist on surfaces. The ability of bacteria to form biofilms is considered a virulence factor, and in fact is central to the pathogenesis of some organisms. Biofilms are inherently resistant to chemotherapy and host immune responses. Clinically, biofilms are considered a primary cause of a majority of infections, such as otitis media, pneumonia in cystic fibrosis patients and endocarditis. However, the vast majority of the data on biofilm formation comes from traditional microtiter-based or flow displacement assays with no consideration given to host factors. These assays, which have been a valuable tool in high-throughput screening for biofilm-related factors, do not mimic a host-pathogen interaction and may contribute to an inappropriate estimation of the role of some factors in clinical biofilm formation. We describe the development of a novel ex vivo model of biofilm formation on a mucosal surface by an important mucosal pathogen, methicillin resistant S. aureus (MRSA). This model is being used for the identification of microbial virulence factors important in mucosal biofilm formation and novel anti-biofilm therapies.

Indexed as

AnimalsBiofilmsMethicillin-Resistant Staphylococcus aureusModels, TheoreticalMucous MembraneOrgan Culture TechniquesSwine

Identifiers

PMID23246911
PMCPMC3570591
OpenAlexW2027398940

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.