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Exploring the key genomic variation in monkeypox virus during the 2022 outbreak
BACKGROUND: In 2022, a global outbreak of monkeypox occurred with a significant shift in its epidemiological characteristics. The monkeypox virus (MPXV) belongs to the B.1 lineage, and its genomic variations that were linked to the outbreak were investigated in this study. Previous studies have sugg...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652487/ https://www.ncbi.nlm.nih.gov/pubmed/37968621 http://dx.doi.org/10.1186/s12863-023-01171-0 |
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author | Zhu, Jie Yu, Jian Qin, Hao Chen, Xinlei Wu, Chuanchang Hong, Xiaodan Zhang, Yafei Zhang, Zhenhua |
author_facet | Zhu, Jie Yu, Jian Qin, Hao Chen, Xinlei Wu, Chuanchang Hong, Xiaodan Zhang, Yafei Zhang, Zhenhua |
author_sort | Zhu, Jie |
collection | PubMed |
description | BACKGROUND: In 2022, a global outbreak of monkeypox occurred with a significant shift in its epidemiological characteristics. The monkeypox virus (MPXV) belongs to the B.1 lineage, and its genomic variations that were linked to the outbreak were investigated in this study. Previous studies have suggested that viral genomic variation plays a crucial role in the pathogenicity and transmissibility of viruses. Therefore, understanding the genomic variation of MPXV is crucial for controlling future outbreaks. METHODS: This study employed bioinformatics and phylogenetic approaches to evaluate the key genomic variation in the B.1 lineage of MPXV. A total of 979 MPXV strains were screened, and 212 representative strains were analyzed to identify specific substitutions in the viral genome. Reference sequences were constructed for each of the 10 lineages based on the most common nucleotide at each site. A total of 49 substitutions were identified, with 23 non-synonymous substitutions. Class I variants, which had significant effects on protein conformation likely to affect viral characteristics, were classified among the non-synonymous substitutions. RESULTS: The phylogenetic analysis revealed 10 relatively monophyletic branches. The study identified 49 substitutions specific to the B.1 lineage, with 23 non-synonymous substitutions that were classified into Class I, II, and III variants. The Class I variants were likely responsible for the observed changes in the characteristics of circulating MPXV in 2022. These key mutations, particularly Class I variants, played a crucial role in the pathogenicity and transmissibility of MPXV. CONCLUSION: This study provides an understanding of the genomic variation of MPXV in the B.1 lineage linked to the recent outbreak of monkeypox. The identification of key mutations, particularly Class I variants, sheds light on the molecular mechanisms underlying the observed changes in the characteristics of circulating MPXV. Further studies can focus on functional domains affected by these mutations, enabling the development of effective control strategies against future monkeypox outbreaks. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12863-023-01171-0. |
format | Online Article Text |
id | pubmed-10652487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106524872023-11-16 Exploring the key genomic variation in monkeypox virus during the 2022 outbreak Zhu, Jie Yu, Jian Qin, Hao Chen, Xinlei Wu, Chuanchang Hong, Xiaodan Zhang, Yafei Zhang, Zhenhua BMC Genom Data Research BACKGROUND: In 2022, a global outbreak of monkeypox occurred with a significant shift in its epidemiological characteristics. The monkeypox virus (MPXV) belongs to the B.1 lineage, and its genomic variations that were linked to the outbreak were investigated in this study. Previous studies have suggested that viral genomic variation plays a crucial role in the pathogenicity and transmissibility of viruses. Therefore, understanding the genomic variation of MPXV is crucial for controlling future outbreaks. METHODS: This study employed bioinformatics and phylogenetic approaches to evaluate the key genomic variation in the B.1 lineage of MPXV. A total of 979 MPXV strains were screened, and 212 representative strains were analyzed to identify specific substitutions in the viral genome. Reference sequences were constructed for each of the 10 lineages based on the most common nucleotide at each site. A total of 49 substitutions were identified, with 23 non-synonymous substitutions. Class I variants, which had significant effects on protein conformation likely to affect viral characteristics, were classified among the non-synonymous substitutions. RESULTS: The phylogenetic analysis revealed 10 relatively monophyletic branches. The study identified 49 substitutions specific to the B.1 lineage, with 23 non-synonymous substitutions that were classified into Class I, II, and III variants. The Class I variants were likely responsible for the observed changes in the characteristics of circulating MPXV in 2022. These key mutations, particularly Class I variants, played a crucial role in the pathogenicity and transmissibility of MPXV. CONCLUSION: This study provides an understanding of the genomic variation of MPXV in the B.1 lineage linked to the recent outbreak of monkeypox. The identification of key mutations, particularly Class I variants, sheds light on the molecular mechanisms underlying the observed changes in the characteristics of circulating MPXV. Further studies can focus on functional domains affected by these mutations, enabling the development of effective control strategies against future monkeypox outbreaks. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12863-023-01171-0. BioMed Central 2023-11-16 /pmc/articles/PMC10652487/ /pubmed/37968621 http://dx.doi.org/10.1186/s12863-023-01171-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zhu, Jie Yu, Jian Qin, Hao Chen, Xinlei Wu, Chuanchang Hong, Xiaodan Zhang, Yafei Zhang, Zhenhua Exploring the key genomic variation in monkeypox virus during the 2022 outbreak |
title | Exploring the key genomic variation in monkeypox virus during the 2022 outbreak |
title_full | Exploring the key genomic variation in monkeypox virus during the 2022 outbreak |
title_fullStr | Exploring the key genomic variation in monkeypox virus during the 2022 outbreak |
title_full_unstemmed | Exploring the key genomic variation in monkeypox virus during the 2022 outbreak |
title_short | Exploring the key genomic variation in monkeypox virus during the 2022 outbreak |
title_sort | exploring the key genomic variation in monkeypox virus during the 2022 outbreak |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652487/ https://www.ncbi.nlm.nih.gov/pubmed/37968621 http://dx.doi.org/10.1186/s12863-023-01171-0 |
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