Comparison of the amniotic fluid and fetal urine peptidome for biomarker discovery in renal developmental disease
Abstract Production of amniotic fluid (AF) is view as predominately driven by excretion of fetal urine (FU). However, the origin of AF peptides, often considered as potential biomarkers of developmental diseases, has never been investigated. Here, we evaluated the FU origin of AF peptides and if the...
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2020-12-01
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doaj-428622a5f2e3402e83de58ba284e7d132020-12-13T12:31:17ZengNature Publishing GroupScientific Reports2045-23222020-12-011011910.1038/s41598-020-78730-3Comparison of the amniotic fluid and fetal urine peptidome for biomarker discovery in renal developmental diseaseCamille Fédou0Benjamin Breuil1Igor Golovko2Stéphane Decramer3Pedro Magalhães4Françoise Muller5Sophie Dreux6Petra Zürbig7Julie Klein8Joost P. Schanstra9Bénédicte Buffin-Meyer10Institut National de La Santé Et de La Recherche Médicale (INSERM), U1048/I2MC-Equipe 12, Institut of Cardiovascular and Metabolic DiseaseInstitut National de La Santé Et de La Recherche Médicale (INSERM), U1048/I2MC-Equipe 12, Institut of Cardiovascular and Metabolic DiseaseMosaiques Diagnostics GmbHInstitut National de La Santé Et de La Recherche Médicale (INSERM), U1048/I2MC-Equipe 12, Institut of Cardiovascular and Metabolic DiseaseMosaiques Diagnostics GmbHUnité de Biochimie Fœto-Placentaire, Laboratoire de Biochimie - Hormonologie CHU Robert Debré, AP-HPUnité de Biochimie Fœto-Placentaire, Laboratoire de Biochimie - Hormonologie CHU Robert Debré, AP-HPMosaiques Diagnostics GmbHInstitut National de La Santé Et de La Recherche Médicale (INSERM), U1048/I2MC-Equipe 12, Institut of Cardiovascular and Metabolic DiseaseInstitut National de La Santé Et de La Recherche Médicale (INSERM), U1048/I2MC-Equipe 12, Institut of Cardiovascular and Metabolic DiseaseInstitut National de La Santé Et de La Recherche Médicale (INSERM), U1048/I2MC-Equipe 12, Institut of Cardiovascular and Metabolic DiseaseAbstract Production of amniotic fluid (AF) is view as predominately driven by excretion of fetal urine (FU). However, the origin of AF peptides, often considered as potential biomarkers of developmental diseases, has never been investigated. Here, we evaluated the FU origin of AF peptides and if the AF peptide content can be used as a surrogate of FU. The abundance of endogenous peptides was analyzed by capillary electrophoresis coupled to mass spectrometry in 216 AF and 64 FU samples. A total of 2668 and 3257 peptides was found in AF and FU respectively. The AF peptidome largely overlapped with the FU peptidome, ranging from 54% in the second pregnancy trimester to 65% in the third trimester. Examination of a subset of 16 paired AF and FU samples revealed that 67 peptides displayed a significant positively correlated abundance in AF and FU, strongly suggesting that their presence in AF was directly associated to FU excretion. As proof-of-concept we showed that measuring the AF abundance of these 67 peptides of FU origin allowed prediction of postnatal renal survival in fetuses with posterior urethral valves. These results demonstrate that the AF peptidome can be considered as a good surrogate of the FU peptidome.https://doi.org/10.1038/s41598-020-78730-3 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Camille Fédou Benjamin Breuil Igor Golovko Stéphane Decramer Pedro Magalhães Françoise Muller Sophie Dreux Petra Zürbig Julie Klein Joost P. Schanstra Bénédicte Buffin-Meyer |
spellingShingle |
Camille Fédou Benjamin Breuil Igor Golovko Stéphane Decramer Pedro Magalhães Françoise Muller Sophie Dreux Petra Zürbig Julie Klein Joost P. Schanstra Bénédicte Buffin-Meyer Comparison of the amniotic fluid and fetal urine peptidome for biomarker discovery in renal developmental disease Scientific Reports |
author_facet |
Camille Fédou Benjamin Breuil Igor Golovko Stéphane Decramer Pedro Magalhães Françoise Muller Sophie Dreux Petra Zürbig Julie Klein Joost P. Schanstra Bénédicte Buffin-Meyer |
author_sort |
Camille Fédou |
title |
Comparison of the amniotic fluid and fetal urine peptidome for biomarker discovery in renal developmental disease |
title_short |
Comparison of the amniotic fluid and fetal urine peptidome for biomarker discovery in renal developmental disease |
title_full |
Comparison of the amniotic fluid and fetal urine peptidome for biomarker discovery in renal developmental disease |
title_fullStr |
Comparison of the amniotic fluid and fetal urine peptidome for biomarker discovery in renal developmental disease |
title_full_unstemmed |
Comparison of the amniotic fluid and fetal urine peptidome for biomarker discovery in renal developmental disease |
title_sort |
comparison of the amniotic fluid and fetal urine peptidome for biomarker discovery in renal developmental disease |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2020-12-01 |
description |
Abstract Production of amniotic fluid (AF) is view as predominately driven by excretion of fetal urine (FU). However, the origin of AF peptides, often considered as potential biomarkers of developmental diseases, has never been investigated. Here, we evaluated the FU origin of AF peptides and if the AF peptide content can be used as a surrogate of FU. The abundance of endogenous peptides was analyzed by capillary electrophoresis coupled to mass spectrometry in 216 AF and 64 FU samples. A total of 2668 and 3257 peptides was found in AF and FU respectively. The AF peptidome largely overlapped with the FU peptidome, ranging from 54% in the second pregnancy trimester to 65% in the third trimester. Examination of a subset of 16 paired AF and FU samples revealed that 67 peptides displayed a significant positively correlated abundance in AF and FU, strongly suggesting that their presence in AF was directly associated to FU excretion. As proof-of-concept we showed that measuring the AF abundance of these 67 peptides of FU origin allowed prediction of postnatal renal survival in fetuses with posterior urethral valves. These results demonstrate that the AF peptidome can be considered as a good surrogate of the FU peptidome. |
url |
https://doi.org/10.1038/s41598-020-78730-3 |
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