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Association of high-risk human papillomavirus infection duration and cervical lesions with vaginal microbiota composition

BACKGROUND: Cervical cancer is reportedly caused by the synergistic effects of persistent high-risk human papillomavirus (HPV) infection. Cervical microbiota represent a unique and dynamically changing microecological system that is directly exposed to the vagina. The relationship between HPV and th...

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Autores principales: Liu, Jun, Luo, Mei, Zhang, Yang, Cao, Guangming, Wang, Shuzhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576078/
https://www.ncbi.nlm.nih.gov/pubmed/33241010
http://dx.doi.org/10.21037/atm-20-5832
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author Liu, Jun
Luo, Mei
Zhang, Yang
Cao, Guangming
Wang, Shuzhen
author_facet Liu, Jun
Luo, Mei
Zhang, Yang
Cao, Guangming
Wang, Shuzhen
author_sort Liu, Jun
collection PubMed
description BACKGROUND: Cervical cancer is reportedly caused by the synergistic effects of persistent high-risk human papillomavirus (HPV) infection. Cervical microbiota represent a unique and dynamically changing microecological system that is directly exposed to the vagina. The relationship between HPV and the composition of the cervical microbiome has long been a primary focus of research. METHODS: To determine the specific differential florae throughout the process of cervical cancer development, in the present study, 16S rRNA sequencing was combined with KEGG pathway enrichment analysis to analyse five groups of cervical scraping samples with increasing durations of HPV infection and cervical intraepithelial neoplasia pathological classification. RESULTS: The findings revealed that decreasing levels of probiotics, including Shuttleworthia, Prevotella, Lactobacillus, and Sneathia, and increasing levels of pathogenic bacteria, including Dispar, Streptococcus, and Faecalibacterium prausnitzii, could be the direct result of early HPV infection. Other pathogenic bacteria, such as Bifidobacteriaceae, might represent key factors in cancer progression. Additionally, KEGG pathway enrichment analysis indicated that HPV infection directly inhibits multiple pathways, including those of sporulation, porphyrin and chlorophyll metabolism, arginine and proline metabolism, isoquinoline alkaloid biosynthesis, and ansamycin biosynthesis, which may lead to the development of early symptoms of cervical cancer. Biomarkers were predicted based on operational taxonomic unit (OTU) abundance data, and OTU851726 and OTU715913 were undoubtedly the best potential indicators of cervical cancer. CONCLUSIONS: The findings of the present study could assist with the development of a guideline for screening new clinical drugs for cervical cancer.
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spelling pubmed-75760782020-11-24 Association of high-risk human papillomavirus infection duration and cervical lesions with vaginal microbiota composition Liu, Jun Luo, Mei Zhang, Yang Cao, Guangming Wang, Shuzhen Ann Transl Med Original Article BACKGROUND: Cervical cancer is reportedly caused by the synergistic effects of persistent high-risk human papillomavirus (HPV) infection. Cervical microbiota represent a unique and dynamically changing microecological system that is directly exposed to the vagina. The relationship between HPV and the composition of the cervical microbiome has long been a primary focus of research. METHODS: To determine the specific differential florae throughout the process of cervical cancer development, in the present study, 16S rRNA sequencing was combined with KEGG pathway enrichment analysis to analyse five groups of cervical scraping samples with increasing durations of HPV infection and cervical intraepithelial neoplasia pathological classification. RESULTS: The findings revealed that decreasing levels of probiotics, including Shuttleworthia, Prevotella, Lactobacillus, and Sneathia, and increasing levels of pathogenic bacteria, including Dispar, Streptococcus, and Faecalibacterium prausnitzii, could be the direct result of early HPV infection. Other pathogenic bacteria, such as Bifidobacteriaceae, might represent key factors in cancer progression. Additionally, KEGG pathway enrichment analysis indicated that HPV infection directly inhibits multiple pathways, including those of sporulation, porphyrin and chlorophyll metabolism, arginine and proline metabolism, isoquinoline alkaloid biosynthesis, and ansamycin biosynthesis, which may lead to the development of early symptoms of cervical cancer. Biomarkers were predicted based on operational taxonomic unit (OTU) abundance data, and OTU851726 and OTU715913 were undoubtedly the best potential indicators of cervical cancer. CONCLUSIONS: The findings of the present study could assist with the development of a guideline for screening new clinical drugs for cervical cancer. AME Publishing Company 2020-09 /pmc/articles/PMC7576078/ /pubmed/33241010 http://dx.doi.org/10.21037/atm-20-5832 Text en 2020 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Liu, Jun
Luo, Mei
Zhang, Yang
Cao, Guangming
Wang, Shuzhen
Association of high-risk human papillomavirus infection duration and cervical lesions with vaginal microbiota composition
title Association of high-risk human papillomavirus infection duration and cervical lesions with vaginal microbiota composition
title_full Association of high-risk human papillomavirus infection duration and cervical lesions with vaginal microbiota composition
title_fullStr Association of high-risk human papillomavirus infection duration and cervical lesions with vaginal microbiota composition
title_full_unstemmed Association of high-risk human papillomavirus infection duration and cervical lesions with vaginal microbiota composition
title_short Association of high-risk human papillomavirus infection duration and cervical lesions with vaginal microbiota composition
title_sort association of high-risk human papillomavirus infection duration and cervical lesions with vaginal microbiota composition
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576078/
https://www.ncbi.nlm.nih.gov/pubmed/33241010
http://dx.doi.org/10.21037/atm-20-5832
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