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Autoinducer-2 May Be a New Biomarker for Monitoring Neonatal Necrotizing Enterocolitis
Autoinducer-2 (AI-2) has a widely accepted role in bacterial intra- and interspecies communication. Little is known about the relationships between AI-2 and NEC. This study found that AI-2 levels in patients and in a NEC mouse model were detected using the Vibrio harveyi BB170 assay system. Bacteria...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7179697/ https://www.ncbi.nlm.nih.gov/pubmed/32373545 http://dx.doi.org/10.3389/fcimb.2020.00140 |
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author | Fu, Chun-Yan Li, Lu-Quan Yang, Ting She, Xiang Ai, Qing Wang, Zheng-Li |
author_facet | Fu, Chun-Yan Li, Lu-Quan Yang, Ting She, Xiang Ai, Qing Wang, Zheng-Li |
author_sort | Fu, Chun-Yan |
collection | PubMed |
description | Autoinducer-2 (AI-2) has a widely accepted role in bacterial intra- and interspecies communication. Little is known about the relationships between AI-2 and NEC. This study found that AI-2 levels in patients and in a NEC mouse model were detected using the Vibrio harveyi BB170 assay system. Bacterial communities of the newborns' stool microbiota (NEC acute group, NEC recovery group, control group, and antibiotics-free group) and of the NEC mouse model (NEC group and control group) were detected by high-throughput sequencing. Intestinal histopathological changes were observed after HE staining. The AI-2 level in the NEC acute group (44.75 [40.17~65.52]) was significantly lower than that in the control group, NEC recovery group and antibiotics-free group. The overall microbiota compositions of each group at the phylum level were not significantly different. The proportions of Enterococcus, Clostridium_sensu_stricto_1, Peptoclostridium, and Veillonella had significant differences among the 4 groups at the genus level. In animal experiments, the AI-2 level in feces of NEC mice (56.89 ± 11.87) was significantly lower than that in the feces of control group mice (102.70 ± 22.97). The microbiota compositions of NEC and control group mice at the phylum level were not significantly different. At the genus level, Klebsiella, Clostridium_sensu_stricto_1, and Peptoclostridium abundances in the NEC group increased significantly compared with those in the control group (P < 0.05). In addition, Lactobacillus, Pasteurella, and Parabacteroides abundances in the NEC group decreased significantly compared with those in the normal control group (P < 0.05), while Lactobacillus, Pasteurella, and Parabacteroides abundances had the opposite trend. The AI-2 concentration decreased significantly in the acute phase of NEC and increased gradually in the convalescent phase. We conclude that the concentration of AI-2 was correlated with intestinal flora disorder and different stages of disease. AI-2 may be a new biomarker for the diagnosis and monitoring of NEC. Trial Registry: ClinicalTrials.gov; ChiCTR-ROC-17013746; URL: www.clinicaltrials.gov |
format | Online Article Text |
id | pubmed-7179697 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71796972020-05-05 Autoinducer-2 May Be a New Biomarker for Monitoring Neonatal Necrotizing Enterocolitis Fu, Chun-Yan Li, Lu-Quan Yang, Ting She, Xiang Ai, Qing Wang, Zheng-Li Front Cell Infect Microbiol Cellular and Infection Microbiology Autoinducer-2 (AI-2) has a widely accepted role in bacterial intra- and interspecies communication. Little is known about the relationships between AI-2 and NEC. This study found that AI-2 levels in patients and in a NEC mouse model were detected using the Vibrio harveyi BB170 assay system. Bacterial communities of the newborns' stool microbiota (NEC acute group, NEC recovery group, control group, and antibiotics-free group) and of the NEC mouse model (NEC group and control group) were detected by high-throughput sequencing. Intestinal histopathological changes were observed after HE staining. The AI-2 level in the NEC acute group (44.75 [40.17~65.52]) was significantly lower than that in the control group, NEC recovery group and antibiotics-free group. The overall microbiota compositions of each group at the phylum level were not significantly different. The proportions of Enterococcus, Clostridium_sensu_stricto_1, Peptoclostridium, and Veillonella had significant differences among the 4 groups at the genus level. In animal experiments, the AI-2 level in feces of NEC mice (56.89 ± 11.87) was significantly lower than that in the feces of control group mice (102.70 ± 22.97). The microbiota compositions of NEC and control group mice at the phylum level were not significantly different. At the genus level, Klebsiella, Clostridium_sensu_stricto_1, and Peptoclostridium abundances in the NEC group increased significantly compared with those in the control group (P < 0.05). In addition, Lactobacillus, Pasteurella, and Parabacteroides abundances in the NEC group decreased significantly compared with those in the normal control group (P < 0.05), while Lactobacillus, Pasteurella, and Parabacteroides abundances had the opposite trend. The AI-2 concentration decreased significantly in the acute phase of NEC and increased gradually in the convalescent phase. We conclude that the concentration of AI-2 was correlated with intestinal flora disorder and different stages of disease. AI-2 may be a new biomarker for the diagnosis and monitoring of NEC. Trial Registry: ClinicalTrials.gov; ChiCTR-ROC-17013746; URL: www.clinicaltrials.gov Frontiers Media S.A. 2020-04-09 /pmc/articles/PMC7179697/ /pubmed/32373545 http://dx.doi.org/10.3389/fcimb.2020.00140 Text en Copyright © 2020 Fu, Li, Yang, She, Ai and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Fu, Chun-Yan Li, Lu-Quan Yang, Ting She, Xiang Ai, Qing Wang, Zheng-Li Autoinducer-2 May Be a New Biomarker for Monitoring Neonatal Necrotizing Enterocolitis |
title | Autoinducer-2 May Be a New Biomarker for Monitoring Neonatal Necrotizing Enterocolitis |
title_full | Autoinducer-2 May Be a New Biomarker for Monitoring Neonatal Necrotizing Enterocolitis |
title_fullStr | Autoinducer-2 May Be a New Biomarker for Monitoring Neonatal Necrotizing Enterocolitis |
title_full_unstemmed | Autoinducer-2 May Be a New Biomarker for Monitoring Neonatal Necrotizing Enterocolitis |
title_short | Autoinducer-2 May Be a New Biomarker for Monitoring Neonatal Necrotizing Enterocolitis |
title_sort | autoinducer-2 may be a new biomarker for monitoring neonatal necrotizing enterocolitis |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7179697/ https://www.ncbi.nlm.nih.gov/pubmed/32373545 http://dx.doi.org/10.3389/fcimb.2020.00140 |
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