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Microbial Diversity of Genital Ulcers of HSV-2 Seropositive Women
We measured the microbial community structure of genital ulcers in women. Swabs from clinically detected ulcers were tested for HSV-2 and Treponema pallidum by polymerase chain reaction (PCR). HSV-2 and T. pallidum were detected by serum antibody testing. Microbial community structure was characteri...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684367/ https://www.ncbi.nlm.nih.gov/pubmed/29133803 http://dx.doi.org/10.1038/s41598-017-15554-8 |
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author | Mehta, Supriya D. Pradhan, Ashish K. Green, Stefan J. Naqib, Ankur Odoyo-June, Elijah Gaydos, Charlotte A. Barry, Sheila Landay, Alan Bailey, Robert C. |
author_facet | Mehta, Supriya D. Pradhan, Ashish K. Green, Stefan J. Naqib, Ankur Odoyo-June, Elijah Gaydos, Charlotte A. Barry, Sheila Landay, Alan Bailey, Robert C. |
author_sort | Mehta, Supriya D. |
collection | PubMed |
description | We measured the microbial community structure of genital ulcers in women. Swabs from clinically detected ulcers were tested for HSV-2 and Treponema pallidum by polymerase chain reaction (PCR). HSV-2 and T. pallidum were detected by serum antibody testing. Microbial community structure was characterized by high-throughput 16 s rRNA gene amplicon sequencing. Multiple group testing and Elastic net and Lasso regressions identified taxa associated with differences in factors of interest. Among 49 ulcer specimens from 49 HSV-2 seropositive women, by PCR HSV-2 was recovered from 28 (57%) specimens and T. pallidum from none; one woman showed serologic evidence of syphilis. Overall, 63% of women were HIV-positive and 49% had an uncircumcised male sex partner. By both multiple group testing and regression, Porphyromonas (FDR p-value = 0.02), Prevotella (FDR p-value = 0.03), Anaerococcus (FDR p-value = 0.07), and Dialister (FDR p-value = 0.09) were detected at higher relative abundance in HSV-2 PCR-positive than negative ulcers. The presence of HSV-2 in a lesion was associated with presumed bacterial agents of Bacterial vaginosis. Differences in bacterial communities may contribute to HSV-2 ulcer pathogenesis, severity, or prolonged healing. If these results are confirmed, future studies may consider the influence of BV treatment on women’s GUD and HSV-2 incidence and recurrence. |
format | Online Article Text |
id | pubmed-5684367 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56843672017-11-21 Microbial Diversity of Genital Ulcers of HSV-2 Seropositive Women Mehta, Supriya D. Pradhan, Ashish K. Green, Stefan J. Naqib, Ankur Odoyo-June, Elijah Gaydos, Charlotte A. Barry, Sheila Landay, Alan Bailey, Robert C. Sci Rep Article We measured the microbial community structure of genital ulcers in women. Swabs from clinically detected ulcers were tested for HSV-2 and Treponema pallidum by polymerase chain reaction (PCR). HSV-2 and T. pallidum were detected by serum antibody testing. Microbial community structure was characterized by high-throughput 16 s rRNA gene amplicon sequencing. Multiple group testing and Elastic net and Lasso regressions identified taxa associated with differences in factors of interest. Among 49 ulcer specimens from 49 HSV-2 seropositive women, by PCR HSV-2 was recovered from 28 (57%) specimens and T. pallidum from none; one woman showed serologic evidence of syphilis. Overall, 63% of women were HIV-positive and 49% had an uncircumcised male sex partner. By both multiple group testing and regression, Porphyromonas (FDR p-value = 0.02), Prevotella (FDR p-value = 0.03), Anaerococcus (FDR p-value = 0.07), and Dialister (FDR p-value = 0.09) were detected at higher relative abundance in HSV-2 PCR-positive than negative ulcers. The presence of HSV-2 in a lesion was associated with presumed bacterial agents of Bacterial vaginosis. Differences in bacterial communities may contribute to HSV-2 ulcer pathogenesis, severity, or prolonged healing. If these results are confirmed, future studies may consider the influence of BV treatment on women’s GUD and HSV-2 incidence and recurrence. Nature Publishing Group UK 2017-11-13 /pmc/articles/PMC5684367/ /pubmed/29133803 http://dx.doi.org/10.1038/s41598-017-15554-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Mehta, Supriya D. Pradhan, Ashish K. Green, Stefan J. Naqib, Ankur Odoyo-June, Elijah Gaydos, Charlotte A. Barry, Sheila Landay, Alan Bailey, Robert C. Microbial Diversity of Genital Ulcers of HSV-2 Seropositive Women |
title | Microbial Diversity of Genital Ulcers of HSV-2 Seropositive Women |
title_full | Microbial Diversity of Genital Ulcers of HSV-2 Seropositive Women |
title_fullStr | Microbial Diversity of Genital Ulcers of HSV-2 Seropositive Women |
title_full_unstemmed | Microbial Diversity of Genital Ulcers of HSV-2 Seropositive Women |
title_short | Microbial Diversity of Genital Ulcers of HSV-2 Seropositive Women |
title_sort | microbial diversity of genital ulcers of hsv-2 seropositive women |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684367/ https://www.ncbi.nlm.nih.gov/pubmed/29133803 http://dx.doi.org/10.1038/s41598-017-15554-8 |
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