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Published on: October 13, 2018
Study of viral infections in infants with biliary atresia
Ramin Yaghobi1, Mahdi Didari, Bita Gramizadeh
1Shiraz Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. rayaviro@yahoo.com
Insights
Hepatitis B virus (HBV), Hepatitis C virus (HCV), and adenovirus were detected in infants with biliary atresia. These viral infections may play a role in the condition
Area of Science:
- Hepatology
- Virology
- Neonatal Research
Background:
- Biliary atresia is a severe neonatal liver disease with incompletely understood pathogenesis.
- Viral infections are suspected contributors to biliary atresia development and progression.
Purpose of the Study:
- To investigate the prevalence of specific viral infections (HBV, HCV, HCMV, adenovirus, BK virus) in neonatal biliary atresia.
- To determine the potential role of these viruses in biliary atresia-related clinical complications.
Main Methods:
- Retrospective analysis of 34 formalin-fixed paraffin-embedded (FFPE) liver tissue samples from neonates with biliary atresia.
- Molecular detection of viral genomes using PCR and RT-PCR.
- Antigenic detection of HBV, HCV, and HCMV using immunohistochemistry (IHC).
Main Results:
- HBV, HCV, and adenovirus genomes were detected in 9%, 6%, and 6% of samples, respectively.
- HBV and HCV co-infection was identified in 6% of FFPE samples.
- No detection of HCMV or BK virus genomes in the studied liver tissues.
Conclusions:
- The presence of HBV, HCV, and adenovirus in biliary atresia tissues suggests a potential role in the disease's pathogenesis.
- Further comprehensive studies are warranted to elucidate the exact contribution of these viral infections to biliary atresia.
Abstract:
Viral infections may have an important role in the pathogenesis of biliary atresia, and related clinical outcomes. In this research for determination of the possible role of HBV, HCV, HCMV, adenovirus, and BK virus infections in biliary atresia related clinical complications, the molecular and antigenic prevalence of these viral agents were studied. In this retrospective study, 34 formalin fixed paraffin embedded (FFPE) biopsy and autopsy liver tissue samples of neonates with biliary atresia were evaluated. The molecular prevalence of these viral infections was assayed by different PCR and RT-PCR methods. The antigenic prevalence of HBV, HCV, and HCMV infections was also studied in these liver tissue samples by immunohistochemistry (IHC) method. HBV, HCV, and adenovirus genomes were detected in 9%, 6%, and 6% of liver autopsy and biopsy tissues of infants with biliary atresia, respectively. HBV and HCV co-infection was confirmed in 6% of FFPE samples. The genome of other investigated viruses was not detected in FFPE liver tissues. Detection of viral infection in FFPE liver tissue samples of newborns with biliary atresia, suggests the need for complete studies for the determination of accurate role of these viral infections in pathogenesis of biliary atresia.
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