Human bocavirus infection in Belgian children with respiratory tract disease
Vanessa Verbeke1, Marijke Reynders2, Katelijne Floré2
1Department of Medical Microbiology, Ghent University Hospital, Corneel Heymanslaan 10, 9000, Ghent, Belgium.
Insights
Human bocavirus (HBoV) can cause respiratory tract disease (RTD) in children. High viral loads of HBoV in infants are linked to wheezing illnesses.
Area of Science:
- Pediatrics
- Virology
- Infectious Diseases
Background:
- Human bocavirus (HBoV) is frequently detected in children with acute lower respiratory tract disease (LRTD).
- The exact role of HBoV in respiratory tract disease (RTD) and its clinical presentation remain unclear.
Purpose of the Study:
- To investigate the prevalence of HBoV in children with RTD.
- To assess the clinical relevance and potential impact of HBoV infection.
Main Methods:
- Molecular testing of 1352 nasopharyngeal samples from children (≤16 years) with RTD in Belgium.
- Detection of HBoV DNA and 20 other respiratory pathogens.
- Analysis of clinical data and viral loads.
Main Results:
- HBoV was detected in 77 children (median age 10.6 months).
- Monoinfection occurred in six infants, with one diagnosed with recurrent wheezing associated with high viral load.
- Coinfections were common (72/77 patients), particularly with rhinovirus and adenovirus.
- High HBoV viral loads were associated with bronchi(oli)tis and wheezing in 17 patients.
Conclusions:
- HBoV infection, particularly at high viral loads in infants, is significantly associated with wheezing.
- Further research is needed to fully elucidate HBoV's role in pediatric respiratory illnesses.
Abstract:
Human bocavirus (HBoV) has been detected primarily in children with acute lower respiratory tract disease (LRTD), but its occurrence, clinical profile, and role as a causative agent of RTD are not clear. The aim of this study was to investigate the prevalence and the potential clinical relevance of HBoV. Using molecular tests, we tested 1352 nasopharyngeal samples obtained between October 1, 2017 and April 30, 2018 from children up to the age of 16 with RTD for the presence of HBoV DNA and 20 other respiratory pathogens at three different hospitals in Belgium. HBoV was detected in 77 children with a median age of 10.6 months. Consecutive samples were available for 15 HBoV-positive children and showed persistent HBoV positivity in four of them. Monoinfection was observed in six infants. Four of them were born prematurely and were infected during hospitalization at the neonatal intensive care unit (NICU). Only one of these six monoinfected children was diagnosed with recurrent wheezing due to HBoV. This child was carried to term and had a high viral load. Coinfections, most frequently with rhinovirus (52.1%) and adenovirus (49.3%), were observed in 72 patients. In seventeen of them in which HBoV was present at high viral load or higher viral load than its copathogens, bronchi(oli)tis (n = 8), recurrent wheezing (n = 8) or episodic wheezing (n = 1) were diagnosed. Our results suggest that HBoV infection at high viral load in infants is associated with wheezing (P = 0.013, Cramer's V = 0.613).
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