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Acute Human Bocavirus 1 Infection in Children Hospitalized for Acute Bronchiolitis: A 2-Year Prospective Study
Tina Uršič1, Lara Lusa2,3, Franc Strle4
1From the Institute of Microbiology and Immunology, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Insights
Human bocavirus 1 (HBoV1) replication was assessed in children hospitalized for acute bronchiolitis (AB). Active HBoV1 infections in AB patients showed high viral DNA and mRNA in nasopharyngeal samples, with plasma DNA detection.
Area of Science:
- Pediatrics
- Virology
- Infectious Diseases
Background:
- Human bocavirus 1 (HBoV1) is a known respiratory pathogen.
- Acute bronchiolitis (AB) is a common respiratory illness in infants and young children.
- The role of HBoV1 replication in the severity of AB requires further investigation.
Purpose of the Study:
- To determine the proportion of HBoV1 replication in children hospitalized with AB.
- To evaluate the clinical significance of HBoV1 replication in these patients.
- To differentiate active HBoV1 infections from inactive ones.
Main Methods:
- Prospective study design.
- Detection of HBoV1 DNA and mRNA in nasopharyngeal (NP) samples from children with AB and healthy controls.
- Analysis of HBoV1 DNA in plasma samples.
Main Results:
- HBoV1 DNA was found in 12.1% of AB patients and 6% of controls.
- A high rate of co-detection with other respiratory viruses was observed in AB patients (75.7%).
- Active HBoV1 infection (DNA and mRNA positive) was confirmed in 24.3% of HBoV1 DNA-positive NP swabs, with concurrent detection of HBoV1 DNA in plasma.
Conclusions:
- Children with acute HBoV1 infection and AB exhibit high viral DNA loads in NP samples.
- Detection of HBoV1 mRNA and plasma DNA indicates active viral replication.
- These findings suggest HBoV1 replication plays a role in the clinical course of acute bronchiolitis.
Background:
The objective of this prospective study was to assess the proportion and clinical consequences of human bocavirus 1 (HBoV1) replication in children hospitalized for acute bronchiolitis (AB) with HBoV1 DNA in the nasopharynx (NP).
Methods:
For this purpose, we detected HBoV1 DNA and mRNA (evidence of viral replication and viable virus) in NP in cases and healthy control children. This research allowed us to distinguish active HBoV1 infections from inactive ones.
Results:
HBoV1 DNA was detected in the NP of 37 of 307 patients with AB (12.1%) and 9 of 150 children in a healthy control group (6%) with a high codetection rate with other respiratory viruses in AB patients, 28 of 37 (75.7%). Only 9 of 37 HBoV1 DNA-positive NP swabs (24.3%) with high DNA load were also HBoV1 mRNA positive, moreover, HBoV1 DNA was also detected in the plasma of these patients.
Conclusions:
Based on the results of our study, we can conclude that children with AB acute HBoV1 infection has a high HBoV1 DNA load in NP samples together with detected HBoV1 mRNA and detected HBoV1 DNA in plasma.
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