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pmid:39366656

Multilevel Proteomics Reveals Epigenetic Signatures in BCG-Mediated Macrophage Activation.

Zoe Schaefer · John Iradukunda · Evelyn N Lumngwena · Kari B Basso · Jonathan M Blackburn · Ivana K Parker

Molecular & cellular proteomics : MCP · 2024 doi:10.1016/j.mcpro.2024.100851

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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title
Multilevel Proteomics Reveals Epigenetic Signatures in BCG-Mediated Macrophage Activation.
doi
10.1016/j.mcpro.2024.100851
pmid
39366656
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[0]
Zoe Schaefer
[1]
John Iradukunda
[2]
Evelyn N Lumngwena
[3]
Kari B Basso
[4]
Jonathan M Blackburn
[5]
Ivana K Parker
journal
Molecular & cellular proteomics : MCP
year
2024
abstract
The bacillus Calmette-Guérin BCG vaccine (Mycobacterium bovis) is primarily used to prevent tuberculosis (TB) infections but has wide-ranging immunogenic effects. One of its most notable properties is its ability to induce trained immunity, a memory-like response in innate immune cells such as macrophages. Through targeted analyses of well-established histone marks, prior research has shown that these changes are generated through epigenetic modification. Mass spectrometry-based proteomic approaches provide a way to globally profile various aspects of the proteome, providing data to further identify unexplored mechanisms of BCG-mediated immunomodulation. Here we use multi-level proteomics (total, histone, and phospho to identify networks and potential mechanisms that mediate BCG-induced immunomodulation in macrophages. Histone-focused proteomics and total proteomics were performed at the University of Cape Town (data available via ProteomeXchange with identifier PXD051187), while phosphoproteomics data was retrieved from the ProteomeXchange Repository (identifier PXD013171). We identify several epigenetic mechanisms that may drive BCG-induced training phenotypes. Evidence across the proteomics and histone-focused proteomics data set pair 6 epigenetic effectors (NuA4, NuRD, NSL, Sin3A, SIRT2, SIRT6) and their substrates.
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Quantitative phosphoproteome analyses of human macrophage-like THP-1 cells following infection with virulent Mycobacterium tuberculosis and avirulent M. bovis BCG, respectively.
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