| Literature DB >> 32209432 |
Frank Yeung1, Ying-Han Chen2, Jian-Da Lin3, Jacqueline M Leung4, Caroline McCauley5, Joseph C Devlin6, Christina Hansen4, Alex Cronkite7, Zac Stephens8, Charlotte Drake-Dunn2, Yi Fulmer9, Bo Shopsin9, Kelly V Ruggles10, June L Round8, P'ng Loke11, Andrea L Graham12, Ken Cadwell13.
Abstract
Free-living mammals, such as humans and wild mice, display heightened immune activation compared with artificially maintained laboratory mice. These differences are partially attributed to microbial exposure as laboratory mice infected with pathogens exhibit immune profiles more closely resembling that of free-living animals. Here, we examine how colonization by microorganisms within the natural environment contributes to immune system maturation by releasing inbred laboratory mice into an outdoor enclosure. In addition to enhancing differentiation of T cell populations previously associated with pathogen exposure, outdoor release increased circulating granulocytes. However, these "rewilded" mice were not infected by pathogens previously implicated in immune activation. Rather, immune system changes were associated with altered microbiota composition with notable increases in intestinal fungi. Fungi isolated from rewilded mice were sufficient in increasing circulating granulocytes. These findings establish a model to investigate how the natural environment impacts immune development and show that sustained fungal exposure impacts granulocyte numbers.Entities:
Keywords: Aspergillus; fungi; granulocytes; laboratory mice; mesocosm; microbiota; mycobiota; neutrophils; rewilding; wild mice
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Year: 2020 PMID: 32209432 PMCID: PMC7276265 DOI: 10.1016/j.chom.2020.02.015
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023