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Updated: Jan 24, 2026

Generation and Assembly of Virus-Specific Nucleocapsids of the Respiratory Syncytial Virus
Published on: July 27, 2021
Immunohistochemical detection of respiratory syncytial virus at autopsy
Tomoya Ikeda1,2, Naoto Tani1,2, Yayoi Aoki1
1Department of Legal Medicine, Osaka City University Medical School, Osaka, Japan.
Insights
Respiratory syncytial virus (RSV) is a fatal threat to infants. Postmortem diagnosis of RSV pathogenicity is challenging but immunopositive bronchial and alveolar cells indicate infection, aiding in infant death investigations.
Area of Science:
- Forensic Pathology
- Pediatric Infectious Diseases
- Virology
Background:
- Respiratory syncytial virus (RSV) infection poses a significant mortality risk in infants under one year old.
- Current diagnostic methods for identifying RSV as a cause of infant death are insufficient and problematic.
- Establishing reliable postmortem diagnostic criteria for RSV pathogenicity is crucial.
Purpose of the Study:
- To establish a reliable postmortem diagnostic method for identifying Respiratory syncytial virus (RSV) pathogenicity in infants.
- To investigate the role of RSV in infant mortality through forensic autopsies.
- To correlate specific cellular findings with RSV infection in deceased infants.
Main Methods:
- Conducted serial forensic autopsies on 55 infants who died within one year of birth.
- Classified causes of death, including viral pneumonia (n=18), bacterial pneumonia (n=12), and other causes (n=25).
- Utilized immunochemical screening and histological staining to identify RSV in airway effusions and lung tissues.
Main Results:
- RSV was identified as the cause of pneumonia in 8 out of 18 viral pneumonia cases.
- Immunohistochemical staining revealed RSV-positive bronchial epithelial and inflammatory cells in infants with RSV pneumonia.
- Bronchial epithelium and intra-alveolar sites showed higher RSV positivity in confirmed RSV pneumonia cases compared to other causes of death.
Conclusions:
- RSV infection was confirmed as the cause of death in only eight infants due to diagnostic difficulties.
- Further investigation into infant deaths is needed to fully ascertain the impact of RSV.
- RSV immunopositivity in bronchial epithelium and intra-alveolar cells suggests a role in augmenting pathogenicity in viral pneumonia.
Background:
Respiratory syncytial virus (RSV) infection can be fatal in infants <1 year after birth. Morphological findings associated with infant death, however, are insufficient, and screening procedures are problematic. The aim of the present study was to establish a postmortem diagnosis of RSV pathogenicity.
Methods:
Serial forensic autopsies of 55 infants who suddenly died ≤1 year after birth due to viral pneumonia (n = 18), bacterial pneumonia (n = 12), or other diseases and trauma (n = 25) were assessed. Causes of viral pneumonia determined on immunochemical screening and histological staining of airway effusions consisted of RSV (n = 8) and other viruses (n = 10).
Results:
Bronchial epithelial and inflammatory cells in the interstitium around bronchioles and alveoli were immunopositive for RSV. Bronchial epithelium was more frequently positive for RSV (5/8, 62.5%) than for bacterial pneumonia and other causes of death (7/47, 14.9%); and intra-alveolar sites were also more frequently positive for RSV pneumonia (3/8, 37.5%) than for bacterial pneumonia and other causes of death (4/47, 8.5%). Screening immunoassays and immunohistochemical staining for RSV can serve as an index of RSV infection when serum antibody titers, viral identification and polymerase chain reaction (PCR) are not informative. Peribronchiolar interstitial RSV positivity was similar between RSV pneumonia (7/8, 87.5%) and other causes of death (34/47, 72.3%).
Conclusions:
RSV was the cause of death in only eight infants because RSV infection was difficult to diagnose. Therefore, more deaths associated with RSV need to be investigated. Bronchial epithelium and intra-alveolar cells that are RSV immunopositive might augment RSV pathogenicity in viral pneumonia.
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