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Etiologies of Acute Bronchiolitis in Children at Risk for Asthma, with Emphasis on the Human Rhinovirus Genotyping
Ahmad R Alsayed1, Anas Abed2, Mahmoud Abu-Samak1
1Department of Clinical Pharmacy and Therapeutics, Applied Science Private University, Amman 11931, Jordan.
Insights
Human Rhinovirus (HRV) is a common cause of acute bronchiolitis in young children. This study developed a method using specific gene regions to accurately identify and classify different HRV types, aiding in diagnosis and research.
Area of Science:
- Pediatric infectious diseases
- Virology
- Molecular diagnostics
Background:
- Acute bronchiolitis is a common respiratory infection in infants and young children.
- Human Rhinovirus (HRV) is a significant, yet often under-characterized, causative agent of acute bronchiolitis.
- Accurate identification of HRV species is crucial for understanding disease epidemiology and developing targeted interventions.
Purpose of the Study:
- To identify the primary viral causes of acute bronchiolitis in young children.
- To establish a reliable protocol for classifying Human Rhinovirus (HRV) species.
- To evaluate specific genetic regions for accurate HRV genotyping.
Main Methods:
- Nasopharyngeal samples from children aged 1-24 months with acute bronchiolitis were analyzed using a viral panel via quantitative polymerase chain reaction (qPCR).
- HRV-positive samples underwent high-throughput sequencing targeting VP4/VP2 and VP3/VP1 regions.
- Phylogenetic analysis, BLAST searching, and sequence divergence were employed to differentiate HRV species and assess genotyping regions.
Main Results:
- Respiratory Syncytial Virus (RSV) was the leading cause, with HRV identified as the second most common viral etiology.
- Sequencing data classified HRV strains into 7 HRV-A, 1 HRV-B, and 7 HRV-C types.
- The VP4/VP2 region exhibited lower nucleotide divergence compared to VP3/VP1, indicating greater utility for differentiating HRV genotypes.
Conclusions:
- HRV is a significant contributor to acute bronchiolitis in children.
- The VP4/VP2 and VP3/VP1 regions are effective for HRV species identification and genotyping.
- Nested and semi-nested PCR methods provide practical approaches for HRV sequencing and genotyping, enhancing diagnostic capabilities.
Abstract:
This research aims to determine acute bronchiolitis' causative virus(es) and establish a viable protocol to classify the Human Rhinovirus (HRV) species. During 2021-2022, we included children 1-24 months of age with acute bronchiolitis at risk for asthma. The nasopharyngeal samples were taken and subjected to a quantitative polymerase chain reaction (qPCR) in a viral panel. For HRV-positive samples, a high-throughput assay was applied, directing the VP4/VP2 and VP3/VP1 regions to confirm species. BLAST searching, phylogenetic analysis, and sequence divergence took place to identify the degree to which these regions were appropriate for identifying and differentiating HRV. HRV ranked second, following RSV, as the etiology of acute bronchiolitis in children. The conclusion of the investigation of all available data in this study distributed sequences into 7 HRV-A, 1 HRV-B, and 7 HRV-C types based on the VP4/VP2 and VP3/VP1 sequences. The nucleotide divergence between the clinical samples and the corresponding reference strains was lower in the VP4/VP2 region than in the VP3/VP1 region. The results demonstrated the potential utility of the VP4/VP2 region and the VP3/VP1 region for differentiating HRV genotypes. Confirmatory outcomes were yielded, indicating how nested and semi-nested PCR can establish practical ways to facilitate HRV sequencing and genotyping.
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