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Updated: Jun 10, 2025

Generation, Amplification, and Titration of Recombinant Respiratory Syncytial Viruses
Published on: April 4, 2019
Genomic characteristics of human respiratory syncytial virus from children in China during 2017-2020
Fei Li1, Yun Zhu1, Qiuping Li1
1Beijing Key Laboratory of Pediatric Respiratory Infection Diseases, Key Laboratory of Major Diseases in Children, Ministry of Education, National Clinical Research Center for Respiratory Diseases, Research Unit of Critical Infection in Children, Chinese Academy of Medical Sciences, 2019RU016, Laboratory of Infection and Virology, Beijing Pediatric Research Institute, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, 100045, China.
Insights
Genetic analysis of respiratory syncytial virus (RSV) reveals specific mutations in ON1 and BA9 genotypes. This genomic data is crucial for developing effective RSV prevention and control strategies, including new vaccines.
Area of Science:
- Virology
- Genomics
- Epidemiology
Background:
- Acute lower respiratory tract infections (ALRTIs) pose a significant global health threat to young children, with human respiratory syncytial virus (RSV) being a primary cause of mortality.
- Understanding the genetic diversity of RSV is essential for effective public health interventions and the development of preventative measures.
Purpose of the Study:
- To monitor genetic variations in human respiratory syncytial virus (RSV) circulating between 2017 and 2020.
- To provide comprehensive genomic data to support the prevention, control, and vaccine development efforts against RSV.
Main Methods:
- Determination of 105 complete RSV genome sequences.
- Phylogenetic analysis of whole genome and G gene sequences.
- Amino acid substitution analysis in viral proteins, particularly the F gene.
Main Results:
- All analyzed RSVA strains belonged to genotype ON1, and all RSVB strains belonged to genotype BA9.
- Whole-genome phylogenetic analysis revealed greater diversity than G-gene analysis.
- Identified simultaneous amino acid substitutions in ON1 and BA9 genotypes, and substitutions in key antigenic sites of the F gene.
Conclusions:
- The study provides critical genomic insights into circulating RSV strains.
- Identified genetic variations can inform the design of targeted RSV vaccines and therapies.
- Genomic surveillance is vital for ongoing RSV prevention and control efforts.
Abstract:
Acute lower respiratory tract infections (ALRTIs) are a leading cause of mortality in young children worldwide due to human respiratory syncytial virus (RSV). The aim of this study was to monitor genetic variations in RSV and provide genomic data support for RSV prevention and control. A total of 105 complete RSV genome sequences were determined during 2017-2020. Phylogenetic analysis showed that all of the RSVA sequences were of genotype ON1, and all of the RSVB sequences were of genotype BA9. Notably, a phylogenetic tree based on the whole genome had more branches than a tree based on the G gene. In comparison to the RSV prototype sequences, 71.43% (50/70) of the ON1 sequences had five amino acid substitutions (T113I, V131N, N178G, H258Q, and H266L) that occurred simultaneously, and 68.57% (24/35) of the BA9 genotype sequences had 12 amino acid substitutions, four of which (A131T, T137I, T288I, and T310I) occurred simultaneously. In the F gene, there were 19 amino acid substitutions, which were mainly located in the antigenic sites Ø, II, V, and VII. Other amino acid substitutions were found in the NS1, NS2, P, SH, and L proteins. No significant evidence of recombination was found in any of the sequences. These findings provide important data that will be useful for prevention, control, and vaccine development against RSV.
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