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The fallopian tube microbiome: implications for reproductive health

OBJECTIVE: There is a paucity of data characterizing the microbiota of the female upper genital tract, which controversially is described as a sterile site. We examine whether the fallopian tube harbours an endogenous microbial community. DESIGN: This prospective study collected from women undergoin...

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Autores principales: Pelzer, Elise S., Willner, Dana, Buttini, Melissa, Hafner, Louise M., Theodoropoulos, Christina, Huygens, Flavia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5940370/
https://www.ncbi.nlm.nih.gov/pubmed/29765558
http://dx.doi.org/10.18632/oncotarget.25059
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author Pelzer, Elise S.
Willner, Dana
Buttini, Melissa
Hafner, Louise M.
Theodoropoulos, Christina
Huygens, Flavia
author_facet Pelzer, Elise S.
Willner, Dana
Buttini, Melissa
Hafner, Louise M.
Theodoropoulos, Christina
Huygens, Flavia
author_sort Pelzer, Elise S.
collection PubMed
description OBJECTIVE: There is a paucity of data characterizing the microbiota of the female upper genital tract, which controversially is described as a sterile site. We examine whether the fallopian tube harbours an endogenous microbial community. DESIGN: This prospective study collected from women undergoing total hysterectomy or salpingectomy-oophorectomy. SETTING: Private hospital gynaecology department. PATIENTS: Fallopian tubes were collected from women diagnosed with benign disease or for prophylaxis. INTERVENTIONS: Samples were interrogated for the presence of microbial DNA using a next generation sequencing technology approach to exploit the V5 to V9 regions of the 16S rRNA gene. MAIN OUTCOME MEASURES: The fallopian tube microbiota was characterized using traditional culture techniques and next generation sequencing. RESULTS: Bacteria were isolated from 50% of cultured samples, and 100% of samples returned positive PCR results. Only 68% of the culture isolates could be confidently identified using automated diagnostic equipment in a clinical microbiology laboratory. Monomicrobial communities were identified only for cultured isolates (50%). Pyrosequencing revealed that all communities were polymicrobial. Lactobacillus spp. were not present in all groups, nor were they the most dominant isolates. Distinct differences in the microbial communities were evident for left compared to right fallopian tubes, ampulla versus isthmus, pre- and post- menopausal tissue, and in secretory phase fallopian tubes with and without Mirena intrauterine devices in situ (all p < 0.05). CONCLUSION: The female upper genital tract is not sterile. Distinct microbial community profiles in the fallopian tubes of healthy women suggest that this genital tract site supports an endogenous microbiota.
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spelling pubmed-59403702018-05-15 The fallopian tube microbiome: implications for reproductive health Pelzer, Elise S. Willner, Dana Buttini, Melissa Hafner, Louise M. Theodoropoulos, Christina Huygens, Flavia Oncotarget Clinical Research Paper OBJECTIVE: There is a paucity of data characterizing the microbiota of the female upper genital tract, which controversially is described as a sterile site. We examine whether the fallopian tube harbours an endogenous microbial community. DESIGN: This prospective study collected from women undergoing total hysterectomy or salpingectomy-oophorectomy. SETTING: Private hospital gynaecology department. PATIENTS: Fallopian tubes were collected from women diagnosed with benign disease or for prophylaxis. INTERVENTIONS: Samples were interrogated for the presence of microbial DNA using a next generation sequencing technology approach to exploit the V5 to V9 regions of the 16S rRNA gene. MAIN OUTCOME MEASURES: The fallopian tube microbiota was characterized using traditional culture techniques and next generation sequencing. RESULTS: Bacteria were isolated from 50% of cultured samples, and 100% of samples returned positive PCR results. Only 68% of the culture isolates could be confidently identified using automated diagnostic equipment in a clinical microbiology laboratory. Monomicrobial communities were identified only for cultured isolates (50%). Pyrosequencing revealed that all communities were polymicrobial. Lactobacillus spp. were not present in all groups, nor were they the most dominant isolates. Distinct differences in the microbial communities were evident for left compared to right fallopian tubes, ampulla versus isthmus, pre- and post- menopausal tissue, and in secretory phase fallopian tubes with and without Mirena intrauterine devices in situ (all p < 0.05). CONCLUSION: The female upper genital tract is not sterile. Distinct microbial community profiles in the fallopian tubes of healthy women suggest that this genital tract site supports an endogenous microbiota. Impact Journals LLC 2018-04-20 /pmc/articles/PMC5940370/ /pubmed/29765558 http://dx.doi.org/10.18632/oncotarget.25059 Text en Copyright: © 2018 Pelzer et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Clinical Research Paper
Pelzer, Elise S.
Willner, Dana
Buttini, Melissa
Hafner, Louise M.
Theodoropoulos, Christina
Huygens, Flavia
The fallopian tube microbiome: implications for reproductive health
title The fallopian tube microbiome: implications for reproductive health
title_full The fallopian tube microbiome: implications for reproductive health
title_fullStr The fallopian tube microbiome: implications for reproductive health
title_full_unstemmed The fallopian tube microbiome: implications for reproductive health
title_short The fallopian tube microbiome: implications for reproductive health
title_sort fallopian tube microbiome: implications for reproductive health
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5940370/
https://www.ncbi.nlm.nih.gov/pubmed/29765558
http://dx.doi.org/10.18632/oncotarget.25059
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