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Urine metabolome in women with Chlamydia trachomatis infection
The aim of this study was to characterize the urine metabolome of women with Chlamydia trachomatis (CT) uro-genital infection (n = 21), comparing it with a group of CT-negative subjects (n = 98). By means of a proton-based nuclear magnetic resonance ((1)H-NMR) spectroscopy, we detected and quantifie...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864028/ https://www.ncbi.nlm.nih.gov/pubmed/29566085 http://dx.doi.org/10.1371/journal.pone.0194827 |
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author | Foschi, Claudio Laghi, Luca D’Antuono, Antonietta Gaspari, Valeria Zhu, Chenglin Dellarosa, Nicolò Salvo, Melissa Marangoni, Antonella |
author_facet | Foschi, Claudio Laghi, Luca D’Antuono, Antonietta Gaspari, Valeria Zhu, Chenglin Dellarosa, Nicolò Salvo, Melissa Marangoni, Antonella |
author_sort | Foschi, Claudio |
collection | PubMed |
description | The aim of this study was to characterize the urine metabolome of women with Chlamydia trachomatis (CT) uro-genital infection (n = 21), comparing it with a group of CT-negative subjects (n = 98). By means of a proton-based nuclear magnetic resonance ((1)H-NMR) spectroscopy, we detected and quantified the urine metabolites of a cohort of 119 pre-menopausal Caucasian women, attending a STI Outpatients Clinic in Italy. In case of a CT positive result, CT molecular genotyping was performed by omp1 gene semi-nested PCR followed by RFLP analysis. We were able to identify several metabolites whose concentrations were significantly higher in the urine samples of CT-positive subjects, including sucrose, mannitol, pyruvate and lactate. In contrast, higher urinary levels of acetone represented the main feature of CT-negative women. These results were not influenced by the age of patients nor by the CT serovars (D, E, F, G, K) responsible of the urethral infections. Since the presence of sugars can increase the stability of chlamydial proteins, higher levels of sucrose and mannitol in the urethral lumen, related to a higher sugar consumption, could have favoured CT infection acquisition or could have been of aid for the bacterial viability. Peculiar dietary habits of the subjects enrolled, in term of type and amount of food consumed, could probably explain these findings. Lactate and pyruvate could result from CT-induced immunopathology, as a product of the inflammatory microenvironment. Further studies are needed to understand the potential role of these metabolites in the pathogenesis of CT infection, as well as their diagnostic/prognostic use. |
format | Online Article Text |
id | pubmed-5864028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58640282018-03-28 Urine metabolome in women with Chlamydia trachomatis infection Foschi, Claudio Laghi, Luca D’Antuono, Antonietta Gaspari, Valeria Zhu, Chenglin Dellarosa, Nicolò Salvo, Melissa Marangoni, Antonella PLoS One Research Article The aim of this study was to characterize the urine metabolome of women with Chlamydia trachomatis (CT) uro-genital infection (n = 21), comparing it with a group of CT-negative subjects (n = 98). By means of a proton-based nuclear magnetic resonance ((1)H-NMR) spectroscopy, we detected and quantified the urine metabolites of a cohort of 119 pre-menopausal Caucasian women, attending a STI Outpatients Clinic in Italy. In case of a CT positive result, CT molecular genotyping was performed by omp1 gene semi-nested PCR followed by RFLP analysis. We were able to identify several metabolites whose concentrations were significantly higher in the urine samples of CT-positive subjects, including sucrose, mannitol, pyruvate and lactate. In contrast, higher urinary levels of acetone represented the main feature of CT-negative women. These results were not influenced by the age of patients nor by the CT serovars (D, E, F, G, K) responsible of the urethral infections. Since the presence of sugars can increase the stability of chlamydial proteins, higher levels of sucrose and mannitol in the urethral lumen, related to a higher sugar consumption, could have favoured CT infection acquisition or could have been of aid for the bacterial viability. Peculiar dietary habits of the subjects enrolled, in term of type and amount of food consumed, could probably explain these findings. Lactate and pyruvate could result from CT-induced immunopathology, as a product of the inflammatory microenvironment. Further studies are needed to understand the potential role of these metabolites in the pathogenesis of CT infection, as well as their diagnostic/prognostic use. Public Library of Science 2018-03-22 /pmc/articles/PMC5864028/ /pubmed/29566085 http://dx.doi.org/10.1371/journal.pone.0194827 Text en © 2018 Foschi et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://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 Foschi, Claudio Laghi, Luca D’Antuono, Antonietta Gaspari, Valeria Zhu, Chenglin Dellarosa, Nicolò Salvo, Melissa Marangoni, Antonella Urine metabolome in women with Chlamydia trachomatis infection |
title | Urine metabolome in women with Chlamydia trachomatis infection |
title_full | Urine metabolome in women with Chlamydia trachomatis infection |
title_fullStr | Urine metabolome in women with Chlamydia trachomatis infection |
title_full_unstemmed | Urine metabolome in women with Chlamydia trachomatis infection |
title_short | Urine metabolome in women with Chlamydia trachomatis infection |
title_sort | urine metabolome in women with chlamydia trachomatis infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864028/ https://www.ncbi.nlm.nih.gov/pubmed/29566085 http://dx.doi.org/10.1371/journal.pone.0194827 |
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