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Host gut resistome in Gulf War chronic multisymptom illness correlates with persistent inflammation
Chronic multisymptom illness (CMI) affects a subsection of elderly and war Veterans and is associated with systemic inflammation. Here, using a mouse model of CMI and a group of Gulf War (GW) Veterans’ with CMI we show the presence of an altered host resistome. Results show that antibiotic resistanc...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174162/ https://www.ncbi.nlm.nih.gov/pubmed/35672382 http://dx.doi.org/10.1038/s42003-022-03494-7 |
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author | Bose, Dipro Chatterjee, Somdatta Older, Ethan Seth, Ratanesh Janulewicz, Patricia Saha, Punnag Mondal, Ayan Carlson, Jeffrey M. Decho, Alan W. Sullivan, Kimberly Klimas, Nancy Lasley, Stephen Li, Jie Chatterjee, Saurabh |
author_facet | Bose, Dipro Chatterjee, Somdatta Older, Ethan Seth, Ratanesh Janulewicz, Patricia Saha, Punnag Mondal, Ayan Carlson, Jeffrey M. Decho, Alan W. Sullivan, Kimberly Klimas, Nancy Lasley, Stephen Li, Jie Chatterjee, Saurabh |
author_sort | Bose, Dipro |
collection | PubMed |
description | Chronic multisymptom illness (CMI) affects a subsection of elderly and war Veterans and is associated with systemic inflammation. Here, using a mouse model of CMI and a group of Gulf War (GW) Veterans’ with CMI we show the presence of an altered host resistome. Results show that antibiotic resistance genes (ARGs) are significantly altered in the CMI group in both mice and GW Veterans when compared to control. Fecal samples from GW Veterans with persistent CMI show a significant increase of resistance to a wide class of antibiotics and exhibited an array of mobile genetic elements (MGEs) distinct from normal healthy controls. The altered resistome and gene signature is correlated with mouse serum IL-6 levels. Altered resistome in mice also is correlated strongly with intestinal inflammation, decreased synaptic plasticity, reversible with fecal microbiota transplant (FMT). The results reported might help in understanding the risks to treating hospital acquired infections in this population. |
format | Online Article Text |
id | pubmed-9174162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91741622022-06-09 Host gut resistome in Gulf War chronic multisymptom illness correlates with persistent inflammation Bose, Dipro Chatterjee, Somdatta Older, Ethan Seth, Ratanesh Janulewicz, Patricia Saha, Punnag Mondal, Ayan Carlson, Jeffrey M. Decho, Alan W. Sullivan, Kimberly Klimas, Nancy Lasley, Stephen Li, Jie Chatterjee, Saurabh Commun Biol Article Chronic multisymptom illness (CMI) affects a subsection of elderly and war Veterans and is associated with systemic inflammation. Here, using a mouse model of CMI and a group of Gulf War (GW) Veterans’ with CMI we show the presence of an altered host resistome. Results show that antibiotic resistance genes (ARGs) are significantly altered in the CMI group in both mice and GW Veterans when compared to control. Fecal samples from GW Veterans with persistent CMI show a significant increase of resistance to a wide class of antibiotics and exhibited an array of mobile genetic elements (MGEs) distinct from normal healthy controls. The altered resistome and gene signature is correlated with mouse serum IL-6 levels. Altered resistome in mice also is correlated strongly with intestinal inflammation, decreased synaptic plasticity, reversible with fecal microbiota transplant (FMT). The results reported might help in understanding the risks to treating hospital acquired infections in this population. Nature Publishing Group UK 2022-06-07 /pmc/articles/PMC9174162/ /pubmed/35672382 http://dx.doi.org/10.1038/s42003-022-03494-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Bose, Dipro Chatterjee, Somdatta Older, Ethan Seth, Ratanesh Janulewicz, Patricia Saha, Punnag Mondal, Ayan Carlson, Jeffrey M. Decho, Alan W. Sullivan, Kimberly Klimas, Nancy Lasley, Stephen Li, Jie Chatterjee, Saurabh Host gut resistome in Gulf War chronic multisymptom illness correlates with persistent inflammation |
title | Host gut resistome in Gulf War chronic multisymptom illness correlates with persistent inflammation |
title_full | Host gut resistome in Gulf War chronic multisymptom illness correlates with persistent inflammation |
title_fullStr | Host gut resistome in Gulf War chronic multisymptom illness correlates with persistent inflammation |
title_full_unstemmed | Host gut resistome in Gulf War chronic multisymptom illness correlates with persistent inflammation |
title_short | Host gut resistome in Gulf War chronic multisymptom illness correlates with persistent inflammation |
title_sort | host gut resistome in gulf war chronic multisymptom illness correlates with persistent inflammation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174162/ https://www.ncbi.nlm.nih.gov/pubmed/35672382 http://dx.doi.org/10.1038/s42003-022-03494-7 |
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