Evidence map›Paper›PMID 42298412›Full record

ArticleBMC microbiology2026

Conserved and context-dependent changes in pathogen and host cell gene expression during Staphylococcus aureus intracellular infection.

Elizabeth A Holmes, Adam Waalkes, Janessa D Lewis, Kelsi Penewit, Dustin R Long, Stephen J Salipante

Abstract read
In one paragraph

Article in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

6 authors.

Elizabeth A HolmesDepartment of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA, USA.
Adam WaalkesDepartment of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA, USA.
Janessa D LewisDepartment of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA, USA.
Kelsi PenewitDepartment of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA, USA.
Dustin R Long *Division of Critical Care Medicine, Department of Anesthesiology and Pain Medicine, University of Washington School of Medicine, Seattle, WA, USA.
Stephen J Salipante *Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA, USA. stevesal@uw.edu.

Funding

Translational Research Center to Expedite Novel Therapies in Cystic FibrosisP30DK089507 · NIDDK · SEATTLE CHILDREN'S HOSPITAL · PI Christopher Hooper Goss, Lucas R Hoffman · 2010 to 2026
$21.4M
Targeting the Patient Microbiome for the Prevention of Surgical Site Infection in Spine SurgeryK23AR080209 · NIAMS · UNIVERSITY OF WASHINGTON · PI Dustin R Long · 2022 to 2026
$833k
Cystic Fibrosis Foundation SINGH24R0National Institute of Allergy and Infectious Diseases K23 AR080209NIAMS NIH HHS K23 AR080209NIDDK NIH HHS P30 DK089507
6 · The paper itself

Abstract

backgroundThe opportunistic intracellular lifestyle of Staphylococcus aureus contributes to its ability to maintain chronic infective states. However, knowledge of pathogen-encoded factors that enable S. aureus to invade and persist within human cells, host cell responses to infection, and how such features vary across different bacterial strains and host cell types remains incomplete. Here, we used dual RNA-seq to examine alterations in S. aureus and host cell transcription following bacterial invasion, comparing results from two different S. aureus strains (JE2 and ATCC29213) and human cell lines (THP-1-derived macrophages and CCL-185 lung epithelial cells) over time.

resultsThe fates of bacteria and host cells, and their changes in gene expression were dependent on the combination of strain and cell type examined. Transcriptional changes largely occurred early in infection (by 3 h), with subtler changes over longer timescales (24 h). Some bacterial alterations, including upregulation of metal ion homeostasis and pyrimidine biosynthesis and downregulation of anaerobic respiration and certain virulence factors, were consistent across infections, indicating general importance to intracellular pathogenesis. Other changes occurred only in particular S. aureus strains or during infection of specific host cell lines. Host cell analysis revealed marked differences in transcriptional response between infected cell types, and specific alterations dependent on the infecting S. aureus strain. Phenotypic contributions of bacterial genes with the most significant expression changes during infection were evaluated using CRISPRi knockdown experiments, most of which confirmed significant alterations in host cell invasion phenotypes under the conditions tested (26 of 32, 81%).

conclusionsThis work identifies a limited number of conserved transcriptional changes occurring during S. aureus intracellular pathogenesis that were common to all host cell-pathogen combinations examined, suggesting these are key to the infection process. However, most transcriptional changes were contingent and specific to the strain of bacteria, type of human cell, or combination of the two, indicating significant variation in context-dependent responses.

Indexed as

Host-Pathogen InteractionsStaphylococcal InfectionsStaphylococcus aureusCell LineEpithelial CellsGene Expression ProfilingGene Expression Regulation, BacterialHumansMacrophagesVirulence FactorsVirulence FactorsCell invasionChronic infectionFacultatively intracellular pathogensGenomicsInfectionMacrophagespersistencePhagocytic uptakeRNA-seqStaphylococcus aureus

Identifiers

PMID42298412
PMCPMC13495183

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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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.