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Emergence and characterization of a putative novel human adenovirus recombinant HAdV-C104 causing pneumonia in Southern China
In 2017, a survey of the molecular epidemiology of human adenovirus (HAdV) infections in Southern China based on hexon and fiber genotype demonstrated that the most prevalent genotypes of HAdV were HAdV-3 (n = 62), HAdV-2 (n = 21), and HAdV-7 (n = 16). In addition, two patients were co-infected with...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953211/ https://www.ncbi.nlm.nih.gov/pubmed/33732504 http://dx.doi.org/10.1093/ve/veab018 |
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author | Ji, Tianxing Li, Ling Li, Wenrui Zheng, Xuehua Ye, Xianmiao Chen, Hongliang Zhou, Qiang Jia, Hongyun Chen, Bo Lin, Zhen Chen, Haoyu Huang, Shiwen Seto, Donald Chen, Ling Feng, Liqiang |
author_facet | Ji, Tianxing Li, Ling Li, Wenrui Zheng, Xuehua Ye, Xianmiao Chen, Hongliang Zhou, Qiang Jia, Hongyun Chen, Bo Lin, Zhen Chen, Haoyu Huang, Shiwen Seto, Donald Chen, Ling Feng, Liqiang |
author_sort | Ji, Tianxing |
collection | PubMed |
description | In 2017, a survey of the molecular epidemiology of human adenovirus (HAdV) infections in Southern China based on hexon and fiber genotype demonstrated that the most prevalent genotypes of HAdV were HAdV-3 (n = 62), HAdV-2 (n = 21), and HAdV-7 (n = 16). In addition, two patients were co-infected with two genotypes of HAdV. Interestingly, a novel human adenovirus C recombinant genotype strain was isolated from one of the pneumonia patients in this survey. Phylogenetic, recombination, and proteotyping analysis showed that this novel pathogen originated from the recombination of parental viruses harboring the HAdV-1 penton and hexon gene, and the HAdV-2 fiber gene. It was named ‘P1H1F2’ and was assigned as HAdV-C104 based on the nomenclature protocol of using three major capsid proteins for characterization. Subsequent in vitro experiments demonstrated that HAdV-C104 had comparable proliferation capacity to HAdV-1, HAdV-2, and another recombination genotype P1H2F2. In addition, the HAdV-C104 infected patient was diagnosed with pneumonia and recovered after antiviral therapy. This report strengthens the hypothesis of recombination as a major pathway for the molecular evolution of HAdV-C species. |
format | Online Article Text |
id | pubmed-7953211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-79532112021-03-16 Emergence and characterization of a putative novel human adenovirus recombinant HAdV-C104 causing pneumonia in Southern China Ji, Tianxing Li, Ling Li, Wenrui Zheng, Xuehua Ye, Xianmiao Chen, Hongliang Zhou, Qiang Jia, Hongyun Chen, Bo Lin, Zhen Chen, Haoyu Huang, Shiwen Seto, Donald Chen, Ling Feng, Liqiang Virus Evol Research Article In 2017, a survey of the molecular epidemiology of human adenovirus (HAdV) infections in Southern China based on hexon and fiber genotype demonstrated that the most prevalent genotypes of HAdV were HAdV-3 (n = 62), HAdV-2 (n = 21), and HAdV-7 (n = 16). In addition, two patients were co-infected with two genotypes of HAdV. Interestingly, a novel human adenovirus C recombinant genotype strain was isolated from one of the pneumonia patients in this survey. Phylogenetic, recombination, and proteotyping analysis showed that this novel pathogen originated from the recombination of parental viruses harboring the HAdV-1 penton and hexon gene, and the HAdV-2 fiber gene. It was named ‘P1H1F2’ and was assigned as HAdV-C104 based on the nomenclature protocol of using three major capsid proteins for characterization. Subsequent in vitro experiments demonstrated that HAdV-C104 had comparable proliferation capacity to HAdV-1, HAdV-2, and another recombination genotype P1H2F2. In addition, the HAdV-C104 infected patient was diagnosed with pneumonia and recovered after antiviral therapy. This report strengthens the hypothesis of recombination as a major pathway for the molecular evolution of HAdV-C species. Oxford University Press 2021-03-02 /pmc/articles/PMC7953211/ /pubmed/33732504 http://dx.doi.org/10.1093/ve/veab018 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Ji, Tianxing Li, Ling Li, Wenrui Zheng, Xuehua Ye, Xianmiao Chen, Hongliang Zhou, Qiang Jia, Hongyun Chen, Bo Lin, Zhen Chen, Haoyu Huang, Shiwen Seto, Donald Chen, Ling Feng, Liqiang Emergence and characterization of a putative novel human adenovirus recombinant HAdV-C104 causing pneumonia in Southern China |
title | Emergence and characterization of a putative novel human adenovirus recombinant HAdV-C104 causing pneumonia in Southern China |
title_full | Emergence and characterization of a putative novel human adenovirus recombinant HAdV-C104 causing pneumonia in Southern China |
title_fullStr | Emergence and characterization of a putative novel human adenovirus recombinant HAdV-C104 causing pneumonia in Southern China |
title_full_unstemmed | Emergence and characterization of a putative novel human adenovirus recombinant HAdV-C104 causing pneumonia in Southern China |
title_short | Emergence and characterization of a putative novel human adenovirus recombinant HAdV-C104 causing pneumonia in Southern China |
title_sort | emergence and characterization of a putative novel human adenovirus recombinant hadv-c104 causing pneumonia in southern china |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953211/ https://www.ncbi.nlm.nih.gov/pubmed/33732504 http://dx.doi.org/10.1093/ve/veab018 |
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