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Altered vaginal eukaryotic virome is associated with different cervical disease status

Viruses are important components of the human body. Growing evidence suggests that they are engaged in the physiology and disease status of the host. Even though the vaginal microbiome is involved in human papillomavirus (HPV) infection and cervical cancer (CC) progression, little is known about the...

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Autores principales: Li, Yanpeng, Cao, Le, Han, Xiao, Ma, Yingying, Liu, Yanmei, Gao, Shujun, Zhang, Chiyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wuhan Institute of Virology, Chinese Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176265/
https://www.ncbi.nlm.nih.gov/pubmed/36565811
http://dx.doi.org/10.1016/j.virs.2022.12.004
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author Li, Yanpeng
Cao, Le
Han, Xiao
Ma, Yingying
Liu, Yanmei
Gao, Shujun
Zhang, Chiyu
author_facet Li, Yanpeng
Cao, Le
Han, Xiao
Ma, Yingying
Liu, Yanmei
Gao, Shujun
Zhang, Chiyu
author_sort Li, Yanpeng
collection PubMed
description Viruses are important components of the human body. Growing evidence suggests that they are engaged in the physiology and disease status of the host. Even though the vaginal microbiome is involved in human papillomavirus (HPV) infection and cervical cancer (CC) progression, little is known about the role of the vaginal virome. In this pilot exploratory study, using unbiased viral metagenomics, we aim to investigate the vaginal eukaryotic virome in women with different levels of cervical lesions, and examine their associations with different cervical disease status. An altered eukaryotic virome was observed in women with different levels of lesions and Lactobacillus profiles. Anelloviruses and papillomaviruses are the most commonly detected eukaryotic viruses of the vaginal virome. Higher abundance and richness of anelloviruses and papillomaviruses were associated with low-grade squamous intraepithelial lesion (LSIL) and CC. Besides, higher anellovirus abundance was also associated with lactobacillus-depleted microbiome profiles and bacterial community state (CST) type IV. Furthermore, increased correlations between Anelloviridae and Papillomaviridae occurred in the women with increased cervical disease severity level from LSIL to CC. These data suggest underlying interactions between different microbes as well as the host physiology. Higher abundance and diversity of both anelloviruses and papillomaviruses shared by LSIL and CC suggest that anellovirus may be used as a potential adjunct biomarker to predict the risk of HPV persistent infection and/or CC. Future studies need to focus on the clinical relevance of anellovirus abundance with cervical disease status, and the evaluation of their potential as a new adjunct biomarker for the prediction and prognoses of CC.
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spelling pubmed-101762652023-05-13 Altered vaginal eukaryotic virome is associated with different cervical disease status Li, Yanpeng Cao, Le Han, Xiao Ma, Yingying Liu, Yanmei Gao, Shujun Zhang, Chiyu Virol Sin Research Article Viruses are important components of the human body. Growing evidence suggests that they are engaged in the physiology and disease status of the host. Even though the vaginal microbiome is involved in human papillomavirus (HPV) infection and cervical cancer (CC) progression, little is known about the role of the vaginal virome. In this pilot exploratory study, using unbiased viral metagenomics, we aim to investigate the vaginal eukaryotic virome in women with different levels of cervical lesions, and examine their associations with different cervical disease status. An altered eukaryotic virome was observed in women with different levels of lesions and Lactobacillus profiles. Anelloviruses and papillomaviruses are the most commonly detected eukaryotic viruses of the vaginal virome. Higher abundance and richness of anelloviruses and papillomaviruses were associated with low-grade squamous intraepithelial lesion (LSIL) and CC. Besides, higher anellovirus abundance was also associated with lactobacillus-depleted microbiome profiles and bacterial community state (CST) type IV. Furthermore, increased correlations between Anelloviridae and Papillomaviridae occurred in the women with increased cervical disease severity level from LSIL to CC. These data suggest underlying interactions between different microbes as well as the host physiology. Higher abundance and diversity of both anelloviruses and papillomaviruses shared by LSIL and CC suggest that anellovirus may be used as a potential adjunct biomarker to predict the risk of HPV persistent infection and/or CC. Future studies need to focus on the clinical relevance of anellovirus abundance with cervical disease status, and the evaluation of their potential as a new adjunct biomarker for the prediction and prognoses of CC. Wuhan Institute of Virology, Chinese Academy of Sciences 2022-12-21 /pmc/articles/PMC10176265/ /pubmed/36565811 http://dx.doi.org/10.1016/j.virs.2022.12.004 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Li, Yanpeng
Cao, Le
Han, Xiao
Ma, Yingying
Liu, Yanmei
Gao, Shujun
Zhang, Chiyu
Altered vaginal eukaryotic virome is associated with different cervical disease status
title Altered vaginal eukaryotic virome is associated with different cervical disease status
title_full Altered vaginal eukaryotic virome is associated with different cervical disease status
title_fullStr Altered vaginal eukaryotic virome is associated with different cervical disease status
title_full_unstemmed Altered vaginal eukaryotic virome is associated with different cervical disease status
title_short Altered vaginal eukaryotic virome is associated with different cervical disease status
title_sort altered vaginal eukaryotic virome is associated with different cervical disease status
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176265/
https://www.ncbi.nlm.nih.gov/pubmed/36565811
http://dx.doi.org/10.1016/j.virs.2022.12.004
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