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Epidemic and molecular evolution of human bocavirus in hospitalized children with acute respiratory tract infection
Human bocavirus (HBoV) is a novel parvovirus, often associated with respiratory tract diseases in children. This study explored the epidemiological characteristics and molecular evolution of HBoV-1 in southeastern China. Nasopharyngeal aspirates were collected from children admitted to hospital with...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087953/ https://www.ncbi.nlm.nih.gov/pubmed/25070494 http://dx.doi.org/10.1007/s10096-014-2215-7 |
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author | Lu, Q.-B. Wo, Y. Wang, H.-Y. Huang, D.-D. Zhao, J. Zhang, X.-A. Zhang, Y.-Y. Liu, E.-M. Liu, W. Cao, W.-C. |
author_facet | Lu, Q.-B. Wo, Y. Wang, H.-Y. Huang, D.-D. Zhao, J. Zhang, X.-A. Zhang, Y.-Y. Liu, E.-M. Liu, W. Cao, W.-C. |
author_sort | Lu, Q.-B. |
collection | PubMed |
description | Human bocavirus (HBoV) is a novel parvovirus, often associated with respiratory tract diseases in children. This study explored the epidemiological characteristics and molecular evolution of HBoV-1 in southeastern China. Nasopharyngeal aspirates were collected from children admitted to hospital with acute respiratory tract infections. HBoV-1 was detected using real-time reverse transcription polymerase chain reaction and further characterized by complete genome sequences analysis. Among the 3,022 recruited children, 386 (12.77 %) were HBoV-1-positive and 300 (77.72 %) had co-detection with other respiratory viruses. Seasonal prevalence peaked in summer. HBoV-1 presence was significantly associated with asthma attack [odds ratio = 1.74; 95 % confidence interval: 1.30, 2.31; p < 0.001]. Similar results were obtained when either single detection or co-detection of HBoV-1 was considered, demonstrating the minor impact of co-detection on the clinical characteristics or epidemic pattern. Phylogenetic analysis based on the complete genome sequences showed that all the HBoV-1 sequences clustered together and no branch was formed that was supported by bootstrap value ≥750. The overall evolutionary rate of the complete genome of HBoV-1 was estimated at 1.08 × 10(−4) nucleotide substitutions per site per year (s/s/y) [95 % highest probability density: (0.40–1.86) × 10(−4) s/s/y]. Selective pressure analysis showed that all the ω-values were less than 1, suggesting that HBoV-1 was under negative selective pressure. Site-by-site analysis identified the codon site 40 of the VP1 gene under positive selection. In conclusion, our study disclosed the epidemiological and genetic dynamics of HBoV-1 epidemics in southeastern China in the most recent 3 years, the information of which might help to further improve our understanding of HBoV-1 infection and guide better surveillance and control strategies in the future. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10096-014-2215-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7087953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-70879532020-03-23 Epidemic and molecular evolution of human bocavirus in hospitalized children with acute respiratory tract infection Lu, Q.-B. Wo, Y. Wang, H.-Y. Huang, D.-D. Zhao, J. Zhang, X.-A. Zhang, Y.-Y. Liu, E.-M. Liu, W. Cao, W.-C. Eur J Clin Microbiol Infect Dis Article Human bocavirus (HBoV) is a novel parvovirus, often associated with respiratory tract diseases in children. This study explored the epidemiological characteristics and molecular evolution of HBoV-1 in southeastern China. Nasopharyngeal aspirates were collected from children admitted to hospital with acute respiratory tract infections. HBoV-1 was detected using real-time reverse transcription polymerase chain reaction and further characterized by complete genome sequences analysis. Among the 3,022 recruited children, 386 (12.77 %) were HBoV-1-positive and 300 (77.72 %) had co-detection with other respiratory viruses. Seasonal prevalence peaked in summer. HBoV-1 presence was significantly associated with asthma attack [odds ratio = 1.74; 95 % confidence interval: 1.30, 2.31; p < 0.001]. Similar results were obtained when either single detection or co-detection of HBoV-1 was considered, demonstrating the minor impact of co-detection on the clinical characteristics or epidemic pattern. Phylogenetic analysis based on the complete genome sequences showed that all the HBoV-1 sequences clustered together and no branch was formed that was supported by bootstrap value ≥750. The overall evolutionary rate of the complete genome of HBoV-1 was estimated at 1.08 × 10(−4) nucleotide substitutions per site per year (s/s/y) [95 % highest probability density: (0.40–1.86) × 10(−4) s/s/y]. Selective pressure analysis showed that all the ω-values were less than 1, suggesting that HBoV-1 was under negative selective pressure. Site-by-site analysis identified the codon site 40 of the VP1 gene under positive selection. In conclusion, our study disclosed the epidemiological and genetic dynamics of HBoV-1 epidemics in southeastern China in the most recent 3 years, the information of which might help to further improve our understanding of HBoV-1 infection and guide better surveillance and control strategies in the future. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10096-014-2215-7) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2014-07-29 2015 /pmc/articles/PMC7087953/ /pubmed/25070494 http://dx.doi.org/10.1007/s10096-014-2215-7 Text en © Springer-Verlag Berlin Heidelberg 2014 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Lu, Q.-B. Wo, Y. Wang, H.-Y. Huang, D.-D. Zhao, J. Zhang, X.-A. Zhang, Y.-Y. Liu, E.-M. Liu, W. Cao, W.-C. Epidemic and molecular evolution of human bocavirus in hospitalized children with acute respiratory tract infection |
title | Epidemic and molecular evolution of human bocavirus in hospitalized children with acute respiratory tract infection |
title_full | Epidemic and molecular evolution of human bocavirus in hospitalized children with acute respiratory tract infection |
title_fullStr | Epidemic and molecular evolution of human bocavirus in hospitalized children with acute respiratory tract infection |
title_full_unstemmed | Epidemic and molecular evolution of human bocavirus in hospitalized children with acute respiratory tract infection |
title_short | Epidemic and molecular evolution of human bocavirus in hospitalized children with acute respiratory tract infection |
title_sort | epidemic and molecular evolution of human bocavirus in hospitalized children with acute respiratory tract infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087953/ https://www.ncbi.nlm.nih.gov/pubmed/25070494 http://dx.doi.org/10.1007/s10096-014-2215-7 |
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