Evidence map›Paper›PMID 25156721›Full record

ArticleInfection and immunity2014

Synergistic interactions of Pseudomonas aeruginosa and Staphylococcus aureus in an in vitro wound model.

Stephanie DeLeon, Allie Clinton, Haley Fowler, Jake Everett, Alexander R Horswill, Kendra P Rumbaugh

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 250 papers.

0numbers the graph read from it
0cells of the map it votes in
250citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

250 citing papers in PubMed, 417 citations in OpenAlex.

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190 more citing papers are in PubMed but not listed here.

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

6 authors at 3 institutions in 1 country.

Stephanie DeLeonDepartment of Surgery, Texas Tech University Health Sciences Center, Lubbock, Texas, USA.
Allie ClintonDepartment of Surgery, Texas Tech University Health Sciences Center, Lubbock, Texas, USA Department of Immunology and Molecular Microbiology, Texas Tech University Health Sciences Center, Lubbock, Texas, USA.
Haley FowlerDepartment of Surgery, Texas Tech University Health Sciences Center, Lubbock, Texas, USA.
Jake EverettDepartment of Surgery, Texas Tech University Health Sciences Center, Lubbock, Texas, USA Department of Immunology and Molecular Microbiology, Texas Tech University Health Sciences Center, Lubbock, Texas, USA.
Alexander R HorswillDepartment of Microbiology, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA.
Kendra P RumbaughDepartment of Surgery, Texas Tech University Health Sciences Center, Lubbock, Texas, USA kendra.rumbaugh@ttuhsc.edu.
Texas Tech University Health Sciences Center · USTexas Tech University · USUniversity of Iowa · US

Funding

The S. aureus biofilm lifecycleP01AI083211 · NIAID · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BAYLES, KENNETH W. · 2009 to 2023
$32.1M
Pseudomonas aeruginosa and Staphylococcus aureus Interspecies Interactions in WouR15AI105763 · NIAID · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI RUMBAUGH, KENDRA P · 2014 to 2014
$448k
Howard Hughes Medical InstituteNIAID NIH HHS AI083211NIAID NIH HHS AI105763NIAID NIH HHS P01 AI083211NIAID NIH HHS R15 AI105763
6 · The paper itself

Abstract

In individuals with polymicrobial infections, microbes often display synergistic interactions that can enhance their colonization, virulence, or persistence. One of the most prevalent types of polymicrobial infection occurs in chronic wounds, where Pseudomonas aeruginosa and Staphylococcus aureus are the two most common causes. Although they are the most commonly associated microbial species in wound infections, very little is known about their interspecies relationship. Evidence suggests that P. aeruginosa-S. aureus coinfections are more virulent than monoculture infection with either species; however, difficulties in growing these two pathogens together in vitro have hampered attempts to uncover the mechanisms involved. Here we describe a simple and clinically relevant in vitro wound model that supported concomitant growth of P. aeruginosa and S. aureus. We observed that the ability of P. aeruginosa and S. aureus to survive antibiotic treatment increased when they were grown together in planktonic cocultures and that antibiotic tolerance was further enhanced when they were grown together in the wound model. We attributed this enhanced tolerance to both the "host-derived" and "bacterium-derived" matrix components. Taken together, our data indicate that P. aeruginosa and S. aureus may benefit each other by coinfecting wounds and that the host-derived matrix may serve as important a role as the bacterium-derived matrix in protecting bacteria from some antibiotics.

Indexed as

Anti-Bacterial AgentsBacteriological TechniquesCoculture TechniquesDrug Resistance, BacterialPseudomonas aeruginosaStaphylococcus aureusAnti-Bacterial Agents

Identifiers

PMID25156721
PMCPMC4249327
OpenAlexW2098455529

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.