Related Experiment Video
Updated: Nov 18, 2025

An In vitro Model to Study Immune Responses of Human Peripheral Blood Mononuclear Cells to Human Respiratory Syncytial Virus Infection
Published on: December 10, 2013
Persistent viral shedding of human adenovirus type 7 in children with severe pneumonia
Sai-Zhen Zeng1,2,3, Le-Yun Xie2,3, Tian Yu2,3
1Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Insights
Human adenovirus (HAdV) shedding in children with severe pneumonia shows HAdV-7 persists longer than HAdV-3. Viral load decreases slower for HAdV-7, impacting control strategies.
Area of Science:
- Virology
- Pediatric Infectious Diseases
- Respiratory Medicine
Background:
- Human adenovirus (HAdV) infections, particularly severe pneumonia in children, necessitate understanding viral shedding dynamics.
- Effective prevention and control strategies depend on characterizing HAdV shedding patterns in pediatric populations.
Purpose of the Study:
- To investigate the characteristics of human adenovirus (HAdV) shedding in hospitalized children with severe HAdV pneumonia.
- To compare the viral load dynamics and shedding duration between HAdV type 7 (HAdV-7) and HAdV type 3 (HAdV-3) infections.
Main Methods:
- Quantitative real-time PCR was used to detect HAdV DNA in nasopharyngeal aspirate (NPA) samples from 132 hospitalized children (<14 years) with severe HAdV pneumonia.
- A total of 1372 NPA samples were analyzed to determine HAdV viral load and shedding duration.
- Statistical analysis, including Spearman correlation and regression, was employed to assess the relationship between viral load, disease course, and shedding duration.
Main Results:
- A significant negative correlation was observed between HAdV viral load and the course of the disease (Spearman r = -0.547, p = .000).
- HAdV-7 viral load decreased slower (0.089 log10 copies/mL/day) with a predicted shedding duration of 96.9 days, while HAdV-3 decreased faster (0.186 log10 copies/mL/day) with a predicted duration of 51.4 days.
- Median viral loads for HAdV-7 were higher than HAdV-3 at weeks 2, 3, and beyond 3 weeks post-infection. No significant differences in shedding duration were found based on gender, age, or underlying conditions.
Conclusions:
- Viral shedding in children with severe HAdV pneumonia is prolonged, with HAdV-7 exhibiting longer shedding duration and slower viral load decline compared to HAdV-3.
- These findings highlight the importance of considering specific HAdV types when developing clinical management and public health interventions for pediatric adenovirus pneumonia.
Abstract:
To understand host-pathogen interactions and develop effective prevention and control strategies for human adenovirus (HAdV), it is essential to explore the characteristics of HAdV shedding. Hospitalized children <14 years who had severe HAdV pneumonia were tested for HAdV DNA by quantitative real-time PCR in nasopharyngeal aspirate (NPA). A total of 132 children were enrolled, including 102 patients with HAdV type 7 (HAdV-7) infection and 12 patients with HAdV type 3 (HAdV-3) infection. A total of 1372 qualified NPA samples were collected. There was a significant negative correlation between the viral load of HAdV and the course of the disease (Spearman r = -0.547, p = .000). HAdV-7 load decreased at a rate of 0.089 log10 copies/mL per day (95% CI: -0.096 to -0.081; R 2 = 0.332), and the duration of viral shedding was predicted to be 96.9 days (y = 8.624-0.089x). However, HAdV-3 load decreased more quickly (95% CI: - 0.229 to - 0.143; R 2 = 0.403), and the duration of viral shedding was 51.4 days (y = 9.558-0.186x). The median viral load of the HAdV-7 group at weeks 2 and 3, and more than 3 weeks postinfection was higher than that of the HAdV-3 group. No significant differences in the duration of viral shedding were found in different gender, age (>2 vs. ≤2 years), and with or without underlying diseases groups. Viral shedding in children with severe HAdV pneumonia persisted, among which HAdV-7 lasted longer than 3 months and the viral load decreased slowly than HAdV-3.
More Related Videos
Related Concept Videos
Pneumonia II: Pathophysiology
Pneumonia I: Introduction
Risk Factors
Various factors influence the likelihood of developing pneumonia. Age plays a crucial role, with infants, children under two, and individuals over 65 at increased risk due to their...
Acute Respiratory Failure-II
The underlying physiological abnormalities that contribute to hypoxemic respiratory failure include:
Pneumonia III: Complications and Assessment

