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Titration of Human Coronaviruses Using an Immunoperoxidase Assay
Published on: April 28, 2008
Human bocavirus 1 epidemiology in children in relation to virus load and codetection
Elina Oldhoff1, Rutger Bennet1, Margareta Eriksson1
1Astrid Lindgren Children's Hospital, Karolinska University Hospital, Stockholm, Sweden.
Human bocavirus 1 (HBoV1) causes respiratory infections in children. High viral loads were linked to younger age and single HBoV1 detection, with mild-to-severe symptoms observed.
Area of Science:
- Pediatric Infectious Diseases
- Virology
- Respiratory Medicine
Background:
- Human bocavirus 1 (HBoV1) is a known cause of respiratory tract infections in children.
- Understanding the clinical significance of HBoV1, particularly in relation to viral load, is crucial for effective management.
Purpose of the Study:
- To describe patient characteristics, seasonality, comorbidities, viral co-detections, clinical manifestations, and complications of HBoV1 infection.
- To elucidate the clinical significance of HBoV1 by analyzing its relationship with viral load in hospitalized children.
Main Methods:
- Retrospective analysis of hospitalized children (0-17 years) with HBoV1-positive nasopharyngeal aspirates from July 2008 to June 2019.
- Analysis of HBoV1 single detection and high viral load (HBoV1-DNA cycle threshold [Ct] < 25) subgroups.
- Information on pre-existing conditions and clinical course was extracted from medical records.
Main Results:
- 768 HBoV1 episodes were identified in 727 children; 64.6% were male, and 60.7% were previously healthy.
- Most infections (62.0%) occurred between December and March; HBoV1 was co-detected with other viruses in 71.5% of cases.
- High viral load (Ct < 25) was associated with younger age, single HBoV1 detection, and early-season presentation, with minimal differences in clinical manifestations between subgroups.
Conclusions:
- HBoV1 infection is associated with mild-to-severe respiratory manifestations in young children.
- The study highlights the clinical significance of HBoV1, especially in relation to viral load and patient demographics.
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