Cargando…
Cervical carcinogenesis risk association of HPV33 E6 and E7 genetic variations in Taizhou, Southeast China
BACKGROUND: Human papillomavirus (HPV) 33 belongs to the Alphapapillomavirus 9 (α-9 HPV) species group, which also contains types 16, 31, 35, 52, 58 and 67. The purpose of this study was to investigate the genetic variations of HPV33 and to explore its carcinogenicity among women in Taizhou, Southea...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354908/ https://www.ncbi.nlm.nih.gov/pubmed/37468974 http://dx.doi.org/10.1186/s12985-023-02125-9 |
_version_ | 1785075022956593152 |
---|---|
author | Yan, Zi-Yi Di, Xing-Hong Qiu, Yi Ying, Yuan-Yuan Gan, Jun Xu, Hui-Hui |
author_facet | Yan, Zi-Yi Di, Xing-Hong Qiu, Yi Ying, Yuan-Yuan Gan, Jun Xu, Hui-Hui |
author_sort | Yan, Zi-Yi |
collection | PubMed |
description | BACKGROUND: Human papillomavirus (HPV) 33 belongs to the Alphapapillomavirus 9 (α-9 HPV) species group, which also contains types 16, 31, 35, 52, 58 and 67. The purpose of this study was to investigate the genetic variations of HPV33 and to explore its carcinogenicity among women in Taizhou, Southeast China. METHODS: Exfoliated cervical cells were collected for HPV genotyping. Only single HPV33 infection cases were selected, and their E6 and E7 genes were sequenced using the ABI 3730xl sequencer and then analysed using MEGA X. RESULTS: From 2014 to 2020, a total of 185 single HPV33-positive specimens were successfully amplified. We obtained 15 distinct HPV33 E6/E7 variants, which were published in GenBank under accession numbers OQ672665-OQ672679. Phylogenetic analysis revealed that all HPV33 E6/E7 variants belonged to lineage A, of which 75.7% belonged to lineage A1. Compared with CIN1, the proportion of sublineage A1 in CIN2/3 was higher, but there was no significant difference (76.5% vs. 80.6%, P > 0.05). Altogether, 20 single nucleotide substitutions were identified, of which 6 were novel substitutions, including T196G (C30G), A447T, G458T (R117L), G531A, A704A, and C740T. In addition, no significant trends were observed between the nucleotide substitutions of HPV33 E6/E7 variants and the risk of cervical lesions. CONCLUSION: This study provides the most comprehensive data on genetic variations, phylogenetics and carcinogenicity of HPV33 E6/E7 variants in Southeast China to date. The data confirmed that cervical lesions among women in Taizhou are attributable to HPV33, which may be due to the high infection rate of sublineage A1 in the population. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12985-023-02125-9. |
format | Online Article Text |
id | pubmed-10354908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103549082023-07-20 Cervical carcinogenesis risk association of HPV33 E6 and E7 genetic variations in Taizhou, Southeast China Yan, Zi-Yi Di, Xing-Hong Qiu, Yi Ying, Yuan-Yuan Gan, Jun Xu, Hui-Hui Virol J Research BACKGROUND: Human papillomavirus (HPV) 33 belongs to the Alphapapillomavirus 9 (α-9 HPV) species group, which also contains types 16, 31, 35, 52, 58 and 67. The purpose of this study was to investigate the genetic variations of HPV33 and to explore its carcinogenicity among women in Taizhou, Southeast China. METHODS: Exfoliated cervical cells were collected for HPV genotyping. Only single HPV33 infection cases were selected, and their E6 and E7 genes were sequenced using the ABI 3730xl sequencer and then analysed using MEGA X. RESULTS: From 2014 to 2020, a total of 185 single HPV33-positive specimens were successfully amplified. We obtained 15 distinct HPV33 E6/E7 variants, which were published in GenBank under accession numbers OQ672665-OQ672679. Phylogenetic analysis revealed that all HPV33 E6/E7 variants belonged to lineage A, of which 75.7% belonged to lineage A1. Compared with CIN1, the proportion of sublineage A1 in CIN2/3 was higher, but there was no significant difference (76.5% vs. 80.6%, P > 0.05). Altogether, 20 single nucleotide substitutions were identified, of which 6 were novel substitutions, including T196G (C30G), A447T, G458T (R117L), G531A, A704A, and C740T. In addition, no significant trends were observed between the nucleotide substitutions of HPV33 E6/E7 variants and the risk of cervical lesions. CONCLUSION: This study provides the most comprehensive data on genetic variations, phylogenetics and carcinogenicity of HPV33 E6/E7 variants in Southeast China to date. The data confirmed that cervical lesions among women in Taizhou are attributable to HPV33, which may be due to the high infection rate of sublineage A1 in the population. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12985-023-02125-9. BioMed Central 2023-07-19 /pmc/articles/PMC10354908/ /pubmed/37468974 http://dx.doi.org/10.1186/s12985-023-02125-9 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 Yan, Zi-Yi Di, Xing-Hong Qiu, Yi Ying, Yuan-Yuan Gan, Jun Xu, Hui-Hui Cervical carcinogenesis risk association of HPV33 E6 and E7 genetic variations in Taizhou, Southeast China |
title | Cervical carcinogenesis risk association of HPV33 E6 and E7 genetic variations in Taizhou, Southeast China |
title_full | Cervical carcinogenesis risk association of HPV33 E6 and E7 genetic variations in Taizhou, Southeast China |
title_fullStr | Cervical carcinogenesis risk association of HPV33 E6 and E7 genetic variations in Taizhou, Southeast China |
title_full_unstemmed | Cervical carcinogenesis risk association of HPV33 E6 and E7 genetic variations in Taizhou, Southeast China |
title_short | Cervical carcinogenesis risk association of HPV33 E6 and E7 genetic variations in Taizhou, Southeast China |
title_sort | cervical carcinogenesis risk association of hpv33 e6 and e7 genetic variations in taizhou, southeast china |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354908/ https://www.ncbi.nlm.nih.gov/pubmed/37468974 http://dx.doi.org/10.1186/s12985-023-02125-9 |
work_keys_str_mv | AT yanziyi cervicalcarcinogenesisriskassociationofhpv33e6ande7geneticvariationsintaizhousoutheastchina AT dixinghong cervicalcarcinogenesisriskassociationofhpv33e6ande7geneticvariationsintaizhousoutheastchina AT qiuyi cervicalcarcinogenesisriskassociationofhpv33e6ande7geneticvariationsintaizhousoutheastchina AT yingyuanyuan cervicalcarcinogenesisriskassociationofhpv33e6ande7geneticvariationsintaizhousoutheastchina AT ganjun cervicalcarcinogenesisriskassociationofhpv33e6ande7geneticvariationsintaizhousoutheastchina AT xuhuihui cervicalcarcinogenesisriskassociationofhpv33e6ande7geneticvariationsintaizhousoutheastchina |