Cervicovaginal DNA Virome Alterations Are Associated with Genital Inflammation and Microbiota Composition
Author
Kaelin, E.A.Skidmore, P.T.
Łaniewski, P.
Holland, L.A.
Chase, D.M.
Herbst-Kralovetz, M.M.
Lim, E.S.
Affiliation
Department of Basic Medical Sciences, College of Medicine-Phoenix, University of ArizonaDepartment of Obstetrics and Gynecology, College of Medicine-Phoenix, University of Arizona
UA Cancer Center, University of Arizona
Issue Date
2022Keywords
anelloviruscervical cancer
cervicovaginal virome
genital inflammation
HPV
human papillomavirus
Lactobacillus species
transkingdom interactions
vaginal microbiome
Metadata
Show full item recordPublisher
American Society for MicrobiologyCitation
Kaelin, E. A., Skidmore, P. T., Łaniewski, P., Holland, L. A., Chase, D. M., Herbst-Kralovetz, M. M., & Lim, E. S. (2022). Cervicovaginal DNA Virome Alterations Are Associated with Genital Inflammation and Microbiota Composition. MSystems, 7(2).Journal
mSystemsRights
Copyright © 2022 Kaelin et al. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International license.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
While the link between the cervicovaginal bacterial microbiome, human papillomavirus (HPV) infection, and cervical cancer is recognized (P. £aniewski, D. Barnes, A. Goulder, H. Cui, et al., Sci. Rep. 8:7593, 2018, http://dx.doi.org/10.1038/s41598-018-25879-7; A. Mitra, D. A. MacIntyre, Y. S. Lee, A. Smith, et al., Sci. Rep. 5:16865, 2015, http://dx.doi.org/ 10.1038/srep16865; A. Mitra, D. A. MacIntyre, J. R. Marchesi, Y. S. Lee, et al., Microbiome 4: 58, 2016, http://dx.doi.org/10.1186/s40168-016-0203-0; J. Norenhag, J. Du, M. Olovsson, H. Verstraelen, et al., BJOG, 127:171-180, 2020, http://dx.doi.org/10.1111/1471-0528.15854; E. O. Dareng, B. Ma, A. O. Famooto, S. N. Adebamowo, et al., Epidemiol. Infect. 144:123-137, 2016, http://dx.doi.org/10.1017/S0950268815000965; A. Audirac-Chalifour, K. Torres-Poveda, M. Bahena-Roman, J. Tellez-Sosa et al., PLoS One 11:e0153274, 2016, http://dx.doi.org/10.1371/journal.pone.0153274; M. Di Paola, C. Sani, A. M. Clemente, A. Iossa, et al., Sci. Rep. 7: 10200, 2017, http://dx.doi.org/10.1038/s41598-017-09842-6), the role of the cervicovaginal virome remains poorly understood. In this pilot study, we conducted metagenomic nextgeneration sequencing of cervicovaginal lavage specimens to investigate the relationship between the cervicovaginal DNA virome, bacterial microbiome, genital inflammation, and HPV infection. Specific virome alterations were associated with features of the local microenvironment related to HPV persistence and progression to cervical cancer. Cervicovaginal viromes clustered distinctly by genital inflammation state. Genital inflammation was associated with decreased virome richness and alpha diversity and an increased abundance of Anelloviridae species from the genus Alphatorquevirus. Lactobacillus bacteriophages were closely associated with increased Lactobacillus abundance, consistent with phage-host relationships. Interestingly, bacteria-bacteriophage transkingdom interactions were linked to genital inflammation and showed specific interactions with bacterial vaginosis-associated bacteria, including Gardnerella, Prevotella, and Sneathia. Taken together, our results reveal prominent virome interactions with features of the cervicovaginal microenvironment that are associated with HPV and cervical cancer. These findings expand our understanding of the cervicovaginal host-microbiome interactions in women's health. Copyright © 2022 Kaelin et al. This is an openaccess article distributed under the terms of the Creative Commons Attribution 4.0 International license.Note
Open access journalISSN
2379-5077Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1128/msystems.00064-22
Scopus Count
Collections
Except where otherwise noted, this item's license is described as Copyright © 2022 Kaelin et al. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

