The Auditory Pathway in Congenitally Cytomegalovirus-Infected Human Fetuses.
Liliana GabrielliMaria Paola BonasoniGiulia PiccirilliEvangelia PetrisliSimona VenturoliAlessia CantianiMatteo PavoniConcetta MarsicoMaria Grazia CaprettiGiuliana SimonazziLazzarotto TizianaPublished in: International journal of molecular sciences (2024)
Congenital cytomegalovirus (CMV) infection is the main cause of non-hereditary sensorineural hearing loss (SNHL). In order to shed light on SNHL pathophysiology, we examined the auditory pathway in CMV-infected fetuses; the temporal lobe, in particular the auditory cortex, and the inner ear. We investigated both inner ears and temporal lobes of 20 human CMV-infected fetuses at 21 weeks of gestation. As a negative group, five fetuses from spontaneous miscarriages without CMV infection were studied. Inner ears and temporal lobes were histologically examined, immunohistochemistry for CMV and CMV-PCR were performed. On the auditory cortex, we evaluated the local microglial reaction to the infection. CMV-positive cells were found in 14/20 brains and the damage was classified as severe, moderate, or mild, according to histological features. Fetuses with severe brain damage had a statistically higher temporal lobe viral load and a higher number of activated microglial cells in the auditory cortex compared to fetuses with mild brain damage ( p : 0.01; p : 0.01). In the inner ears, the marginal cells of the stria vascularis were the most CMV positive. In our study, CMV affected the auditory pathway, suggesting a tropism for this route. In addition, in the auditory cortex, microglial activation may favor further tissue damage contributing to hearing loss.
Keyphrases
- hearing loss
- gestational age
- working memory
- induced apoptosis
- functional connectivity
- oxidative stress
- cell cycle arrest
- resting state
- endothelial cells
- inflammatory response
- lipopolysaccharide induced
- signaling pathway
- white matter
- high intensity
- preterm infants
- cell death
- pi k akt
- multiple sclerosis
- mass spectrometry
- spinal cord
- spinal cord injury
- blood brain barrier
- cell proliferation
- atomic force microscopy