Cargando…
The polymorphism analysis and epitope predicted of Alphapapillomavirus 9 E6 in Sichuan, China
BACKGROUND: The Alphapapillomavirus 9 (α-9 HPV) is a member of the Alphapapillomavirus genus and Papillomaviridae family. These viruses are almost all carcinogenic HPV, which is closely related to 75% of invasive cervical cancer worldwide, and has a high prevalence in Sichuan. The carcinogenic funct...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8772103/ https://www.ncbi.nlm.nih.gov/pubmed/35057815 http://dx.doi.org/10.1186/s12985-021-01728-4 |
_version_ | 1784635771950465024 |
---|---|
author | He, Jiaoyu Li, Qiufu Ma, Shiyu Li, Tianjun Chen, Yuning Liu, Yiran Cui, Yanru Peng, Jianying Shi, Yunfan Wei, Xia Ding, Xianping |
author_facet | He, Jiaoyu Li, Qiufu Ma, Shiyu Li, Tianjun Chen, Yuning Liu, Yiran Cui, Yanru Peng, Jianying Shi, Yunfan Wei, Xia Ding, Xianping |
author_sort | He, Jiaoyu |
collection | PubMed |
description | BACKGROUND: The Alphapapillomavirus 9 (α-9 HPV) is a member of the Alphapapillomavirus genus and Papillomaviridae family. These viruses are almost all carcinogenic HPV, which is closely related to 75% of invasive cervical cancer worldwide, and has a high prevalence in Sichuan. The carcinogenic function is mainly realized by its E6 oncoprotein. METHODS: Cell samples were collected by cervical scraped for HPV detecting and typing. HPV-16, HPV-31, HPV-33, HPV-52, HPV-58 5 α-9 genus HPV subtype positive samples were selected, their E6 gene was sequenced and analyzed. The positive selection sites of HPV E6 genes were estimated by PAML 4.8 server. The secondary and tertiary structure of E6 protein were predicted by PSIPred and Swiss-model. The T-cell antigen epitopes of E6 protein were predicted by IEDB. RESULTS: α-9 HPV has a high prevalence in Sichuan, China. From 2012 to 2017, 18,067 cell cervical samples were collected, and 3135 were detected with α-9 HPV infection. Among which, 250 cases HPV-16 E6, 96 cases HPV-31 E6, 216 cases HPV-33 E6, 288 cases HPV-52 E6 and 405 cases HPV-58 E6 were successfully amplified, 17, 6, 6, 13, and 4 non-synonymous nucleotide mutations were respectively detected in HPV-16, 31, 33, 52, and 58 E6, 7 positive selection sites of α-9 HPV E6 were selected out (D32E of HPV-16 E6, K35N, K93N and R145I of HPV-33 E6, K93R of HPV-52 E6, K93N and R145K of HPV-58 E6). The structure and antigen epitopes of E6 protein with amino acid substitution differ from those of wild-type E6 protein, especially for the mutation located in the E6 positive selection site. CONCLUSIONS: HPV E6 nucleotide non-synonymous mutation in the positive selection site influence the protein structure and decrease the antigen epitopes affinity of the E6 protein overall, making it more difficult for the HPV-infected cells to be detected by the immune system, and enhancing the HPV adaptability to the environment. Mutations influence the validity of HPV clinical diagnostic probes, the polymorphism analysis of α-9 HPV E6 enrich the data of HR-risk HPV in Sichuan China, and the detection probes designed with the polymorphism data in mind can improve the efficiency of clinical detection; Mutations influence epitopes affinity, the association of E6 polymorphism and epitope affinity can improve the design of therapeutic vaccine with good immunity and high generality antigen epitope; The above study all provide a good theoretical basis for the prevention and treatment of HPV-related diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12985-021-01728-4. |
format | Online Article Text |
id | pubmed-8772103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-87721032022-01-20 The polymorphism analysis and epitope predicted of Alphapapillomavirus 9 E6 in Sichuan, China He, Jiaoyu Li, Qiufu Ma, Shiyu Li, Tianjun Chen, Yuning Liu, Yiran Cui, Yanru Peng, Jianying Shi, Yunfan Wei, Xia Ding, Xianping Virol J Research BACKGROUND: The Alphapapillomavirus 9 (α-9 HPV) is a member of the Alphapapillomavirus genus and Papillomaviridae family. These viruses are almost all carcinogenic HPV, which is closely related to 75% of invasive cervical cancer worldwide, and has a high prevalence in Sichuan. The carcinogenic function is mainly realized by its E6 oncoprotein. METHODS: Cell samples were collected by cervical scraped for HPV detecting and typing. HPV-16, HPV-31, HPV-33, HPV-52, HPV-58 5 α-9 genus HPV subtype positive samples were selected, their E6 gene was sequenced and analyzed. The positive selection sites of HPV E6 genes were estimated by PAML 4.8 server. The secondary and tertiary structure of E6 protein were predicted by PSIPred and Swiss-model. The T-cell antigen epitopes of E6 protein were predicted by IEDB. RESULTS: α-9 HPV has a high prevalence in Sichuan, China. From 2012 to 2017, 18,067 cell cervical samples were collected, and 3135 were detected with α-9 HPV infection. Among which, 250 cases HPV-16 E6, 96 cases HPV-31 E6, 216 cases HPV-33 E6, 288 cases HPV-52 E6 and 405 cases HPV-58 E6 were successfully amplified, 17, 6, 6, 13, and 4 non-synonymous nucleotide mutations were respectively detected in HPV-16, 31, 33, 52, and 58 E6, 7 positive selection sites of α-9 HPV E6 were selected out (D32E of HPV-16 E6, K35N, K93N and R145I of HPV-33 E6, K93R of HPV-52 E6, K93N and R145K of HPV-58 E6). The structure and antigen epitopes of E6 protein with amino acid substitution differ from those of wild-type E6 protein, especially for the mutation located in the E6 positive selection site. CONCLUSIONS: HPV E6 nucleotide non-synonymous mutation in the positive selection site influence the protein structure and decrease the antigen epitopes affinity of the E6 protein overall, making it more difficult for the HPV-infected cells to be detected by the immune system, and enhancing the HPV adaptability to the environment. Mutations influence the validity of HPV clinical diagnostic probes, the polymorphism analysis of α-9 HPV E6 enrich the data of HR-risk HPV in Sichuan China, and the detection probes designed with the polymorphism data in mind can improve the efficiency of clinical detection; Mutations influence epitopes affinity, the association of E6 polymorphism and epitope affinity can improve the design of therapeutic vaccine with good immunity and high generality antigen epitope; The above study all provide a good theoretical basis for the prevention and treatment of HPV-related diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12985-021-01728-4. BioMed Central 2022-01-20 /pmc/articles/PMC8772103/ /pubmed/35057815 http://dx.doi.org/10.1186/s12985-021-01728-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 He, Jiaoyu Li, Qiufu Ma, Shiyu Li, Tianjun Chen, Yuning Liu, Yiran Cui, Yanru Peng, Jianying Shi, Yunfan Wei, Xia Ding, Xianping The polymorphism analysis and epitope predicted of Alphapapillomavirus 9 E6 in Sichuan, China |
title | The polymorphism analysis and epitope predicted of Alphapapillomavirus 9 E6 in Sichuan, China |
title_full | The polymorphism analysis and epitope predicted of Alphapapillomavirus 9 E6 in Sichuan, China |
title_fullStr | The polymorphism analysis and epitope predicted of Alphapapillomavirus 9 E6 in Sichuan, China |
title_full_unstemmed | The polymorphism analysis and epitope predicted of Alphapapillomavirus 9 E6 in Sichuan, China |
title_short | The polymorphism analysis and epitope predicted of Alphapapillomavirus 9 E6 in Sichuan, China |
title_sort | polymorphism analysis and epitope predicted of alphapapillomavirus 9 e6 in sichuan, china |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8772103/ https://www.ncbi.nlm.nih.gov/pubmed/35057815 http://dx.doi.org/10.1186/s12985-021-01728-4 |
work_keys_str_mv | AT hejiaoyu thepolymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT liqiufu thepolymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT mashiyu thepolymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT litianjun thepolymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT chenyuning thepolymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT liuyiran thepolymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT cuiyanru thepolymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT pengjianying thepolymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT shiyunfan thepolymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT weixia thepolymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT dingxianping thepolymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT hejiaoyu polymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT liqiufu polymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT mashiyu polymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT litianjun polymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT chenyuning polymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT liuyiran polymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT cuiyanru polymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT pengjianying polymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT shiyunfan polymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT weixia polymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina AT dingxianping polymorphismanalysisandepitopepredictedofalphapapillomavirus9e6insichuanchina |