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Relationship between the Cervical Microbiome, HIV Status, and Precancerous Lesions
Nearly all cervical cancers are causally associated with human papillomavirus (HPV). The burden of HPV-associated dysplasias in sub-Saharan Africa is influenced by HIV. To investigate the role of the bacterial microbiome in cervical dysplasia, cytobrush samples were collected directly from cervical...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381280/ https://www.ncbi.nlm.nih.gov/pubmed/30782659 http://dx.doi.org/10.1128/mBio.02785-18 |
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author | Klein, Cameron Gonzalez, Daniela Samwel, Kandali Kahesa, Crispin Mwaiselage, Julius Aluthge, Nirosh Fernando, Samodha West, John T. Wood, Charles Angeletti, Peter C. |
author_facet | Klein, Cameron Gonzalez, Daniela Samwel, Kandali Kahesa, Crispin Mwaiselage, Julius Aluthge, Nirosh Fernando, Samodha West, John T. Wood, Charles Angeletti, Peter C. |
author_sort | Klein, Cameron |
collection | PubMed |
description | Nearly all cervical cancers are causally associated with human papillomavirus (HPV). The burden of HPV-associated dysplasias in sub-Saharan Africa is influenced by HIV. To investigate the role of the bacterial microbiome in cervical dysplasia, cytobrush samples were collected directly from cervical lesions of 144 Tanzanian women. The V4 hypervariable region of the 16S rRNA gene was amplified and deep sequenced. Alpha diversity metrics (Chao1, PD whole tree, and operational taxonomic unit [OTU] estimates) displayed significantly higher bacterial richness in HIV-positive patients (P = 0.01) than in HIV-negative patients. In HIV-positive patients, there was higher bacterial richness in patients with high-grade squamous intraepithelial lesions (HSIL) (P = 0.13) than those without lesions. The most abundant OTUs associated with high-grade squamous intraepithelial lesions were Mycoplasmatales, Pseudomonadales, and Staphylococcus. We suggest that a chronic mycoplasma infection of the cervix may contribute to HPV-dependent dysplasia by sustained inflammatory signals. |
format | Online Article Text |
id | pubmed-6381280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-63812802019-02-22 Relationship between the Cervical Microbiome, HIV Status, and Precancerous Lesions Klein, Cameron Gonzalez, Daniela Samwel, Kandali Kahesa, Crispin Mwaiselage, Julius Aluthge, Nirosh Fernando, Samodha West, John T. Wood, Charles Angeletti, Peter C. mBio Research Article Nearly all cervical cancers are causally associated with human papillomavirus (HPV). The burden of HPV-associated dysplasias in sub-Saharan Africa is influenced by HIV. To investigate the role of the bacterial microbiome in cervical dysplasia, cytobrush samples were collected directly from cervical lesions of 144 Tanzanian women. The V4 hypervariable region of the 16S rRNA gene was amplified and deep sequenced. Alpha diversity metrics (Chao1, PD whole tree, and operational taxonomic unit [OTU] estimates) displayed significantly higher bacterial richness in HIV-positive patients (P = 0.01) than in HIV-negative patients. In HIV-positive patients, there was higher bacterial richness in patients with high-grade squamous intraepithelial lesions (HSIL) (P = 0.13) than those without lesions. The most abundant OTUs associated with high-grade squamous intraepithelial lesions were Mycoplasmatales, Pseudomonadales, and Staphylococcus. We suggest that a chronic mycoplasma infection of the cervix may contribute to HPV-dependent dysplasia by sustained inflammatory signals. American Society for Microbiology 2019-02-19 /pmc/articles/PMC6381280/ /pubmed/30782659 http://dx.doi.org/10.1128/mBio.02785-18 Text en Copyright © 2019 Klein et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Klein, Cameron Gonzalez, Daniela Samwel, Kandali Kahesa, Crispin Mwaiselage, Julius Aluthge, Nirosh Fernando, Samodha West, John T. Wood, Charles Angeletti, Peter C. Relationship between the Cervical Microbiome, HIV Status, and Precancerous Lesions |
title | Relationship between the Cervical Microbiome, HIV Status, and Precancerous Lesions |
title_full | Relationship between the Cervical Microbiome, HIV Status, and Precancerous Lesions |
title_fullStr | Relationship between the Cervical Microbiome, HIV Status, and Precancerous Lesions |
title_full_unstemmed | Relationship between the Cervical Microbiome, HIV Status, and Precancerous Lesions |
title_short | Relationship between the Cervical Microbiome, HIV Status, and Precancerous Lesions |
title_sort | relationship between the cervical microbiome, hiv status, and precancerous lesions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381280/ https://www.ncbi.nlm.nih.gov/pubmed/30782659 http://dx.doi.org/10.1128/mBio.02785-18 |
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