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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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.
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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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