Evidence map›Paper›PMID 41407717›Full record

ArticleNPJ biofilms and microbiomes2025

Surgical revision in the presence of an S. aureus infection increases virulence factor expression and activates a multi-tissue inflammatory response.

Carly J Smith, Arianna J Moniodes, Amanda R Watkins, Autumn G Melvage, Thomas P Thompson, Eirene Choi, Abigail A Lucas, Brendan F Gilmore, Thomas P Schaer, Noreen J Hickok and 1 more

Abstract read
In one paragraph

Article in NPJ biofilms and microbiomes, 2025. 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

11 authors.

Carly J SmithThomas Jefferson University, Department of Orthopedic Surgery Research, Philadelphia, PA, USA.
Arianna J MoniodesThomas Jefferson University, Department of Orthopedic Surgery Research, Philadelphia, PA, USA.
Amanda R WatkinsUniversity of Pennsylvania School of Veterinary Medicine, New Bolton Center Department of Clinical Studies, Philadelphia, PA, USA.
Autumn G MelvageThomas Jefferson University, Department of Orthopedic Surgery Research, Philadelphia, PA, USA.
Thomas P ThompsonSchool of Pharmacy, Queen's University Belfast, Belfast, UK.
Eirene ChoiThomas Jefferson University, Department of Orthopedic Surgery Research, Philadelphia, PA, USA.
Abigail A LucasThomas Jefferson University, Department of Orthopedic Surgery Research, Philadelphia, PA, USA.
Brendan F GilmoreSchool of Pharmacy, Queen's University Belfast, Belfast, UK.
Thomas P SchaerUniversity of Pennsylvania School of Veterinary Medicine, New Bolton Center Department of Clinical Studies, Philadelphia, PA, USA.
Noreen J HickokThomas Jefferson University, Department of Orthopedic Surgery Research, Philadelphia, PA, USA.
Theresa A FreemanThomas Jefferson University, Department of Orthopedic Surgery Research, Philadelphia, PA, USA. Theresa.Freeman@jefferson.edu.

Funding

Overall: Resource-based Center for Musculoskeletal Disorders Research (Overall Application)P30AR069619 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI LOUIS J SOSLOWSKY · 2016 to 2026
$9.1M
Plasma-based therapies for bone infection: A tripartite USA/Northern Ireland/Republic of Ireland consortiumR01AR076941 · NIAMS · THOMAS JEFFERSON UNIVERSITY · PI BOURKE, PAULA, FREEMAN, THERESA A · 2020 to 2025
$3.3M
National Institute of Arthritic and Musculoskeletal and Skin Diseases R01AR076941NIAMS NIH HHS P30 AR069619NIAMS NIH HHS R01 AR076941University of Pennsylvania Center for Musculoskeletal Disorders Histology Core P30AR069619
6 · The paper itself

Abstract

Replacing implanted medical hardware due to infection often requires one or more revision surgeries. Each surgery triggers a tissue injury response and disrupts the established bacterial biofilm. However, the complex tissue response to reinjury and biofilm disturbance is not well understood. Our results show that with an existing infection, immunological niches such as the bone marrow, lymph nodes, and circulating blood further upregulate pro-inflammatory programs in response to revision. Rather than reducing bacterial burden, this heightened inflammation provokes virulence factor expression and tissue damage, including bone osteolysis and muscle fibrosis. While muscle fibrosis appears transient and begins resolving by 14 days post-revision, osteolysis continues to progress. This study defines the timing and pathophysiology of coordinated multi-tissue responses to revision during infection. Understanding how host-pathogen interactions influence tissue recovery after revision can help identify risks and guide interventions that minimize damage and maximize bacterial clearance.

Indexed as

InflammationReoperationStaphylococcal InfectionsStaphylococcus aureusVirulence FactorsAnimalsBiofilmsHost-Pathogen InteractionsHumansMiceVirulence Factors

Identifiers

PMID41407717
PMCPMC12820204

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.