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Evaluation of DNA extraction protocols from liquid-based cytology specimens for studying cervical microbiota

Cervical microbiota (CM) are considered an important factor affecting the progression of cervical intraepithelial neoplasia (CIN) and are implicated in the persistence of human papillomavirus (HPV). Collection of liquid-based cytology (LBC) samples is routine for cervical cancer screening and HPV ge...

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Autores principales: Shibata, Takeo, Nakagawa, Mayumi, Coleman, Hannah N., Owens, Sarah M., Greenfield, William W., Sasagawa, Toshiyuki, Robeson, Michael S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404996/
https://www.ncbi.nlm.nih.gov/pubmed/34460815
http://dx.doi.org/10.1371/journal.pone.0237556
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author Shibata, Takeo
Nakagawa, Mayumi
Coleman, Hannah N.
Owens, Sarah M.
Greenfield, William W.
Sasagawa, Toshiyuki
Robeson, Michael S.
author_facet Shibata, Takeo
Nakagawa, Mayumi
Coleman, Hannah N.
Owens, Sarah M.
Greenfield, William W.
Sasagawa, Toshiyuki
Robeson, Michael S.
author_sort Shibata, Takeo
collection PubMed
description Cervical microbiota (CM) are considered an important factor affecting the progression of cervical intraepithelial neoplasia (CIN) and are implicated in the persistence of human papillomavirus (HPV). Collection of liquid-based cytology (LBC) samples is routine for cervical cancer screening and HPV genotyping and can be used for long-term cytological biobanking. We sought to determine whether it is possible to access microbial DNA from LBC specimens, and compared the performance of four different extraction protocols: (ZymoBIOMICS DNA Miniprep Kit; QIAamp PowerFecal Pro DNA Kit; QIAamp DNA Mini Kit; and IndiSpin Pathogen Kit) and their ability to capture the diversity of CM from LBC specimens. LBC specimens from 20 patients (stored for 716 ± 105 days) with CIN values of 2 or 3 were each aliquoted for each of the four kits. Loss of microbial diversity due to long-term LBC storage could not be assessed due to lack of fresh LBC samples. Comparisons with other types of cervical sampling were not performed. We observed that all DNA extraction kits provided equivalent accessibility to the cervical microbial DNA within stored LBC samples. Approximately 80% microbial genera were shared among all DNA extraction protocols. Potential kit contaminants were observed as well. Variation between individuals was a significantly greater influence on the observed microbial composition than was the method of DNA extraction. We also observed that HPV16 was significantly associated with community types that were not dominated by Lactobacillus iners.
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spelling pubmed-84049962021-08-31 Evaluation of DNA extraction protocols from liquid-based cytology specimens for studying cervical microbiota Shibata, Takeo Nakagawa, Mayumi Coleman, Hannah N. Owens, Sarah M. Greenfield, William W. Sasagawa, Toshiyuki Robeson, Michael S. PLoS One Research Article Cervical microbiota (CM) are considered an important factor affecting the progression of cervical intraepithelial neoplasia (CIN) and are implicated in the persistence of human papillomavirus (HPV). Collection of liquid-based cytology (LBC) samples is routine for cervical cancer screening and HPV genotyping and can be used for long-term cytological biobanking. We sought to determine whether it is possible to access microbial DNA from LBC specimens, and compared the performance of four different extraction protocols: (ZymoBIOMICS DNA Miniprep Kit; QIAamp PowerFecal Pro DNA Kit; QIAamp DNA Mini Kit; and IndiSpin Pathogen Kit) and their ability to capture the diversity of CM from LBC specimens. LBC specimens from 20 patients (stored for 716 ± 105 days) with CIN values of 2 or 3 were each aliquoted for each of the four kits. Loss of microbial diversity due to long-term LBC storage could not be assessed due to lack of fresh LBC samples. Comparisons with other types of cervical sampling were not performed. We observed that all DNA extraction kits provided equivalent accessibility to the cervical microbial DNA within stored LBC samples. Approximately 80% microbial genera were shared among all DNA extraction protocols. Potential kit contaminants were observed as well. Variation between individuals was a significantly greater influence on the observed microbial composition than was the method of DNA extraction. We also observed that HPV16 was significantly associated with community types that were not dominated by Lactobacillus iners. Public Library of Science 2021-08-30 /pmc/articles/PMC8404996/ /pubmed/34460815 http://dx.doi.org/10.1371/journal.pone.0237556 Text en © 2021 Shibata et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Shibata, Takeo
Nakagawa, Mayumi
Coleman, Hannah N.
Owens, Sarah M.
Greenfield, William W.
Sasagawa, Toshiyuki
Robeson, Michael S.
Evaluation of DNA extraction protocols from liquid-based cytology specimens for studying cervical microbiota
title Evaluation of DNA extraction protocols from liquid-based cytology specimens for studying cervical microbiota
title_full Evaluation of DNA extraction protocols from liquid-based cytology specimens for studying cervical microbiota
title_fullStr Evaluation of DNA extraction protocols from liquid-based cytology specimens for studying cervical microbiota
title_full_unstemmed Evaluation of DNA extraction protocols from liquid-based cytology specimens for studying cervical microbiota
title_short Evaluation of DNA extraction protocols from liquid-based cytology specimens for studying cervical microbiota
title_sort evaluation of dna extraction protocols from liquid-based cytology specimens for studying cervical microbiota
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404996/
https://www.ncbi.nlm.nih.gov/pubmed/34460815
http://dx.doi.org/10.1371/journal.pone.0237556
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