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Human Alcohol-Microbiota Mice have Increased Susceptibility to Bacterial Pneumonia
Preclinical studies have shown that chronic alcohol abuse leads to alterations in the gastrointestinal microbiota that are associated with behavior changes, physiological alterations, and immunological effects. However, such studies have been limited in their ability to evaluate the direct effects o...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10526526/ https://www.ncbi.nlm.nih.gov/pubmed/37759490 http://dx.doi.org/10.3390/cells12182267 |
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author | Cunningham, Kelly C. Smith, Deandra R. Villageliú, Daniel N. Ellis, Christi M. Ramer-Tait, Amanda E. Price, Jeffrey D. Wyatt, Todd A. Knoell, Daren L. Samuelson, Mystera M. Molina, Patricia E. Welsh, David A. Samuelson, Derrick R. |
author_facet | Cunningham, Kelly C. Smith, Deandra R. Villageliú, Daniel N. Ellis, Christi M. Ramer-Tait, Amanda E. Price, Jeffrey D. Wyatt, Todd A. Knoell, Daren L. Samuelson, Mystera M. Molina, Patricia E. Welsh, David A. Samuelson, Derrick R. |
author_sort | Cunningham, Kelly C. |
collection | PubMed |
description | Preclinical studies have shown that chronic alcohol abuse leads to alterations in the gastrointestinal microbiota that are associated with behavior changes, physiological alterations, and immunological effects. However, such studies have been limited in their ability to evaluate the direct effects of alcohol-associated dysbiosis. To address this, we developed a humanized alcohol-microbiota mouse model to systematically evaluate the immunological effects of chronic alcohol abuse mediated by intestinal dysbiosis. Germ-free mice were colonized with human fecal microbiota from individuals with high and low Alcohol Use Disorders Identification Test (AUDIT) scores and bred to produce human alcohol-associated microbiota or human control-microbiota F1 progenies. F1 offspring colonized with fecal microbiota from individuals with high AUDIT scores had increased susceptibility to Klebsiella pneumoniae and Streptococcus pneumoniae pneumonia, as determined by increased mortality rates, pulmonary bacterial burden, and post-infection lung damage. These findings highlight the importance of considering both the direct effects of alcohol and alcohol-induced dysbiosis when investigating the mechanisms behind alcohol-related disorders and treatment strategies. |
format | Online Article Text |
id | pubmed-10526526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105265262023-09-28 Human Alcohol-Microbiota Mice have Increased Susceptibility to Bacterial Pneumonia Cunningham, Kelly C. Smith, Deandra R. Villageliú, Daniel N. Ellis, Christi M. Ramer-Tait, Amanda E. Price, Jeffrey D. Wyatt, Todd A. Knoell, Daren L. Samuelson, Mystera M. Molina, Patricia E. Welsh, David A. Samuelson, Derrick R. Cells Article Preclinical studies have shown that chronic alcohol abuse leads to alterations in the gastrointestinal microbiota that are associated with behavior changes, physiological alterations, and immunological effects. However, such studies have been limited in their ability to evaluate the direct effects of alcohol-associated dysbiosis. To address this, we developed a humanized alcohol-microbiota mouse model to systematically evaluate the immunological effects of chronic alcohol abuse mediated by intestinal dysbiosis. Germ-free mice were colonized with human fecal microbiota from individuals with high and low Alcohol Use Disorders Identification Test (AUDIT) scores and bred to produce human alcohol-associated microbiota or human control-microbiota F1 progenies. F1 offspring colonized with fecal microbiota from individuals with high AUDIT scores had increased susceptibility to Klebsiella pneumoniae and Streptococcus pneumoniae pneumonia, as determined by increased mortality rates, pulmonary bacterial burden, and post-infection lung damage. These findings highlight the importance of considering both the direct effects of alcohol and alcohol-induced dysbiosis when investigating the mechanisms behind alcohol-related disorders and treatment strategies. MDPI 2023-09-13 /pmc/articles/PMC10526526/ /pubmed/37759490 http://dx.doi.org/10.3390/cells12182267 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Cunningham, Kelly C. Smith, Deandra R. Villageliú, Daniel N. Ellis, Christi M. Ramer-Tait, Amanda E. Price, Jeffrey D. Wyatt, Todd A. Knoell, Daren L. Samuelson, Mystera M. Molina, Patricia E. Welsh, David A. Samuelson, Derrick R. Human Alcohol-Microbiota Mice have Increased Susceptibility to Bacterial Pneumonia |
title | Human Alcohol-Microbiota Mice have Increased Susceptibility to Bacterial Pneumonia |
title_full | Human Alcohol-Microbiota Mice have Increased Susceptibility to Bacterial Pneumonia |
title_fullStr | Human Alcohol-Microbiota Mice have Increased Susceptibility to Bacterial Pneumonia |
title_full_unstemmed | Human Alcohol-Microbiota Mice have Increased Susceptibility to Bacterial Pneumonia |
title_short | Human Alcohol-Microbiota Mice have Increased Susceptibility to Bacterial Pneumonia |
title_sort | human alcohol-microbiota mice have increased susceptibility to bacterial pneumonia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10526526/ https://www.ncbi.nlm.nih.gov/pubmed/37759490 http://dx.doi.org/10.3390/cells12182267 |
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