Evidence map›Paper›PMID 41915017›Full record

ArticleInternational forum of allergy & rhinology2026

Interspecies Biofilm Dynamics Among Staphylococci: Inflammatory Contributions to Chronic Rhinosinusitis.

Sintayehu Ambachew, Mahnaz Ramezanpour, Clare M Cooksley, Sholeh Feizi, Muhammed Awad, Kevin Aaron Fenix, Peter-John Wormald, Alkis J Psaltis, Sarah Vreugde

Abstract read
In one paragraph

Article in International forum of allergy & rhinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Sintayehu AmbachewAdelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, Australia.ORCID https://orcid.org/0000-0002-9220-0928
Mahnaz RamezanpourAdelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, Australia.ORCID https://orcid.org/0000-0001-6218-2071
Clare M CooksleyAdelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, Australia.
Sholeh FeiziAdelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, Australia.ORCID https://orcid.org/0000-0001-5489-4650
Muhammed AwadAdelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, Australia.ORCID https://orcid.org/0000-0002-0402-6406
Kevin Aaron FenixAdelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, Australia.
Peter-John WormaldAdelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, Australia.
Alkis J PsaltisAdelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, Australia.
Sarah VreugdeAdelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, Australia.ORCID https://orcid.org/0000-0003-4719-9785

Funding

Australian National Health and Medical Research Council (NHMRC) 0006008606Passe and Williams Foundation Senior FellowshipUniversity of Adelaide Research Scholarship
6 · The paper itself

Abstract

introductionStaphylococcus species are frequently isolated from the sinonasal niche of chronic rhinosinusitis (CRS) patients. While Staphylococcus aureus is often associated with recalcitrant CRS, Staphylococcus epidermidis and Staphylococcus lugdunensis are largely deemed commensal. The purpose of this study was to investigate interspecies interactions and how those might influence inflammation and susceptibility to antibiotics.

methodsTwelve staphylococcal isolates were harvested from six CRS patients, each infected with S. aureus and S. epidermidis, or with S. aureus and S. lugdunensis. Bacteria were cultured to allow biofilm formation in direct and indirect interspecies interactions, followed by measuring their biofilm biomass, antibiotic sensitivity, and toxicity and inflammatory potential when applied to human nasal epithelial cells (HNECs).

resultsS. epidermidis produced up to 7.4-fold higher biomass than S. aureus in monocultures, with a reduction in S. epidermidis biomass under indirect coculture conditions with S. aureus biofilm (p < 0.05). In contrast, the biofilm biomass values of both S. lugdunensis and S. aureus were higher under indirect coculture conditions compared to monocultures for 2/3 paired isolates (p < 0.05). S. epidermidis monocultures and S. aureus/S. epidermidis cocultures were less toxic to HNECs than S. aureus monocultures. S. aureus and S. lugdunensis monocultures and S. aureus/S. lugdunensis cocultures induced interleukin-6 (IL-6) and toxicity to a similar extent versus controls. An increased tolerance to amoxicillin was observed for 2/3 S. epidermidis biofilm and for 3/3 S. lugdunensis biofilm when in indirect contact with S. aureus biofilm (p < 0.05).

conclusionOverall, staphylococcal interactions were highly strain specific, with S. aureus influencing the biofilm-forming capacity and increasing the tolerance to amoxicillin of both S. epidermidis and S. lugdunensis. S. epidermidis but not S. lugdunensis could mitigate S. aureus induced epithelial cytotoxicity. These findings support the complex nature of interactions among staphylococci with S. aureus and potentially S. lugdunensis having a pathogenic role and S. epidermidis a protective role within polymicrobial biofilms. Our findings have implications for the inflammatory potential and response to therapy of mixed biofilms.

Indexed as

BiofilmsRhinitisRhinosinusitisSinusitisStaphylococcal InfectionsStaphylococcus aureusStaphylococcus epidermidisStaphylococcus lugdunensisAnti-Bacterial AgentsChronic DiseaseCoculture TechniquesEpithelial CellsHumansInterleukin-6Anti-Bacterial AgentsInterleukin-6biofilmbiomasschronic rhinosinusitisS. aureusS. epidermidisS. lugdunensis

Identifiers

PMID41915017
PMCPMC13544510

What Socratic 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 Socratic graph.