TY - JOUR
T1 - Chronic toxoplasma gondii infection enhances susceptibility to colitis
AU - Saraav, Iti
AU - Cervantes-Barragan, Luisa
AU - Olias, Philipp
AU - Fu, Yong
AU - Wang, Qiuling
AU - Wang, Leran
AU - Wang, Yi
AU - Mack, Matthias
AU - Baldridge, Megan T.
AU - Stappenbeck, Thaddeus
AU - Colonna, Marco
AU - Sibley, L. David
N1 - Funding Information:
ACKNOWLEDGMENTS. We thank Kymberli May for assistance with processing histology samples, Advanced Imaging and Tissue Analysis Core of the Digestive Disease Research Core Center. We acknowledge the core facilities: Flow Cytometry and Fluorescence-Activated Cell Sorting Core, Center for Genome Sciences and Systems Biology, Immunomonitoring Laboratory, and the Bursky Center for Human Immunology and Immunotherapy Programs, at Washington University School of Medicine in St. Louis. The Digestive Disease Research Core Center is supported by Grant P30DK052574. The Center for Genome Sciences and Systems Biology at Washington University in St. Louis is partially supported by NCI Cancer Center Support Grant P30 CA91842 to the Siteman Cancer Center and by Institute of Clinical and Translational Sciences/CTSA Grant UL1TR002345 from the National Center for Research Resources. This study was supported by grants from the NIH (AI118426) and the German Academy of Sciences Leopoldina (LPDS 2012-10).
Funding Information:
We thank Kymberli May for assistance with processing histology samples, Advanced Imaging and Tissue Analysis Core of the Digestive Disease Research Core Center. We acknowledge the core facilities: Flow Cytometry and Fluorescence-Activated Cell Sorting Core, Center for Genome Sciences and Systems Biology, Immunomonitoring Laboratory, and the Bursky Center for Human Immunology and Immunotherapy Programs, at Washington University School of Medicine in St. Louis. The Digestive Disease Research Core Center is supported by Grant P30DK052574. The Center for Genome Sciences and Systems Biology at Washington University in St. Louis is partially supported by NCI Cancer Center Support Grant P30 CA91842 to the Siteman Cancer Center and by Institute of Clinical and Translational Sciences/CTSA Grant UL1TR002345 from the National Center for Research Resources. This study was supported by grants from the NIH (AI118426) and the German Academy of Sciences Leopoldina (LPDS 2012-10).
Publisher Copyright:
© 2021 National Academy of Sciences. All rights reserved.
PY - 2021/9/7
Y1 - 2021/9/7
N2 - Oral infection with Toxoplasma gondii results in dysbiosis and enteritis, both of which revert to normal during chronic infection. However, whether infection leaves a lasting impact on mucosal responses remains uncertain. Here we examined the effect of the chemical irritant dextran sodium sulfate (DSS) on intestinal damage and wound healing in chronically infected mice. Our findings indicate that prior infection with T. gondii exacerbates damage to the colon caused by DSS and impairs wound healing by suppressing stem cell regeneration of the epithelium. Enhanced tissue damage was attributable to inflammatory monocytes that emerge preactivated from bone marrow, migrate to the intestine, and release inflammatory mediators, including nitric oxide. Tissue damage was reversed by neutralization of inflammatory monocytes or nitric oxide, revealing a causal mechanism for tissue damage. Our findings suggest that chronic infection with T. gondii enhances monocyte activation to increase inflammation associated with a secondary environmental insult.
AB - Oral infection with Toxoplasma gondii results in dysbiosis and enteritis, both of which revert to normal during chronic infection. However, whether infection leaves a lasting impact on mucosal responses remains uncertain. Here we examined the effect of the chemical irritant dextran sodium sulfate (DSS) on intestinal damage and wound healing in chronically infected mice. Our findings indicate that prior infection with T. gondii exacerbates damage to the colon caused by DSS and impairs wound healing by suppressing stem cell regeneration of the epithelium. Enhanced tissue damage was attributable to inflammatory monocytes that emerge preactivated from bone marrow, migrate to the intestine, and release inflammatory mediators, including nitric oxide. Tissue damage was reversed by neutralization of inflammatory monocytes or nitric oxide, revealing a causal mechanism for tissue damage. Our findings suggest that chronic infection with T. gondii enhances monocyte activation to increase inflammation associated with a secondary environmental insult.
KW - Disbiosis
KW - Inflammation
KW - Monocytes
KW - Nitric oxide
KW - Toxoplasmosis
UR - http://www.scopus.com/inward/record.url?scp=85114115435&partnerID=8YFLogxK
U2 - 10.1073/pnas.2106730118
DO - 10.1073/pnas.2106730118
M3 - Article
C2 - 34462359
AN - SCOPUS:85114115435
SN - 0027-8424
VL - 118
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 36
M1 - e2106730118
ER -