Epigenetic Changes in Cerebrospinal Fluid and Blood of People With Neurosyphilis

Epigenetic changes within immune cells may contribute to neuroinflammation during bacterial infection, but their role in neurosyphilis (NS) pathogenesis and response has not yet been established. We longitudinally analyzed DNA methylation and RNA expression in cerebrospinal fluid (CSF) cells and peripheral blood mononuclear cells (PBMCs) from 11 participants with laboratory-confirmed NS (CSF Venereal Disease Research Laboratory test positive) and 11 matched controls with syphilis without NS (non-NS). DNA methylation profiles from CSF and PBMCs of participants with NS significantly differed from those of participants with non-NS. Some genes associated with these differentially methylated sites had corresponding RNA expression changes in the CSF (111/1097 [10.1%]), and included genes involved in B cell activation and insulin-response pathways. Despite antibiotic treatment, approximately 80% of CSF methylation changes associated with NS persisted, suggesting that epigenetic scars accompanying NS may persistently affect immunity following infection. Future studies must examine whether these sequelae are clinically meaningful.

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Publication Details

Journal
The Journal of Infectious Diseases
Published
2024-10-02
DOI
https://doi.org/10.1093/infdis/jiae476
Citations
2
Primary Topic
Syphilis Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.65

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article

Epigenetic Changes in Cerebrospinal Fluid and Blood of People With Neurosyphilis

Shelli Farhadian, Darius Mostaghimi, Priya Kosana, Michael J. Corley et al.
2 citations
The Journal of Infectious Diseases
Syphilis Diagnosis and Treatment
0.65
article

Epigenetic Changes in Cerebrospinal Fluid and Blood of People With Neurosyphilis

Shelli Farhadian, Darius Mostaghimi, Priya Kosana, Michael J. Corley, Jennifer Yoon, Sameet Mehta, Christina Marra
article en
2 citations

Abstract

Epigenetic changes within immune cells may contribute to neuroinflammation during bacterial infection, but their role in neurosyphilis (NS) pathogenesis and response has not yet been established. We longitudinally analyzed DNA methylation and RNA expression in cerebrospinal fluid (CSF) cells and peripheral blood mononuclear cells (PBMCs) from 11 participants with laboratory-confirmed NS (CSF Venereal Disease Research Laboratory test positive) and 11 matched controls with syphilis without NS (non-NS). DNA methylation profiles from CSF and PBMCs of participants with NS significantly differed from those of participants with non-NS. Some genes associated with these differentially methylated sites had corresponding RNA expression changes in the CSF (111/1097 [10.1%]), and included genes involved in B cell activation and insulin-response pathways. Despite antibiotic treatment, approximately 80% of CSF methylation changes associated with NS persisted, suggesting that epigenetic scars accompanying NS may persistently affect immunity following infection. Future studies must examine whether these sequelae are clinically meaningful.

The Journal of Infectious DiseasesVol. 231(4)
University of Washington (US), Cornell University (US), Yale University (US), Weill Cornell Medicine (US)
Yale University, National Institutes of Health
Good health and well-being
Openalex Percentile: Top 29%
Syphilis Diagnosis and Treatment
0.65
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