Human Alcohol-Microbiota Mice have Increased Susceptibility to Bacterial Pneumonia.
Kelly C CunninghamDeandra R SmithDaniel N VillageliúChristi M EllisAmanda E Ramer-TaitJeffrey D PriceTodd A WyattDaren L KnoellMystera M SamuelsonPatricia E MolinaDavid A WelshDerrick R SamuelsonPublished in: Cells (2023)
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.
Keyphrases
- endothelial cells
- alcohol consumption
- mouse model
- klebsiella pneumoniae
- escherichia coli
- induced pluripotent stem cells
- pluripotent stem cells
- high glucose
- pulmonary hypertension
- stem cells
- oxidative stress
- multidrug resistant
- high fat diet induced
- insulin resistance
- diabetic rats
- mechanical ventilation
- stress induced