Exploratory Proteomics of Amniotic Fluid Extracellular Vesicles in Congenital Cytomegalovirus

ABSTRACT Introduction Congenital cytomegalovirus (cCMV) is the most common congenital viral infection and a leading non-genetic cause of neurodevelopmental impairment. Current diagnostic methods using fetal biofluids provide limited insight into fetal pathophysiology. Extracellular vesicles (EVs) in amniotic fluid (AF) are a promising source of stable biomolecules that reflect real-time fetal physiology. This proof-of-concept study compared amniotic fluid EV (AF-EV) characteristics in fetuses with severe CMV infection with those of uninfected fetuses and aimed to develop hypotheses about fetal response to cCMV in utero . Methods AF samples were collected from pregnancies with symptomatic CMV infection and gestational-age-matched uninfected controls (4 pairs, n=8 total). EVs were isolated and characterised by Western blotting, cryo-electron microscopy, and nanoparticle tracking analysis. Label-free quantitative proteomics identified CMV-associated changes in the AF-EV proteome. Results CMV-infected AF showed higher vesicle levels (Hedges’ g = 1.55), indicating inflammation and virus-induced changes in EV biogenesis. Proteomic analysis found 8.6% of proteins dysregulated. Upregulated proteins included haemoglobin subunits, immunoglobulin heavy chain mu, and myeloperoxidase (Hedges’ g = 1.51 to 1.88), indicating haemolysis and immune activation. Eleven host proteins related to neurodevelopment, mitochondrial function, lipid metabolism, and Golgi trafficking were absent in infected cases, indicating viral disruption of host pathways. Protein enrichment analysis revealed differences in neurological, haematological, and immune pathways, aligning with severe cCMV pathology. Conclusion This study acts as a proof-of-principle investigation of the AF-EV proteome in cCMV. Although the results highlight key protein signatures associated with severe fetal outcomes, they primarily serve to generate hypotheses and inform larger prospective studies.

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Journal
Viruses
Published
2026-11-02
DOI
https://doi.org/10.3390/v18111209
Primary Topic
Cytomegalovirus and herpesvirus research
Type
article
Field-Weighted Citation Impact
0.00

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article

Exploratory Proteomics of Amniotic Fluid Extracellular Vesicles in Congenital Cytomegalovirus

Sepideh Valimehr, Sally Beard, Lisa Hui, Luc De Catte et al.
1 links
Viruses
Cytomegalovirus and herpesvirus research
article

Exploratory Proteomics of Amniotic Fluid Extracellular Vesicles in Congenital Cytomegalovirus

Sepideh Valimehr, Sally Beard, Lisa Hui, Luc De Catte, Ching‐Seng Ang, Ishara Atukorala, Natalie Hannan
article en

Abstract

ABSTRACT Introduction Congenital cytomegalovirus (cCMV) is the most common congenital viral infection and a leading non-genetic cause of neurodevelopmental impairment. Current diagnostic methods using fetal biofluids provide limited insight into fetal pathophysiology. Extracellular vesicles (EVs) in amniotic fluid (AF) are a promising source of stable biomolecules that reflect real-time fetal physiology. This proof-of-concept study compared amniotic fluid EV (AF-EV) characteristics in fetuses with severe CMV infection with those of uninfected fetuses and aimed to develop hypotheses about fetal response to cCMV in utero . Methods AF samples were collected from pregnancies with symptomatic CMV infection and gestational-age-matched uninfected controls (4 pairs, n=8 total). EVs were isolated and characterised by Western blotting, cryo-electron microscopy, and nanoparticle tracking analysis. Label-free quantitative proteomics identified CMV-associated changes in the AF-EV proteome. Results CMV-infected AF showed higher vesicle levels (Hedges’ g = 1.55), indicating inflammation and virus-induced changes in EV biogenesis. Proteomic analysis found 8.6% of proteins dysregulated. Upregulated proteins included haemoglobin subunits, immunoglobulin heavy chain mu, and myeloperoxidase (Hedges’ g = 1.51 to 1.88), indicating haemolysis and immune activation. Eleven host proteins related to neurodevelopment, mitochondrial function, lipid metabolism, and Golgi trafficking were absent in infected cases, indicating viral disruption of host pathways. Protein enrichment analysis revealed differences in neurological, haematological, and immune pathways, aligning with severe cCMV pathology. Conclusion This study acts as a proof-of-principle investigation of the AF-EV proteome in cCMV. Although the results highlight key protein signatures associated with severe fetal outcomes, they primarily serve to generate hypotheses and inform larger prospective studies.

VirusesVol. 18(11)
The University of Melbourne (AU), Northern Health (AU), Walter and Eliza Hall Institute of Medical Research (AU), Universitair Ziekenhuis Leuven (BE), Mercy Hospital for Women (AU), Northern Hospital (AU), Murdoch Children's Research Institute (AU)
Austin Medical Research Foundation, Norman Beischer Medical Research Foundation, Department of Health and Aged Care, Australian Government, National Health and Medical Research Council
Good health and well-being
Openalex Percentile: Top 49%
Cytomegalovirus and herpesvirus research
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